14025	1	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029266	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029266	GSM352202	SRA009988	SRX012330	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	2	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029267	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029267	GSM352202	SRA009988	SRX012330	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	3	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029268	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029268	GSM352202	SRA009988	SRX012330	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	4	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029269	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029269	GSM352202	SRA009988	SRX012330	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	5	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029270	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029270	GSM352202	SRA009988	SRX012330	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	6	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029271	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029271	GSM352203	SRA009988	SRX012331	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	7	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029272	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029272	GSM352203	SRA009988	SRX012331	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	8	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029273	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029273	GSM352203	SRA009988	SRX012331	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	9	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029274	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029274	GSM352203	SRA009988	SRX012331	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	10	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029275	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029275	GSM352203	SRA009988	SRX012331	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	11	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029238	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029238	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	12	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029239	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029239	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	13	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029240	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029240	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	14	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029241	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029241	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	15	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029242	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029242	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	16	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029243	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029243	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	17	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029244	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029244	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	18	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029245	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029245	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	19	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029246	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029246	GSM352204	SRA009988	SRX012313	OTHER	SINGLE	SRP001343	PRJNA112449
14025	20	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029276	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029276	GSM419463	SRA009988	SRX012332	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14025	21	Gert Jan Veenstra	A Hierarchy of H3K4me3 and H3K27me3 Acquisition in Spatial Gene Regulation in Xenopus Embryos	Epigenetic mechanisms set apart the active and inactive regions in the genome of multicellular organisms to produce distinct cell fates during embryog	Gert Jan Veenstra, Robert Akkers, Simon van Heeringen, Ulrike Jacobi, Eva Janssen-Megens, Kees-Jan Françoijs, Hendrik Stunnenberg, Gert Veenstra	ChIP-seq profiles of two histone modifications (H3K4me3 and H3K27me3) and RNA Polymerase II, and a RNA-seq profile, of gastrula stage Xenopus tropicalis embryos	19758566	40368	SRP001343	SRR029277	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000028/SRR029277	GSM419463	SRA009988	SRX012332	ChIP-Seq	SINGLE	SRP001343	PRJNA112449
14952	1	Mike Gilchrist	High-throughput sequencing of small RNAs from Xenopus tropicalis	High-throughput sequencing of small RNAs from Xenopus tropicalis (adult liver, adult skin, oocytes stage I, II, III, IV, V, VI).total RNA, ~18-42 nt 	Mike Gilchrist	Illumina/Solexa sequencing of adult liver, adult skin, oocytes stage I, II, III, IV, V, VI	19628731	40115	SRP001036	SRR020456	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000019/SRR020456	GSM372598	SRA009325	SRX007332	OTHER	SINGLE	SRP001036	PRJNA111817
14952	2	Mike Gilchrist	High-throughput sequencing of small RNAs from Xenopus tropicalis	High-throughput sequencing of small RNAs from Xenopus tropicalis (adult liver, adult skin, oocytes stage I, II, III, IV, V, VI).total RNA, ~18-42 nt 	Mike Gilchrist	Illumina/Solexa sequencing of adult liver, adult skin, oocytes stage I, II, III, IV, V, VI	19628731	40115	SRP001036	SRR020457	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000019/SRR020457	GSM372601	SRA009325	SRX007333	OTHER	SINGLE	SRP001036	PRJNA111817
14952	3	Mike Gilchrist	High-throughput sequencing of small RNAs from Xenopus tropicalis	High-throughput sequencing of small RNAs from Xenopus tropicalis (adult liver, adult skin, oocytes stage I, II, III, IV, V, VI).total RNA, ~18-42 nt 	Mike Gilchrist	Illumina/Solexa sequencing of adult liver, adult skin, oocytes stage I, II, III, IV, V, VI	19628731	40115	SRP001036	SRR020458	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000019/SRR020458	GSM372602	SRA009325	SRX007334	OTHER	SINGLE	SRP001036	PRJNA111817
14952	4	Mike Gilchrist	High-throughput sequencing of small RNAs from Xenopus tropicalis	High-throughput sequencing of small RNAs from Xenopus tropicalis (adult liver, adult skin, oocytes stage I, II, III, IV, V, VI).total RNA, ~18-42 nt 	Mike Gilchrist	Illumina/Solexa sequencing of adult liver, adult skin, oocytes stage I, II, III, IV, V, VI	19628731	40115	SRP001036	SRR020459	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000019/SRR020459	GSM372603	SRA009325	SRX007335	OTHER	SINGLE	SRP001036	PRJNA111817
14952	5	Mike Gilchrist	High-throughput sequencing of small RNAs from Xenopus tropicalis	High-throughput sequencing of small RNAs from Xenopus tropicalis (adult liver, adult skin, oocytes stage I, II, III, IV, V, VI).total RNA, ~18-42 nt 	Mike Gilchrist	Illumina/Solexa sequencing of adult liver, adult skin, oocytes stage I, II, III, IV, V, VI	19628731	40115	SRP001036	SRR020460	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000019/SRR020460	GSM372604	SRA009325	SRX007336	OTHER	SINGLE	SRP001036	PRJNA111817
19173	1	Nicolas Robine	Xenopus egg small RNA associated with Y12 antibody	We examined in Xenopus tropicalis eggs piRNAs that are associated with Y12 antibody, which binds symmetrically methylated arginines that are present o	Nicolas Robine, Nelson Lau, Eric Lai	Sequencing of a cDNA library from small RNAs from the Y12 immunoprecipitate	20022248	40809	SRP001702	SRR033660	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/000032/SRR033660	GSM475282	SRA010774	SRX015664	RNA-Seq	SINGLE	SRP001702	PRJNA120587
21482	1	Gert Jan Veenstra	Nucleotide composition-linked divergence of vertebrate core promoter architecture	Transcription initiation involves the recruitment of basal transcription factors to the core promoter. A variety of core promoter elements exists, how	Gert Jan Veenstra, Simon van Heeringen, Waseem Akhtar, Ulrike Jacobi, Robert Akkers, Yutaka Suzuki, Gert Veenstra	ChIP-seq profiles of TBP in Xenopus tropicalis stage 12 embryos and TSS-seq profiles of Xenopus oocytes and stage 12 embryos	21284373	42761	SRP002372	SRR040482	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000039/SRR040482	GSM537039	SRA012595	SRX019583	ChIP-Seq	SINGLE	SRP002372	PRJNA126041
21482	2	Gert Jan Veenstra	Nucleotide composition-linked divergence of vertebrate core promoter architecture	Transcription initiation involves the recruitment of basal transcription factors to the core promoter. A variety of core promoter elements exists, how	Gert Jan Veenstra, Simon van Heeringen, Waseem Akhtar, Ulrike Jacobi, Robert Akkers, Yutaka Suzuki, Gert Veenstra	ChIP-seq profiles of TBP in Xenopus tropicalis stage 12 embryos and TSS-seq profiles of Xenopus oocytes and stage 12 embryos	21284373	42761	SRP002372	SRR040483	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000039/SRR040483	GSM537039	SRA012595	SRX019583	ChIP-Seq	SINGLE	SRP002372	PRJNA126041
21482	3	Gert Jan Veenstra	Nucleotide composition-linked divergence of vertebrate core promoter architecture	Transcription initiation involves the recruitment of basal transcription factors to the core promoter. A variety of core promoter elements exists, how	Gert Jan Veenstra, Simon van Heeringen, Waseem Akhtar, Ulrike Jacobi, Robert Akkers, Yutaka Suzuki, Gert Veenstra	ChIP-seq profiles of TBP in Xenopus tropicalis stage 12 embryos and TSS-seq profiles of Xenopus oocytes and stage 12 embryos	21284373	42761	SRP002372	SRR085448	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000083/SRR085448	GSM632116	SRA012595	SRX035149	RNA-Seq	SINGLE	SRP002372	PRJNA126041
21482	4	Gert Jan Veenstra	Nucleotide composition-linked divergence of vertebrate core promoter architecture	Transcription initiation involves the recruitment of basal transcription factors to the core promoter. A variety of core promoter elements exists, how	Gert Jan Veenstra, Simon van Heeringen, Waseem Akhtar, Ulrike Jacobi, Robert Akkers, Yutaka Suzuki, Gert Veenstra	ChIP-seq profiles of TBP in Xenopus tropicalis stage 12 embryos and TSS-seq profiles of Xenopus oocytes and stage 12 embryos	21284373	42761	SRP002372	SRR085449	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000083/SRR085449	GSM632116	SRA012595	SRX035149	RNA-Seq	SINGLE	SRP002372	PRJNA126041
21482	5	Gert Jan Veenstra	Nucleotide composition-linked divergence of vertebrate core promoter architecture	Transcription initiation involves the recruitment of basal transcription factors to the core promoter. A variety of core promoter elements exists, how	Gert Jan Veenstra, Simon van Heeringen, Waseem Akhtar, Ulrike Jacobi, Robert Akkers, Yutaka Suzuki, Gert Veenstra	ChIP-seq profiles of TBP in Xenopus tropicalis stage 12 embryos and TSS-seq profiles of Xenopus oocytes and stage 12 embryos	21284373	42761	SRP002372	SRR085450	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000083/SRR085450	GSM632117	SRA012595	SRX035150	RNA-Seq	SINGLE	SRP002372	PRJNA126041
21482	6	Gert Jan Veenstra	Nucleotide composition-linked divergence of vertebrate core promoter architecture	Transcription initiation involves the recruitment of basal transcription factors to the core promoter. A variety of core promoter elements exists, how	Gert Jan Veenstra, Simon van Heeringen, Waseem Akhtar, Ulrike Jacobi, Robert Akkers, Yutaka Suzuki, Gert Veenstra	ChIP-seq profiles of TBP in Xenopus tropicalis stage 12 embryos and TSS-seq profiles of Xenopus oocytes and stage 12 embryos	21284373	42761	SRP002372	SRR085451	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000083/SRR085451	GSM632117	SRA012595	SRX035150	RNA-Seq	SINGLE	SRP002372	PRJNA126041
22146	1	Kevin Lebrigand	microRNAs signatures of Xenopus laevis embryo epidermis at stage 11 (non ciliated) and 26 (ciliated) using high throughput sequencing	Epidermis of Xenopus embryos forms a mucociliary epithelium constituted of basal, scattered, secreting and ciliated cells and is histologically simila	Kevin Lebrigand, B Marcet, P Barbry, K Lebrigand	2 technical replicates of a pool of 50 explants for each stage 11.5 (non ciliated)  and 26 (ciliated) of Xenopus laevis development	21602795	43315	SRP002578	SRR057341	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000055/SRR057341	GSM550779	SRA020109	SRX021834	RNA-Seq	SINGLE	SRP002578	PRJNA129201
22146	2	Kevin Lebrigand	microRNAs signatures of Xenopus laevis embryo epidermis at stage 11 (non ciliated) and 26 (ciliated) using high throughput sequencing	Epidermis of Xenopus embryos forms a mucociliary epithelium constituted of basal, scattered, secreting and ciliated cells and is histologically simila	Kevin Lebrigand, B Marcet, P Barbry, K Lebrigand	2 technical replicates of a pool of 50 explants for each stage 11.5 (non ciliated)  and 26 (ciliated) of Xenopus laevis development	21602795	43315	SRP002578	SRR057342	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000055/SRR057342	GSM550780	SRA020109	SRX021835	RNA-Seq	SINGLE	SRP002578	PRJNA129201
22146	3	Kevin Lebrigand	microRNAs signatures of Xenopus laevis embryo epidermis at stage 11 (non ciliated) and 26 (ciliated) using high throughput sequencing	Epidermis of Xenopus embryos forms a mucociliary epithelium constituted of basal, scattered, secreting and ciliated cells and is histologically simila	Kevin Lebrigand, B Marcet, P Barbry, K Lebrigand	2 technical replicates of a pool of 50 explants for each stage 11.5 (non ciliated)  and 26 (ciliated) of Xenopus laevis development	21602795	43315	SRP002578	SRR057343	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000055/SRR057343	GSM550781	SRA020109	SRX021836	RNA-Seq	SINGLE	SRP002578	PRJNA129201
22146	4	Kevin Lebrigand	microRNAs signatures of Xenopus laevis embryo epidermis at stage 11 (non ciliated) and 26 (ciliated) using high throughput sequencing	Epidermis of Xenopus embryos forms a mucociliary epithelium constituted of basal, scattered, secreting and ciliated cells and is histologically simila	Kevin Lebrigand, B Marcet, P Barbry, K Lebrigand	2 technical replicates of a pool of 50 explants for each stage 11.5 (non ciliated)  and 26 (ciliated) of Xenopus laevis development	21602795	43315	SRP002578	SRR057344	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000056/SRR057344	GSM550782	SRA020109	SRX021837	RNA-Seq	SINGLE	SRP002578	PRJNA129201
23913	1	Ozren Bogdanovic	Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis	DNA methylation is a tightly regulated epigenetic mark associated with transcriptional repression. Next-generation sequencing of purified methylated D	Ozren Bogdanovic, Simon van Heeringen, Steven Long, Arjen Brinkman, Hendrik Stunnenberg, Peter Jones, Gert-Jan Veenstra	MethylCap (methylated DNA affinity capture with the MBD domain of MeCP2), 500mM and 700mM elution fractions of stage 9 (blastula) and stage 12.5 (gastrula) Xenopus tropicalis DNA	21636662	43338	SRP003559	SRR065795	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000064/SRR065795	GSM589696	SRA023915	SRX026883	OTHER	SINGLE	SRP003559	PRJNA130531
23913	2	Ozren Bogdanovic	Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis	DNA methylation is a tightly regulated epigenetic mark associated with transcriptional repression. Next-generation sequencing of purified methylated D	Ozren Bogdanovic, Simon van Heeringen, Steven Long, Arjen Brinkman, Hendrik Stunnenberg, Peter Jones, Gert-Jan Veenstra	MethylCap (methylated DNA affinity capture with the MBD domain of MeCP2), 500mM and 700mM elution fractions of stage 9 (blastula) and stage 12.5 (gastrula) Xenopus tropicalis DNA	21636662	43338	SRP003559	SRR065796	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000064/SRR065796	GSM589697	SRA023915	SRX026884	OTHER	SINGLE	SRP003559	PRJNA130531
23913	3	Ozren Bogdanovic	Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis	DNA methylation is a tightly regulated epigenetic mark associated with transcriptional repression. Next-generation sequencing of purified methylated D	Ozren Bogdanovic, Simon van Heeringen, Steven Long, Arjen Brinkman, Hendrik Stunnenberg, Peter Jones, Gert-Jan Veenstra	MethylCap (methylated DNA affinity capture with the MBD domain of MeCP2), 500mM and 700mM elution fractions of stage 9 (blastula) and stage 12.5 (gastrula) Xenopus tropicalis DNA	21636662	43338	SRP003559	SRR065797	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000064/SRR065797	GSM589698	SRA023915	SRX026885	OTHER	SINGLE	SRP003559	PRJNA130531
23913	4	Ozren Bogdanovic	Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis	DNA methylation is a tightly regulated epigenetic mark associated with transcriptional repression. Next-generation sequencing of purified methylated D	Ozren Bogdanovic, Simon van Heeringen, Steven Long, Arjen Brinkman, Hendrik Stunnenberg, Peter Jones, Gert-Jan Veenstra	MethylCap (methylated DNA affinity capture with the MBD domain of MeCP2), 500mM and 700mM elution fractions of stage 9 (blastula) and stage 12.5 (gastrula) Xenopus tropicalis DNA	21636662	43338	SRP003559	SRR065798	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000064/SRR065798	GSM589699	SRA023915	SRX026886	OTHER	SINGLE	SRP003559	PRJNA130531
30067	1	Juan Larrain	Deep sequencing of small RNAs in the Xenopus tropicalis gastrula	Transposable elements comprise a large proportion of animal genomes. Transcripts of transposable elements are a source for the synthesis of endogenous	Juan Larrain, Fernando Faunes, Natalia Sanchez, Mauricio Moreno, Gonzalo Olivares, Dasfne Lee-Liu, Leonardo Almonacid, Alex Slater, Tomas Norambuena, Ryan Taft, John Mattick, Francisco Melo	Analysis of small RNAs expressed in the Xenopus tropicalis gastrula.	21818339	43632	SRP007217	SRR285186	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/000278/SRR285186	GSM744253	SRA038449	SRX077929	RNA-Seq	SINGLE	SRP007217	PRJNA144001
30067	2	Juan Larrain	Deep sequencing of small RNAs in the Xenopus tropicalis gastrula	Transposable elements comprise a large proportion of animal genomes. Transcripts of transposable elements are a source for the synthesis of endogenous	Juan Larrain, Fernando Faunes, Natalia Sanchez, Mauricio Moreno, Gonzalo Olivares, Dasfne Lee-Liu, Leonardo Almonacid, Alex Slater, Tomas Norambuena, Ryan Taft, John Mattick, Francisco Melo	Analysis of small RNAs expressed in the Xenopus tropicalis gastrula.	21818339	43632	SRP007217	SRR285187	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/000278/SRR285187	GSM744254	SRA038449	SRX077930	RNA-Seq	SINGLE	SRP007217	PRJNA144001
30146	1	Se-Jin Yoon	HEB and E2A function as SMAD/FOXH1 cofactors	Nodal signaling, mediated through SMAD transcription factors, is necessary for pluripotency maintenance and endoderm commitment. We have identified a 	Se-Jin Yoon, Andrea Wills, Edward Chuong, Rakhi Gupta, Julie Baker	ChIP-seq of Smad2/3 and Input in X.tropicalis, stage 10.5 embryo.	21828274	43683	SRP007355	SRR299084	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/000292/SRR299084	GSM746611	SRA039282	SRX080197	ChIP-Seq	SINGLE	SRP007355	PRJNA143851
30146	2	Se-Jin Yoon	HEB and E2A function as SMAD/FOXH1 cofactors	Nodal signaling, mediated through SMAD transcription factors, is necessary for pluripotency maintenance and endoderm commitment. We have identified a 	Se-Jin Yoon, Andrea Wills, Edward Chuong, Rakhi Gupta, Julie Baker	ChIP-seq of Smad2/3 and Input in X.tropicalis, stage 10.5 embryo.	21828274	43683	SRP007355	SRR299085	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/000292/SRR299085	GSM746612	SRA039282	SRX080198	ChIP-Seq	SINGLE	SRP007355	PRJNA143851
33444	1	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360852	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360852	GSM827025	SRA047840	SRX104181	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	2	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360853	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360853	GSM827026	SRA047840	SRX104182	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	3	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360854	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360854	GSM827027	SRA047840	SRX104183	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	4	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360855	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360855	GSM827028	SRA047840	SRX104184	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	5	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360856	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360856	GSM827029	SRA047840	SRX104185	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	6	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360857	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360857	GSM827030	SRA047840	SRX104186	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	7	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360858	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360858	GSM827031	SRA047840	SRX104187	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	8	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360859	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360859	GSM827032	SRA047840	SRX104188	RNA-Seq	SINGLE	SRP009183	PRJNA148701
33444	9	Cei Abreu-Goodger	miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones	During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of 	Cei Abreu-Goodger, Marie-Laure Baudet, Krishna Zivraj, Alistair Muldal, Javier Armisen, Cherie Blenkiron, Leonard Goldstein, Erik Miska, Christine Holt	Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.	22138647	44540	SRP009183	SRR360860	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/000352/SRR360860	GSM827033	SRA047840	SRX104189	RNA-Seq	SINGLE	SRP009183	PRJNA148701
37452	1	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489439	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489439	GSM919922	SRA051954	SRX143516	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	2	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489440	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489440	GSM919923	SRA051954	SRX143517	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	3	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489441	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489441	GSM919924	SRA051954	SRX143518	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	4	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489442	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489442	GSM919925	SRA051954	SRX143519	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	5	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489443	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489443	GSM919926	SRA051954	SRX143520	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	6	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489444	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489444	GSM919927	SRA051954	SRX143521	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	7	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489445	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489445	GSM919928	SRA051954	SRX143522	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	8	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489446	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489446	GSM919929	SRA051954	SRX143523	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	9	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489447	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489447	GSM919930	SRA051954	SRX143524	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	10	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489448	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489448	GSM919931	SRA051954	SRX143525	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	11	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489449	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489449	GSM919932	SRA051954	SRX143526	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	12	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489450	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489450	GSM919933	SRA051954	SRX143527	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	13	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489451	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489451	GSM919934	SRA051954	SRX143528	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	14	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489452	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489452	GSM919935	SRA051954	SRX143529	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	15	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489453	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489453	GSM919936	SRA051954	SRX143530	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	16	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489454	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489454	GSM919937	SRA051954	SRX143531	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	17	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489455	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489455	GSM919938	SRA051954	SRX143532	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	18	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489456	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489456	GSM919939	SRA051954	SRX143533	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	19	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489457	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489457	GSM919940	SRA051954	SRX143534	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	20	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489458	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489458	GSM919941	SRA051954	SRX143535	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	21	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489459	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489459	GSM919942	SRA051954	SRX143536	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	22	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489460	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489460	GSM919943	SRA051954	SRX143537	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	23	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489461	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489461	GSM919944	SRA051954	SRX143538	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	24	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489462	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489462	GSM919945	SRA051954	SRX143539	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	25	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489463	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489463	GSM919946	SRA051954	SRX143540	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	26	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489464	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489464	GSM919947	SRA051954	SRX143541	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	27	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489465	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489465	GSM919948	SRA051954	SRX143542	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	28	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489466	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489466	GSM919949	SRA051954	SRX143543	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	29	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489467	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489467	GSM919950	SRA051954	SRX143544	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	30	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489468	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489468	GSM919951	SRA051954	SRX143545	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	31	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489469	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489469	GSM919952	SRA051954	SRX143546	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	32	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489470	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489470	GSM919953	SRA051954	SRX143547	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	33	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489471	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000477/SRR489471	GSM919954	SRA051954	SRX143548	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	34	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489472	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000478/SRR489472	GSM919955	SRA051954	SRX143549	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	35	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489473	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000478/SRR489473	GSM919956	SRA051954	SRX143550	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	36	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489474	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000478/SRR489474	GSM919957	SRA051954	SRX143551	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	37	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489475	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000478/SRR489475	GSM919958	SRA051954	SRX143552	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	38	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489476	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000478/SRR489476	GSM919959	SRA051954	SRX143553	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	39	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489477	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000478/SRR489477	GSM919960	SRA051954	SRX143554	RNA-Seq	PAIRED	SRP012375	PRJNA160141
37452	40	Kin Fai Au	RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.	We report the application of paired-end RNA sequencing for high throughput profiling of the Xenopus transcriptome in 23 distinct developmental stages.	Kin Fai Au, Meng Tan, Kin Au, Arielle Yablonovitch, Andrea Wills, Julie Baker, Wing Wong, Jin Li	Examination of the transcriptome of Xenopus tropicalis from a 2-cell fertilized embryo to a stage 45 feeding tapole	22960373	45933	SRP012375	SRR489478	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000478/SRR489478	GSM919961	SRA051954	SRX143555	RNA-Seq	PAIRED	SRP012375	PRJNA160141
38605	1	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505561	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505561	GSM945997	SRA053593	SRX152563	RNA-Seq	SINGLE	SRP013627	PRJNA168208
38605	2	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505562	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505562	GSM945998	SRA053593	SRX152564	RNA-Seq	SINGLE	SRP013627	PRJNA168208
38605	3	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505563	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505563	GSM945999	SRA053593	SRX152565	RNA-Seq	SINGLE	SRP013627	PRJNA168208
38605	4	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505564	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505564	GSM946000	SRA053593	SRX152566	RNA-Seq	SINGLE	SRP013627	PRJNA168208
38605	5	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505565	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505565	GSM946001	SRA053593	SRX152567	RNA-Seq	SINGLE	SRP013627	PRJNA168208
38605	6	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505566	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505566	GSM946002	SRA053593	SRX152568	RNA-Seq	SINGLE	SRP013627	PRJNA168208
38605	7	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505567	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505567	GSM946003	SRA053593	SRX152569	RNA-Seq	SINGLE	SRP013627	PRJNA168208
38605	8	Caroline Hill	Genome-wide small RNA profiling and mRNA profiling of Xenopus embryos	Here we report on genome-wide small RNA and transcriptome profiling of blastula, gastrula and neurula-stage Xenopus tropicalis embryos using deep sequ	Caroline Hill, Joanne Harding, Stuart Horswell, Javier Armisen, Lyle Zimmerman, Eric Miska, Caroline Hill	Examination of small RNAs and mRNA at 3 stages of Xenopus embryonic development.	24065776	47876	SRP013627	SRR505568	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/000493/SRR505568	GSM946004	SRA053593	SRX152570	RNA-Seq	SINGLE	SRP013627	PRJNA168208
41161	1	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576762	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576762	GSM1009589	SRA059058	SRX189700	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	2	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576763	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576763	GSM1009590	SRA059058	SRX189701	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	3	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576764	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576764	GSM1009591	SRA059058	SRX189702	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	4	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576765	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576765	GSM1009592	SRA059058	SRX189703	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	5	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576766	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576766	GSM1009593	SRA059058	SRX189704	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	6	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576767	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576767	GSM1009594	SRA059058	SRX189705	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	7	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576768	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576768	GSM1009595	SRA059058	SRX189706	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	8	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576769	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576769	GSM1009596	SRA059058	SRX189707	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	9	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576770	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576770	GSM1009597	SRA059058	SRX189708	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	10	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576771	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576771	GSM1009598	SRA059058	SRX189709	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	11	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576772	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576772	GSM1009599	SRA059058	SRX189710	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	12	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576773	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576773	GSM1009600	SRA059058	SRX189711	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	13	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576774	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576774	GSM1009601	SRA059058	SRX189712	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	14	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576775	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576775	GSM1009602	SRA059058	SRX189713	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	15	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576776	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/000563/SRR576776	GSM1009603	SRA059058	SRX189714	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41161	16	Gert Jan Veenstra	Principles of nucleation of H3K27 methylation during embryonic development	During embryonic development, maintenance of cell identity and lineage commitment requires the Polycomb-group PRC2 complex, which catalyzes histone H3	Gert Jan Veenstra, Simon van Heeringen, Robert Akkers, Ila van Kruijsbergen, Lars Hanssen, Nilofar Sharifi, Gert-Jan Veenstra, M. Asif Arif	ChIP-seq profiles of three histone modifications (H3K4me3, H3K27me3 and H3K4me1) and RNA Polymerase II, EZH2 and Jarid2 of Xenopus tropicalis embryos during development	24336765	47807	SRP015902	SRR576777	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000563/SRR576777	GSM1009604	SRA059058	SRX189715	ChIP-Seq	SINGLE	SRP015902	PRJNA175996
41338	1	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579545	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579545	GSM1015150	SRA059267	SRX191149	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	2	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579546	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579546	GSM1015151	SRA059267	SRX191150	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	3	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579547	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579547	GSM1015152	SRA059267	SRX191151	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	4	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579548	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579548	GSM1015153	SRA059267	SRX191152	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	5	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579549	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579549	GSM1015154	SRA059267	SRX191153	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	6	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579550	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579550	GSM1015155	SRA059267	SRX191154	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	7	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579551	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579551	GSM1015156	SRA059267	SRX191155	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	8	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579552	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579552	GSM1015157	SRA059267	SRX191156	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	9	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579553	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579553	GSM1015158	SRA059267	SRX191157	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	10	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579554	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579554	GSM1015159	SRA059267	SRX191158	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	11	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579555	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579555	GSM1015160	SRA059267	SRX191159	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	12	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579556	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579556	GSM1015161	SRA059267	SRX191160	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	13	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579557	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579557	GSM1015162	SRA059267	SRX191161	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	14	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579558	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579558	GSM1015163	SRA059267	SRX191162	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	15	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579559	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579559	GSM1015164	SRA059267	SRX191163	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	16	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579560	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579560	GSM1015165	SRA059267	SRX191164	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	17	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579561	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579561	GSM1015166	SRA059267	SRX191165	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	18	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579562	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579562	GSM1015167	SRA059267	SRX191166	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	19	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579563	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579563	GSM1015168	SRA059267	SRX191167	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	20	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579564	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579564	GSM1015169	SRA059267	SRX191168	RNA-Seq	PAIRED	SRP015997	PRJNA176589
41338	21	Nuno Barbosa-Morais	The evolutionary landscape of alternative splicing in vertebrate species	How species with similar repertoires of protein coding genes differ so dramatically at the phenotypic level is poorly understood. From comparing the t	Nuno Barbosa-Morais, Claudia Kutter, Stephen Watt, Duncan Odom, Benjamin Blencowe	mRNA profiles of several organs (brain, liver, kidney, heart, skeletal muscle) in multiple vertebrate species (mouse, chicken, lizard, frog, pufferfish) generated by deep sequencing using Illumina HiSeq	23258890	46474	SRP015997	SRR579565	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/000565/SRR579565	GSM1015170	SRA059267	SRX191169	RNA-Seq	PAIRED	SRP015997	PRJNA176589
43512	1	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648795	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648795	GSM1064674	SRA064777	SRX217137	OTHER	SINGLE	SRP017952	PRJNA186672
43512	2	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648796	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648796	GSM1064675	SRA064777	SRX217138	OTHER	SINGLE	SRP017952	PRJNA186672
43512	3	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648797	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648797	GSM1064675	SRA064777	SRX217138	OTHER	SINGLE	SRP017952	PRJNA186672
43512	4	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648798	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648798	GSM1064676	SRA064777	SRX217139	OTHER	SINGLE	SRP017952	PRJNA186672
43512	5	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648799	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648799	GSM1064676	SRA064777	SRX217139	OTHER	SINGLE	SRP017952	PRJNA186672
43512	6	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648800	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648800	GSM1064677	SRA064777	SRX217140	OTHER	SINGLE	SRP017952	PRJNA186672
43512	7	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648801	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648801	GSM1064678	SRA064777	SRX217141	OTHER	SINGLE	SRP017952	PRJNA186672
43512	8	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648802	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648802	GSM1064678	SRA064777	SRX217141	OTHER	SINGLE	SRP017952	PRJNA186672
43512	9	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648803	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648803	GSM1064679	SRA064777	SRX217142	OTHER	SINGLE	SRP017952	PRJNA186672
43512	10	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648804	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648804	GSM1064679	SRA064777	SRX217142	OTHER	SINGLE	SRP017952	PRJNA186672
43512	11	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648805	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648805	GSM1064680	SRA064777	SRX217143	OTHER	SINGLE	SRP017952	PRJNA186672
43512	12	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648806	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648806	GSM1064680	SRA064777	SRX217143	OTHER	SINGLE	SRP017952	PRJNA186672
43512	13	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648807	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648807	GSM1064681	SRA064777	SRX217144	OTHER	SINGLE	SRP017952	PRJNA186672
43512	14	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648808	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648808	GSM1064682	SRA064777	SRX217145	OTHER	SINGLE	SRP017952	PRJNA186672
43512	15	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648809	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648809	GSM1064682	SRA064777	SRX217145	OTHER	SINGLE	SRP017952	PRJNA186672
43512	16	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648810	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648810	GSM1064683	SRA064777	SRX217146	OTHER	SINGLE	SRP017952	PRJNA186672
43512	17	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648811	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648811	GSM1064683	SRA064777	SRX217146	OTHER	SINGLE	SRP017952	PRJNA186672
43512	18	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648812	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648812	GSM1064684	SRA064777	SRX217147	OTHER	SINGLE	SRP017952	PRJNA186672
43512	19	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648813	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648813	GSM1064685	SRA064777	SRX217148	OTHER	SINGLE	SRP017952	PRJNA186672
43512	20	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648814	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648814	GSM1064685	SRA064777	SRX217148	OTHER	SINGLE	SRP017952	PRJNA186672
43512	21	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648815	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648815	GSM1064686	SRA064777	SRX217149	OTHER	SINGLE	SRP017952	PRJNA186672
43512	22	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648816	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648816	GSM1064686	SRA064777	SRX217149	OTHER	SINGLE	SRP017952	PRJNA186672
43512	23	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648817	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648817	GSM1064687	SRA064777	SRX217150	OTHER	SINGLE	SRP017952	PRJNA186672
43512	24	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648818	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648818	GSM1064688	SRA064777	SRX217151	OTHER	SINGLE	SRP017952	PRJNA186672
43512	25	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648819	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648819	GSM1064688	SRA064777	SRX217151	OTHER	SINGLE	SRP017952	PRJNA186672
43512	26	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648820	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648820	GSM1064689	SRA064777	SRX217152	OTHER	SINGLE	SRP017952	PRJNA186672
43512	27	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648821	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648821	GSM1064689	SRA064777	SRX217152	OTHER	SINGLE	SRP017952	PRJNA186672
43512	28	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648822	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648822	GSM1064690	SRA064777	SRX217153	OTHER	SINGLE	SRP017952	PRJNA186672
43512	29	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648823	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648823	GSM1064691	SRA064777	SRX217154	OTHER	SINGLE	SRP017952	PRJNA186672
43512	30	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648824	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648824	GSM1064691	SRA064777	SRX217154	OTHER	SINGLE	SRP017952	PRJNA186672
43512	31	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648825	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648825	GSM1064692	SRA064777	SRX217155	OTHER	SINGLE	SRP017952	PRJNA186672
43512	32	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648826	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648826	GSM1064692	SRA064777	SRX217155	OTHER	SINGLE	SRP017952	PRJNA186672
43512	33	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648827	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648827	GSM1064693	SRA064777	SRX217156	OTHER	SINGLE	SRP017952	PRJNA186672
43512	34	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648828	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648828	GSM1064693	SRA064777	SRX217156	OTHER	SINGLE	SRP017952	PRJNA186672
43512	35	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648829	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648829	GSM1064694	SRA064777	SRX217157	OTHER	SINGLE	SRP017952	PRJNA186672
43512	36	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648830	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648830	GSM1064695	SRA064777	SRX217158	OTHER	SINGLE	SRP017952	PRJNA186672
43512	37	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648831	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648831	GSM1064695	SRA064777	SRX217158	OTHER	SINGLE	SRP017952	PRJNA186672
43512	38	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648832	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648832	GSM1064696	SRA064777	SRX217159	OTHER	SINGLE	SRP017952	PRJNA186672
43512	39	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648833	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648833	GSM1064696	SRA064777	SRX217159	OTHER	SINGLE	SRP017952	PRJNA186672
43512	40	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648834	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648834	GSM1064697	SRA064777	SRX217160	OTHER	SINGLE	SRP017952	PRJNA186672
43512	41	David Sims	Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates	Two-thirds of gene promoters in mammals are associated with regions of non-methylated DNA, called CpG islands (CGIs), which counteract the repressive 	David Sims, Hannah Long, Chris Ponting, Robert Klose	Bio-CAP was used to identify non-methylated regions of the genome in seven diverse vertebrates (human, mouse, platypus, chicken, lizard, frog and zebrafish) across a number of tissues.	23467541	46753	SRP017952	SRR648835	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000633/SRR648835	GSM1064697	SRA064777	SRX217160	OTHER	SINGLE	SRP017952	PRJNA186672
43520	1	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649360	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000634/SRR649360	GSM1064822	SRA064905	SRX217680	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	2	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649361	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649361	GSM1064824	SRA064905	SRX217681	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	3	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649362	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649362	GSM1064826	SRA064905	SRX217682	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	4	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649363	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649363	GSM1064828	SRA064905	SRX217683	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	5	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649364	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649364	GSM1064829	SRA064905	SRX217684	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	6	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649365	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000634/SRR649365	GSM1064832	SRA064905	SRX217685	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	7	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649366	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000634/SRR649366	GSM1064834	SRA064905	SRX217686	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	8	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649367	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000634/SRR649367	GSM1064834	SRA064905	SRX217686	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	9	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649368	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000634/SRR649368	GSM1064837	SRA064905	SRX217687	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	10	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649369	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000634/SRR649369	GSM1064840	SRA064905	SRX217688	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	11	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649370	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/000634/SRR649370	GSM1064840	SRA064905	SRX217688	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	12	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649371	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649371	GSM1064841	SRA064905	SRX217689	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	13	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649372	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649372	GSM1064842	SRA064905	SRX217690	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	14	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649373	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649373	GSM1064843	SRA064905	SRX217691	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	15	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649374	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649374	GSM1064844	SRA064905	SRX217692	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	16	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649375	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649375	GSM1064845	SRA064905	SRX217693	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	17	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649376	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649376	GSM1064846	SRA064905	SRX217694	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	18	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649377	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649377	GSM1064847	SRA064905	SRX217695	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	19	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649378	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649378	GSM1064848	SRA064905	SRX217696	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	20	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649379	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649379	GSM1064849	SRA064905	SRX217697	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	21	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649380	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649380	GSM1064849	SRA064905	SRX217697	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	22	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649381	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649381	GSM1064850	SRA064905	SRX217698	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	23	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649382	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649382	GSM1064851	SRA064905	SRX217699	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	24	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649383	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649383	GSM1064852	SRA064905	SRX217700	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	25	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649384	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649384	GSM1064852	SRA064905	SRX217700	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	26	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649385	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649385	GSM1064853	SRA064905	SRX217701	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	27	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649386	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649386	GSM1064854	SRA064905	SRX217702	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	28	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649387	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649387	GSM1064854	SRA064905	SRX217702	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	29	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649388	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649388	GSM1064854	SRA064905	SRX217702	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	30	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649389	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649389	GSM1064855	SRA064905	SRX217703	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	31	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649390	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649390	GSM1064855	SRA064905	SRX217703	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	32	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649391	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649391	GSM1064856	SRA064905	SRX217704	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	33	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649392	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649392	GSM1064857	SRA064905	SRX217705	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	34	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649393	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649393	GSM1064858	SRA064905	SRX217706	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	35	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649394	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649394	GSM1064859	SRA064905	SRX217707	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	36	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649395	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649395	GSM1064860	SRA064905	SRX217708	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	37	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649396	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649396	GSM1064861	SRA064905	SRX217709	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	38	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649397	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649397	GSM1064862	SRA064905	SRX217710	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	39	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649398	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649398	GSM1064863	SRA064905	SRX217711	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	40	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649399	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649399	GSM1064864	SRA064905	SRX217712	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	41	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR649400	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000634/SRR649400	GSM1064865	SRA064905	SRX217713	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	42	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943339	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943339	GSM1196040	SRA064905	SRX328074	RNA-Seq	PAIRED	SRP017959	PRJNA186646
43520	43	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943357	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943357	GSM1196041	SRA064905	SRX328092	RNA-Seq	PAIRED	SRP017959	PRJNA186646
43520	44	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943358	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943358	GSM1196042	SRA064905	SRX328093	RNA-Seq	PAIRED	SRP017959	PRJNA186646
43520	45	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943359	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943359	GSM1196043	SRA064905	SRX328094	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	46	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943340	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943340	GSM1196044	SRA064905	SRX328075	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	47	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943341	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943341	GSM1196045	SRA064905	SRX328076	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	48	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943342	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943342	GSM1196046	SRA064905	SRX328077	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	49	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943343	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943343	GSM1196047	SRA064905	SRX328078	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	50	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943344	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943344	GSM1196048	SRA064905	SRX328079	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	51	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943345	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943345	GSM1196049	SRA064905	SRX328080	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	52	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943346	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943346	GSM1196050	SRA064905	SRX328081	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	53	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943347	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943347	GSM1196051	SRA064905	SRX328082	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	54	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943348	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943348	GSM1196052	SRA064905	SRX328083	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	55	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943349	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943349	GSM1196053	SRA064905	SRX328084	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	56	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943350	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943350	GSM1196054	SRA064905	SRX328085	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	57	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943351	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943351	GSM1196055	SRA064905	SRX328086	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	58	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943352	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943352	GSM1196056	SRA064905	SRX328087	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	59	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943353	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943353	GSM1196057	SRA064905	SRX328088	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	60	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943354	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943354	GSM1196058	SRA064905	SRX328089	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	61	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943355	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943355	GSM1196059	SRA064905	SRX328090	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43520	62	Anamaria Necsulea	The evolution of lncRNA repertoires and expression patterns in tetrapods	Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into thei	Anamaria Necsulea, Magali Soumillon, Angélica Liechti, Tasman Daish, Ulrich Zeller, Julie Baker, Frank Grutzner, Henrik Kaessmann, Maria Warnefors	[Batch 1 and 2] To broaden our understanding of lncRNA evolution, we used an extensive RNA-seq dataset to establish lncRNA repertoires and homologous gene families in 11 tetrapod species. We analyzed the poly- adenylated transcriptomes of 8 organs (cortex/whole brain without cerebellum, cerebellum, heart, kidney, liver, placenta, ovary and testis) and 11 species (human, chimpanzee, bonobo, gorilla, orangutan, macaque, mouse, opossum, platypus, chicken and the frog Xenopus tropicalis), which shared a common ancestor ~370 millions of years (MY) ago. Our dataset included 47 strand-specific samples, which allowed us to confirm the orientation of gene predictions and to address the evolution of sense-antisense transcripts. See also GSE43721 (Soumillon et al, Cell Reports, 2013) for three strand-specific samples for mouse brain, liver and testis.	24463510	54076	SRP017959	SRR943356	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/000921/SRR943356	GSM1196060	SRA064905	SRX328091	RNA-Seq	SINGLE	SRP017959	PRJNA186646
43652	1	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651117	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651117	GSM1067623	SRA065319	SRX218733	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	2	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651118	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651118	GSM1067623	SRA065319	SRX218733	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	3	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651119	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651119	GSM1067624	SRA065319	SRX218734	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	4	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651120	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651120	GSM1067624	SRA065319	SRX218734	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	5	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651121	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651121	GSM1067625	SRA065319	SRX218735	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	6	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651122	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651122	GSM1067626	SRA065319	SRX218736	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	7	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651123	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651123	GSM1067626	SRA065319	SRX218736	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	8	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651124	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651124	GSM1067627	SRA065319	SRX218737	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	9	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651125	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651125	GSM1067628	SRA065319	SRX218738	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	10	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651126	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651126	GSM1067629	SRA065319	SRX218739	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	11	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651127	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651127	GSM1067630	SRA065319	SRX218740	RNA-Seq	SINGLE	SRP018091	PRJNA186932
43652	12	Gert Jan Veenstra	A Genome-Wide Survey of Maternal and Embryonic Transcripts during Xenopus tropicalis Development	To analyze the dynamics and diversity of coding and non-coding transcripts during development, both polyadenylated mRNA and ribosomal RNA-depleted tot	Gert Jan Veenstra, Sarita Paranjpe, Ulrike Jacobi, Simon van Heeringen, Gert Veenstra	Profiles of polyadenylated mRNA (6 stages) and ribosomal RNA-depleted total RNA (3 stages) through early Xenopus tropicalis development	24195446	47572	SRP018091	SRR651128	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/000635/SRR651128	GSM1067631	SRA065319	SRX218741	RNA-Seq	SINGLE	SRP018091	PRJNA186932
45786	1	Panna Tandon	Cardiac transcriptome of Tcf21-depleted Xenopus embryos	The aim of the approach was to use RNAseq analysis to identify genes expressed in  Xenopus epicardium that were affected by embryonic depletion of the	Panna Tandon, Frank Conlon, Nirav Amin	mRNA profiles of stage 44-45 Xenopus laevis sibling hearts from control or Tcf21-depleted embryos, were generated by deep sequencing using Illumina GAII.	23637334	47035	SRP020536	SRR808992	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/000790/SRR808992	GSM1115088	SRA072600	SRX260070	RNA-Seq	SINGLE	SRP020536	PRJNA196315
45786	2	Panna Tandon	Cardiac transcriptome of Tcf21-depleted Xenopus embryos	The aim of the approach was to use RNAseq analysis to identify genes expressed in  Xenopus epicardium that were affected by embryonic depletion of the	Panna Tandon, Frank Conlon, Nirav Amin	mRNA profiles of stage 44-45 Xenopus laevis sibling hearts from control or Tcf21-depleted embryos, were generated by deep sequencing using Illumina GAII.	23637334	47035	SRP020536	SRR808993	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/000790/SRR808993	GSM1115089	SRA072600	SRX260071	RNA-Seq	SINGLE	SRP020536	PRJNA196315
48560	1	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926401	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926401	GSM1180932	SRA092176	SRX318201	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	2	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926402	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926402	GSM1180933	SRA092176	SRX318202	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	3	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926403	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926403	GSM1180934	SRA092176	SRX318203	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	4	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926404	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926404	GSM1180935	SRA092176	SRX318204	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	5	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926405	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926405	GSM1180936	SRA092176	SRX318205	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	6	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926406	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926406	GSM1180937	SRA092176	SRX318206	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	7	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926407	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926407	GSM1180938	SRA092176	SRX318207	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	8	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926408	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926408	GSM1180939	SRA092176	SRX318208	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	9	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926409	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926409	GSM1180940	SRA092176	SRX318209	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48560	10	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency.	We defined genome-wide regulatory inputs of the T-box transcription factors Brachyury (Xbra), Eomesodermin (Eomes) and VegT that maintain neuro-mesode	George Gentsch, George Gentsch, James Smith	Binding profiles for Xbra, Eomes and VegT in X. tropicalis embryos (ChIP-Seq)	24055059	47416	SRP026570	SRR926410	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/000904/SRR926410	GSM1180941	SRA092176	SRX318210	ChIP-Seq	SINGLE	SRP026570	PRJNA210646
48663	1	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency	Brachyury (Xbra/Xbra3) knock-down embryos of the frog Xenopus tropicalis were profiled to quantify neuro-mesodermal cell fate switches at a transcript	George Gentsch, George Gentsch, James Smith	Transcriptional profiling of Xbra/Xbra3 double morphants at early tadpole stage (RNA-Seq) in biological triplicates.	24055059	47416	SRP026685	SRR929119	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/000907/SRR929119	GSM1183056	SRA092415	SRX319533	RNA-Seq	PAIRED	SRP026685	PRJNA210967
48663	2	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency	Brachyury (Xbra/Xbra3) knock-down embryos of the frog Xenopus tropicalis were profiled to quantify neuro-mesodermal cell fate switches at a transcript	George Gentsch, George Gentsch, James Smith	Transcriptional profiling of Xbra/Xbra3 double morphants at early tadpole stage (RNA-Seq) in biological triplicates.	24055059	47416	SRP026685	SRR929120	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/000907/SRR929120	GSM1183057	SRA092415	SRX319534	RNA-Seq	PAIRED	SRP026685	PRJNA210967
48663	3	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency	Brachyury (Xbra/Xbra3) knock-down embryos of the frog Xenopus tropicalis were profiled to quantify neuro-mesodermal cell fate switches at a transcript	George Gentsch, George Gentsch, James Smith	Transcriptional profiling of Xbra/Xbra3 double morphants at early tadpole stage (RNA-Seq) in biological triplicates.	24055059	47416	SRP026685	SRR929121	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/000907/SRR929121	GSM1183058	SRA092415	SRX319535	RNA-Seq	PAIRED	SRP026685	PRJNA210967
48663	4	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency	Brachyury (Xbra/Xbra3) knock-down embryos of the frog Xenopus tropicalis were profiled to quantify neuro-mesodermal cell fate switches at a transcript	George Gentsch, George Gentsch, James Smith	Transcriptional profiling of Xbra/Xbra3 double morphants at early tadpole stage (RNA-Seq) in biological triplicates.	24055059	47416	SRP026685	SRR929122	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/000907/SRR929122	GSM1183059	SRA092415	SRX319536	RNA-Seq	PAIRED	SRP026685	PRJNA210967
48663	5	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency	Brachyury (Xbra/Xbra3) knock-down embryos of the frog Xenopus tropicalis were profiled to quantify neuro-mesodermal cell fate switches at a transcript	George Gentsch, George Gentsch, James Smith	Transcriptional profiling of Xbra/Xbra3 double morphants at early tadpole stage (RNA-Seq) in biological triplicates.	24055059	47416	SRP026685	SRR929123	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/000907/SRR929123	GSM1183060	SRA092415	SRX319537	RNA-Seq	PAIRED	SRP026685	PRJNA210967
48663	6	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency	Brachyury (Xbra/Xbra3) knock-down embryos of the frog Xenopus tropicalis were profiled to quantify neuro-mesodermal cell fate switches at a transcript	George Gentsch, George Gentsch, James Smith	Transcriptional profiling of Xbra/Xbra3 double morphants at early tadpole stage (RNA-Seq) in biological triplicates.	24055059	47416	SRP026685	SRR929124	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/000907/SRR929124	GSM1183061	SRA092415	SRX319538	RNA-Seq	PAIRED	SRP026685	PRJNA210967
48663	7	George Gentsch	In vivo T-box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuro-mesodermal Bipotency	Brachyury (Xbra/Xbra3) knock-down embryos of the frog Xenopus tropicalis were profiled to quantify neuro-mesodermal cell fate switches at a transcript	George Gentsch, George Gentsch, James Smith	Transcriptional profiling of Xbra/Xbra3 double morphants at early tadpole stage (RNA-Seq) in biological triplicates.	24055059	47416	SRP026685	SRR929125	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/000907/SRR929125	GSM1183062	SRA092415	SRX319539	RNA-Seq	PAIRED	SRP026685	PRJNA210967
50593	1	Taejoon Kwon	Coordinated genomic control of ciliogenesis and cell movement by Rfx2	We have performed a systems-level analysis of the RFX/Daf-19 family transcription factor, Rfx2. Using a combination of high-throughput sequencing of R	Taejoon Kwon, Mei-I Chung, Rakhi Gupta, Julie Baker, Edward Marcotte, John Wallingford	RNA-seq: two biological replicates for control and RFX2 knockdown by morpholino injection, ChIP-seq: RFX2-GFP pulldown with GFP antibody, GFP only expression used as control	24424412	51735	SRP029582	SRR1276213	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/001246/SRR1276213	GSM1224372	SRA100059	SRX345032	RNA-Seq	PAIRED	SRP029582	PRJNA218018
50593	2	Taejoon Kwon	Coordinated genomic control of ciliogenesis and cell movement by Rfx2	We have performed a systems-level analysis of the RFX/Daf-19 family transcription factor, Rfx2. Using a combination of high-throughput sequencing of R	Taejoon Kwon, Mei-I Chung, Rakhi Gupta, Julie Baker, Edward Marcotte, John Wallingford	RNA-seq: two biological replicates for control and RFX2 knockdown by morpholino injection, ChIP-seq: RFX2-GFP pulldown with GFP antibody, GFP only expression used as control	24424412	51735	SRP029582	SRR1276214	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/001246/SRR1276214	GSM1224373	SRA100059	SRX345033	RNA-Seq	PAIRED	SRP029582	PRJNA218018
50593	3	Taejoon Kwon	Coordinated genomic control of ciliogenesis and cell movement by Rfx2	We have performed a systems-level analysis of the RFX/Daf-19 family transcription factor, Rfx2. Using a combination of high-throughput sequencing of R	Taejoon Kwon, Mei-I Chung, Rakhi Gupta, Julie Baker, Edward Marcotte, John Wallingford	RNA-seq: two biological replicates for control and RFX2 knockdown by morpholino injection, ChIP-seq: RFX2-GFP pulldown with GFP antibody, GFP only expression used as control	24424412	51735	SRP029582	SRR1276215	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/001246/SRR1276215	GSM1224374	SRA100059	SRX345034	RNA-Seq	PAIRED	SRP029582	PRJNA218018
50593	4	Taejoon Kwon	Coordinated genomic control of ciliogenesis and cell movement by Rfx2	We have performed a systems-level analysis of the RFX/Daf-19 family transcription factor, Rfx2. Using a combination of high-throughput sequencing of R	Taejoon Kwon, Mei-I Chung, Rakhi Gupta, Julie Baker, Edward Marcotte, John Wallingford	RNA-seq: two biological replicates for control and RFX2 knockdown by morpholino injection, ChIP-seq: RFX2-GFP pulldown with GFP antibody, GFP only expression used as control	24424412	51735	SRP029582	SRR1276216	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/001246/SRR1276216	GSM1224375	SRA100059	SRX345035	RNA-Seq	PAIRED	SRP029582	PRJNA218018
50593	5	Taejoon Kwon	Coordinated genomic control of ciliogenesis and cell movement by Rfx2	We have performed a systems-level analysis of the RFX/Daf-19 family transcription factor, Rfx2. Using a combination of high-throughput sequencing of R	Taejoon Kwon, Mei-I Chung, Rakhi Gupta, Julie Baker, Edward Marcotte, John Wallingford	RNA-seq: two biological replicates for control and RFX2 knockdown by morpholino injection, ChIP-seq: RFX2-GFP pulldown with GFP antibody, GFP only expression used as control	24424412	51735	SRP029582	SRR965781	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000943/SRR965781	GSM1224376	SRA100059	SRX345036	ChIP-Seq	SINGLE	SRP029582	PRJNA218018
50593	6	Taejoon Kwon	Coordinated genomic control of ciliogenesis and cell movement by Rfx2	We have performed a systems-level analysis of the RFX/Daf-19 family transcription factor, Rfx2. Using a combination of high-throughput sequencing of R	Taejoon Kwon, Mei-I Chung, Rakhi Gupta, Julie Baker, Edward Marcotte, John Wallingford	RNA-seq: two biological replicates for control and RFX2 knockdown by morpholino injection, ChIP-seq: RFX2-GFP pulldown with GFP antibody, GFP only expression used as control	24424412	51735	SRP029582	SRR965782	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/000943/SRR965782	GSM1224377	SRA100059	SRX345037	ChIP-Seq	SINGLE	SRP029582	PRJNA218018
52809	1	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039856	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039856	GSM1276537	SRA114402	SRX384666	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	2	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039857	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039857	GSM1276538	SRA114402	SRX384667	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	3	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039858	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039858	GSM1276539	SRA114402	SRX384668	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	4	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039859	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039859	GSM1276540	SRA114402	SRX384669	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	5	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039860	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039860	GSM1276541	SRA114402	SRX384670	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	6	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039861	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039861	GSM1276542	SRA114402	SRX384671	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	7	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039862	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001015/SRR1039862	GSM1276543	SRA114402	SRX384672	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	8	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039863	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001015/SRR1039863	GSM1276544	SRA114402	SRX384673	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	9	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039864	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039864	GSM1276545	SRA114402	SRX384674	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	10	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039865	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001015/SRR1039865	GSM1276546	SRA114402	SRX384675	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	11	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039866	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039866	GSM1276547	SRA114402	SRX384676	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	12	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039867	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039867	GSM1276548	SRA114402	SRX384677	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	13	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146617	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146617	GSM1276549	SRA114402	SRX384678	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	14	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039869	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039869	GSM1276550	SRA114402	SRX384679	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	15	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039870	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039870	GSM1276551	SRA114402	SRX384680	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	16	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039871	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039871	GSM1276552	SRA114402	SRX384681	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	17	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039872	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039872	GSM1276553	SRA114402	SRX384682	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	18	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039873	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039873	GSM1276554	SRA114402	SRX384683	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	19	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039874	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001015/SRR1039874	GSM1276555	SRA114402	SRX384684	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	20	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039875	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039875	GSM1276556	SRA114402	SRX384685	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	21	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039876	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039876	GSM1276557	SRA114402	SRX384686	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	22	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039877	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001015/SRR1039877	GSM1276558	SRA114402	SRX384687	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	23	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039878	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039878	GSM1276559	SRA114402	SRX384688	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	24	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039879	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039879	GSM1276560	SRA114402	SRX384689	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	25	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039880	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001015/SRR1039880	GSM1276561	SRA114402	SRX384690	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	26	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039881	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039881	GSM1276562	SRA114402	SRX384691	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	27	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039882	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039882	GSM1276563	SRA114402	SRX384692	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	28	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146618	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001119/SRR1146618	GSM1276564	SRA114402	SRX384693	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	29	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1039884	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/001015/SRR1039884	GSM1276565	SRA114402	SRX384694	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	30	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146615	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146615	GSM1276566	SRA114402	SRX384695	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	31	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146542	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146542	GSM1316794	SRA114402	SRX451671	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	32	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146543	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146543	GSM1316795	SRA114402	SRX451672	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	33	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146544	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146544	GSM1316796	SRA114402	SRX451673	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	34	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146545	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146545	GSM1316797	SRA114402	SRX451674	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	35	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146546	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146546	GSM1316798	SRA114402	SRX451675	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	36	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146547	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146547	GSM1316799	SRA114402	SRX451676	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	37	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146548	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146548	GSM1316800	SRA114402	SRX451677	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	38	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146549	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146549	GSM1316801	SRA114402	SRX451678	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	39	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146550	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146550	GSM1316802	SRA114402	SRX451679	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	40	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146551	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146551	GSM1316803	SRA114402	SRX451680	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	41	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146552	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146552	GSM1316804	SRA114402	SRX451681	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	42	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146553	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146553	GSM1316805	SRA114402	SRX451682	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	43	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146554	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146554	GSM1316806	SRA114402	SRX451683	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	44	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146555	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146555	GSM1316807	SRA114402	SRX451684	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	45	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146556	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146556	GSM1316808	SRA114402	SRX451685	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	46	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146557	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146557	GSM1316809	SRA114402	SRX451686	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	47	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146558	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146558	GSM1316810	SRA114402	SRX451687	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	48	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146559	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146559	GSM1316811	SRA114402	SRX451688	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	49	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146560	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/001119/SRR1146560	GSM1316812	SRA114402	SRX451689	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	50	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146561	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146561	GSM1316813	SRA114402	SRX451690	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	51	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146562	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146562	GSM1316814	SRA114402	SRX451691	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	52	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146563	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146563	GSM1316815	SRA114402	SRX451692	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	53	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146564	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146564	GSM1316816	SRA114402	SRX451693	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	54	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146565	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146565	GSM1316817	SRA114402	SRX451694	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	55	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146566	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146566	GSM1316818	SRA114402	SRX451695	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	56	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146567	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146567	GSM1316819	SRA114402	SRX451696	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	57	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146568	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146568	GSM1316820	SRA114402	SRX451697	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	58	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146569	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146569	GSM1316821	SRA114402	SRX451698	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	59	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146570	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146570	GSM1316822	SRA114402	SRX451699	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	60	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146571	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146571	GSM1316823	SRA114402	SRX451700	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	61	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146572	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146572	GSM1316824	SRA114402	SRX451701	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	62	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146573	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146573	GSM1316825	SRA114402	SRX451702	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	63	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146574	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146574	GSM1316826	SRA114402	SRX451703	RNA-Seq	SINGLE	SRP033369	PRJNA230112
52809	64	Stephen Eichhorn	Poly(A)-tail profiling reveals an embryonic switch in translational control	Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths hav	Stephen Eichhorn, Alexander Subtelny, Stephen Eichhorn, Grace Chen, Hazel Sive, David Bartel	64 samples from a variety of species	24476825	48919	SRP033369	SRR1146575	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001119/SRR1146575	GSM1316827	SRA114402	SRX451704	RNA-Seq	SINGLE	SRP033369	PRJNA230112
53652	1	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [ChIP-seq]	We defined the genome-wide binding regions of Smad2/3 and Foxh1 at mid-gastrula stage Xenopus tropicalis embryos, at which Nodal signaling and Foxh1 a	William Chiu, William Chiu, Ken Cho	Binding profile of the TFs Smad2/3 and Foxh1 in gastrula stage (st10.5) Xenopus tropicalis embryos using ChIP-seq approach.	25359723	49634	SRP034730	SRR1060744	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/001035/SRR1060744	GSM1298090	SRA122377	SRX399447	ChIP-Seq	SINGLE	SRP034730	PRJNA232589
53652	2	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [ChIP-seq]	We defined the genome-wide binding regions of Smad2/3 and Foxh1 at mid-gastrula stage Xenopus tropicalis embryos, at which Nodal signaling and Foxh1 a	William Chiu, William Chiu, Ken Cho	Binding profile of the TFs Smad2/3 and Foxh1 in gastrula stage (st10.5) Xenopus tropicalis embryos using ChIP-seq approach.	25359723	49634	SRP034730	SRR1060745	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/001035/SRR1060745	GSM1298091	SRA122377	SRX399448	ChIP-Seq	SINGLE	SRP034730	PRJNA232589
53652	3	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [ChIP-seq]	We defined the genome-wide binding regions of Smad2/3 and Foxh1 at mid-gastrula stage Xenopus tropicalis embryos, at which Nodal signaling and Foxh1 a	William Chiu, William Chiu, Ken Cho	Binding profile of the TFs Smad2/3 and Foxh1 in gastrula stage (st10.5) Xenopus tropicalis embryos using ChIP-seq approach.	25359723	49634	SRP034730	SRR1060746	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/001035/SRR1060746	GSM1298092	SRA122377	SRX399449	ChIP-Seq	SINGLE	SRP034730	PRJNA232589
53652	4	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [ChIP-seq]	We defined the genome-wide binding regions of Smad2/3 and Foxh1 at mid-gastrula stage Xenopus tropicalis embryos, at which Nodal signaling and Foxh1 a	William Chiu, William Chiu, Ken Cho	Binding profile of the TFs Smad2/3 and Foxh1 in gastrula stage (st10.5) Xenopus tropicalis embryos using ChIP-seq approach.	25359723	49634	SRP034730	SRR1060747	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/001035/SRR1060747	GSM1298093	SRA122377	SRX399450	ChIP-Seq	SINGLE	SRP034730	PRJNA232589
53652	5	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [ChIP-seq]	We defined the genome-wide binding regions of Smad2/3 and Foxh1 at mid-gastrula stage Xenopus tropicalis embryos, at which Nodal signaling and Foxh1 a	William Chiu, William Chiu, Ken Cho	Binding profile of the TFs Smad2/3 and Foxh1 in gastrula stage (st10.5) Xenopus tropicalis embryos using ChIP-seq approach.	25359723	49634	SRP034730	SRR1060748	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/001035/SRR1060748	GSM1298094	SRA122377	SRX399451	ChIP-Seq	SINGLE	SRP034730	PRJNA232589
53653	1	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [RNA-seq]	We identified Nodal and Foxh1 downstream targets by performing RNA-seq of embryos either treated with small molecule SB431542 or microinjected morphol	William Chiu, William Chiu, Ken Cho	Differential gene expression analyses of perturbed embryos (SB431542 treated, or Foxh1 MO injected) using RNA-seq	25359723	49634	SRP034731	SRR1060749	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/001035/SRR1060749	GSM1298095	SRA122378	SRX399452	RNA-Seq	SINGLE	SRP034731	PRJNA232590
53653	2	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [RNA-seq]	We identified Nodal and Foxh1 downstream targets by performing RNA-seq of embryos either treated with small molecule SB431542 or microinjected morphol	William Chiu, William Chiu, Ken Cho	Differential gene expression analyses of perturbed embryos (SB431542 treated, or Foxh1 MO injected) using RNA-seq	25359723	49634	SRP034731	SRR1060750	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/001035/SRR1060750	GSM1298096	SRA122378	SRX399453	RNA-Seq	SINGLE	SRP034731	PRJNA232590
53653	3	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [RNA-seq]	We identified Nodal and Foxh1 downstream targets by performing RNA-seq of embryos either treated with small molecule SB431542 or microinjected morphol	William Chiu, William Chiu, Ken Cho	Differential gene expression analyses of perturbed embryos (SB431542 treated, or Foxh1 MO injected) using RNA-seq	25359723	49634	SRP034731	SRR1060751	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001035/SRR1060751	GSM1298097	SRA122378	SRX399454	RNA-Seq	SINGLE	SRP034731	PRJNA232590
53653	4	William Chiu	Genome-wide view of TGFb/Foxh1 regulation of the early mesendoderm program [RNA-seq]	We identified Nodal and Foxh1 downstream targets by performing RNA-seq of embryos either treated with small molecule SB431542 or microinjected morphol	William Chiu, William Chiu, Ken Cho	Differential gene expression analyses of perturbed embryos (SB431542 treated, or Foxh1 MO injected) using RNA-seq	25359723	49634	SRP034731	SRR1060752	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001035/SRR1060752	GSM1298098	SRA122378	SRX399455	RNA-Seq	SINGLE	SRP034731	PRJNA232590
56000	1	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199229	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001171/SRR1199229	GSM1350502	SRA147084	SRX495638	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	2	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199230	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001171/SRR1199230	GSM1350503	SRA147084	SRX495639	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	3	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199231	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001171/SRR1199231	GSM1350504	SRA147084	SRX495640	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	4	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199232	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199232	GSM1350505	SRA147084	SRX495641	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	5	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199233	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199233	GSM1350506	SRA147084	SRX495642	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	6	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199234	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001171/SRR1199234	GSM1350506	SRA147084	SRX495642	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	7	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199235	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199235	GSM1350507	SRA147084	SRX495643	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	8	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199236	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199236	GSM1350508	SRA147084	SRX495644	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	9	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793867	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793867	GSM1350508	SRA147084	SRX495644	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	10	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793868	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793868	GSM1350509	SRA147084	SRX495645	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	11	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199237	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001171/SRR1199237	GSM1350509	SRA147084	SRX495645	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	12	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199238	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001171/SRR1199238	GSM1350510	SRA147084	SRX495646	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	13	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793869	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793869	GSM1350510	SRA147084	SRX495646	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	14	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793870	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793870	GSM1350511	SRA147084	SRX495647	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	15	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199239	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/001171/SRR1199239	GSM1350511	SRA147084	SRX495647	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	16	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199240	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/001171/SRR1199240	GSM1350512	SRA147084	SRX495648	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	17	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793871	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793871	GSM1350512	SRA147084	SRX495648	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	18	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793933	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793933	GSM1350512	SRA147084	SRX495648	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	19	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793935	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/001751/SRR1793935	GSM1350512	SRA147084	SRX495648	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	20	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793872	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793872	GSM1350513	SRA147084	SRX495649	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	21	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199241	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199241	GSM1350513	SRA147084	SRX495649	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	22	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199242	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199242	GSM1350514	SRA147084	SRX495650	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	23	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793873	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793873	GSM1350514	SRA147084	SRX495650	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	24	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793874	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793874	GSM1350515	SRA147084	SRX495651	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	25	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199243	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199243	GSM1350515	SRA147084	SRX495651	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	26	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199244	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001171/SRR1199244	GSM1350516	SRA147084	SRX495652	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	27	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793875	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001751/SRR1793875	GSM1350516	SRA147084	SRX495652	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	28	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793828	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/001751/SRR1793828	GSM1350517	SRA147084	SRX495653	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	29	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199245	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001171/SRR1199245	GSM1350517	SRA147084	SRX495653	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	30	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199246	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/001171/SRR1199246	GSM1350518	SRA147084	SRX495654	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	31	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793829	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/001751/SRR1793829	GSM1350518	SRA147084	SRX495654	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	32	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1793830	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/001751/SRR1793830	GSM1350519	SRA147084	SRX495655	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	33	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199247	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/001171/SRR1199247	GSM1350519	SRA147084	SRX495655	ChIP-Seq	PAIRED	SRP040298	PRJNA242234
56000	34	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199248	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199248	GSM1350520	SRA147084	SRX495656	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	35	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199249	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199249	GSM1350521	SRA147084	SRX495657	ChIP-Seq	SINGLE	SRP040298	PRJNA242234
56000	36	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199250	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199250	GSM1350522	SRA147084	SRX495658	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56000	37	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199251	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199251	GSM1350522	SRA147084	SRX495658	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56000	38	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199252	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199252	GSM1350523	SRA147084	SRX495659	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56000	39	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199253	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199253	GSM1350523	SRA147084	SRX495659	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56000	40	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199254	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199254	GSM1350524	SRA147084	SRX495660	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56000	41	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199255	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199255	GSM1350524	SRA147084	SRX495660	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56000	42	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199256	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199256	GSM1350525	SRA147084	SRX495661	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56000	43	Julie Baker	Enhancer chromatin signatures predict Smad2/3 binding in Xenopus	In this study we have examine the deposition of H3K4me1,H3K4Me3 and H3K27Ac and the Nodal transcription factor, Smad2/3, immediately following zygotic	Julie Baker, Rakhi Gupta	We profiled 4 histone modifications (H3K4Me3, H3K27Me3, H3K27AC, H3K4Me1) and one transcription factor smad2/3 (+ chromatin input) using ChIP-Seq, and expression profiles (3' RNA-Seq) for Xenopus tropicalis embryos stage8, stage9 and stage10.5. Furthermore, we have profile two histone modifications (H3K4Me1 and H3K27Ac) in absance of nodal signaling in stage9 Xenopus tropicalis embryos using ChIP-seq and 3-seq	25205067	49423	SRP040298	SRR1199257	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001171/SRR1199257	GSM1350525	SRA147084	SRX495661	RNA-Seq	SINGLE	SRP040298	PRJNA242234
56169	1	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204599	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001176/SRR1204599	GSM1357032	SRA149110	SRX500916	ChIP-Seq	SINGLE	SRP040548	PRJNA242626
56169	2	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204600	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204600	GSM1357033	SRA149110	SRX500917	ChIP-Seq	SINGLE	SRP040548	PRJNA242626
56169	3	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204601	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204601	GSM1357034	SRA149110	SRX500918	ChIP-Seq	SINGLE	SRP040548	PRJNA242626
56169	4	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204602	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204602	GSM1357035	SRA149110	SRX500919	ChIP-Seq	SINGLE	SRP040548	PRJNA242626
56169	5	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204604	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204604	GSM1357037	SRA149110	SRX500921	ChIP-Seq	SINGLE	SRP040548	PRJNA242626
56169	6	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204605	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204605	GSM1357038	SRA149110	SRX500922	ChIP-Seq	SINGLE	SRP040548	PRJNA242626
56169	7	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204606	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204606	GSM1357039	SRA149110	SRX500923	RNA-Seq	SINGLE	SRP040548	PRJNA242626
56169	8	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204607	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204607	GSM1357040	SRA149110	SRX500924	RNA-Seq	SINGLE	SRP040548	PRJNA242626
56169	9	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204608	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204608	GSM1357041	SRA149110	SRX500925	RNA-Seq	SINGLE	SRP040548	PRJNA242626
56169	10	Andrea Wills	E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty	We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription 	Andrea Wills, Andrea Wills, Julie Baker	For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos.  For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.	25669884	50519	SRP040548	SRR1204609	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/001176/SRR1204609	GSM1357042	SRA149110	SRX500926	RNA-Seq	SINGLE	SRP040548	PRJNA242626
56242	1	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205735	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205735	GSM1357541	SRA149315	SRX501597	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	2	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205736	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205736	GSM1357542	SRA149315	SRX501598	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	3	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205737	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205737	GSM1357543	SRA149315	SRX501599	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	4	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205738	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205738	GSM1357544	SRA149315	SRX501600	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	5	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205739	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205739	GSM1357545	SRA149315	SRX501601	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	6	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205740	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205740	GSM1357546	SRA149315	SRX501602	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	7	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205741	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205741	GSM1357547	SRA149315	SRX501603	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	8	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205742	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205742	GSM1357548	SRA149315	SRX501604	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	9	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205743	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205743	GSM1357549	SRA149315	SRX501605	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	10	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205744	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205744	GSM1357550	SRA149315	SRX501606	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	11	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205745	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205745	GSM1357551	SRA149315	SRX501607	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	12	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205746	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205746	GSM1357552	SRA149315	SRX501608	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	13	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205747	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205747	GSM1357553	SRA149315	SRX501609	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	14	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205748	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205748	GSM1357554	SRA149315	SRX501610	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	15	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205749	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205749	GSM1357555	SRA149315	SRX501611	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	16	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205750	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205750	GSM1357556	SRA149315	SRX501612	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	17	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205751	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205751	GSM1357557	SRA149315	SRX501613	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	18	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205752	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205752	GSM1357558	SRA149315	SRX501614	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	19	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205753	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205753	GSM1357559	SRA149315	SRX501615	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	20	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205754	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205754	GSM1357560	SRA149315	SRX501616	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	21	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205755	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205755	GSM1357561	SRA149315	SRX501617	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	22	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205756	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205756	GSM1357562	SRA149315	SRX501618	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	23	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205757	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205757	GSM1357563	SRA149315	SRX501619	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	24	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205758	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/001177/SRR1205758	GSM1357564	SRA149315	SRX501620	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	25	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205759	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205759	GSM1357565	SRA149315	SRX501621	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	26	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205760	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205760	GSM1357566	SRA149315	SRX501622	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	27	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205761	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205761	GSM1357567	SRA149315	SRX501623	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	28	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205762	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205762	GSM1357568	SRA149315	SRX501624	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	29	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205763	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205763	GSM1357569	SRA149315	SRX501625	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	30	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205764	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205764	GSM1357570	SRA149315	SRX501626	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	31	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205765	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205765	GSM1357571	SRA149315	SRX501627	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	32	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205766	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205766	GSM1357572	SRA149315	SRX501628	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	33	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205767	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205767	GSM1357573	SRA149315	SRX501629	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	34	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205768	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205768	GSM1357574	SRA149315	SRX501630	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	35	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205769	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205769	GSM1357575	SRA149315	SRX501631	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	36	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205770	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205770	GSM1357576	SRA149315	SRX501632	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	37	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205771	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205771	GSM1357577	SRA149315	SRX501633	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	38	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205772	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205772	GSM1357578	SRA149315	SRX501634	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	39	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205773	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205773	GSM1357579	SRA149315	SRX501635	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	40	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205774	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205774	GSM1357580	SRA149315	SRX501636	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	41	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205775	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205775	GSM1357581	SRA149315	SRX501637	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	42	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205776	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205776	GSM1357582	SRA149315	SRX501638	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	43	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205777	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205777	GSM1357583	SRA149315	SRX501639	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	44	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205778	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205778	GSM1357584	SRA149315	SRX501640	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	45	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205779	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205779	GSM1357585	SRA149315	SRX501641	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	46	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205780	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205780	GSM1357586	SRA149315	SRX501642	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	47	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205781	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205781	GSM1357587	SRA149315	SRX501643	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	48	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205782	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205782	GSM1357588	SRA149315	SRX501644	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	49	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205783	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205783	GSM1357589	SRA149315	SRX501645	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	50	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205784	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205784	GSM1357590	SRA149315	SRX501646	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	51	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205785	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205785	GSM1357591	SRA149315	SRX501647	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56242	52	Mike Gilchrist	High-resolution analysis of gene activity during the Xenopus mid-blastula transition	The Xenopus mid-blastula transition (MBT) marks the onset of large-scale zygotic transcription, as well as an increase in cell cycle length and a loss	Mike Gilchrist, Clara Collart, Nick Owens, Leena Bhaw-Rosun, Brook Cooper, Elena De Domenico, Ilya Patrushev, Abdul Sesay, James Smith, James Smith, Michael Gilchrist	Time series polyA+ and RiboZero RNA sequencing of Xenopus Embryos covering 0-9.5 hours post fertilization	24757007	48872	SRP040589	SRR1205786	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001177/SRR1205786	GSM1357592	SRA149315	SRX501648	RNA-Seq	PAIRED	SRP040589	PRJNA242712
56586	1	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1222414	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001193/SRR1222414	GSM1364749	SRA156772	SRX512838	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	2	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1222415	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001193/SRR1222415	GSM1364750	SRA156772	SRX512839	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	3	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1222416	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001193/SRR1222416	GSM1364751	SRA156772	SRX512840	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	4	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1222417	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001193/SRR1222417	GSM1364752	SRA156772	SRX512841	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	5	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1222418	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001193/SRR1222418	GSM1364753	SRA156772	SRX512842	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	6	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509447	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509447	GSM1430926	SRA156772	SRX648247	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	7	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509448	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509448	GSM1430927	SRA156772	SRX648248	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	8	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509449	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509449	GSM1430928	SRA156772	SRX648249	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	9	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509450	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509450	GSM1430929	SRA156772	SRX648250	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	10	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509451	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509451	GSM1430930	SRA156772	SRX648251	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	11	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509452	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509452	GSM1430931	SRA156772	SRX648252	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	12	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509453	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509453	GSM1430932	SRA156772	SRX648253	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56586	13	Gert Jan Veenstra	Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs	Recent developments in genomic sequencing technology have enabled comprehensive transcriptome analyses of single cells. In contrast, single cell prote	Gert Jan Veenstra, Arne Smits, Rik Lindeboom, Matteo Perino, Simon van Heeringen, GertJan Veenstra, Michiel Vermeulen	RNA-seq in Xenopus laevis of 5 replicates of both single eggs and single embryos.	25056316	49279	SRP041021	SRR1509454	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001474/SRR1509454	GSM1430933	SRA156772	SRX648254	RNA-Seq	SINGLE	SRP041021	PRJNA244000
56680	1	Maria Warnefors	MicroRNA editing in Xenopus tropicalis	We collected small RNA sequencing data from brain and heart of an adult Xenopus tropicalis individual to investigate the conservation of site-specific	Maria Warnefors, Angélica Liechti, Jean Halbert, Delphine Valloton, Henrik Kaessmann	Sequencing of 2 small RNA sequencing libraries	24964909	50469	SRP041076	SRR1231993	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001203/SRR1231993	GSM1366781	SRA157273	SRX514968	miRNA-Seq	SINGLE	SRP041076	PRJNA244299
56680	2	Maria Warnefors	MicroRNA editing in Xenopus tropicalis	We collected small RNA sequencing data from brain and heart of an adult Xenopus tropicalis individual to investigate the conservation of site-specific	Maria Warnefors, Angélica Liechti, Jean Halbert, Delphine Valloton, Henrik Kaessmann	Sequencing of 2 small RNA sequencing libraries	24964909	50469	SRP041076	SRR1231994	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/001203/SRR1231994	GSM1366782	SRA157273	SRX514969	miRNA-Seq	SINGLE	SRP041076	PRJNA244299
58420	1	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382030	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382030	GSM1410597	SRA170144	SRX591680	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	2	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382031	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382031	GSM1410598	SRA170144	SRX591681	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	3	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382032	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382032	GSM1410599	SRA170144	SRX591682	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	4	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382033	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382033	GSM1410600	SRA170144	SRX591683	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	5	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382034	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382034	GSM1410601	SRA170144	SRX591684	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	6	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382035	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382035	GSM1410602	SRA170144	SRX591685	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	7	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382036	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382036	GSM1410603	SRA170144	SRX591686	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	8	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382037	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382037	GSM1410604	SRA170144	SRX591687	RNA-Seq	PAIRED	SRP043147	PRJNA252563
58420	9	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382038	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382038	GSM1410605	SRA170144	SRX591688	RNA-Seq	SINGLE	SRP043147	PRJNA252563
58420	10	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382039	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382039	GSM1410606	SRA170144	SRX591689	RNA-Seq	SINGLE	SRP043147	PRJNA252563
58420	11	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382040	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382040	GSM1410607	SRA170144	SRX591690	RNA-Seq	SINGLE	SRP043147	PRJNA252563
58420	12	Gabriela Salinas-Riester	Next generation sequencing identifies differentially localized transcripts in Xenopus laevis and Xenopus tropicalis oocytes	RNA-seq technology was used to identify differentially localized transcripts from Xenopus laevis and Xenopus tropicalis stage VI oocytes. Besides the 	Gabriela Salinas-Riester, Maike Claußen, Tomas Pieler	mRNA profiles of Xenopus laevis and Xenopus tropicalis animal and vegetal oocyte halves were generated by RNA-seq technology. For Xenopus laevis, animal and vegetal oocyte RNA preparations from two different females were generated in duplicates. For Xenopus tropicalis, animal and vegetal oocyte RNA preparations from two different females were analyzed.	26337391	51224	SRP043147	SRR1382041	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/001349/SRR1382041	GSM1410608	SRA170144	SRX591691	RNA-Seq	SINGLE	SRP043147	PRJNA252563
59309	1	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511454	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511454	GSM1434771	SRA174832	SRX649157	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	2	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511455	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511455	GSM1434772	SRA174832	SRX649158	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	3	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511456	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511456	GSM1434773	SRA174832	SRX649159	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	4	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511457	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511457	GSM1434774	SRA174832	SRX649160	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	5	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511458	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511458	GSM1434775	SRA174832	SRX649161	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	6	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511459	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511459	GSM1434776	SRA174832	SRX649162	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	7	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511460	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511460	GSM1434777	SRA174832	SRX649163	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	8	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511461	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511461	GSM1434778	SRA174832	SRX649164	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	9	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511462	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511462	GSM1434779	SRA174832	SRX649165	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	10	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511463	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511463	GSM1434780	SRA174832	SRX649166	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	11	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511464	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511464	GSM1434781	SRA174832	SRX649167	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	12	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511465	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511465	GSM1434782	SRA174832	SRX649168	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	13	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511466	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511466	GSM1434783	SRA174832	SRX649169	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	14	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511467	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511467	GSM1434784	SRA174832	SRX649170	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	15	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511468	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511468	GSM1434785	SRA174832	SRX649171	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	16	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511469	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511469	GSM1434786	SRA174832	SRX649172	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	17	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511470	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511470	GSM1434787	SRA174832	SRX649173	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	18	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511471	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511471	GSM1434788	SRA174832	SRX649174	RNA-Seq	SINGLE	SRP044238	PRJNA255038
59309	19	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511472	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511472	GSM1434789	SRA174832	SRX649175	ChIP-Seq	SINGLE	SRP044238	PRJNA255038
59309	20	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511473	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511473	GSM1434789	SRA174832	SRX649175	ChIP-Seq	SINGLE	SRP044238	PRJNA255038
59309	21	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511474	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511474	GSM1434790	SRA174832	SRX649176	ChIP-Seq	SINGLE	SRP044238	PRJNA255038
59309	22	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511475	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511475	GSM1434790	SRA174832	SRX649176	ChIP-Seq	SINGLE	SRP044238	PRJNA255038
59309	23	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511476	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511476	GSM1434791	SRA174832	SRX649177	ChIP-Seq	SINGLE	SRP044238	PRJNA255038
59309	24	Ian Quigley	Multicilin drives centriole biogenesis via E2f proteins	Biochemistry suggests e2f4 forms a complex with the coiled-coiled protein multicilin (MCIDAS), a protein that is necessary and sufficient to specify m	Ian Quigley, Lina Ma, Chris Kintner	RNAseq: misexpression of multicilin-HGR +/- dominant-negative e2f4 messenger RNAs in X. laevis animal caps, multicilin induced with dexamethasone at mid-stage 11 and harvested at 3 timepoints (3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18) with 3 biological replicates.
ChIPseq: misexpression of e2f4-GFP +/- multicilin-HGR messenger RNAs in X. laevis animal caps, multicilin induced at mid-stage 11 and harvested at one timepoint (6 hours after induction, roughly corresponding to stage 16), immunoprecipitated with anti-GFP and sequenced;  2 biological replicates. Background was input prior to IP.	24934224	49750	SRP044238	SRR1511477	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001476/SRR1511477	GSM1434792	SRA174832	SRX649178	ChIP-Seq	SINGLE	SRP044238	PRJNA255038
63228	1	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649292	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649292	GSM1544070	SRA200904	SRX758227	RNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	2	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649293	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649293	GSM1544071	SRA200904	SRX758228	RNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	3	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649294	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649294	GSM1544072	SRA200904	SRX758229	RNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	4	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649295	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649295	GSM1544073	SRA200904	SRX758230	RNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	5	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649296	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649296	GSM1544074	SRA200904	SRX758231	RNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	6	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649297	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649297	GSM1544075	SRA200904	SRX758232	RNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	7	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649298	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649298	GSM1544076	SRA200904	SRX758233	ncRNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	8	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649299	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649299	GSM1544077	SRA200904	SRX758234	ncRNA-Seq	SINGLE	SRP049739	PRJNA267016
63228	9	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649300	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649300	GSM1544078	SRA200904	SRX758235	RIP-Seq	SINGLE	SRP049739	PRJNA267016
63228	10	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649301	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649301	GSM1544079	SRA200904	SRX758236	RIP-Seq	SINGLE	SRP049739	PRJNA267016
63228	11	Nelson Lau	Xenopus Piwi protein associated transcripts indicate regulation beyond transposons	This study examines the population of transcripts associated with the Xenopus Piwi proteins, Xiwi and Xili, from X.laevis and X.tropicalis. RIP-seq, C	Nelson Lau, Trey Toombs, Yuliya Sytnkova, Gungwei Chirn, Michael Blower	We performed several replicates of a Piw CLIP-Seq experiment to isolate RNA fragments as CLIP-tags to discover which transcripts are preferentially bound by the Piwi protein.  Then we performed several types of mRNA expression profiling experiments using several forms of mRNA-Seq library construction formats.  Finally, we sequenced the piRNAs from the OSS cells	28031481	52877	SRP049739	SRR1649302	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/001610/SRR1649302	GSM1544080	SRA200904	SRX758237	RNA-Seq	SINGLE	SRP049739	PRJNA267016
64551	1	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736289	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736289	GSM1574071	SRA221631	SRX825218	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	2	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736290	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736290	GSM1574072	SRA221631	SRX825219	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	3	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736291	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736291	GSM1574073	SRA221631	SRX825220	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	4	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736292	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736292	GSM1574074	SRA221631	SRX825221	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	5	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736293	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736293	GSM1574075	SRA221631	SRX825222	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	6	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736294	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736294	GSM1574076	SRA221631	SRX825223	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	7	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736295	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736295	GSM1574077	SRA221631	SRX825224	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	8	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736296	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736296	GSM1574078	SRA221631	SRX825225	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	9	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736297	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736297	GSM1574079	SRA221631	SRX825226	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	10	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736298	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736298	GSM1574080	SRA221631	SRX825227	RNA-Seq	SINGLE	SRP051597	PRJNA271289
64551	11	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736299	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736299	GSM1574081	SRA221631	SRX825228	ChIP-Seq	SINGLE	SRP051597	PRJNA271289
64551	12	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736300	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736300	GSM1574082	SRA221631	SRX825229	ChIP-Seq	SINGLE	SRP051597	PRJNA271289
64551	13	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736301	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736301	GSM1574083	SRA221631	SRX825230	ChIP-Seq	SINGLE	SRP051597	PRJNA271289
64551	14	Ian Quigley	Occupancy and transcriptional profile of Prdm12 in posteriorized neural tissue	V1 interneurons are a class of inhibitory neurons that play an essential role in vertebrate locomotion; however, the factors contributing to their spe	Ian Quigley, Kristine Henningfeld, Chris Kintner, Eric Bellefroid, Claude Van Campenhout	X. laevis embryos were injected with mRNAs encoding prdm12 constructs, along with the bmp inhibitor noggin. Presumptive ectoderm (neuralized by noggin) was dissected and treated with retinoic acid. Samples were then processed into RNAseq libraries or prdm12-FLAG was immunoprecipitated and its targets sequenced. Background was input prior to IP.	26443638	51355	SRP051597	SRR1736302	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/001695/SRR1736302	GSM1574084	SRA221631	SRX825231	ChIP-Seq	SINGLE	SRP051597	PRJNA271289
65785	1	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795628	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795628	GSM1606268	SRA237121	SRX870931	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	2	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795629	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795629	GSM1606269	SRA237121	SRX870932	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	3	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795630	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795630	GSM1606270	SRA237121	SRX870933	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	4	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795631	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795631	GSM1606271	SRA237121	SRX870934	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	5	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795632	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795632	GSM1606272	SRA237121	SRX870935	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	6	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795633	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795633	GSM1606273	SRA237121	SRX870936	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	7	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795634	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795634	GSM1606274	SRA237121	SRX870937	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	8	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795635	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795635	GSM1606275	SRA237121	SRX870938	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	9	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795636	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795636	GSM1606276	SRA237121	SRX870939	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	10	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795637	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795637	GSM1606277	SRA237121	SRX870940	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	11	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795638	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795638	GSM1606278	SRA237121	SRX870941	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	12	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795639	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795639	GSM1606279	SRA237121	SRX870942	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	13	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795640	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795640	GSM1606280	SRA237121	SRX870943	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	14	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795641	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795641	GSM1606281	SRA237121	SRX870944	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	15	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795642	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795642	GSM1606282	SRA237121	SRX870945	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	16	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795643	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795643	GSM1606283	SRA237121	SRX870946	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	17	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795644	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795644	GSM1606284	SRA237121	SRX870947	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	18	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795645	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795645	GSM1606285	SRA237121	SRX870948	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	19	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795646	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795646	GSM1606286	SRA237121	SRX870949	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	20	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795647	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795647	GSM1606287	SRA237121	SRX870950	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	21	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795648	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795648	GSM1606288	SRA237121	SRX870951	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	22	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795649	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795649	GSM1606289	SRA237121	SRX870952	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	23	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795650	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795650	GSM1606290	SRA237121	SRX870953	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	24	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795651	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795651	GSM1606291	SRA237121	SRX870954	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	25	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795652	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795652	GSM1606292	SRA237121	SRX870955	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	26	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795653	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795653	GSM1606293	SRA237121	SRX870956	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	27	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795654	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795654	GSM1606294	SRA237121	SRX870957	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	28	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795655	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795655	GSM1606295	SRA237121	SRX870958	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	29	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795656	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795656	GSM1606296	SRA237121	SRX870959	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	30	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795657	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795657	GSM1606297	SRA237121	SRX870960	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	31	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795658	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795658	GSM1606298	SRA237121	SRX870961	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	32	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795659	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795659	GSM1606299	SRA237121	SRX870962	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	33	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795660	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795660	GSM1606300	SRA237121	SRX870963	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	34	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795661	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795661	GSM1606301	SRA237121	SRX870964	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	35	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795662	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795662	GSM1606302	SRA237121	SRX870965	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	36	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795663	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795663	GSM1606303	SRA237121	SRX870966	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	37	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795664	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795664	GSM1606304	SRA237121	SRX870967	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	38	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795665	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795665	GSM1606305	SRA237121	SRX870968	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	39	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795666	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795666	GSM1606306	SRA237121	SRX870969	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	40	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795667	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795667	GSM1606307	SRA237121	SRX870970	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	41	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795668	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795668	GSM1606308	SRA237121	SRX870971	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	42	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795669	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795669	GSM1606309	SRA237121	SRX870972	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	43	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795670	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795670	GSM1606310	SRA237121	SRX870973	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	44	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795671	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795671	GSM1606311	SRA237121	SRX870974	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	45	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795672	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795672	GSM1606312	SRA237121	SRX870975	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	46	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795673	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795673	GSM1606313	SRA237121	SRX870976	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	47	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795674	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795674	GSM1606314	SRA237121	SRX870977	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	48	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795675	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795675	GSM1606315	SRA237121	SRX870978	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	49	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795676	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795676	GSM1606316	SRA237121	SRX870979	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	50	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795677	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795677	GSM1606317	SRA237121	SRX870980	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	51	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795678	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795678	GSM1606318	SRA237121	SRX870981	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	52	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795679	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795679	GSM1606319	SRA237121	SRX870982	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	53	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795680	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795680	GSM1606320	SRA237121	SRX870983	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	54	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795681	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795681	GSM1606321	SRA237121	SRX870984	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	55	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795682	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795682	GSM1606322	SRA237121	SRX870985	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	56	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795683	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795683	GSM1606323	SRA237121	SRX870986	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	57	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795684	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795684	GSM1606324	SRA237121	SRX870987	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	58	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795685	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795685	GSM1606325	SRA237121	SRX870988	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	59	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795686	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795686	GSM1606326	SRA237121	SRX870989	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	60	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795687	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795687	GSM1606327	SRA237121	SRX870990	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	61	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795688	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795688	GSM1606328	SRA237121	SRX870991	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	62	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795689	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795689	GSM1606329	SRA237121	SRX870992	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	63	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795690	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795690	GSM1606330	SRA237121	SRX870993	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	64	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795691	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795691	GSM1606331	SRA237121	SRX870994	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	65	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795692	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795692	GSM1606332	SRA237121	SRX870995	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	66	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795693	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795693	GSM1606333	SRA237121	SRX870996	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	67	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795694	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795694	GSM1606334	SRA237121	SRX870997	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	68	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795695	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795695	GSM1606335	SRA237121	SRX870998	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	69	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795696	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795696	GSM1606336	SRA237121	SRX870999	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	70	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795697	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795697	GSM1606337	SRA237121	SRX871000	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	71	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795698	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795698	GSM1606338	SRA237121	SRX871001	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	72	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR2972862	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002903/SRR2972862	GSM1606339	SRA237121	SRX871002	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	73	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR2972863	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002903/SRR2972863	GSM1606340	SRA237121	SRX871003	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	74	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795701	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795701	GSM1606341	SRA237121	SRX871004	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	75	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795702	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795702	GSM1606342	SRA237121	SRX871005	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	76	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795703	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795703	GSM1606343	SRA237121	SRX871006	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	77	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795704	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795704	GSM1606344	SRA237121	SRX871007	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	78	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795705	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795705	GSM1606345	SRA237121	SRX871008	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	79	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795706	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795706	GSM1606346	SRA237121	SRX871009	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	80	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795707	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795707	GSM1606347	SRA237121	SRX871010	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	81	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795708	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795708	GSM1606348	SRA237121	SRX871011	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	82	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795709	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795709	GSM1606349	SRA237121	SRX871012	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	83	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795710	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795710	GSM1606350	SRA237121	SRX871013	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	84	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795711	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795711	GSM1606351	SRA237121	SRX871014	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	85	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795712	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795712	GSM1606352	SRA237121	SRX871015	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	86	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795713	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795713	GSM1606353	SRA237121	SRX871016	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	87	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR2972864	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002903/SRR2972864	GSM1606354	SRA237121	SRX871017	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	88	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR2972865	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002903/SRR2972865	GSM1606355	SRA237121	SRX871018	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	89	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795716	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795716	GSM1606356	SRA237121	SRX871019	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	90	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795717	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795717	GSM1606357	SRA237121	SRX871020	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	91	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795718	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795718	GSM1606358	SRA237121	SRX871021	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	92	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795719	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795719	GSM1606359	SRA237121	SRX871022	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	93	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795720	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795720	GSM1606360	SRA237121	SRX871023	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	94	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795721	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795721	GSM1606361	SRA237121	SRX871024	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	95	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795722	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795722	GSM1606362	SRA237121	SRX871025	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	96	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795723	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795723	GSM1606363	SRA237121	SRX871026	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	97	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795724	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795724	GSM1606364	SRA237121	SRX871027	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	98	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795725	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795725	GSM1606365	SRA237121	SRX871028	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	99	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795726	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795726	GSM1606366	SRA237121	SRX871029	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	100	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795727	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795727	GSM1606367	SRA237121	SRX871030	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	101	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795535	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795535	GSM1606175	SRA237121	SRX870838	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	102	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795536	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795536	GSM1606176	SRA237121	SRX870839	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	103	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795537	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795537	GSM1606177	SRA237121	SRX870840	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	104	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795538	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795538	GSM1606178	SRA237121	SRX870841	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	105	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795539	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795539	GSM1606179	SRA237121	SRX870842	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	106	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795540	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795540	GSM1606180	SRA237121	SRX870843	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	107	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795541	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795541	GSM1606181	SRA237121	SRX870844	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	108	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795542	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795542	GSM1606182	SRA237121	SRX870845	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	109	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795543	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795543	GSM1606183	SRA237121	SRX870846	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	110	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795544	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795544	GSM1606184	SRA237121	SRX870847	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	111	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795545	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795545	GSM1606185	SRA237121	SRX870848	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	112	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795546	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795546	GSM1606186	SRA237121	SRX870849	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	113	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795547	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795547	GSM1606187	SRA237121	SRX870850	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	114	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795548	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795548	GSM1606188	SRA237121	SRX870851	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	115	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795549	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795549	GSM1606189	SRA237121	SRX870852	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	116	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795550	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795550	GSM1606190	SRA237121	SRX870853	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	117	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795551	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795551	GSM1606191	SRA237121	SRX870854	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	118	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795552	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795552	GSM1606192	SRA237121	SRX870855	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	119	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795553	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795553	GSM1606193	SRA237121	SRX870856	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	120	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795554	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795554	GSM1606194	SRA237121	SRX870857	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	121	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795555	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795555	GSM1606195	SRA237121	SRX870858	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	122	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795556	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795556	GSM1606196	SRA237121	SRX870859	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	123	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795557	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795557	GSM1606197	SRA237121	SRX870860	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	124	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795558	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795558	GSM1606198	SRA237121	SRX870861	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	125	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795559	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795559	GSM1606199	SRA237121	SRX870862	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	126	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795560	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795560	GSM1606200	SRA237121	SRX870863	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	127	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795561	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795561	GSM1606201	SRA237121	SRX870864	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	128	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795562	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795562	GSM1606202	SRA237121	SRX870865	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	129	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795563	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795563	GSM1606203	SRA237121	SRX870866	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	130	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795564	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795564	GSM1606204	SRA237121	SRX870867	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	131	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795565	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795565	GSM1606205	SRA237121	SRX870868	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	132	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795566	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795566	GSM1606206	SRA237121	SRX870869	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	133	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795567	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795567	GSM1606207	SRA237121	SRX870870	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	134	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795568	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795568	GSM1606208	SRA237121	SRX870871	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	135	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795569	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795569	GSM1606209	SRA237121	SRX870872	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	136	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795570	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795570	GSM1606210	SRA237121	SRX870873	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	137	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795571	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795571	GSM1606211	SRA237121	SRX870874	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	138	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795572	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795572	GSM1606212	SRA237121	SRX870875	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	139	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795573	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795573	GSM1606213	SRA237121	SRX870876	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	140	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795574	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795574	GSM1606214	SRA237121	SRX870877	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	141	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795575	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795575	GSM1606215	SRA237121	SRX870878	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	142	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795576	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795576	GSM1606216	SRA237121	SRX870879	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	143	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795577	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795577	GSM1606217	SRA237121	SRX870880	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	144	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795578	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795578	GSM1606218	SRA237121	SRX870881	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	145	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795579	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795579	GSM1606219	SRA237121	SRX870882	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	146	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795580	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795580	GSM1606220	SRA237121	SRX870883	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	147	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795581	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795581	GSM1606221	SRA237121	SRX870884	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	148	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795582	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795582	GSM1606222	SRA237121	SRX870885	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	149	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795583	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795583	GSM1606223	SRA237121	SRX870886	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	150	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795584	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795584	GSM1606224	SRA237121	SRX870887	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	151	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795585	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795585	GSM1606225	SRA237121	SRX870888	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	152	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795586	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795586	GSM1606226	SRA237121	SRX870889	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	153	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795587	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795587	GSM1606227	SRA237121	SRX870890	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	154	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795588	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795588	GSM1606228	SRA237121	SRX870891	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	155	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795589	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795589	GSM1606229	SRA237121	SRX870892	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	156	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795590	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795590	GSM1606230	SRA237121	SRX870893	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	157	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795591	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795591	GSM1606231	SRA237121	SRX870894	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	158	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795592	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795592	GSM1606232	SRA237121	SRX870895	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	159	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795593	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795593	GSM1606233	SRA237121	SRX870896	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	160	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795594	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795594	GSM1606234	SRA237121	SRX870897	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	161	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795595	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795595	GSM1606235	SRA237121	SRX870898	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	162	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795596	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795596	GSM1606236	SRA237121	SRX870899	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	163	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795597	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795597	GSM1606237	SRA237121	SRX870900	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	164	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795598	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795598	GSM1606238	SRA237121	SRX870901	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	165	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795599	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795599	GSM1606239	SRA237121	SRX870902	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	166	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795600	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795600	GSM1606240	SRA237121	SRX870903	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	167	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795601	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795601	GSM1606241	SRA237121	SRX870904	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	168	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795602	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795602	GSM1606242	SRA237121	SRX870905	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	169	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795603	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795603	GSM1606243	SRA237121	SRX870906	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	170	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795604	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795604	GSM1606244	SRA237121	SRX870907	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	171	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795605	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795605	GSM1606245	SRA237121	SRX870908	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	172	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795606	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795606	GSM1606246	SRA237121	SRX870909	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	173	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795607	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795607	GSM1606247	SRA237121	SRX870910	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	174	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795608	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795608	GSM1606248	SRA237121	SRX870911	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	175	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795609	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795609	GSM1606249	SRA237121	SRX870912	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	176	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795610	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795610	GSM1606250	SRA237121	SRX870913	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	177	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795611	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795611	GSM1606251	SRA237121	SRX870914	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	178	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795612	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795612	GSM1606252	SRA237121	SRX870915	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	179	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795613	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795613	GSM1606253	SRA237121	SRX870916	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	180	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795614	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795614	GSM1606254	SRA237121	SRX870917	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	181	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795615	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795615	GSM1606255	SRA237121	SRX870918	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	182	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795616	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795616	GSM1606256	SRA237121	SRX870919	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	183	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795617	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795617	GSM1606257	SRA237121	SRX870920	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	184	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795618	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795618	GSM1606258	SRA237121	SRX870921	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	185	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795619	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795619	GSM1606259	SRA237121	SRX870922	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	186	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795620	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795620	GSM1606260	SRA237121	SRX870923	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	187	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795621	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795621	GSM1606261	SRA237121	SRX870924	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	188	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795622	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795622	GSM1606262	SRA237121	SRX870925	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	189	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795623	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795623	GSM1606263	SRA237121	SRX870926	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	190	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795624	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795624	GSM1606264	SRA237121	SRX870927	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	191	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795625	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795625	GSM1606265	SRA237121	SRX870928	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	192	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795626	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795626	GSM1606266	SRA237121	SRX870929	RNA-Seq	PAIRED	SRP053406	PRJNA275011
65785	193	Mike Gilchrist	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development	Transcript regulation is essential for cell function, and misregulation can lead to disease. Despite technologies to survey the transcriptome, we lack	Mike Gilchrist, Nick Owens, Ira Blitz, Maura Lane, Ilya Patrushev, John Overton, Michael Gilchrist, Ken Cho, Mustafa Khokha	High Resolution Time series covering the first 66 hours of development of Xenopus tropicalis with PolyA+ and ribosomal depletion sequencing.	26774488	51804	SRP053406	SRR1795627	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/001753/SRR1795627	GSM1606267	SRA237121	SRX870930	RNA-Seq	PAIRED	SRP053406	PRJNA275011
67974	1	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980165	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980165	GSM1659896	SRA259887	SRX999324	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	2	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980166	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980166	GSM1659897	SRA259887	SRX999325	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	3	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980167	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980167	GSM1659898	SRA259887	SRX999326	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	4	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980168	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980168	GSM1659899	SRA259887	SRX999327	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	5	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980169	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980169	GSM1659900	SRA259887	SRX999328	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	6	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980170	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980170	GSM1659901	SRA259887	SRX999329	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	7	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980171	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980171	GSM1659902	SRA259887	SRX999330	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	8	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980172	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980172	GSM1659903	SRA259887	SRX999331	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	9	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980173	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980173	GSM1659904	SRA259887	SRX999332	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	10	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980174	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980174	GSM1659905	SRA259887	SRX999333	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	11	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980175	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001933/SRR1980175	GSM1659906	SRA259887	SRX999334	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	12	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980176	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001933/SRR1980176	GSM1659907	SRA259887	SRX999335	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	13	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980177	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/001933/SRR1980177	GSM1659908	SRA259887	SRX999336	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	14	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980178	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980178	GSM1659909	SRA259887	SRX999337	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	15	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980179	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980179	GSM1659910	SRA259887	SRX999338	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	16	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980180	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980180	GSM1659911	SRA259887	SRX999339	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	17	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980181	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980181	GSM1659912	SRA259887	SRX999340	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	18	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980182	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980182	GSM1659913	SRA259887	SRX999341	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	19	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980183	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980183	GSM1659914	SRA259887	SRX999342	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	20	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980184	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980184	GSM1659915	SRA259887	SRX999343	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	21	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980185	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980185	GSM1659916	SRA259887	SRX999344	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	22	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980186	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980186	GSM1659917	SRA259887	SRX999345	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	23	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980187	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980187	GSM1659918	SRA259887	SRX999346	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	24	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980188	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980188	GSM1659919	SRA259887	SRX999347	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	25	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980189	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980189	GSM1659920	SRA259887	SRX999348	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	26	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980190	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980190	GSM1659921	SRA259887	SRX999349	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	27	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980191	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980191	GSM1659922	SRA259887	SRX999350	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	28	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980192	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980192	GSM1659923	SRA259887	SRX999351	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	29	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980193	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980193	GSM1659924	SRA259887	SRX999352	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	30	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980194	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980194	GSM1659925	SRA259887	SRX999353	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	31	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980195	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980195	GSM1659926	SRA259887	SRX999354	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	32	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980196	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980196	GSM1659927	SRA259887	SRX999355	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	33	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980197	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980197	GSM1659928	SRA259887	SRX999356	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	34	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980198	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980198	GSM1659929	SRA259887	SRX999357	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	35	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980199	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980199	GSM1659930	SRA259887	SRX999358	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	36	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980200	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980200	GSM1659931	SRA259887	SRX999359	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	37	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980201	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980201	GSM1659932	SRA259887	SRX999360	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	38	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980202	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980202	GSM1659933	SRA259887	SRX999361	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	39	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980203	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980203	GSM1659934	SRA259887	SRX999362	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	40	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980204	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980204	GSM1659935	SRA259887	SRX999363	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	41	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980205	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980205	GSM1659936	SRA259887	SRX999364	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	42	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980206	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980206	GSM1659937	SRA259887	SRX999365	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	43	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980207	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980207	GSM1659938	SRA259887	SRX999366	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	44	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980208	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980208	GSM1659939	SRA259887	SRX999367	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	45	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980209	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980209	GSM1659940	SRA259887	SRX999368	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	46	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980210	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980210	GSM1659941	SRA259887	SRX999369	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	47	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980211	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980211	GSM1659942	SRA259887	SRX999370	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	48	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980212	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980212	GSM1659943	SRA259887	SRX999371	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	49	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980213	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980213	GSM1659944	SRA259887	SRX999372	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	50	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980214	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980214	GSM1659945	SRA259887	SRX999373	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	51	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980215	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980215	GSM1659946	SRA259887	SRX999374	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	52	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980216	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980216	GSM1659947	SRA259887	SRX999375	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	53	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980217	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980217	GSM1659948	SRA259887	SRX999376	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	54	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980218	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980218	GSM1659949	SRA259887	SRX999377	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	55	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980219	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980219	GSM1659950	SRA259887	SRX999378	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	56	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980220	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980220	GSM1659951	SRA259887	SRX999379	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	57	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980221	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980221	GSM1659952	SRA259887	SRX999380	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	58	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980222	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980222	GSM1659953	SRA259887	SRX999381	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	59	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980223	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980223	GSM1659954	SRA259887	SRX999382	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	60	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR1980224	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001933/SRR1980224	GSM1659955	SRA259887	SRX999383	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	61	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2011510	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001964/SRR2011510	GSM1677167	SRA259887	SRX1020033	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	62	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353007	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353007	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	63	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353008	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353008	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	64	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353009	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353009	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	65	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353010	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353010	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	66	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353011	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353011	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	67	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353012	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353012	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	68	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353013	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353013	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	69	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353014	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353014	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	70	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353015	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353015	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	71	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353016	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353016	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	72	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353017	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353017	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	73	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353018	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353018	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	74	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR2353019	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002297/SRR2353019	GSM1875285	SRA259887	SRX1225083	Bisulfite-Seq	SINGLE	SRP057395	PRJNA281501
67974	75	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027514	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002956/SRR3027514	GSM1974223	SRA259887	SRX1488584	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	76	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027515	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002956/SRR3027515	GSM1974224	SRA259887	SRX1488585	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	77	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027516	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002956/SRR3027516	GSM1974225	SRA259887	SRX1488586	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	78	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027517	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002956/SRR3027517	GSM1974226	SRA259887	SRX1488587	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	79	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027518	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002956/SRR3027518	GSM1974227	SRA259887	SRX1488588	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	80	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027519	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002956/SRR3027519	GSM1974228	SRA259887	SRX1488589	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	81	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027520	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002956/SRR3027520	GSM1974229	SRA259887	SRX1488590	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	82	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027521	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002956/SRR3027521	GSM1974230	SRA259887	SRX1488591	ChIP-Seq	SINGLE	SRP057395	PRJNA281501
67974	83	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027522	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002956/SRR3027522	GSM1974231	SRA259887	SRX1488592	RNA-Seq	SINGLE	SRP057395	PRJNA281501
67974	84	Saartje Hontelez	Embryonic transcription is controlled by maternally defined chromatin state	During development histone modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origi	Saartje Hontelez, GertJan Veenstra	We have performed ChIP-sequencing of eight histone modifications, RNA polymerase II (RNAPII) and the enhancer protein p300 at five stages of development: blastula (st. 9), gastrula (st. 10.5, 12.5), neurula (st. 16) and tailbud (st. 30). These experiments allow identification of enhancers (H3K4me1, p300), promoters (H3K4me3, H3K9ac), transcribed regions (H3K36me3, RNAPII) and repressed and heterochromatic domains (H3K27me3, H3K9me2, H3K9me3, H4K20me3). In addition we generated pre-MBT (st. 8) maps for three histone modifications (H3K4me3, H3K9ac, H3K27me3) and single-base resolution DNA methylome maps using whole genome bisulfite sequencing of blastula and gastrula (st. 9 and 10.5) embryos. To determine the maternal and zygotic contributions to chromatin state, we used alpha-amanitin to block embryonic transcription. Fertilised eggs were injected with 2.3 nl of 2.67 ng/ul alpha-amanitin and developed until the control embryos reached mid-gastrulation. Alpha-amanitin and control embryos were used for RNA-seq and ChIP-seq of RNAPII, H3K4me3, H3K27me3 and p300. For all ChIP-seq samples of the epigenome reference maps and RNAPII ChIP-seq samples of the α-amanitin experiments three biological replicates of different chromatin isolations of 45 embryos were pooled. Two biological replicates for H3K4me3 (α-amanitin injected: resp. 90 and 56 embryo equivalents (eeq); control: resp. 45 and 67 eeq), H3K27me3 (α-amanitin injected: resp. 90 and 180 eeq; control: resp. 45 and 202 eeq) and p300 (α-amanitin injected: resp. 112 and 56 eeq; control: resp. 112 and 67 eeq) ChIP-seq samples of the α-amanitin experiments were generated. For RNA-seq samples of the α-amanitin experiments RNA from 5 embryos from one biological replicate was isolated and depleted of ribosomal RNA	26679111	51677	SRP057395	SRR3027523	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002956/SRR3027523	GSM1974232	SRA259887	SRX1488593	RNA-Seq	SINGLE	SRP057395	PRJNA281501
68087	1	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983665	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983665	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	2	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983666	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983666	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	3	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983667	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983667	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	4	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983668	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983668	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	5	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983669	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983669	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	6	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983670	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983670	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	7	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983671	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983671	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	8	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983672	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983672	GSM1662779	SRA260956	SRX1002590	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	9	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983673	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983673	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	10	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983674	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983674	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	11	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983675	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983675	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	12	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983676	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983676	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	13	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983677	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983677	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	14	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983678	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983678	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	15	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983679	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983679	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	16	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983680	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983680	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	17	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983681	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983681	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	18	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983682	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983682	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	19	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983683	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983683	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	20	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983684	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983684	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	21	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983685	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983685	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	22	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983686	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983686	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	23	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983687	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983687	GSM1662780	SRA260956	SRX1002591	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	24	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983688	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983688	GSM1662781	SRA260956	SRX1002592	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	25	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983689	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983689	GSM1662781	SRA260956	SRX1002592	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	26	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983690	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983690	GSM1662781	SRA260956	SRX1002592	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	27	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983691	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983691	GSM1662781	SRA260956	SRX1002592	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	28	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983692	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983692	GSM1662781	SRA260956	SRX1002592	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	29	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983693	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983693	GSM1662781	SRA260956	SRX1002592	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	30	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983694	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983694	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	31	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983695	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983695	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	32	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983696	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983696	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	33	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983697	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983697	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	34	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983698	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983698	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	35	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983699	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983699	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	36	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983700	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983700	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	37	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983701	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983701	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	38	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983702	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983702	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	39	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983703	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983703	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	40	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983704	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983704	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	41	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983705	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983705	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	42	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983706	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983706	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	43	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983707	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983707	GSM1662782	SRA260956	SRX1002593	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	44	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983708	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983708	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	45	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983709	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983709	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	46	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983710	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983710	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	47	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983711	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983711	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	48	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983712	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983712	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	49	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983713	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983713	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	50	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983714	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983714	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	51	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983715	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983715	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	52	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983716	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983716	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	53	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983717	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983717	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	54	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983718	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983718	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	55	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983719	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983719	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	56	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983720	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983720	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	57	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983721	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983721	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	58	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983722	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983722	GSM1662783	SRA260956	SRX1002594	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	59	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983723	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983723	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	60	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983724	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983724	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	61	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983725	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983725	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	62	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983726	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983726	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	63	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983727	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983727	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	64	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983728	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983728	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	65	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983729	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983729	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	66	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983730	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983730	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	67	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983731	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983731	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	68	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983732	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983732	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	69	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983733	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983733	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	70	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983734	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983734	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	71	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983735	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983735	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	72	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983736	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983736	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	73	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983737	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983737	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	74	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983738	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983738	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	75	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983739	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983739	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	76	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983740	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983740	GSM1662784	SRA260956	SRX1002595	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	77	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983741	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983741	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	78	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983742	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983742	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	79	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983743	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983743	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	80	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983744	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983744	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	81	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983745	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983745	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	82	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983746	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983746	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	83	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983747	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983747	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	84	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983748	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983748	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	85	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983749	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983749	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	86	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983750	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983750	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	87	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983751	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983751	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	88	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983752	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983752	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	89	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983753	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983753	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	90	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983754	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983754	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	91	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983755	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983755	GSM1662785	SRA260956	SRX1002596	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	92	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983756	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983756	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	93	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983757	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983757	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	94	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983758	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983758	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	95	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983759	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983759	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	96	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983760	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983760	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	97	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983761	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983761	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	98	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983762	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983762	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	99	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983763	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983763	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	100	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983764	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983764	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	101	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983765	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983765	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	102	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983766	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983766	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	103	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983767	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983767	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	104	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983768	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983768	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	105	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983769	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983769	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	106	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983770	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983770	GSM1662786	SRA260956	SRX1002597	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	107	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983771	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983771	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	108	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983772	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983772	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	109	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983773	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983773	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	110	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983774	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983774	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	111	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983775	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983775	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	112	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983776	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983776	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	113	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983777	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983777	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	114	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983778	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983778	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	115	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983779	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983779	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	116	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983780	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983780	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	117	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983781	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983781	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	118	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983782	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983782	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	119	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983783	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983783	GSM1662787	SRA260956	SRX1002598	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	120	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983784	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983784	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	121	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983785	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983785	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	122	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983786	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983786	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	123	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983787	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983787	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	124	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983788	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983788	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	125	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983789	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983789	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	126	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983790	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983790	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	127	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983791	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983791	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	128	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983792	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983792	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	129	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983793	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983793	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	130	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983794	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983794	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	131	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983795	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983795	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	132	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983796	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983796	GSM1662788	SRA260956	SRX1002599	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	133	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983797	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983797	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	134	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983798	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983798	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	135	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983799	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983799	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	136	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983800	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983800	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	137	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983801	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983801	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	138	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983802	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983802	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	139	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983803	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983803	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	140	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983804	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983804	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	141	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983805	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983805	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	142	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983806	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983806	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	143	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983807	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983807	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	144	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983808	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983808	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	145	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983809	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983809	GSM1662789	SRA260956	SRX1002600	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	146	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983810	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983810	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	147	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983811	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983811	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	148	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983812	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983812	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	149	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983813	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983813	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	150	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983814	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983814	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	151	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983815	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983815	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	152	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983816	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983816	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	153	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983817	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983817	GSM1662790	SRA260956	SRX1002601	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	154	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983818	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983818	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	155	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983819	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983819	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	156	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983820	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983820	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	157	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983821	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983821	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	158	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983822	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983822	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	159	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983823	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983823	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	160	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983824	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983824	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	161	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983825	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983825	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	162	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983826	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983826	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	163	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983827	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983827	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	164	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983828	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983828	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	165	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983829	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983829	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	166	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983830	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983830	GSM1662791	SRA260956	SRX1002602	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	167	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983831	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983831	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	168	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983832	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983832	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	169	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983833	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983833	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	170	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983834	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983834	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	171	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983835	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983835	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	172	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983836	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983836	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	173	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983837	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983837	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	174	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR1983838	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001937/SRR1983838	GSM1662792	SRA260956	SRX1002603	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	175	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179966	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179966	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	176	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179967	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179967	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	177	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179968	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179968	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	178	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179969	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179969	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	179	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179970	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179970	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	180	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179971	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179971	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	181	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179972	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179972	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	182	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179973	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179973	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	183	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179974	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179974	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	184	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179975	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179975	GSM1859497	SRA260956	SRX1162703	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	185	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179976	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179976	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	186	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179977	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179977	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	187	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179978	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179978	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	188	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179979	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179979	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	189	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179980	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179980	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	190	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179981	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179981	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	191	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179982	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179982	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	192	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179983	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179983	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	193	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179984	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179984	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	194	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179985	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179985	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	195	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179986	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179986	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	196	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179987	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179987	GSM1859498	SRA260956	SRX1162704	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	197	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179988	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179988	GSM1859499	SRA260956	SRX1162705	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	198	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179989	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179989	GSM1859499	SRA260956	SRX1162705	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	199	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179990	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179990	GSM1859499	SRA260956	SRX1162705	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	200	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179991	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179991	GSM1859499	SRA260956	SRX1162705	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	201	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179992	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179992	GSM1859499	SRA260956	SRX1162705	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	202	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179993	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179993	GSM1859499	SRA260956	SRX1162705	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	203	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179994	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179994	GSM1859499	SRA260956	SRX1162705	Bisulfite-Seq	SINGLE	SRP057505	PRJNA281741
68087	204	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179995	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179995	GSM1859500	SRA260956	SRX1162706	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	205	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179996	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179996	GSM1859501	SRA260956	SRX1162707	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	206	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179997	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179997	GSM1859502	SRA260956	SRX1162708	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	207	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179998	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179998	GSM1859503	SRA260956	SRX1162709	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	208	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2179999	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2179999	GSM1859504	SRA260956	SRX1162710	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	209	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180000	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180000	GSM1859505	SRA260956	SRX1162711	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	210	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180001	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180001	GSM1859506	SRA260956	SRX1162712	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	211	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180002	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180002	GSM1859507	SRA260956	SRX1162713	RNA-Seq	SINGLE	SRP057505	PRJNA281741
68087	212	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180003	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180003	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	213	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180004	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180004	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	214	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180005	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180005	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	215	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180006	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180006	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	216	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180007	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180007	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	217	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180008	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180008	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	218	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180009	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180009	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	219	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180010	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180010	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	220	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180011	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180011	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	221	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180012	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180012	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	222	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180013	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180013	GSM1859508	SRA260956	SRX1162714	OTHER	SINGLE	SRP057505	PRJNA281741
68087	223	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180014	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180014	GSM1859509	SRA260956	SRX1162715	OTHER	PAIRED	SRP057505	PRJNA281741
68087	224	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180015	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180015	GSM1859510	SRA260956	SRX1162716	OTHER	PAIRED	SRP057505	PRJNA281741
68087	225	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180016	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180016	GSM1859511	SRA260956	SRX1162717	OTHER	PAIRED	SRP057505	PRJNA281741
68087	226	Ozren Bogdanovic	Active DNA demethylation at enhancers during the vertebrate phylotypic period	The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage, however the mechanisms that guide the e	Ozren Bogdanovic, Ryan Lister	MethylC-Seq in zebrafish embryos, MethylC-seq in Xenopus tropicalis embryos, MethylC-seq in mouse embryos, MethylC-seq in zebrafish tissues, MethylC-seq in Xenopus tropicalis tissues, TAB-seq in zebrafish embryos, TAB-seq in Xenopus tropicalis embryos, TAB-seq in mouse embryos, RNA-seq in zebrafish embryos, RNA-seq in mouse embryos	26928226	51922	SRP057505	SRR2180017	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002128/SRR2180017	GSM1859512	SRA260956	SRX1162718	OTHER	PAIRED	SRP057505	PRJNA281741
68972	1	Xiaopeng Ma	The identification of differentially expressed genes between animal and vegetal blastomeres in Xenopus laevis	To identify asymmetrically localized maternal mRNAs along the animal-vegetal axis in cleavage Xenopus embryos, we isolated animal and vegetal blastome	Xiaopeng Ma, Guanni Sun, Zhirui Hu, Zheying Min, Xiaohua Yan, Zhenpo Guan, Hanxia Su, Yu Fu, YeGuang Chen, Michael Zhang, Qinghua Tao, Wei Wu	RNAseq of animal and vegetal blastomeres with 2 biological replicates	26013826	50741	SRP058428	SRR2029779	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/001982/SRR2029779	GSM1689109	SRA268729	SRX1030262	RNA-Seq	PAIRED	SRP058428	PRJNA284242
68972	2	Xiaopeng Ma	The identification of differentially expressed genes between animal and vegetal blastomeres in Xenopus laevis	To identify asymmetrically localized maternal mRNAs along the animal-vegetal axis in cleavage Xenopus embryos, we isolated animal and vegetal blastome	Xiaopeng Ma, Guanni Sun, Zhirui Hu, Zheying Min, Xiaohua Yan, Zhenpo Guan, Hanxia Su, Yu Fu, YeGuang Chen, Michael Zhang, Qinghua Tao, Wei Wu	RNAseq of animal and vegetal blastomeres with 2 biological replicates	26013826	50741	SRP058428	SRR2029780	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/001982/SRR2029780	GSM1689110	SRA268729	SRX1030263	RNA-Seq	PAIRED	SRP058428	PRJNA284242
68972	3	Xiaopeng Ma	The identification of differentially expressed genes between animal and vegetal blastomeres in Xenopus laevis	To identify asymmetrically localized maternal mRNAs along the animal-vegetal axis in cleavage Xenopus embryos, we isolated animal and vegetal blastome	Xiaopeng Ma, Guanni Sun, Zhirui Hu, Zheying Min, Xiaohua Yan, Zhenpo Guan, Hanxia Su, Yu Fu, YeGuang Chen, Michael Zhang, Qinghua Tao, Wei Wu	RNAseq of animal and vegetal blastomeres with 2 biological replicates	26013826	50741	SRP058428	SRR2029781	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001982/SRR2029781	GSM1689111	SRA268729	SRX1030264	RNA-Seq	PAIRED	SRP058428	PRJNA284242
68972	4	Xiaopeng Ma	The identification of differentially expressed genes between animal and vegetal blastomeres in Xenopus laevis	To identify asymmetrically localized maternal mRNAs along the animal-vegetal axis in cleavage Xenopus embryos, we isolated animal and vegetal blastome	Xiaopeng Ma, Guanni Sun, Zhirui Hu, Zheying Min, Xiaohua Yan, Zhenpo Guan, Hanxia Su, Yu Fu, YeGuang Chen, Michael Zhang, Qinghua Tao, Wei Wu	RNAseq of animal and vegetal blastomeres with 2 biological replicates	26013826	50741	SRP058428	SRR2029782	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/001982/SRR2029782	GSM1689112	SRA268729	SRX1030265	RNA-Seq	PAIRED	SRP058428	PRJNA284242
69701	1	Daniel Ramire-Gordillo	RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM® genes for hereditary disorders of hearing and balance	Purpose: To identify orthologous genes in Xenopus that are implicated in deafness and vestibular disorders in humans and to compare RNA-Seq and microa	Daniel Ramire-Gordillo, Daniel Ramirez-Gordillo, TuShun Powers, Casilda Trujillo-Provencio, Jennifer van Velkinburgh, Faye Schilkey, Elba Serrano	Inner ear RNA from X. laevis larval stages 56-58 was isolated and shipped to the National Center for Genome Resources, for Illumina-Solexa sequencing or to the Massachusetts Institute of Technology BioMicro Center for microarray analysis with the Affymetrix GeneChip® X. laevis Genome 2.0 Array. RNA-Sequencing was completed using the Illumina-Solexa platform for sequencing by synthesis.  Short-insert paired end (SIPE) libraries were prepared from total RNA according to Illumina’s mRNA-Seq Sample Prep Protocol v2.0 (Illumina, San Diego, CA, USA).  The resultant double-stranded cDNA concentration was measured on a NanoDrop spectrophotometer, and size and purity were determined on the 2100 Bioanalyzer using a DNA 1000 Nano kit. The cDNA libraries were cluster amplified on Illumina flowcells, sequenced on the GAII Sequencer as 36-cycle single-end reads, and processed using Illumina software v1.0.  Illumina reads were aligned to the X. tropicalis genome using the algorithm for genomic mapping and alignment program (GMAP) and Alpheus® Sequence Variant Detection System v3.1.	26582541	51592	SRP059283	SRR2057655	https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRR/002009/SRR2057655	GSM1707665	SRA272228	SRX1054490	RNA-Seq	SINGLE	SRP059283	PRJNA286217
71006	1	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105075	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105075	GSM1825040	SRA278301	SRX1099252	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	2	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105076	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105076	GSM1825041	SRA278301	SRX1099254	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	3	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105077	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105077	GSM1825042	SRA278301	SRX1099255	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	4	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105078	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105078	GSM1825043	SRA278301	SRX1099256	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	5	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105079	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105079	GSM1825044	SRA278301	SRX1099257	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	6	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105080	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105080	GSM1825045	SRA278301	SRX1099258	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	7	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105081	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105081	GSM1825046	SRA278301	SRX1099259	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	8	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105082	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105082	GSM1825047	SRA278301	SRX1099260	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	9	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105083	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105083	GSM1825048	SRA278301	SRX1099261	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	10	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105084	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105084	GSM1825049	SRA278301	SRX1099262	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	11	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105085	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105085	GSM1825050	SRA278301	SRX1099263	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	12	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105086	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105086	GSM1825051	SRA278301	SRX1099264	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	13	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105087	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105087	GSM1825052	SRA278301	SRX1099265	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	14	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105088	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105088	GSM1825053	SRA278301	SRX1099266	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	15	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105089	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105089	GSM1825054	SRA278301	SRX1099267	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	16	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105090	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105090	GSM1825055	SRA278301	SRX1099268	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	17	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105091	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105091	GSM1825056	SRA278301	SRX1099269	RNA-Seq	PAIRED	SRP061238	PRJNA290093
71006	18	Ferdinand Marlétaz	Cdx ParaHox genes acquired distinct developmental roles after gene duplication in vertebrate evolution	We examined the degree of regulatory and functional overlap between the three vertebrate Cdx genes using single and triple morpholino knock-down in Xe	Ferdinand Marlétaz, Harv Isaacs, Peter Holland	Stage 14 (early neurula) embryos derived from eggs injected with morpholinos against Cdx1, Cdx2, Cdx4 and a mixture of all three plus corresponding uninjected embryos. All in triplicates.	26231746	51076	SRP061238	SRR2105092	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/002055/SRR2105092	GSM1825057	SRA278301	SRX1099270	RNA-Seq	PAIRED	SRP061238	PRJNA290093
72657	1	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230067	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230067	GSM1867400	SRA293747	SRX1178590	ChIP-Seq	SINGLE	SRP063109	PRJNA294599
72657	2	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230068	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230068	GSM1867401	SRA293747	SRX1178591	ChIP-Seq	SINGLE	SRP063109	PRJNA294599
72657	3	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230069	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230069	GSM1867402	SRA293747	SRX1178592	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	4	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230070	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230070	GSM1867403	SRA293747	SRX1178593	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	5	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230071	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230071	GSM1867404	SRA293747	SRX1178594	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	6	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230072	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230072	GSM1867405	SRA293747	SRX1178595	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	7	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230073	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230073	GSM1867406	SRA293747	SRX1178596	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	8	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230074	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230074	GSM1867407	SRA293747	SRX1178597	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	9	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230075	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230075	GSM1867408	SRA293747	SRX1178598	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	10	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230076	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230076	GSM1867409	SRA293747	SRX1178599	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	11	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230077	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230077	GSM1867410	SRA293747	SRX1178600	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	12	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230078	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230078	GSM1867411	SRA293747	SRX1178601	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	13	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230079	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230079	GSM1867412	SRA293747	SRX1178602	RNA-Seq	PAIRED	SRP063109	PRJNA294599
72657	14	Stefan Hoppler	Tissue- and stage-specific cellular context regulates Wnt target gene expression subsequent to β-catenin recruitment	The aim of our study is to identify direct target genes of Wnt/β-catenin signaling operating in gastrula-stage X. tropicalis embryos. We characterize	Stefan Hoppler, Yukio Nakamura, Eduardo Alves	For ChIP-seq, one ChIP DNA and one input control DNA samples pooled from three independent ChIP experiments using early gastrula embryos were sequenced. For RNA-seq, Twelve total RNA samples (triplicates of each experimental samples: uninjected, CoMO-injected, wnt8aMO-injected, wnt8aMO and pCSKA-wnt8a-coinjected) from early gastrula embryos were sequenced.	27068107	52077	SRP063109	SRR2230080	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/002177/SRR2230080	GSM1867413	SRA293747	SRX1178603	RNA-Seq	PAIRED	SRP063109	PRJNA294599
73419	1	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515135	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515135	GSM1893239	SRA300938	SRX1286458	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	2	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515136	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515136	GSM1893240	SRA300938	SRX1286459	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	3	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515137	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515137	GSM1893241	SRA300938	SRX1286460	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	4	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515138	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515138	GSM1893242	SRA300938	SRX1286461	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	5	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515139	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515139	GSM1893243	SRA300938	SRX1286462	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	6	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515140	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515140	GSM1893244	SRA300938	SRX1286463	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	7	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515141	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515141	GSM1893245	SRA300938	SRX1286464	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	8	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515142	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515142	GSM1893246	SRA300938	SRX1286465	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	9	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515143	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515143	GSM1893247	SRA300938	SRX1286466	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	10	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515144	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515144	GSM1893248	SRA300938	SRX1286467	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	11	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515145	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515145	GSM1893249	SRA300938	SRX1286468	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	12	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515146	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515146	GSM1893250	SRA300938	SRX1286469	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	13	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515147	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515147	GSM1893251	SRA300938	SRX1286470	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	14	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515148	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515148	GSM1893252	SRA300938	SRX1286471	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	15	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515149	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515149	GSM1893253	SRA300938	SRX1286472	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	16	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515150	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515150	GSM1893254	SRA300938	SRX1286473	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	17	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515151	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515151	GSM1893255	SRA300938	SRX1286474	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	18	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515152	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515152	GSM1893256	SRA300938	SRX1286475	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	19	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515153	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515153	GSM1893257	SRA300938	SRX1286476	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	20	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515154	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515154	GSM1893258	SRA300938	SRX1286477	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	21	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515155	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515155	GSM1893259	SRA300938	SRX1286478	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	22	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515156	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515156	GSM1893260	SRA300938	SRX1286479	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	23	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515157	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515157	GSM1893261	SRA300938	SRX1286480	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	24	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515158	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515158	GSM1893262	SRA300938	SRX1286481	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	25	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515159	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515159	GSM1893263	SRA300938	SRX1286482	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	26	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515160	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515160	GSM1893264	SRA300938	SRX1286483	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	27	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515161	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515161	GSM1893265	SRA300938	SRX1286484	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73419	28	Taejoon Kwon	Tissue gene expression of Xenopus laevis J strain [tissue]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. Th	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole tissue; two female frogs were used as donors for most tissues (Taira dataset for one frog, Ueno dataset for the other frog); testis samples were collected from two male frogs (sibling of two female donors)	27762356	52612	SRP064167	SRR2515162	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002456/SRR2515162	GSM1893266	SRA300938	SRX1286485	RNA-Seq	PAIRED	SRP064167	PRJNA296921
73430	1	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517972	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517972	GSM1893583	SRA300995	SRX1287707	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	2	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517973	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517973	GSM1893584	SRA300995	SRX1287708	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	3	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517974	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517974	GSM1893585	SRA300995	SRX1287709	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	4	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517975	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517975	GSM1893586	SRA300995	SRX1287710	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	5	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517976	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517976	GSM1893587	SRA300995	SRX1287711	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	6	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517977	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517977	GSM1893588	SRA300995	SRX1287712	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	7	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517978	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517978	GSM1893589	SRA300995	SRX1287713	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	8	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517979	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517979	GSM1893590	SRA300995	SRX1287714	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	9	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517980	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517980	GSM1893591	SRA300995	SRX1287715	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	10	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517981	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517981	GSM1893592	SRA300995	SRX1287716	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	11	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517982	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517982	GSM1893593	SRA300995	SRX1287717	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	12	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517983	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517983	GSM1893594	SRA300995	SRX1287718	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	13	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517984	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517984	GSM1893595	SRA300995	SRX1287719	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	14	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517985	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517985	GSM1893596	SRA300995	SRX1287720	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	15	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517986	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517986	GSM1893597	SRA300995	SRX1287721	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	16	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517987	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517987	GSM1893598	SRA300995	SRX1287722	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	17	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517988	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517988	GSM1893599	SRA300995	SRX1287723	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	18	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517989	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517989	GSM1893600	SRA300995	SRX1287724	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	19	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517990	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517990	GSM1893601	SRA300995	SRX1287725	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	20	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517991	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517991	GSM1893602	SRA300995	SRX1287726	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	21	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517992	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517992	GSM1893603	SRA300995	SRX1287727	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	22	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517993	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517993	GSM1893604	SRA300995	SRX1287728	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	23	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517994	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517994	GSM1893605	SRA300995	SRX1287729	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	24	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517995	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517995	GSM1893606	SRA300995	SRX1287730	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	25	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517996	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517996	GSM1893607	SRA300995	SRX1287731	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	26	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517997	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517997	GSM1893608	SRA300995	SRX1287732	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	27	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517998	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517998	GSM1893609	SRA300995	SRX1287733	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73430	28	Taejoon Kwon	Developmental gene expression of Xenopus laevis J strain [stage]	Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genom	Taejoon Kwon, Shuji Takahashi, Yutaka Suzuki, Atsushi Toyoda, Naoto Ueno, Masanori Taira	Collect mRNA from whole embryos; two clutches were used (Taira dataset for one pair, Ueno dataset for the other pair)	27762356	52612	SRP064186	SRR2517999	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/002458/SRR2517999	GSM1893610	SRA300995	SRX1287734	RNA-Seq	PAIRED	SRP064186	PRJNA296953
73870	1	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589787	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589787	GSM1904663	SRA304013	SRX1319030	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	2	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589788	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002529/SRR2589788	GSM1904664	SRA304013	SRX1319031	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	3	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589789	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589789	GSM1904665	SRA304013	SRX1319032	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	4	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589790	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589790	GSM1904666	SRA304013	SRX1319033	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	5	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589791	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589791	GSM1904667	SRA304013	SRX1319034	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	6	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589792	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002529/SRR2589792	GSM1904668	SRA304013	SRX1319035	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	7	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589793	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589793	GSM1904669	SRA304013	SRX1319036	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	8	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589794	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589794	GSM1904670	SRA304013	SRX1319037	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	9	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589795	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002529/SRR2589795	GSM1904671	SRA304013	SRX1319038	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	10	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589796	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589796	GSM1904672	SRA304013	SRX1319039	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	11	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589797	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589797	GSM1904673	SRA304013	SRX1319040	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	12	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589798	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002529/SRR2589798	GSM1904674	SRA304013	SRX1319041	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	13	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589799	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002529/SRR2589799	GSM1904675	SRA304013	SRX1319042	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	14	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589800	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589800	GSM1904676	SRA304013	SRX1319043	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	15	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589801	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002529/SRR2589801	GSM1904677	SRA304013	SRX1319044	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	16	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589802	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589802	GSM1904678	SRA304013	SRX1319045	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	17	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589803	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002529/SRR2589803	GSM1904679	SRA304013	SRX1319046	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73870	18	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [polyA]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by Poly(A) extraction using Dynabeads (invitrogen) and the EpiCenter ScripSeq kit V1 using 50-300ng input RNA, and 10 cycles amplification.	26555057	51556	SRP064629	SRR2589804	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002529/SRR2589804	GSM1904680	SRA304013	SRX1319047	RNA-Seq	PAIRED	SRP064629	PRJNA298254
73904	1	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614099	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614099	GSM1905637	SRA304196	SRX1325663	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	2	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614100	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614100	GSM1905638	SRA304196	SRX1325665	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	3	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614101	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614101	GSM1905639	SRA304196	SRX1325666	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	4	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614102	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614102	GSM1905640	SRA304196	SRX1325667	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	5	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614103	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614103	GSM1905641	SRA304196	SRX1325668	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	6	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614104	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614104	GSM1905642	SRA304196	SRX1325669	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	7	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614105	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614105	GSM1905643	SRA304196	SRX1325670	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	8	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614106	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614106	GSM1905644	SRA304196	SRX1325671	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	9	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614107	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614107	GSM1905645	SRA304196	SRX1325672	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	10	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614108	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614108	GSM1905646	SRA304196	SRX1325673	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	11	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614109	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614109	GSM1905647	SRA304196	SRX1325674	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	12	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614110	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614110	GSM1905648	SRA304196	SRX1325675	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	13	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614111	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614111	GSM1905649	SRA304196	SRX1325676	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	14	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614112	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614112	GSM1905650	SRA304196	SRX1325677	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	15	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614113	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614113	GSM1905651	SRA304196	SRX1325678	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	16	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614114	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614114	GSM1905652	SRA304196	SRX1325679	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	17	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614115	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614115	GSM1905653	SRA304196	SRX1325680	RNA-Seq	PAIRED	SRP064686	PRJNA298393
73904	18	Esther Pearl	On the relationship of protein and mRNA dynamics in vertebrate embryonic development [RiboZero]	A biochemical explanation of development from the fertilized egg to the adult anatomy requires an understanding of the complement of proteins and RNAs	Esther Pearl, Leonid Peshkin, Martin Wuhr, Esther Pearl, Wilhelm Haas, Robert Freeman, John Gerhart, Allon Klein, Marko Horb, Steven Gygi, Marc Kirscher	mRNA from 18 samples each at a different developmental stage. Libraries were constructed using RNA enriched for mRNA by rRNA depletion using the EpiCenter RiboZero kit and the EpiCenter ScripSeq kit V2 using 50ng input RNA, and 12 cycles amplification.	26555057	51556	SRP064686	SRR2614116	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002552/SRR2614116	GSM1905654	SRA304196	SRX1325681	RNA-Seq	PAIRED	SRP064686	PRJNA298393
74184	1	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732219	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732219	GSM1912879	SRA306257	SRX1356590	OTHER	SINGLE	SRP065025	PRJNA299278
74184	2	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732220	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732220	GSM1912880	SRA306257	SRX1356591	OTHER	SINGLE	SRP065025	PRJNA299278
74184	3	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732221	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732221	GSM1912881	SRA306257	SRX1356592	OTHER	SINGLE	SRP065025	PRJNA299278
74184	4	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732222	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732222	GSM1912882	SRA306257	SRX1356593	OTHER	SINGLE	SRP065025	PRJNA299278
74184	5	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732223	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732223	GSM1912883	SRA306257	SRX1356594	OTHER	SINGLE	SRP065025	PRJNA299278
74184	6	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732224	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732224	GSM1912884	SRA306257	SRX1356595	OTHER	SINGLE	SRP065025	PRJNA299278
74184	7	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732225	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732225	GSM1912885	SRA306257	SRX1356596	OTHER	SINGLE	SRP065025	PRJNA299278
74184	8	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732226	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732226	GSM1912886	SRA306257	SRX1356597	OTHER	SINGLE	SRP065025	PRJNA299278
74184	9	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732227	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732227	GSM1912887	SRA306257	SRX1356598	OTHER	SINGLE	SRP065025	PRJNA299278
74184	10	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732228	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/002668/SRR2732228	GSM1912888	SRA306257	SRX1356599	OTHER	SINGLE	SRP065025	PRJNA299278
74184	11	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732229	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732229	GSM1912889	SRA306257	SRX1356600	OTHER	SINGLE	SRP065025	PRJNA299278
74184	12	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732230	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732230	GSM1912890	SRA306257	SRX1356601	OTHER	SINGLE	SRP065025	PRJNA299278
74184	13	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732231	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732231	GSM1912891	SRA306257	SRX1356602	OTHER	SINGLE	SRP065025	PRJNA299278
74184	14	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732232	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732232	GSM1912892	SRA306257	SRX1356603	OTHER	SINGLE	SRP065025	PRJNA299278
74184	15	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732233	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/002668/SRR2732233	GSM1912893	SRA306257	SRX1356604	OTHER	SINGLE	SRP065025	PRJNA299278
74184	16	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732234	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732234	GSM1912894	SRA306257	SRX1356605	OTHER	SINGLE	SRP065025	PRJNA299278
74184	17	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732235	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732235	GSM1912895	SRA306257	SRX1356606	OTHER	SINGLE	SRP065025	PRJNA299278
74184	18	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732236	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732236	GSM1912896	SRA306257	SRX1356607	OTHER	SINGLE	SRP065025	PRJNA299278
74184	19	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732237	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732237	GSM1912897	SRA306257	SRX1356608	OTHER	SINGLE	SRP065025	PRJNA299278
74184	20	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732238	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732238	GSM1912898	SRA306257	SRX1356609	OTHER	SINGLE	SRP065025	PRJNA299278
74184	21	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732239	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/002668/SRR2732239	GSM1912899	SRA306257	SRX1356610	OTHER	SINGLE	SRP065025	PRJNA299278
74184	22	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732240	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/002668/SRR2732240	GSM1912900	SRA306257	SRX1356611	OTHER	SINGLE	SRP065025	PRJNA299278
74184	23	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732241	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732241	GSM1912901	SRA306257	SRX1356612	OTHER	SINGLE	SRP065025	PRJNA299278
74184	24	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732242	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732242	GSM1912902	SRA306257	SRX1356613	OTHER	SINGLE	SRP065025	PRJNA299278
74184	25	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732243	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732243	GSM1912903	SRA306257	SRX1356614	OTHER	SINGLE	SRP065025	PRJNA299278
74184	26	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732244	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732244	GSM1912904	SRA306257	SRX1356615	OTHER	SINGLE	SRP065025	PRJNA299278
74184	27	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732245	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732245	GSM1912905	SRA306257	SRX1356616	OTHER	SINGLE	SRP065025	PRJNA299278
74184	28	Charles Bradshaw	Methylome analysis of deoxyadenosines in higher eukaryotes	Here, we report that we detected N-6-methyl-deoxyadenosine (dA6m) not only in frog DNA, but also in other species including mouse and humans. Our meth	Charles Bradshaw, Magdalena Koziol, Charles Bradshaw, George Allen, Ana Costa, Christian Frezza, John Gurdon	Determining regions of deoxyadenosine methylation in  M. musculus kidney and X. laevis fat, oviduct and testes	26689968	51669	SRP065025	SRR2732246	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/002668/SRR2732246	GSM1912906	SRA306257	SRX1356617	OTHER	SINGLE	SRP065025	PRJNA299278
74470	1	Leonid Peshkin	Transcriptomic Insights into Genetic Diversity of  Protein-Coding Genes in X. laevis	We characterize the genetic diversity of Xenopus laevis strains using allele-specific RNA-seq data analysis and provide a catalogue of coding variatio	Leonid Peshkin, Virginia Savova, Esther Pearl, Elvan Boke, Marko Horb, Sasha Gimelbrant	We successfully performed natural mating of the two Xenopus strains: two reciprocal (BxJ, JxB) and two straight self (JxJ, BxB) crosses. We then collected tadpoles at a single developmental timepoint (stage NF 42), pooled ten tadpoles per cross, and isolated RNA from each pool. After RiboZero treatment, we constructed Illumina libraries, and performed RNAseq on HiSeq 2000, resulting in approximately 30 to 47 million reads per library with paired-end 100 base reads.	28283406	53166	SRP065480	SRR2858152	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002791/SRR2858152	GSM1921263	SRA307973	SRX1397134	RNA-Seq	PAIRED	SRP065480	PRJNA300520
74470	2	Leonid Peshkin	Transcriptomic Insights into Genetic Diversity of  Protein-Coding Genes in X. laevis	We characterize the genetic diversity of Xenopus laevis strains using allele-specific RNA-seq data analysis and provide a catalogue of coding variatio	Leonid Peshkin, Virginia Savova, Esther Pearl, Elvan Boke, Marko Horb, Sasha Gimelbrant	We successfully performed natural mating of the two Xenopus strains: two reciprocal (BxJ, JxB) and two straight self (JxJ, BxB) crosses. We then collected tadpoles at a single developmental timepoint (stage NF 42), pooled ten tadpoles per cross, and isolated RNA from each pool. After RiboZero treatment, we constructed Illumina libraries, and performed RNAseq on HiSeq 2000, resulting in approximately 30 to 47 million reads per library with paired-end 100 base reads.	28283406	53166	SRP065480	SRR2858153	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002791/SRR2858153	GSM1921264	SRA307973	SRX1397135	RNA-Seq	PAIRED	SRP065480	PRJNA300520
74470	3	Leonid Peshkin	Transcriptomic Insights into Genetic Diversity of  Protein-Coding Genes in X. laevis	We characterize the genetic diversity of Xenopus laevis strains using allele-specific RNA-seq data analysis and provide a catalogue of coding variatio	Leonid Peshkin, Virginia Savova, Esther Pearl, Elvan Boke, Marko Horb, Sasha Gimelbrant	We successfully performed natural mating of the two Xenopus strains: two reciprocal (BxJ, JxB) and two straight self (JxJ, BxB) crosses. We then collected tadpoles at a single developmental timepoint (stage NF 42), pooled ten tadpoles per cross, and isolated RNA from each pool. After RiboZero treatment, we constructed Illumina libraries, and performed RNAseq on HiSeq 2000, resulting in approximately 30 to 47 million reads per library with paired-end 100 base reads.	28283406	53166	SRP065480	SRR2858154	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002791/SRR2858154	GSM1921265	SRA307973	SRX1397136	RNA-Seq	PAIRED	SRP065480	PRJNA300520
74919	1	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932716	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932716	GSM1937543	SRA310866	SRX1427057	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	2	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932717	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932717	GSM1937544	SRA310866	SRX1427058	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	3	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932718	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932718	GSM1937545	SRA310866	SRX1427059	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	4	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932719	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932719	GSM1937546	SRA310866	SRX1427060	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	5	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932720	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932720	GSM1937547	SRA310866	SRX1427061	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	6	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932721	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932721	GSM1937548	SRA310866	SRX1427062	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	7	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932722	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932722	GSM1937549	SRA310866	SRX1427063	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	8	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932723	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932723	GSM1937550	SRA310866	SRX1427064	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	9	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932724	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932724	GSM1937551	SRA310866	SRX1427065	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	10	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932725	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932725	GSM1937552	SRA310866	SRX1427066	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	11	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932726	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932726	GSM1937553	SRA310866	SRX1427067	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	12	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932727	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932727	GSM1937554	SRA310866	SRX1427068	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	13	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932728	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932728	GSM1937555	SRA310866	SRX1427069	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	14	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932729	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932729	GSM1937556	SRA310866	SRX1427070	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	15	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932730	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932730	GSM1937557	SRA310866	SRX1427071	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	16	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932731	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932731	GSM1937558	SRA310866	SRX1427072	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	17	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932732	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932732	GSM1937559	SRA310866	SRX1427073	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	18	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932733	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932733	GSM1937560	SRA310866	SRX1427074	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	19	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932734	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932734	GSM1937561	SRA310866	SRX1427075	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	20	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932735	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002863/SRR2932735	GSM1937562	SRA310866	SRX1427076	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	21	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932736	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002864/SRR2932736	GSM1937563	SRA310866	SRX1427077	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	22	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932737	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002864/SRR2932737	GSM1937564	SRA310866	SRX1427078	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	23	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932738	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002864/SRR2932738	GSM1937565	SRA310866	SRX1427079	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	24	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932739	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002864/SRR2932739	GSM1937566	SRA310866	SRX1427080	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	25	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932740	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002864/SRR2932740	GSM1937567	SRA310866	SRX1427081	RNA-Seq	SINGLE	SRP066064	PRJNA301904
74919	26	Zhihua Jiang	Whole transcriptome target sequencing: profiling  gene expression and alternative polyadenylation with one pipeline.	We have developed a deep sequencing method called Whole Transcriptome Target Sequencing (WTTS), which sequences the 3’ ends of polyA+ RNA. This meth	Zhihua Jiang, Xiang Zhou, Rui Li, Jennifer Michal, Richard Harland	A pooled total RNA sample derived from three male and three female adult frogs was used in seven trials to develop the WTTS assay.  The same sample was sequenced using RNA-seq as control. Technical replicates of the same female adult frog were analyzed using the finalized WTTS library preparation method.  Biological replicates, which included 10 embryo pools collected from two families at stages 6, 8, 11, 15 and 28 were subsequently analyzed to validate the finalized WTTS method.  Six embryo samples collected at stages of 6, 8 and 11 were also sequenced using RNA-seq.  Therefore, this submission involved a total of 26 libraries.	27098915	52200	SRP066064	SRR2932741	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002864/SRR2932741	GSM1937568	SRA310866	SRX1427082	RNA-Seq	SINGLE	SRP066064	PRJNA301904
75164	1	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924614	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924614	GSM1944406	SRA312236	SRX1437960	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	2	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924615	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924615	GSM1944407	SRA312236	SRX1437961	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	3	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924616	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924616	GSM1944408	SRA312236	SRX1437962	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	4	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924617	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924617	GSM1944409	SRA312236	SRX1437963	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	5	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924618	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924618	GSM1944410	SRA312236	SRX1437964	RNA-Seq	PAIRED	SRP066384	PRJNA302662
75164	6	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924619	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924619	GSM1944411	SRA312236	SRX1437965	RNA-Seq	PAIRED	SRP066384	PRJNA302662
75164	7	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924620	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924620	GSM1944412	SRA312236	SRX1437966	RNA-Seq	PAIRED	SRP066384	PRJNA302662
75164	8	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924621	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924621	GSM1944413	SRA312236	SRX1437967	RNA-Seq	PAIRED	SRP066384	PRJNA302662
75164	9	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924622	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924622	GSM1944414	SRA312236	SRX1437968	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	10	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924623	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924623	GSM1944415	SRA312236	SRX1437969	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	11	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924624	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924624	GSM1944416	SRA312236	SRX1437970	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	12	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924625	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924625	GSM1944417	SRA312236	SRX1437971	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	13	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924626	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924626	GSM1944418	SRA312236	SRX1437972	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	14	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924627	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924627	GSM1944419	SRA312236	SRX1437973	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	15	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924628	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924628	GSM1944420	SRA312236	SRX1437974	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	16	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924629	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924629	GSM1944421	SRA312236	SRX1437975	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	17	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924630	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924630	GSM1944422	SRA312236	SRX1437976	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	18	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924631	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924631	GSM1944423	SRA312236	SRX1437977	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	19	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924632	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924632	GSM1944424	SRA312236	SRX1437978	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	20	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924633	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924633	GSM1944425	SRA312236	SRX1437979	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	21	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924634	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924634	GSM1944426	SRA312236	SRX1437980	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	22	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924635	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924635	GSM1944427	SRA312236	SRX1437981	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	23	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924636	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924636	GSM1944428	SRA312236	SRX1437982	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	24	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924637	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924637	GSM1944429	SRA312236	SRX1437983	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	25	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924638	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924638	GSM1944430	SRA312236	SRX1437984	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	26	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924639	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924639	GSM1944431	SRA312236	SRX1437985	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	27	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924640	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924640	GSM1944432	SRA312236	SRX1437986	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	28	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924641	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924641	GSM1944433	SRA312236	SRX1437987	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	29	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924642	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924642	GSM1944434	SRA312236	SRX1437988	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	30	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924643	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924643	GSM1944435	SRA312236	SRX1437989	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	31	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924644	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924644	GSM1944436	SRA312236	SRX1437990	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	32	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924645	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924645	GSM1944437	SRA312236	SRX1437991	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	33	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924646	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924646	GSM1944438	SRA312236	SRX1437992	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	34	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924647	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924647	GSM1944439	SRA312236	SRX1437993	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	35	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924648	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924648	GSM1944440	SRA312236	SRX1437994	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	36	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924649	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924649	GSM1944441	SRA312236	SRX1437995	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	37	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924650	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924650	GSM1944442	SRA312236	SRX1437996	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	38	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924651	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924651	GSM1944443	SRA312236	SRX1437997	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	39	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924652	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924652	GSM1944444	SRA312236	SRX1437998	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	40	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924653	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924653	GSM1944445	SRA312236	SRX1437999	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	41	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924654	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924654	GSM1944446	SRA312236	SRX1438000	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	42	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924655	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924655	GSM1944447	SRA312236	SRX1438001	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	43	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924656	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924656	GSM1944448	SRA312236	SRX1438002	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	44	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924657	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924657	GSM1944449	SRA312236	SRX1438003	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	45	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924658	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924658	GSM1944450	SRA312236	SRX1438004	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	46	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924659	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924659	GSM1944451	SRA312236	SRX1438005	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	47	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924660	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924660	GSM1944452	SRA312236	SRX1438006	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	48	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924661	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924661	GSM1944453	SRA312236	SRX1438007	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	49	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924662	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924662	GSM1944454	SRA312236	SRX1438008	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	50	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924663	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924663	GSM1944455	SRA312236	SRX1438009	MNase-Seq	SINGLE	SRP066384	PRJNA302662
75164	51	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924664	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924664	GSM1944456	SRA312236	SRX1438010	MNase-Seq	SINGLE	SRP066384	PRJNA302662
75164	52	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924665	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924665	GSM1944457	SRA312236	SRX1438011	MNase-Seq	SINGLE	SRP066384	PRJNA302662
75164	53	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924666	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924666	GSM1944458	SRA312236	SRX1438012	MNase-Seq	SINGLE	SRP066384	PRJNA302662
75164	54	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924667	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924667	GSM1944459	SRA312236	SRX1438013	MNase-Seq	SINGLE	SRP066384	PRJNA302662
75164	55	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924668	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924668	GSM1944460	SRA312236	SRX1438014	MNase-Seq	SINGLE	SRP066384	PRJNA302662
75164	56	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924669	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924669	GSM1944461	SRA312236	SRX1438015	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	57	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924670	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924670	GSM1944462	SRA312236	SRX1438016	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	58	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924671	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924671	GSM1944463	SRA312236	SRX1438017	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	59	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924672	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924672	GSM1944464	SRA312236	SRX1438018	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	60	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924673	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924673	GSM1944465	SRA312236	SRX1438019	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	61	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924674	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924674	GSM1944466	SRA312236	SRX1438020	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	62	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924675	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924675	GSM1944467	SRA312236	SRX1438021	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	63	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924676	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924676	GSM1944468	SRA312236	SRX1438022	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	64	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924677	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924677	GSM1944469	SRA312236	SRX1438023	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	65	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924678	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924678	GSM1944470	SRA312236	SRX1438024	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	66	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924679	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924679	GSM1944471	SRA312236	SRX1438025	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	67	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924680	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924680	GSM1944472	SRA312236	SRX1438026	MBD-Seq	SINGLE	SRP066384	PRJNA302662
75164	68	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924681	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924681	GSM1944473	SRA312236	SRX1438027	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	69	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924682	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924682	GSM1944474	SRA312236	SRX1438028	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	70	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924683	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924683	GSM1944475	SRA312236	SRX1438029	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	71	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924684	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924684	GSM1944476	SRA312236	SRX1438030	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	72	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924685	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924685	GSM1944477	SRA312236	SRX1438031	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	73	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924686	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924686	GSM1944478	SRA312236	SRX1438032	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	74	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924687	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924687	GSM1944479	SRA312236	SRX1438033	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	75	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924688	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924688	GSM1944480	SRA312236	SRX1438034	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	76	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924689	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924689	GSM1944481	SRA312236	SRX1438035	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	77	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924690	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924690	GSM1944482	SRA312236	SRX1438036	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	78	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924691	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924691	GSM1944483	SRA312236	SRX1438037	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	79	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924692	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924692	GSM1944484	SRA312236	SRX1438038	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	80	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924693	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924693	GSM1944485	SRA312236	SRX1438039	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	81	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924694	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924694	GSM1944486	SRA312236	SRX1438040	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	82	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924695	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924695	GSM1944487	SRA312236	SRX1438041	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	83	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924696	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924696	GSM1944488	SRA312236	SRX1438042	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	84	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924697	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924697	GSM1944489	SRA312236	SRX1438043	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	85	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924698	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924698	GSM1944490	SRA312236	SRX1438044	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	86	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924699	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924699	GSM1944491	SRA312236	SRX1438045	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	87	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924700	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924700	GSM1944492	SRA312236	SRX1438046	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	88	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924701	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924701	GSM1944493	SRA312236	SRX1438047	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	89	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924702	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924702	GSM1944494	SRA312236	SRX1438048	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	90	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924703	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924703	GSM1944495	SRA312236	SRX1438049	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	91	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924704	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924704	GSM1944496	SRA312236	SRX1438050	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	92	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924705	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924705	GSM1944497	SRA312236	SRX1438051	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	93	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924706	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924706	GSM1944498	SRA312236	SRX1438052	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	94	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924707	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924707	GSM1944499	SRA312236	SRX1438053	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	95	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924708	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924708	GSM1944500	SRA312236	SRX1438054	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	96	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924709	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924709	GSM1944501	SRA312236	SRX1438055	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	97	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924710	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924710	GSM1944502	SRA312236	SRX1438056	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	98	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924711	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924711	GSM1944503	SRA312236	SRX1438057	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	99	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924712	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924712	GSM1944504	SRA312236	SRX1438058	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	100	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924713	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924713	GSM1944505	SRA312236	SRX1438059	ChIP-Seq	SINGLE	SRP066384	PRJNA302662
75164	101	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924608	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924608	GSM1944400	SRA312236	SRX1437954	RNA-Seq	PAIRED	SRP066384	PRJNA302662
75164	102	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924609	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924609	GSM1944401	SRA312236	SRX1437955	RNA-Seq	PAIRED	SRP066384	PRJNA302662
75164	103	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924610	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924610	GSM1944402	SRA312236	SRX1437956	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	104	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924611	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924611	GSM1944403	SRA312236	SRX1437957	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	105	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924612	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924612	GSM1944404	SRA312236	SRX1437958	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75164	106	Charles Bradshaw	Sperm is epigenetically programmed to regulate gene transcription in embryo	Using the frog Xenopus laevis as a model system we profile epigenetic features of sperm and spermatid to study how they relate to gene expression in e	Charles Bradshaw, Marta Teperek, Angela Simeone, Vincent Gaggioli, Kei Miiyamoto, George Allen, Serap Erkek, Taejoon Kwon, Edward Marcotte, Philip Zegermann, Charles Bradshaw, Antoine Peters, John Gurdon, Jerome Jullien	48 samples, single-ended ChIP-seq libraries from sperm- and spermatid-derived haploid embryos pulling down H3K4me2, H3K4me3, H3K27me3 and H3K9me3, 3 replicates for each histone modification pull-down.
14  samples of both single-ended and pair-ended RNA-seq libraries for sperm- and spermatid-derived embryos. 
3 replicates of single-ended RNA-seq libraries for spermatid cells.
22 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm5b
16 samples of single-ended RNA-seq form sperm- and spermatid-derived embryos overexpressing Kdm6b
6 samples of single-ended MNase-seq from sperm and spermatid chromatin
12 samples of MBD-seq from sperm and spermatid chromatin	27034506	53997	SRP066384	SRR2924613	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/002856/SRR2924613	GSM1944405	SRA312236	SRX1437959	RNA-Seq	SINGLE	SRP066384	PRJNA302662
75278	1	Edward De Robertis	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula	RNA sequencing has allowed high-throughput screening of differential gene expression in many tissues and organisms. Xenopus laevis is a classical embr	Edward De Robertis, Yi Ding, Gabriele Colozza, Kelvin Zhang, Yuki Moriyama, Diego Ploper, Eric Sosa, Maria Benitez	One stage 10.5 wild type whole embryo and triplicates of stage 10.5 dorsal lips and ventral lips are sequenced.	27016259	51980	SRP066508	SRR2939617	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002870/SRR2939617	GSM1948717	SRA312669	SRX1441880	RNA-Seq	SINGLE	SRP066508	PRJNA303056
75278	2	Edward De Robertis	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula	RNA sequencing has allowed high-throughput screening of differential gene expression in many tissues and organisms. Xenopus laevis is a classical embr	Edward De Robertis, Yi Ding, Gabriele Colozza, Kelvin Zhang, Yuki Moriyama, Diego Ploper, Eric Sosa, Maria Benitez	One stage 10.5 wild type whole embryo and triplicates of stage 10.5 dorsal lips and ventral lips are sequenced.	27016259	51980	SRP066508	SRR2939618	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002870/SRR2939618	GSM1948718	SRA312669	SRX1441881	RNA-Seq	SINGLE	SRP066508	PRJNA303056
75278	3	Edward De Robertis	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula	RNA sequencing has allowed high-throughput screening of differential gene expression in many tissues and organisms. Xenopus laevis is a classical embr	Edward De Robertis, Yi Ding, Gabriele Colozza, Kelvin Zhang, Yuki Moriyama, Diego Ploper, Eric Sosa, Maria Benitez	One stage 10.5 wild type whole embryo and triplicates of stage 10.5 dorsal lips and ventral lips are sequenced.	27016259	51980	SRP066508	SRR2939619	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002870/SRR2939619	GSM1948719	SRA312669	SRX1441882	RNA-Seq	SINGLE	SRP066508	PRJNA303056
75278	4	Edward De Robertis	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula	RNA sequencing has allowed high-throughput screening of differential gene expression in many tissues and organisms. Xenopus laevis is a classical embr	Edward De Robertis, Yi Ding, Gabriele Colozza, Kelvin Zhang, Yuki Moriyama, Diego Ploper, Eric Sosa, Maria Benitez	One stage 10.5 wild type whole embryo and triplicates of stage 10.5 dorsal lips and ventral lips are sequenced.	27016259	51980	SRP066508	SRR2939620	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002870/SRR2939620	GSM1948720	SRA312669	SRX1441883	RNA-Seq	SINGLE	SRP066508	PRJNA303056
75278	5	Edward De Robertis	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula	RNA sequencing has allowed high-throughput screening of differential gene expression in many tissues and organisms. Xenopus laevis is a classical embr	Edward De Robertis, Yi Ding, Gabriele Colozza, Kelvin Zhang, Yuki Moriyama, Diego Ploper, Eric Sosa, Maria Benitez	One stage 10.5 wild type whole embryo and triplicates of stage 10.5 dorsal lips and ventral lips are sequenced.	27016259	51980	SRP066508	SRR2939621	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002870/SRR2939621	GSM1948721	SRA312669	SRX1441884	RNA-Seq	SINGLE	SRP066508	PRJNA303056
75278	6	Edward De Robertis	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula	RNA sequencing has allowed high-throughput screening of differential gene expression in many tissues and organisms. Xenopus laevis is a classical embr	Edward De Robertis, Yi Ding, Gabriele Colozza, Kelvin Zhang, Yuki Moriyama, Diego Ploper, Eric Sosa, Maria Benitez	One stage 10.5 wild type whole embryo and triplicates of stage 10.5 dorsal lips and ventral lips are sequenced.	27016259	51980	SRP066508	SRR2939622	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002870/SRR2939622	GSM1948722	SRA312669	SRX1441885	RNA-Seq	SINGLE	SRP066508	PRJNA303056
75278	7	Edward De Robertis	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula	RNA sequencing has allowed high-throughput screening of differential gene expression in many tissues and organisms. Xenopus laevis is a classical embr	Edward De Robertis, Yi Ding, Gabriele Colozza, Kelvin Zhang, Yuki Moriyama, Diego Ploper, Eric Sosa, Maria Benitez	One stage 10.5 wild type whole embryo and triplicates of stage 10.5 dorsal lips and ventral lips are sequenced.	27016259	51980	SRP066508	SRR2939623	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002870/SRR2939623	GSM1948723	SRA312669	SRX1441886	RNA-Seq	SINGLE	SRP066508	PRJNA303056
76059	1	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017195	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017195	GSM1973491	SRA320052	SRX1485087	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	2	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017196	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017196	GSM1973492	SRA320052	SRX1485088	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	3	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017197	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017197	GSM1973493	SRA320052	SRX1485089	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	4	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017198	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017198	GSM1973494	SRA320052	SRX1485090	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	5	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017199	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017199	GSM1973495	SRA320052	SRX1485091	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	6	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017200	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002946/SRR3017200	GSM1973496	SRA320052	SRX1485092	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	7	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017201	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017201	GSM1973497	SRA320052	SRX1485093	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	8	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017202	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017202	GSM1973498	SRA320052	SRX1485094	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	9	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017203	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002946/SRR3017203	GSM1973499	SRA320052	SRX1485095	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	10	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017204	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017204	GSM1973500	SRA320052	SRX1485096	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	11	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017205	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017205	GSM1973500	SRA320052	SRX1485096	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76059	12	Simon van Heeringen	ChIP-sequencing in stage 10.5 Xenopus laevis embryos	Epigenomic profiling (H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II) of Xenopus laevis stage 10.5 embryos.                                   	Simon van Heeringen, Simon van Heeringen, Sarita Paranjpe, Gert-Jan Veenstra	ChIP-seq of H3K4me1, H3K4me3, H3K36me3, p300 and RNA Polymerase II in duplicate.
BAM processed data files (a format not accepted by GEO) were generated for H3K4me1, H3K36me3, RNAPII samples.	27762356	52612	SRP067434	SRR3017206	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/002946/SRR3017206	GSM1973501	SRA320052	SRX1485097	ChIP-Seq	SINGLE	SRP067434	PRJNA306102
76247	1	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044220	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044220	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	2	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044221	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044221	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	3	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044222	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044222	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	4	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044223	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044223	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	5	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044224	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044224	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	6	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044225	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044225	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	7	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044226	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044226	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	8	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044227	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044227	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	9	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044228	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044228	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	10	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044229	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044229	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	11	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044230	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044230	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	12	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044231	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044231	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	13	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044232	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044232	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	14	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044233	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044233	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	15	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044234	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044234	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	16	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044235	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044235	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	17	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044236	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044236	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	18	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044237	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044237	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	19	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044238	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044238	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	20	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044239	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044239	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	21	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044240	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044240	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	22	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044241	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044241	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	23	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044242	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044242	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	24	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044243	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044243	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	25	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044244	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044244	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	26	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044245	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044245	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	27	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044246	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044246	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	28	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044247	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044247	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	29	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044248	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044248	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76247	30	Ozren Bogdanovic	Single-base resolution methylome of Xenopus laevis embryos	Here we describe a base-resolution DNA methylation map of Xenopus laevis gastrula (st.10.5) embryos generated by whole genome bisulfite sequencing    	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus laevis st.10.5 embryos	27762356	52612	SRP067679	SRR3044249	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002972/SRR3044249	GSM1977638	SRA321210	SRX1496284	Bisulfite-Seq	SINGLE	SRP067679	PRJNA306718
76342	1	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055524	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055524	GSM1981745	SRA322724	SRX1502297	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	2	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055525	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055525	GSM1981746	SRA322724	SRX1502298	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	3	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055526	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055526	GSM1981747	SRA322724	SRX1502299	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	4	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055527	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055527	GSM1981748	SRA322724	SRX1502300	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	5	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055528	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/002983/SRR3055528	GSM1981749	SRA322724	SRX1502301	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	6	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055529	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055529	GSM1981750	SRA322724	SRX1502302	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	7	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055530	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/002983/SRR3055530	GSM1981751	SRA322724	SRX1502303	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	8	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055531	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055531	GSM1981752	SRA322724	SRX1502304	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	9	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055532	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055532	GSM1981753	SRA322724	SRX1502305	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	10	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055533	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055533	GSM1981754	SRA322724	SRX1502306	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	11	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055534	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/002983/SRR3055534	GSM1981755	SRA322724	SRX1502307	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	12	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055535	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055535	GSM1981756	SRA322724	SRX1502308	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	13	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055536	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055536	GSM1981757	SRA322724	SRX1502309	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	14	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055537	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055537	GSM1981758	SRA322724	SRX1502310	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	15	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055538	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055538	GSM1981759	SRA322724	SRX1502311	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	16	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055539	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055539	GSM1981760	SRA322724	SRX1502312	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	17	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055540	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055540	GSM1981761	SRA322724	SRX1502313	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	18	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055541	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055541	GSM1981762	SRA322724	SRX1502314	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	19	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055542	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055542	GSM1981763	SRA322724	SRX1502315	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	20	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055543	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055543	GSM1981764	SRA322724	SRX1502316	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	21	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055544	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055544	GSM1981765	SRA322724	SRX1502317	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	22	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055545	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/002983/SRR3055545	GSM1981766	SRA322724	SRX1502318	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	23	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055546	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/002983/SRR3055546	GSM1981767	SRA322724	SRX1502319	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	24	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055547	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/002983/SRR3055547	GSM1981768	SRA322724	SRX1502320	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	25	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055548	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055548	GSM1981769	SRA322724	SRX1502321	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	26	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055549	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055549	GSM1981770	SRA322724	SRX1502322	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	27	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055550	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055550	GSM1981771	SRA322724	SRX1502323	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	28	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055551	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055551	GSM1981772	SRA322724	SRX1502324	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	29	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055552	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055552	GSM1981773	SRA322724	SRX1502325	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	30	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055553	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055553	GSM1981774	SRA322724	SRX1502326	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	31	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055554	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055554	GSM1981775	SRA322724	SRX1502327	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	32	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055555	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055555	GSM1981776	SRA322724	SRX1502328	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	33	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055556	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055556	GSM1981777	SRA322724	SRX1502329	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	34	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055557	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055557	GSM1981778	SRA322724	SRX1502330	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	35	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055558	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/002983/SRR3055558	GSM1981779	SRA322724	SRX1502331	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76342	36	Ian Quigley	RNAseq profiling of multiciliated cells	To determine what genes are upregulated in multiciliated cells, we manipulated Xenopus laevis ectoderm to either make more or fewer of this cell type 	Ian Quigley, Chris Kintner	We suppressed multiciliated cell development by activating the notch pathway with an injected mRNA encoding the intracellular domain of notch (icd) or by injecting an mRNA encoding a dominant-negative form of multicilin (dnmcidas). Conversely, we promoted multiciliated cell differentiation by blocking notch signaling with a DNA-binding mutant of Suppressor of Hairless (dbm), or by overexpressing an inducible form of multicilin (mcidas). We also coinjected these constructs in a way aimed at causing the greatest change in multiciliated cells and reducing background transcriptional programs not associated with these cells: for example, we coinjected icd with mcidas, in order to reduce other cell types specified by notch. After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA at 3, 6, and 9 hours after induction, roughly corresponding to stages 13, 16, and 18 and performed poly-a+  RNAseq (Illumina Truseq v2). We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) and took the intersection of genes differentially expressed between all comparisons in which the multiciliated cell number dramatically changed (icd vs. icd + mcidas, icd vs. dbm, dbm vs. dbm + dnmcidas) to obtain a core list of  multiciliated cell genes.	28103240	53709	SRP067781	SRR3055559	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/002983/SRR3055559	GSM1981780	SRA322724	SRX1502332	RNA-Seq	SINGLE	SRP067781	PRJNA306946
76363	1	Ian Quigley	3D chromosomal capture of X. laevis	To determine 3D chromosomal structure in differentating ectoderm of the frog  Xenopus laevis, we performed tethered conformation capture (TCC) (PMID: 	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types (stage 10). In other experiments, we injected some embryos with mRNAs encoding an inducible form of multicilin (mcidas-HGR).  After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed tethered conformation capture on all harvested tissues (PMID: 22198700). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1 to interrogate 3D structure and the more fragmented genome version 7.1 to assist with chromosome assembly). TADs were called with HOMER, and chromosomes were assembled with both Lachesis (PMID: 24185095) and HighRise (arXiv:1502.05331).	28103240	53709	SRP067835	SRR3057323	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002985/SRR3057323	GSM1982232	SRA322996	SRX1503157	OTHER	PAIRED	SRP067835	PRJNA307102
76363	2	Ian Quigley	3D chromosomal capture of X. laevis	To determine 3D chromosomal structure in differentating ectoderm of the frog  Xenopus laevis, we performed tethered conformation capture (TCC) (PMID: 	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types (stage 10). In other experiments, we injected some embryos with mRNAs encoding an inducible form of multicilin (mcidas-HGR).  After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed tethered conformation capture on all harvested tissues (PMID: 22198700). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1 to interrogate 3D structure and the more fragmented genome version 7.1 to assist with chromosome assembly). TADs were called with HOMER, and chromosomes were assembled with both Lachesis (PMID: 24185095) and HighRise (arXiv:1502.05331).	28103240	53709	SRP067835	SRR3057324	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/002985/SRR3057324	GSM1982233	SRA322996	SRX1503158	OTHER	PAIRED	SRP067835	PRJNA307102
76363	3	Ian Quigley	3D chromosomal capture of X. laevis	To determine 3D chromosomal structure in differentating ectoderm of the frog  Xenopus laevis, we performed tethered conformation capture (TCC) (PMID: 	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types (stage 10). In other experiments, we injected some embryos with mRNAs encoding an inducible form of multicilin (mcidas-HGR).  After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed tethered conformation capture on all harvested tissues (PMID: 22198700). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1 to interrogate 3D structure and the more fragmented genome version 7.1 to assist with chromosome assembly). TADs were called with HOMER, and chromosomes were assembled with both Lachesis (PMID: 24185095) and HighRise (arXiv:1502.05331).	28103240	53709	SRP067835	SRR3057325	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002985/SRR3057325	GSM1982234	SRA322996	SRX1503159	OTHER	PAIRED	SRP067835	PRJNA307102
76363	4	Ian Quigley	3D chromosomal capture of X. laevis	To determine 3D chromosomal structure in differentating ectoderm of the frog  Xenopus laevis, we performed tethered conformation capture (TCC) (PMID: 	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types (stage 10). In other experiments, we injected some embryos with mRNAs encoding an inducible form of multicilin (mcidas-HGR).  After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed tethered conformation capture on all harvested tissues (PMID: 22198700). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1 to interrogate 3D structure and the more fragmented genome version 7.1 to assist with chromosome assembly). TADs were called with HOMER, and chromosomes were assembled with both Lachesis (PMID: 24185095) and HighRise (arXiv:1502.05331).	28103240	53709	SRP067835	SRR3057326	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/002985/SRR3057326	GSM1982235	SRA322996	SRX1503160	OTHER	PAIRED	SRP067835	PRJNA307102
76915	1	Li Gao	A novel role for ASCL1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT function	Maternally expressed proteins function in vertebrates to establish the major body axes of the embryo, and to establish a pre-pattern that sets the sta	Li Gao, Xin Ma, Qinghua Tao	Examination of genes expression in control (cMO) and Ascl1 MO knockdown (AMOs) embryos by deep sequencing.	26700681	51664	SRP068506	SRR3103472	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003030/SRR3103472	GSM2040681	SRA335063	SRX1532122	RNA-Seq	PAIRED	SRP068506	PRJNA308931
76915	2	Li Gao	A novel role for ASCL1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT function	Maternally expressed proteins function in vertebrates to establish the major body axes of the embryo, and to establish a pre-pattern that sets the sta	Li Gao, Xin Ma, Qinghua Tao	Examination of genes expression in control (cMO) and Ascl1 MO knockdown (AMOs) embryos by deep sequencing.	26700681	51664	SRP068506	SRR3103473	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003030/SRR3103473	GSM2040682	SRA335063	SRX1532123	RNA-Seq	PAIRED	SRP068506	PRJNA308931
76915	3	Li Gao	A novel role for ASCL1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT function	Maternally expressed proteins function in vertebrates to establish the major body axes of the embryo, and to establish a pre-pattern that sets the sta	Li Gao, Xin Ma, Qinghua Tao	Examination of genes expression in control (cMO) and Ascl1 MO knockdown (AMOs) embryos by deep sequencing.	26700681	51664	SRP068506	SRR3103474	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003030/SRR3103474	GSM2040683	SRA335063	SRX1532124	RNA-Seq	PAIRED	SRP068506	PRJNA308931
76915	4	Li Gao	A novel role for ASCL1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT function	Maternally expressed proteins function in vertebrates to establish the major body axes of the embryo, and to establish a pre-pattern that sets the sta	Li Gao, Xin Ma, Qinghua Tao	Examination of genes expression in control (cMO) and Ascl1 MO knockdown (AMOs) embryos by deep sequencing.	26700681	51664	SRP068506	SRR3103475	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003030/SRR3103475	GSM2040684	SRA335063	SRX1532125	RNA-Seq	PAIRED	SRP068506	PRJNA308931
76915	5	Li Gao	A novel role for ASCL1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT function	Maternally expressed proteins function in vertebrates to establish the major body axes of the embryo, and to establish a pre-pattern that sets the sta	Li Gao, Xin Ma, Qinghua Tao	Examination of genes expression in control (cMO) and Ascl1 MO knockdown (AMOs) embryos by deep sequencing.	26700681	51664	SRP068506	SRR3103476	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003030/SRR3103476	GSM2040685	SRA335063	SRX1532126	RNA-Seq	PAIRED	SRP068506	PRJNA308931
76915	6	Li Gao	A novel role for ASCL1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT function	Maternally expressed proteins function in vertebrates to establish the major body axes of the embryo, and to establish a pre-pattern that sets the sta	Li Gao, Xin Ma, Qinghua Tao	Examination of genes expression in control (cMO) and Ascl1 MO knockdown (AMOs) embryos by deep sequencing.	26700681	51664	SRP068506	SRR3103477	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003030/SRR3103477	GSM2040686	SRA335063	SRX1532127	RNA-Seq	PAIRED	SRP068506	PRJNA308931
76991	1	Gert Veenstra	Differential expression analysis of Gcn5 knockdown embryos at early developmental stage 10.5 in Xenopus laevis	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos injected with Gcn5-antisense oligonucleotides and with water to crea	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068637	SRR3109284	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003036/SRR3109284	GSM2042204	SRA336546	SRX1537590	RNA-Seq	SINGLE	SRP068637	PRJNA309195
76991	2	Gert Veenstra	Differential expression analysis of Gcn5 knockdown embryos at early developmental stage 10.5 in Xenopus laevis	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos injected with Gcn5-antisense oligonucleotides and with water to crea	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068637	SRR3109285	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003036/SRR3109285	GSM2042205	SRA336546	SRX1537591	RNA-Seq	SINGLE	SRP068637	PRJNA309195
76991	3	Gert Veenstra	Differential expression analysis of Gcn5 knockdown embryos at early developmental stage 10.5 in Xenopus laevis	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos injected with Gcn5-antisense oligonucleotides and with water to crea	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068637	SRR3109286	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003036/SRR3109286	GSM2042206	SRA336546	SRX1537592	RNA-Seq	SINGLE	SRP068637	PRJNA309195
76991	4	Gert Veenstra	Differential expression analysis of Gcn5 knockdown embryos at early developmental stage 10.5 in Xenopus laevis	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos injected with Gcn5-antisense oligonucleotides and with water to crea	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068637	SRR3109287	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003036/SRR3109287	GSM2042207	SRA336546	SRX1537593	RNA-Seq	SINGLE	SRP068637	PRJNA309195
76994	1	Gert Veenstra	Differential expression analysis of triple knockdown of TBP and TBP-related factors (TKD) in Xenopus laevis embryos at early developmental stage 10.5	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos co-injected with TBP-,TBP2- and TLF-AS antisense oligonucleotides an	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068680	SRR3107014	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003034/SRR3107014	GSM2042215	SRA335990	SRX1535321	RNA-Seq	SINGLE	SRP068680	PRJNA309218
76994	2	Gert Veenstra	Differential expression analysis of triple knockdown of TBP and TBP-related factors (TKD) in Xenopus laevis embryos at early developmental stage 10.5	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos co-injected with TBP-,TBP2- and TLF-AS antisense oligonucleotides an	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068680	SRR3107015	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003034/SRR3107015	GSM2042216	SRA335990	SRX1535322	RNA-Seq	SINGLE	SRP068680	PRJNA309218
76994	3	Gert Veenstra	Differential expression analysis of triple knockdown of TBP and TBP-related factors (TKD) in Xenopus laevis embryos at early developmental stage 10.5	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos co-injected with TBP-,TBP2- and TLF-AS antisense oligonucleotides an	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068680	SRR3107016	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003034/SRR3107016	GSM2042217	SRA335990	SRX1535323	RNA-Seq	SINGLE	SRP068680	PRJNA309218
76994	4	Gert Veenstra	Differential expression analysis of triple knockdown of TBP and TBP-related factors (TKD) in Xenopus laevis embryos at early developmental stage 10.5	We sequenced cDNA prepared from ribosomal RNA depleted total RNA of 10-10 embryos co-injected with TBP-,TBP2- and TLF-AS antisense oligonucleotides an	Gert Veenstra, E Gazdag, I Kruijsbergen, G Veenstra	Differential expression analysis using RNA sequencing	26952988	51942	SRP068680	SRR3107017	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003034/SRR3107017	GSM2042218	SRA335990	SRX1535324	RNA-Seq	SINGLE	SRP068680	PRJNA309218
77281	1	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126253	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126253/SRR3126253.1	GSM2047228	SRA341991	SRX1548330	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	2	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126254	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126254/SRR3126254.1	GSM2047229	SRA341991	SRX1548331	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	3	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126255	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126255/SRR3126255.1	GSM2047230	SRA341991	SRX1548332	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	4	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126256	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126256/SRR3126256.1	GSM2047231	SRA341991	SRX1548333	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	5	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126257	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126257/SRR3126257.1	GSM2047232	SRA341991	SRX1548334	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	6	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126258	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126258/SRR3126258.1	GSM2047233	SRA341991	SRX1548335	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	7	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126259	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126259/SRR3126259.1	GSM2047234	SRA341991	SRX1548336	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	8	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126260	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126260/SRR3126260.1	GSM2047235	SRA341991	SRX1548337	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	9	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126261	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126261/SRR3126261.1	GSM2047236	SRA341991	SRX1548338	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	10	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126262	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126262/SRR3126262.1	GSM2047237	SRA341991	SRX1548339	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	11	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126263	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126263/SRR3126263.1	GSM2047238	SRA341991	SRX1548340	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	12	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126264	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126264/SRR3126264.1	GSM2047239	SRA341991	SRX1548341	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	13	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126265	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126265/SRR3126265.1	GSM2047240	SRA341991	SRX1548342	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	14	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126266	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126266/SRR3126266.1	GSM2047241	SRA341991	SRX1548343	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77281	15	Toshi Shioda	RNA-seq based identification of potential RARgamma target genes in Xenopus laevis	The development of massively parallel sequencing technologies has revolutionized transcriptome analysis. Sequencing of total cDNA (RNA-Seq) can determ	Toshi Shioda, Amanda Janesick, Weiyi Tang, Bruce Blumberg	Xenopus laevis early blastula stage embyos were exposed to (1) 0.1% EtOH as vehicle, (2) an RARgamma-selective dose (10 nM) NRX204647, and (3) a high dose (1 microM) of NRX204647, which activates all three RAR subtypes (RARalpha, beta, gamma). Each exposure group cosisted of five single-clutch replicates.	0	57140	SRP068951	SRR3126267	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR3126267/SRR3126267.1	GSM2047242	SRA341991	SRX1548344	RNA-Seq	SINGLE	SRP068951	PRJNA309946
77363	1	Richard Harland	Genome-wide binding pattern of β-catenin during Xenopus gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Xenopus laevis emrbyos were injected with a triple FLAG tagged beta-catenin at levels that did not effect phenotype. Pools of about 500 embryos were fixed for ChIP processing. An input sample was taken prior to immunoprecipitation with a Flag antibody. Both input and ChIP material were used to make sequencing libraries.	27091726	52028	SRP069034	SRR3133151	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133151	GSM2050738	SRA342793	SRX1552576	ChIP-Seq	SINGLE	SRP069034	PRJNA310141
77363	2	Richard Harland	Genome-wide binding pattern of β-catenin during Xenopus gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Xenopus laevis emrbyos were injected with a triple FLAG tagged beta-catenin at levels that did not effect phenotype. Pools of about 500 embryos were fixed for ChIP processing. An input sample was taken prior to immunoprecipitation with a Flag antibody. Both input and ChIP material were used to make sequencing libraries.	27091726	52028	SRP069034	SRR3133152	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133152	GSM2050739	SRA342793	SRX1552577	ChIP-Seq	SINGLE	SRP069034	PRJNA310141
77363	3	Richard Harland	Genome-wide binding pattern of β-catenin during Xenopus gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Xenopus laevis emrbyos were injected with a triple FLAG tagged beta-catenin at levels that did not effect phenotype. Pools of about 500 embryos were fixed for ChIP processing. An input sample was taken prior to immunoprecipitation with a Flag antibody. Both input and ChIP material were used to make sequencing libraries.	27091726	52028	SRP069034	SRR3133153	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133153	GSM2050740	SRA342793	SRX1552578	ChIP-Seq	SINGLE	SRP069034	PRJNA310141
77363	4	Richard Harland	Genome-wide binding pattern of β-catenin during Xenopus gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Xenopus laevis emrbyos were injected with a triple FLAG tagged beta-catenin at levels that did not effect phenotype. Pools of about 500 embryos were fixed for ChIP processing. An input sample was taken prior to immunoprecipitation with a Flag antibody. Both input and ChIP material were used to make sequencing libraries.	27091726	52028	SRP069034	SRR3133154	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133154	GSM2050741	SRA342793	SRX1552579	ChIP-Seq	SINGLE	SRP069034	PRJNA310141
77363	5	Richard Harland	Genome-wide binding pattern of β-catenin during Xenopus gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Xenopus laevis emrbyos were injected with a triple FLAG tagged beta-catenin at levels that did not effect phenotype. Pools of about 500 embryos were fixed for ChIP processing. An input sample was taken prior to immunoprecipitation with a Flag antibody. Both input and ChIP material were used to make sequencing libraries.	27091726	52028	SRP069034	SRR3133155	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133155	GSM2050742	SRA342793	SRX1552580	ChIP-Seq	SINGLE	SRP069034	PRJNA310141
77363	6	Richard Harland	Genome-wide binding pattern of β-catenin during Xenopus gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Xenopus laevis emrbyos were injected with a triple FLAG tagged beta-catenin at levels that did not effect phenotype. Pools of about 500 embryos were fixed for ChIP processing. An input sample was taken prior to immunoprecipitation with a Flag antibody. Both input and ChIP material were used to make sequencing libraries.	27091726	52028	SRP069034	SRR3133156	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133156	GSM2050743	SRA342793	SRX1552581	ChIP-Seq	SINGLE	SRP069034	PRJNA310141
77364	1	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133166	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133166	GSM2050744	SRA342794	SRX1552582	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	2	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133167	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133167	GSM2050744	SRA342794	SRX1552582	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	3	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133168	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133168	GSM2050744	SRA342794	SRX1552582	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	4	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133169	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133169	GSM2050744	SRA342794	SRX1552582	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	5	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133170	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133170	GSM2050744	SRA342794	SRX1552582	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	6	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133171	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133171	GSM2050744	SRA342794	SRX1552582	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	7	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133172	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133172	GSM2050744	SRA342794	SRX1552582	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	8	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133173	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133173	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	9	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133174	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133174	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	10	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133175	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133175	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	11	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133176	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133176	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	12	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133177	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133177	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	13	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133178	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133178	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	14	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133179	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133179	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	15	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133180	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133180	GSM2050745	SRA342794	SRX1552583	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	16	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133181	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133181	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	17	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133182	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133182	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	18	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133183	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133183	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	19	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133184	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133184	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	20	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133185	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133185	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	21	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133186	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133186	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	22	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133187	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133187	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	23	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133188	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133188	GSM2050746	SRA342794	SRX1552584	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	24	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133189	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133189	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	25	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133190	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133190	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	26	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133191	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133191	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	27	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133192	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133192	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	28	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133193	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133193	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	29	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133194	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133194	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	30	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133195	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133195	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	31	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133196	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133196	GSM2050747	SRA342794	SRX1552585	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	32	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133197	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133197	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	33	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133198	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133198	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	34	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133199	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133199	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	35	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133200	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133200	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	36	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133201	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133201	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	37	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133202	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133202	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	38	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133203	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133203	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	39	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133204	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133204	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	40	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133205	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133205	GSM2050748	SRA342794	SRX1552586	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	41	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133206	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133206	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	42	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133207	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133207	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	43	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133208	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133208	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	44	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133209	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133209	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	45	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133210	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133210	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	46	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133211	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133211	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	47	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133212	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133212	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	48	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133213	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133213	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	49	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133214	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003059/SRR3133214	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77364	50	Richard Harland	Transcriptome analysis of Wnt knockdown embryos reveals candidate canonical Wnt/β-catenin target genes during Xenopus laevis gastrulation	The canonical Wnt/β-catenin signaling pathway plays multiple roles during Xenopus gastrulation, including posteriorization of the neural plate, patte	Richard Harland, Rachel Kjolby, Richard Harland	Total RNA was extracted from a single uninjected control and a single dkk injected embryo from the same mating and used to make sequencing libraries. There are three replicates, each pair from a different mating pair.	27091726	52028	SRP069035	SRR3133215	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003059/SRR3133215	GSM2050749	SRA342794	SRX1552587	RNA-Seq	PAIRED	SRP069035	PRJNA310139
77724	1	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157346	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157346	GSM2057921	SRA352385	SRX1568298	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	2	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157347	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157347	GSM2057922	SRA352385	SRX1568299	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	3	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157348	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157348	GSM2057923	SRA352385	SRX1568300	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	4	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157349	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157349	GSM2057924	SRA352385	SRX1568301	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	5	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157350	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003083/SRR3157350	GSM2057925	SRA352385	SRX1568302	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	6	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157351	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157351	GSM2057926	SRA352385	SRX1568303	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	7	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157352	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157352	GSM2057927	SRA352385	SRX1568304	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	8	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157353	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157353	GSM2057928	SRA352385	SRX1568305	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	9	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157354	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003083/SRR3157354	GSM2057929	SRA352385	SRX1568306	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	10	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157355	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157355	GSM2057930	SRA352385	SRX1568307	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	11	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157356	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003083/SRR3157356	GSM2057931	SRA352385	SRX1568308	RNA-Seq	SINGLE	SRP069816	PRJNA311315
77724	12	Gregg Whitworth	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis	Unlike adult mammals, adult frogs regrow and regenerate their optic nerve following a crush injury. Using Translational Ribosome Affinity Purification	Gregg Whitworth, Gregg Whitworth, Bayan Misaghi, Andrew Watson, David Heinen, Nicholas Marsh-Armstrong, Fiona Watson	To investigate the changes in gene expression that occur as retinal ganglion cells (RGCs) recover and regrow following injury, we have used the TRAP method.  With TRAP we are able to isolate the actively translating pool of mRNAs from a specific cell type, in this case RGCs.  To do this, we created lines of transgenic frogs which express an eGFP-tagged variant of the large ribosomal protein rpl10a under the control of an RGC-specific promoter from the islet2b locus.  In our experimental framework, we quantify gene expression changes in RGCs recovering from optic nerve crush by comparing mRNA levels in samples collected from the eye undergoing a surgical crush (right) to the contralateral eye (left).  At discrete time points following optic nerve crush in the left eye, both eyes are rapidly dissected and the ribosome-associated RNAs purified from tissue extracts using eGFP antibodies conjugated to magnetic beads.  To control for the effects of surgery on RGCs, gene expression was also quantified in animals that underwent sham surgeries with no optic nerve crush ("sham" samples).  To control for the systemic effects of the surgical procedure per se, gene expression was also quantified in animals that did not undergo any surgery ("naive" sample).  These mRNA pools were used to construct libraries for RNA-Seq using poly(A) selection and 2x multiplexing.	27471010	52302	SRP069816	SRR3157357	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003083/SRR3157357	GSM2057932	SRA352385	SRX1568309	RNA-Seq	SINGLE	SRP069816	PRJNA311315
78176	1	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182668	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182668	GSM2068802	SRA356925	SRX1596710	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	2	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182669	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003108/SRR3182669	GSM2068802	SRA356925	SRX1596710	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	3	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182670	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182670	GSM2068803	SRA356925	SRX1596711	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	4	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182671	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182671	GSM2068804	SRA356925	SRX1596712	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	5	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182672	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182672	GSM2068804	SRA356925	SRX1596712	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	6	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182673	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003108/SRR3182673	GSM2068805	SRA356925	SRX1596713	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	7	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182674	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182674	GSM2068806	SRA356925	SRX1596714	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	8	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182675	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003108/SRR3182675	GSM2068807	SRA356925	SRX1596715	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	9	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182676	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182676	GSM2068808	SRA356925	SRX1596716	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	10	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182677	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182677	GSM2068809	SRA356925	SRX1596717	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	11	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182678	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182678	GSM2068810	SRA356925	SRX1596718	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	12	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182679	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003108/SRR3182679	GSM2068811	SRA356925	SRX1596719	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	13	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182680	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182680	GSM2068812	SRA356925	SRX1596720	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	14	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182681	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/003108/SRR3182681	GSM2068813	SRA356925	SRX1596721	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	15	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182682	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182682	GSM2068814	SRA356925	SRX1596722	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78176	16	Ian Quigley	Histone modification and transcription factor ChIPseq of Xenopus laevis epithelial progenitors	To determine the positions of promoters and enhancers in developing Xenopus laevis epithelial progenitors, we performed ChIPseq on the histone modific	Ian Quigley, Chris Kintner	Some embryos were harvested as wild-types; in other experiments, we injected  embryos with mRNAs encoding FLAG-foxj1 (with and without rfx2 morpholino) or GFP-myb (with and without an inducible form of multicilin (mcidas-HGR)).  We then isolated epithelial progenitors surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested chromatin at 9 hours after induction (roughly stage 18) and performed ChIPseq using antibodies against endogenous targets (H3K4me3, H3K27ac, rad21) or protein tags (FLAG, GFP). We then sequenced these libraries, aligned the reads to the X. laevis genome (version 9.1) with bwa mem and called peaks with HOMER, using input as background.	28103240	53709	SRP070664	SRR3182683	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003108/SRR3182683	GSM2068815	SRA356925	SRX1596723	ChIP-Seq	SINGLE	SRP070664	PRJNA312836
78854	1	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201255	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201255	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	2	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201256	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201256	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	3	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201257	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201257	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	4	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201258	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201258	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	5	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201259	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201259	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	6	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201260	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201260	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	7	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201261	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201261	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	8	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201262	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201262	GSM2079619	SRA366069	SRX1610974	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	9	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201263	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201263	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	10	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201264	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201264	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	11	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201265	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201265	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	12	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201266	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201266	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	13	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201267	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201267	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	14	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201268	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201268	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	15	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201269	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201269	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	16	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201270	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201270	GSM2079620	SRA366069	SRX1610975	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	17	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201271	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201271	GSM2079621	SRA366069	SRX1610976	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	18	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201272	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201272	GSM2079621	SRA366069	SRX1610976	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	19	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201273	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201273	GSM2079621	SRA366069	SRX1610976	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	20	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201274	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201274	GSM2079621	SRA366069	SRX1610976	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	21	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201275	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201275	GSM2079621	SRA366069	SRX1610976	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	22	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201276	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201276	GSM2079621	SRA366069	SRX1610976	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
78854	23	Giordano Lippi	Peptide-signaling and miRNA regulation of transmitter switching affecting social preference	Sensory circuit activation can induce neurotransmitter respecification. To understand the consequences and mechanisms of this neuroplasticity we inves	Giordano Lippi, Davide Dulcis, Christiana Stark, Long Do, Darwin Berg, Nicholas Spitzer	The AOBs of 15 larvae (stage 45) raised in sibling, orphan, or non-sibling conditions were frozen, cryosectioned at 50 μm and neuronal tissue was harvested with scalpels for clean dissection. Total RNA was extracted from tissue with the “Recover All Total Nucleic Acid” isolation kit. RNA quality was assessed on a Bioanalyzer and degraded samples excluded from RNA sequencing. Library preparation and RNA sequencing were performed at the UCSD Biogem core.	28867550	53988	SRP071089	SRR3201277	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003126/SRR3201277	GSM2079621	SRA366069	SRX1610976	miRNA-Seq	SINGLE	SRP071089	PRJNA314143
80971	1	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469769	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469769	GSM2139449	SRA422827	SRX1738127	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	2	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469770	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469770	GSM2139449	SRA422827	SRX1738127	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	3	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469771	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469771	GSM2139450	SRA422827	SRX1738128	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	4	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469772	https://sra-download.ncbi.nlm.nih.gov/traces/sra40/SRR/003388/SRR3469772	GSM2139450	SRA422827	SRX1738128	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	5	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469773	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469773	GSM2139451	SRA422827	SRX1738129	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	6	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469774	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469774	GSM2139451	SRA422827	SRX1738129	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	7	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469775	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469775	GSM2139452	SRA422827	SRX1738130	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	8	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469776	https://sra-download.ncbi.nlm.nih.gov/traces/sra40/SRR/003388/SRR3469776	GSM2139452	SRA422827	SRX1738130	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	9	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469777	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469777	GSM2139453	SRA422827	SRX1738131	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	10	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469778	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/003388/SRR3469778	GSM2139453	SRA422827	SRX1738131	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	11	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469779	https://sra-download.ncbi.nlm.nih.gov/traces/sra40/SRR/003388/SRR3469779	GSM2139454	SRA422827	SRX1738132	RNA-Seq	PAIRED	SRP074230	PRJNA320214
80971	12	Mary King	High Throughput Analysis Reveals Novel Maternal Germline RNAs Critical for PGC Preservation and Proper Migration	During oogenesis hundreds of RNAs are selectively localized to either the animal or vegetal cortical region. These maternal RNAs include determinants 	Mary King, Dawn Owens, Amanda Butler, Mary King	Examination of animal and vegetal pole samples of stg. VI X. laevis oocyte to determine vegetally enriched genes that may contribute to germ plasm and PGCs.	28096217	53019	SRP074230	SRR3469780	https://sra-download.ncbi.nlm.nih.gov/traces/sra40/SRR/003388/SRR3469780	GSM2139454	SRA422827	SRX1738132	RNA-Seq	PAIRED	SRP074230	PRJNA320214
81458	1	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509723	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003427/SRR3509723	GSM2152748	SRA425738	SRX1763440	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	2	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509724	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/003427/SRR3509724	GSM2152749	SRA425738	SRX1763441	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	3	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509725	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003427/SRR3509725	GSM2152750	SRA425738	SRX1763442	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	4	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509726	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/003427/SRR3509726	GSM2152751	SRA425738	SRX1763443	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	5	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509727	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003427/SRR3509727	GSM2152752	SRA425738	SRX1763444	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	6	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509728	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/003427/SRR3509728	GSM2152753	SRA425738	SRX1763445	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	7	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509729	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003427/SRR3509729	GSM2152754	SRA425738	SRX1763446	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	8	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509730	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/003427/SRR3509730	GSM2152755	SRA425738	SRX1763447	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	9	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509731	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003427/SRR3509731	GSM2152756	SRA425738	SRX1763448	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	10	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509732	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/003427/SRR3509732	GSM2152757	SRA425738	SRX1763449	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	11	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509733	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/003427/SRR3509733	GSM2152758	SRA425738	SRX1763450	RNA-Seq	SINGLE	SRP075201	PRJNA321667
81458	12	Kitt Paraiso	Regional expression of X. tropicalis transcription factors in early gastrula embryos	Purpose: We wished to obtain spatial expression profiles of transcription factor gene expression and expression of other genes.Methods: Embryos were 	Kitt Paraiso, Ira Blitz, Kitt Paraiso	mRNA-seq performed on 5 dissected regions of NF stage 10.5 X. tropicalis embryos and stage-matched sibling whole embryos. Experiment performed in duplicate.	27475627	52307	SRP075201	SRR3509734	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/003427/SRR3509734	GSM2152759	SRA425738	SRX1763451	RNA-Seq	SINGLE	SRP075201	PRJNA321667
82153	1	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620839	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620839/SRR3620839.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	2	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620840	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620840/SRR3620840.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	3	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620841	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620841/SRR3620841.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	4	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620842	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620842/SRR3620842.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	5	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620843	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620843/SRR3620843.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	6	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620844	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620844/SRR3620844.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	7	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620845	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620845/SRR3620845.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	8	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620846	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620846/SRR3620846.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	9	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620847	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620847/SRR3620847.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	10	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620848	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620848/SRR3620848.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	11	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620849	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620849/SRR3620849.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	12	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620850	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620850/SRR3620850.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	13	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620851	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620851/SRR3620851.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	14	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620852	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620852/SRR3620852.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	15	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620853	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620853/SRR3620853.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	16	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620854	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620854/SRR3620854.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	17	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620855	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620855/SRR3620855.1	GSM2184890	SRA430469	SRX1816638	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	18	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620856	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620856/SRR3620856.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	19	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620857	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620857/SRR3620857.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	20	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620858	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620858/SRR3620858.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	21	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620859	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620859/SRR3620859.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	22	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620860	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620860/SRR3620860.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	23	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620861	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620861/SRR3620861.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	24	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620862	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620862/SRR3620862.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	25	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620863	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620863/SRR3620863.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	26	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620864	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620864/SRR3620864.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	27	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620865	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620865/SRR3620865.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	28	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620866	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620866/SRR3620866.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	29	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620867	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620867/SRR3620867.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	30	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620868	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620868/SRR3620868.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	31	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620869	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620869/SRR3620869.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
82153	32	Saartje Hontelez	CDK9 knock-out Xenopus tropicalis	To study the role of CDK9 in RNAPII pausing                                                                                                           	Saartje Hontelez, GertJan Veenstra, Marta Marin-Barba, Grant Wheeler, Ines Desanlis	Knock-down of CDK9 by injection of CDK9.S morpholino	0	57687	SRP076016	SRR3620870	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-1/SRR3620870/SRR3620870.1	GSM2184891	SRA430469	SRX1816639	ChIP-Seq	SINGLE	SRP076016	PRJNA324187
83784	1	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723149	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723149	GSM2218802	SRA436183	SRX1880836	miRNA-Seq	SINGLE	SRP077327	PRJNA326974
83784	2	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723150	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723150	GSM2218803	SRA436183	SRX1880837	miRNA-Seq	SINGLE	SRP077327	PRJNA326974
83784	3	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723151	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723151	GSM2218804	SRA436183	SRX1880838	miRNA-Seq	SINGLE	SRP077327	PRJNA326974
83784	4	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723152	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723152	GSM2218805	SRA436183	SRX1880839	miRNA-Seq	SINGLE	SRP077327	PRJNA326974
83784	5	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723153	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723153	GSM2218806	SRA436183	SRX1880840	miRNA-Seq	SINGLE	SRP077327	PRJNA326974
83784	6	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723154	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723154	GSM2218807	SRA436183	SRX1880841	miRNA-Seq	SINGLE	SRP077327	PRJNA326974
83784	7	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723155	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723155	GSM2218808	SRA436183	SRX1880842	OTHER	PAIRED	SRP077327	PRJNA326974
83784	8	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723156	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723156	GSM2218809	SRA436183	SRX1880843	OTHER	PAIRED	SRP077327	PRJNA326974
83784	9	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723157	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723157	GSM2218810	SRA436183	SRX1880844	OTHER	PAIRED	SRP077327	PRJNA326974
83784	10	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723158	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723158	GSM2218811	SRA436183	SRX1880845	OTHER	PAIRED	SRP077327	PRJNA326974
83784	11	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723159	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723159	GSM2218812	SRA436183	SRX1880846	OTHER	PAIRED	SRP077327	PRJNA326974
83784	12	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723160	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723160	GSM2218813	SRA436183	SRX1880847	OTHER	PAIRED	SRP077327	PRJNA326974
83784	13	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723161	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723161	GSM2218814	SRA436183	SRX1880848	OTHER	PAIRED	SRP077327	PRJNA326974
83784	14	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723162	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723162	GSM2218815	SRA436183	SRX1880849	OTHER	PAIRED	SRP077327	PRJNA326974
83784	15	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723163	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723163	GSM2218816	SRA436183	SRX1880850	OTHER	PAIRED	SRP077327	PRJNA326974
83784	16	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723164	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723164	GSM2218817	SRA436183	SRX1880851	OTHER	PAIRED	SRP077327	PRJNA326974
83784	17	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723165	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723165	GSM2218818	SRA436183	SRX1880852	OTHER	PAIRED	SRP077327	PRJNA326974
83784	18	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723166	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723166	GSM2218819	SRA436183	SRX1880853	RNA-Seq	PAIRED	SRP077327	PRJNA326974
83784	19	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723167	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723167	GSM2218820	SRA436183	SRX1880854	RNA-Seq	PAIRED	SRP077327	PRJNA326974
83784	20	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723168	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723168	GSM2218821	SRA436183	SRX1880855	RNA-Seq	PAIRED	SRP077327	PRJNA326974
83784	21	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723169	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723169	GSM2218822	SRA436183	SRX1880856	RNA-Seq	PAIRED	SRP077327	PRJNA326974
83784	22	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723170	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723170	GSM2218823	SRA436183	SRX1880857	RNA-Seq	PAIRED	SRP077327	PRJNA326974
83784	23	Amy Sater	Identification of microRNAs and microRNA targets in Xenopus ectoderm	Purpose: The establishment of cell lineages occurs via a dynamic progression of gene regulatory networks that underlie developmental commitment and di	Amy Sater, Vrutant Shah	Identification of microRNAs and microRNA targets in establishment of early ectodermal tissues in Xenopus.	27623002	52452	SRP077327	SRR3723171	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/003635/SRR3723171	GSM2218824	SRA436183	SRX1880858	RNA-Seq	PAIRED	SRP077327	PRJNA326974
85273	1	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011696	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011696	GSM2263590	SRA449640	SRX2007793	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	2	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011697	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011697	GSM2263590	SRA449640	SRX2007793	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	3	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011698	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011698	GSM2263591	SRA449640	SRX2007794	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	4	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011699	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011699	GSM2263591	SRA449640	SRX2007794	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	5	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011700	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011700	GSM2263592	SRA449640	SRX2007795	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	6	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011701	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011701	GSM2263593	SRA449640	SRX2007796	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	7	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011702	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011702	GSM2263593	SRA449640	SRX2007796	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	8	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011703	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011703	GSM2263594	SRA449640	SRX2007797	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	9	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011704	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011704	GSM2263594	SRA449640	SRX2007797	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	10	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011705	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011705	GSM2263595	SRA449640	SRX2007798	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	11	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011706	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011706	GSM2263595	SRA449640	SRX2007798	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	12	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011707	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011707	GSM2263596	SRA449640	SRX2007799	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	13	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011708	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011708	GSM2263596	SRA449640	SRX2007799	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	14	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011709	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011709	GSM2263597	SRA449640	SRX2007800	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	15	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011710	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011710	GSM2263598	SRA449640	SRX2007801	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	16	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011711	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011711	GSM2263599	SRA449640	SRX2007802	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	17	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011712	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011712	GSM2263599	SRA449640	SRX2007802	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
85273	18	Rebekah Charney	Foxh1 marks the embryonic genome prior to the activation of the mesendoderm gene regulatory program	We examined the binding dynamics of the maternal TF Foxh1 over a time course of germ layer development. Foxh1 binding was compared to the onset of zyg	Rebekah Charney, Ken Cho	ChIP-seq analysis of transcription factors Foxh1 and Foxa, RNA Polymerase II and the co-repressor TLE, during zygotic gene activation and germ layer development. Includes biological replicates and stage-matched input controls. Five Samples from GSE53652 are included in this study. The reanalyzed processed data for these Samples are on the Series record.	28325473	53575	SRP081096	SRR4011713	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/003917/SRR4011713	GSM2263600	SRA449640	SRX2007803	ChIP-Seq	SINGLE	SRP081096	PRJNA338166
86382	1	Stephanie Ceman	RISC factor MOV10 is required for normal development and viability in both mouse and Xenopus	MOV10 is an RNA helicase that functions in the miRNA pathway. Our study shows that a knockdown of MOV10 in mouse is embryonic lethal. To determine the	Stephanie Ceman, Geena Skariah	The analysis includes 5 samples. Three of these are control morpholino injected stage 10.5 embryos. The remaining 2 are MOV10 morpholino treated embryos from the same stage. The samples are biological replicates.	29266590	54381	SRP084249	SRR4120004	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004023/SRR4120004	GSM2301411	SRA459848	SRX2100827	RNA-Seq	SINGLE	SRP084249	PRJNA341579
86382	2	Stephanie Ceman	RISC factor MOV10 is required for normal development and viability in both mouse and Xenopus	MOV10 is an RNA helicase that functions in the miRNA pathway. Our study shows that a knockdown of MOV10 in mouse is embryonic lethal. To determine the	Stephanie Ceman, Geena Skariah	The analysis includes 5 samples. Three of these are control morpholino injected stage 10.5 embryos. The remaining 2 are MOV10 morpholino treated embryos from the same stage. The samples are biological replicates.	29266590	54381	SRP084249	SRR4120005	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004023/SRR4120005	GSM2301412	SRA459848	SRX2100828	RNA-Seq	SINGLE	SRP084249	PRJNA341579
86382	3	Stephanie Ceman	RISC factor MOV10 is required for normal development and viability in both mouse and Xenopus	MOV10 is an RNA helicase that functions in the miRNA pathway. Our study shows that a knockdown of MOV10 in mouse is embryonic lethal. To determine the	Stephanie Ceman, Geena Skariah	The analysis includes 5 samples. Three of these are control morpholino injected stage 10.5 embryos. The remaining 2 are MOV10 morpholino treated embryos from the same stage. The samples are biological replicates.	29266590	54381	SRP084249	SRR4120006	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004023/SRR4120006	GSM2301413	SRA459848	SRX2100829	RNA-Seq	SINGLE	SRP084249	PRJNA341579
86382	4	Stephanie Ceman	RISC factor MOV10 is required for normal development and viability in both mouse and Xenopus	MOV10 is an RNA helicase that functions in the miRNA pathway. Our study shows that a knockdown of MOV10 in mouse is embryonic lethal. To determine the	Stephanie Ceman, Geena Skariah	The analysis includes 5 samples. Three of these are control morpholino injected stage 10.5 embryos. The remaining 2 are MOV10 morpholino treated embryos from the same stage. The samples are biological replicates.	29266590	54381	SRP084249	SRR4120007	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004023/SRR4120007	GSM2301414	SRA459848	SRX2100830	RNA-Seq	SINGLE	SRP084249	PRJNA341579
86382	5	Stephanie Ceman	RISC factor MOV10 is required for normal development and viability in both mouse and Xenopus	MOV10 is an RNA helicase that functions in the miRNA pathway. Our study shows that a knockdown of MOV10 in mouse is embryonic lethal. To determine the	Stephanie Ceman, Geena Skariah	The analysis includes 5 samples. Three of these are control morpholino injected stage 10.5 embryos. The remaining 2 are MOV10 morpholino treated embryos from the same stage. The samples are biological replicates.	29266590	54381	SRP084249	SRR4120008	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004023/SRR4120008	GSM2301415	SRA459848	SRX2100831	RNA-Seq	SINGLE	SRP084249	PRJNA341579
86649	1	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241282	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241282	GSM2308328	SRA470686	SRX2162254	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	2	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241283	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241283	GSM2308329	SRA470686	SRX2162255	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	3	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241284	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241284	GSM2308330	SRA470686	SRX2162256	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	4	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241285	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241285	GSM2308331	SRA470686	SRX2162257	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	5	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241286	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241286	GSM2308332	SRA470686	SRX2162258	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	6	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241287	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241287	GSM2308333	SRA470686	SRX2162259	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	7	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241288	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241288	GSM2308334	SRA470686	SRX2162260	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	8	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241289	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241289	GSM2308335	SRA470686	SRX2162261	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	9	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241290	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241290	GSM2308336	SRA470686	SRX2162262	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	10	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241291	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241291	GSM2308337	SRA470686	SRX2162263	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	11	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241292	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241292	GSM2308338	SRA470686	SRX2162264	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	12	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241293	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241293	GSM2308339	SRA470686	SRX2162265	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	13	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241294	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241294	GSM2308340	SRA470686	SRX2162266	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	14	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241295	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241295	GSM2308341	SRA470686	SRX2162267	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	15	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241296	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241296	GSM2308342	SRA470686	SRX2162268	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86649	16	Gabriela Salinas-Riester	Comparative temporal analysis of wild-type Ptf1a, Neurog2 and mutant Ptf1a (Ptf1aW224A/W242A) overexpressing Xenopus explant transcriptomes after 6 and 25 hours of DEX induction.	RNA-seq reveals the downstream gene regulatory network of wild-type Ptf1a, Neurog2 and Ptf1aW224A/W242A                                               	Gabriela Salinas-Riester, Kristine Henningfeld, Tomas Pieler, Marie Hedderich, Thomas Lingner	X.laevis embryos were injected in the animal pole of both blastomeres at the two-cell stage with 20 pg mRNA encoding for ptf1a-GR, GR-neurog2 or ptf1aW224A/W242A-GR. At blastula stage, inijected DEX-treated animal caps served as controls (CC).	0	57684	SRP089812	SRR4241297	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004141/SRR4241297	GSM2308343	SRA470686	SRX2162269	RNA-Seq	PAIRED	SRP089812	PRJNA342823
86883	1	Cei Abreu-Goodger	miR-182 regulates Slit2-mediated axon guidance by modulating the local translation of a specific mRNA	During brain wiring, mRNAs are trafficked into axons and growth cones where they are differentially translated in response to extrinsic signals. Diffe	Cei Abreu-Goodger, Anaïs Bellon, Archana Iyer, Simone Bridi, Flora Lee, Cesaré Ovando-Vázquez, Eloina Corradi, Sara Longhi, Michela Rocuzzo, Stephanie Strohbuecker, Sindhu Naik, Peter Sarkies, Eric Miska, Christine Holt, Marie-Laure Baudet	Two biological replicates, one condition	28147273	53046	SRP089815	SRR4241439	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004142/SRR4241439	GSM2309835	SRA470711	SRX2162412	miRNA-Seq	SINGLE	SRP089815	PRJNA342827
86883	2	Cei Abreu-Goodger	miR-182 regulates Slit2-mediated axon guidance by modulating the local translation of a specific mRNA	During brain wiring, mRNAs are trafficked into axons and growth cones where they are differentially translated in response to extrinsic signals. Diffe	Cei Abreu-Goodger, Anaïs Bellon, Archana Iyer, Simone Bridi, Flora Lee, Cesaré Ovando-Vázquez, Eloina Corradi, Sara Longhi, Michela Rocuzzo, Stephanie Strohbuecker, Sindhu Naik, Peter Sarkies, Eric Miska, Christine Holt, Marie-Laure Baudet	Two biological replicates, one condition	28147273	53046	SRP089815	SRR4241440	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/004142/SRR4241440	GSM2309836	SRA470711	SRX2162413	miRNA-Seq	SINGLE	SRP089815	PRJNA342827
87652	1	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346390	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346390	GSM2337671	SRA482196	SRX2213215	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	2	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346391	https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/004244/SRR4346391	GSM2337672	SRA482196	SRX2213216	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	3	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346392	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004244/SRR4346392	GSM2337673	SRA482196	SRX2213217	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	4	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346393	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004244/SRR4346393	GSM2337674	SRA482196	SRX2213218	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	5	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346394	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/004244/SRR4346394	GSM2337675	SRA482196	SRX2213219	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	6	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346395	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/004244/SRR4346395	GSM2337676	SRA482196	SRX2213220	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	7	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346396	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004244/SRR4346396	GSM2337677	SRA482196	SRX2213221	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	8	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346397	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346397	GSM2337678	SRA482196	SRX2213222	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	9	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346398	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004244/SRR4346398	GSM2337679	SRA482196	SRX2213223	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	10	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346399	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004244/SRR4346399	GSM2337680	SRA482196	SRX2213224	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	11	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346400	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004244/SRR4346400	GSM2337681	SRA482196	SRX2213225	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	12	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346401	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346401	GSM2337682	SRA482196	SRX2213226	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	13	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346402	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004244/SRR4346402	GSM2337683	SRA482196	SRX2213227	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	14	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346403	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004244/SRR4346403	GSM2337684	SRA482196	SRX2213228	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	15	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346404	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/004244/SRR4346404	GSM2337685	SRA482196	SRX2213229	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	16	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346405	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346405	GSM2337686	SRA482196	SRX2213230	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	17	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346406	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004244/SRR4346406	GSM2337687	SRA482196	SRX2213231	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	18	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346407	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004244/SRR4346407	GSM2337688	SRA482196	SRX2213232	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	19	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346408	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004244/SRR4346408	GSM2337689	SRA482196	SRX2213233	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87652	20	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [ChIP-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	ChIP of whole embryos, foregut and hindgut explants for 3 different antibodies (b-catenin, Smad1 and p300).	28219948	53106	SRP090888	SRR4346409	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004244/SRR4346409	GSM2337690	SRA482196	SRX2213234	ChIP-Seq	SINGLE	SRP090888	PRJNA345495
87653	1	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346410	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004244/SRR4346410	GSM2337691	SRA482197	SRX2213235	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	2	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346411	https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/004244/SRR4346411	GSM2337692	SRA482197	SRX2213236	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	3	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346412	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004244/SRR4346412	GSM2337693	SRA482197	SRX2213237	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	4	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346413	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004244/SRR4346413	GSM2337694	SRA482197	SRX2213238	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	5	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346414	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004244/SRR4346414	GSM2337695	SRA482197	SRX2213239	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	6	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346415	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004244/SRR4346415	GSM2337696	SRA482197	SRX2213240	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	7	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346416	https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/004244/SRR4346416	GSM2337697	SRA482197	SRX2213241	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	8	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346417	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346417	GSM2337698	SRA482197	SRX2213242	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	9	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346418	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004244/SRR4346418	GSM2337699	SRA482197	SRX2213243	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	10	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346419	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004244/SRR4346419	GSM2337700	SRA482197	SRX2213244	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	11	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346420	https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/004244/SRR4346420	GSM2337701	SRA482197	SRX2213245	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	12	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346421	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004244/SRR4346421	GSM2337702	SRA482197	SRX2213246	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	13	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346422	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004244/SRR4346422	GSM2337703	SRA482197	SRX2213247	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	14	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346423	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004244/SRR4346423	GSM2337704	SRA482197	SRX2213248	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	15	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346424	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004244/SRR4346424	GSM2337705	SRA482197	SRX2213249	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	16	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346425	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/004244/SRR4346425	GSM2337706	SRA482197	SRX2213250	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	17	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346426	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004244/SRR4346426	GSM2337707	SRA482197	SRX2213251	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	18	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346427	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/004244/SRR4346427	GSM2337708	SRA482197	SRX2213252	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	19	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346428	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004244/SRR4346428	GSM2337709	SRA482197	SRX2213253	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	20	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346429	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004244/SRR4346429	GSM2337710	SRA482197	SRX2213254	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	21	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346430	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346430	GSM2337711	SRA482197	SRX2213255	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	22	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346431	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/004244/SRR4346431	GSM2337712	SRA482197	SRX2213256	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	23	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346432	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004244/SRR4346432	GSM2337713	SRA482197	SRX2213257	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	24	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346433	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004244/SRR4346433	GSM2337714	SRA482197	SRX2213258	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	25	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346434	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/004244/SRR4346434	GSM2337715	SRA482197	SRX2213259	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	26	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346435	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346435	GSM2337716	SRA482197	SRX2213260	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	27	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346436	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/004244/SRR4346436	GSM2337717	SRA482197	SRX2213261	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	28	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346437	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/004244/SRR4346437	GSM2337718	SRA482197	SRX2213262	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	29	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346438	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/004244/SRR4346438	GSM2337719	SRA482197	SRX2213263	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	30	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346439	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/004244/SRR4346439	GSM2337720	SRA482197	SRX2213264	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	31	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346440	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004244/SRR4346440	GSM2337721	SRA482197	SRX2213265	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	32	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346441	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004244/SRR4346441	GSM2337722	SRA482197	SRX2213266	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	33	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346442	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/004244/SRR4346442	GSM2337723	SRA482197	SRX2213267	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	34	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346443	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004244/SRR4346443	GSM2337724	SRA482197	SRX2213268	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	35	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346444	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004244/SRR4346444	GSM2337725	SRA482197	SRX2213269	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	36	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346445	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/004244/SRR4346445	GSM2337726	SRA482197	SRX2213270	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87653	37	Aaron Zorn	Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors [RNA-seq]	Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how they are integrated in the	Aaron Zorn, Mariana Stevens, Praneet Chaturvedi, Scott Rankin, Melissa Macdonald, Sajjeev Jagannathan, Masashi Yukawa, Artem Barski	mRNA profile of foregut and hindgut explants from BMP and Wnt manipulated embryos.	28219948	53106	SRP090889	SRR4346446	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004244/SRR4346446	GSM2337727	SRA482197	SRX2213271	RNA-Seq	SINGLE	SRP090889	PRJNA345496
87872	1	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417743	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004314/SRR4417743	GSM2342126	SRA483678	SRX2240126	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	2	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417744	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417744	GSM2342127	SRA483678	SRX2240127	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	3	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417745	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/004314/SRR4417745	GSM2342128	SRA483678	SRX2240128	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	4	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417746	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/004314/SRR4417746	GSM2342129	SRA483678	SRX2240129	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	5	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417747	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417747	GSM2342130	SRA483678	SRX2240130	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	6	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417748	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/004314/SRR4417748	GSM2342131	SRA483678	SRX2240131	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	7	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417749	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/004314/SRR4417749	GSM2342132	SRA483678	SRX2240132	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	8	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417750	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004314/SRR4417750	GSM2342133	SRA483678	SRX2240133	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	9	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417751	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417751	GSM2342134	SRA483678	SRX2240134	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	10	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417752	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/004314/SRR4417752	GSM2342135	SRA483678	SRX2240135	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	11	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417753	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004314/SRR4417753	GSM2342136	SRA483678	SRX2240136	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	12	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417754	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417754	GSM2342137	SRA483678	SRX2240137	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	13	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417755	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004314/SRR4417755	GSM2342138	SRA483678	SRX2240138	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	14	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417756	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417756	GSM2342139	SRA483678	SRX2240139	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	15	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417757	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004314/SRR4417757	GSM2342140	SRA483678	SRX2240140	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	16	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417758	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004314/SRR4417758	GSM2342141	SRA483678	SRX2240141	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	17	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417759	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004314/SRR4417759	GSM2342142	SRA483678	SRX2240142	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	18	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417760	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417760	GSM2342143	SRA483678	SRX2240143	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	19	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417761	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004314/SRR4417761	GSM2342144	SRA483678	SRX2240144	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	20	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417762	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004314/SRR4417762	GSM2342145	SRA483678	SRX2240145	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	21	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417763	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417763	GSM2342146	SRA483678	SRX2240146	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	22	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417764	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004314/SRR4417764	GSM2342147	SRA483678	SRX2240147	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	23	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417765	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004314/SRR4417765	GSM2342148	SRA483678	SRX2240148	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	24	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417766	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004314/SRR4417766	GSM2342149	SRA483678	SRX2240149	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	25	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417767	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004314/SRR4417767	GSM2342150	SRA483678	SRX2240150	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	26	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417768	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004314/SRR4417768	GSM2342151	SRA483678	SRX2240151	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	27	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417769	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004314/SRR4417769	GSM2342152	SRA483678	SRX2240152	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	28	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417770	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004314/SRR4417770	GSM2342153	SRA483678	SRX2240153	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	29	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417771	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004314/SRR4417771	GSM2342154	SRA483678	SRX2240154	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	30	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417772	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/004314/SRR4417772	GSM2342155	SRA483678	SRX2240155	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	31	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417773	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417773	GSM2342156	SRA483678	SRX2240156	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	32	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417774	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004314/SRR4417774	GSM2342157	SRA483678	SRX2240157	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	33	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417775	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/004314/SRR4417775	GSM2342158	SRA483678	SRX2240158	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	34	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417776	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417776	GSM2342159	SRA483678	SRX2240159	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	35	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417777	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/004314/SRR4417777	GSM2342160	SRA483678	SRX2240160	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	36	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417778	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004314/SRR4417778	GSM2342161	SRA483678	SRX2240161	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	37	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417779	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004314/SRR4417779	GSM2342162	SRA483678	SRX2240162	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	38	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417780	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004314/SRR4417780	GSM2342163	SRA483678	SRX2240163	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	39	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417781	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/004314/SRR4417781	GSM2342164	SRA483678	SRX2240164	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	40	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417782	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/004314/SRR4417782	GSM2342165	SRA483678	SRX2240165	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	41	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417783	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/004314/SRR4417783	GSM2342166	SRA483678	SRX2240166	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	42	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417784	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/004314/SRR4417784	GSM2342167	SRA483678	SRX2240167	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	43	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417785	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004314/SRR4417785	GSM2342168	SRA483678	SRX2240168	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	44	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417786	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004314/SRR4417786	GSM2342169	SRA483678	SRX2240169	RNA-Seq	SINGLE	SRP091439	PRJNA347982
87872	45	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417787	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/004314/SRR4417787	GSM2342170	SRA483678	SRX2240170	ChIP-Seq	SINGLE	SRP091439	PRJNA347982
87872	46	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417788	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/004314/SRR4417788	GSM2342171	SRA483678	SRX2240171	ChIP-Seq	SINGLE	SRP091439	PRJNA347982
87872	47	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417789	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/004314/SRR4417789	GSM2342172	SRA483678	SRX2240172	ChIP-Seq	SINGLE	SRP091439	PRJNA347982
87872	48	Charles Bradshaw	Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin repressive pathways	Understanding the mechanism of resistance of certain genes to reactivation will help improving the success of nuclear reprogramming. Here, in a Xenopu	Charles Bradshaw, Jerome Jullien, Munender Vodnala, George Allen, Charles Bradshaw, Vincent Pasque, Nathalie Beaujean, Stan Wang, Haruhiko Koseki, Vitorio Sartorelli, John Gurdon	36 samples, single-ended RNA-seq libraries from MEF or mES nuclei transplanted to Xenopus oocytes; 8 samples, single-ended RNA-seq libraries from mES  cloned two-cell stage embryos; 4 samples single-ended ChIP-seq librarys (H2Aub antibody) from MEF transplanted to Xenopus oocytes.	28257702	53077	SRP091439	SRR4417790	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004314/SRR4417790	GSM2342173	SRA483678	SRX2240173	ChIP-Seq	SINGLE	SRP091439	PRJNA347982
88975	1	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435588	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004331/SRR4435588	GSM2356631	SRA486089	SRX2254815	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	2	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435589	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004331/SRR4435589	GSM2356632	SRA486089	SRX2254816	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	3	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435590	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/004331/SRR4435590	GSM2356633	SRA486089	SRX2254817	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	4	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435591	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004331/SRR4435591	GSM2356634	SRA486089	SRX2254818	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	5	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435592	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004331/SRR4435592	GSM2356635	SRA486089	SRX2254819	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	6	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435593	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/004331/SRR4435593	GSM2356636	SRA486089	SRX2254820	RNA-Seq	PAIRED	SRP091865	PRJNA349464
88975	7	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435594	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004331/SRR4435594	GSM2356637	SRA486089	SRX2254821	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	8	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435595	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004331/SRR4435595	GSM2356638	SRA486089	SRX2254822	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	9	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435596	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004331/SRR4435596	GSM2356639	SRA486089	SRX2254823	RNA-Seq	SINGLE	SRP091865	PRJNA349464
88975	10	Jessica Chang	RNA-Seq of Xenopus tail regeneration	In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail am	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Whole tail (WT) samples were obtained from an an initial amputation.  Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples.  The 0 hpa time point samples the tissue directly adjacent to the initial cut site.  Regenerating tail samples collected up to 72 hpa.
Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.	28095651	53040	SRP091865	SRR4435597	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/004331/SRR4435597	GSM2356640	SRA486089	SRX2254824	RNA-Seq	SINGLE	SRP091865	PRJNA349464
89165	1	Zhihua Jiang	Usage of Alternative Polyadenylation Sites Differs Dramatically Between Male and Female Xenopus tropicalis.	We applied our recently released Whole Transcriptome Termini Site sequencing protocol to profile usage of alternative polyadenylation sites in Xenopus	Zhihua Jiang, Xiang Zhou, Jennifer Michal, Yangzi Zhang	Total RNA samples derived from whole body homogenates of individual adult frogs were used to construct WTTS-seq libraries. Four WTTS-seq libraries from two male frogs and two female frogs were involved in this submission.	30729254	55685	SRP092052	SRR4449921	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/004345/SRR4449921	GSM2359906	SRA486795	SRX2268037	RNA-Seq	SINGLE	SRP092052	PRJNA350509
89165	2	Zhihua Jiang	Usage of Alternative Polyadenylation Sites Differs Dramatically Between Male and Female Xenopus tropicalis.	We applied our recently released Whole Transcriptome Termini Site sequencing protocol to profile usage of alternative polyadenylation sites in Xenopus	Zhihua Jiang, Xiang Zhou, Jennifer Michal, Yangzi Zhang	Total RNA samples derived from whole body homogenates of individual adult frogs were used to construct WTTS-seq libraries. Four WTTS-seq libraries from two male frogs and two female frogs were involved in this submission.	30729254	55685	SRP092052	SRR4449922	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004345/SRR4449922	GSM2359907	SRA486795	SRX2268038	RNA-Seq	SINGLE	SRP092052	PRJNA350509
89165	3	Zhihua Jiang	Usage of Alternative Polyadenylation Sites Differs Dramatically Between Male and Female Xenopus tropicalis.	We applied our recently released Whole Transcriptome Termini Site sequencing protocol to profile usage of alternative polyadenylation sites in Xenopus	Zhihua Jiang, Xiang Zhou, Jennifer Michal, Yangzi Zhang	Total RNA samples derived from whole body homogenates of individual adult frogs were used to construct WTTS-seq libraries. Four WTTS-seq libraries from two male frogs and two female frogs were involved in this submission.	30729254	55685	SRP092052	SRR4449923	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004345/SRR4449923	GSM2359908	SRA486795	SRX2268039	RNA-Seq	SINGLE	SRP092052	PRJNA350509
89165	4	Zhihua Jiang	Usage of Alternative Polyadenylation Sites Differs Dramatically Between Male and Female Xenopus tropicalis.	We applied our recently released Whole Transcriptome Termini Site sequencing protocol to profile usage of alternative polyadenylation sites in Xenopus	Zhihua Jiang, Xiang Zhou, Jennifer Michal, Yangzi Zhang	Total RNA samples derived from whole body homogenates of individual adult frogs were used to construct WTTS-seq libraries. Four WTTS-seq libraries from two male frogs and two female frogs were involved in this submission.	30729254	55685	SRP092052	SRR4449924	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/004345/SRR4449924	GSM2359909	SRA486795	SRX2268040	RNA-Seq	SINGLE	SRP092052	PRJNA350509
89271	1	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473800	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004368/SRR4473800	GSM2363456	SRA487358	SRX2279685	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	2	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473801	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/004368/SRR4473801	GSM2363457	SRA487358	SRX2279686	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	3	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473802	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004368/SRR4473802	GSM2363458	SRA487358	SRX2279687	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	4	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473803	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/004368/SRR4473803	GSM2363459	SRA487358	SRX2279688	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	5	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473804	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004368/SRR4473804	GSM2363460	SRA487358	SRX2279689	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	6	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473805	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/004368/SRR4473805	GSM2363461	SRA487358	SRX2279690	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	7	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473806	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/004368/SRR4473806	GSM2363462	SRA487358	SRX2279691	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	8	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473807	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/004368/SRR4473807	GSM2363463	SRA487358	SRX2279692	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	9	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473808	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004368/SRR4473808	GSM2363464	SRA487358	SRX2279693	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	10	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473809	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/004368/SRR4473809	GSM2363465	SRA487358	SRX2279694	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	11	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473810	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/004368/SRR4473810	GSM2363466	SRA487358	SRX2279695	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	12	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473811	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004368/SRR4473811	GSM2363467	SRA487358	SRX2279696	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	13	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473812	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/004368/SRR4473812	GSM2363468	SRA487358	SRX2279697	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	14	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4473813	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/004368/SRR4473813	GSM2363469	SRA487358	SRX2279698	ChIP-Seq	SINGLE	SRP092243	PRJNA351216
89271	15	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4478521	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/004373/SRR4478521	GSM2364660	SRA487358	SRX2281883	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	16	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4478522	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/004373/SRR4478522	GSM2364661	SRA487358	SRX2281884	RNA-Seq	SINGLE	SRP092243	PRJNA351216
89271	17	Ian Quigley	RNAseq and ChIPseq profiling of Foxn4 and Foxj1 in multiciliated cells	Foxn4 and Foxj1 are expressed in multiciliated cells. Here, we dissect their role with knockdowns using two different technologies (morpholinos and CR	Ian Quigley, Chris Kintner	To examine Foxn4 and Foxj1's effect on multiciliated cells, we knocked them down in tissue where we also overexpressed an inducible form of multicilin (also known as mcidas; Stubbs et al., 2012). After injecting, we isolated ectoderm surgically and, when injected with multicilin, induced at mid-stage 11. We then harvested RNA or chromatin at 9 hours after induction, roughly corresponding to stage 18 and performed poly-a+  RNAseq (Illumina Truseq v2) or ChIPseq. We then aligned reads to X. laevis gene models (Mayball version, Chung and Kwon et al. 2014) or the genome (v7.1) and determined differential expression or binding targets. To determine differential expression, we compared RNAseq reads from ectoderm isolated from embryos injected with multicilin alone, as reported in Ma et al. 2014 (PMID: 24934224, NCBI GEO:GSE59309) with samples here injected with multicilin and Foxn4 or Foxj1 perturbations.	27864379	52793	SRP092243	SRR4478523	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/004373/SRR4478523	GSM2364662	SRA487358	SRX2281885	RNA-Seq	SINGLE	SRP092243	PRJNA351216
90898	1	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077831	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077831	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	2	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077832	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077832	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	3	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077833	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077833	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	4	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077834	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077834	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	5	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077835	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077835	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	6	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077836	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077836	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	7	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077837	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077837	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	8	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077838	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077838	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	9	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077839	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077839	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	10	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077840	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077840	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	11	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077841	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077841	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	12	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077842	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077842	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	13	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077843	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077843	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	14	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077844	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077844	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	15	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077845	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077845	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	16	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077846	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077846	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	17	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077847	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077847	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	18	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077848	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077848	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	19	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077849	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077849	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	20	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077850	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077850	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	21	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077851	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077851	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	22	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077852	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077852	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	23	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077853	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077853	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	24	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077854	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077854	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	25	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077855	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077855	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	26	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077856	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077856	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	27	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077857	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077857	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	28	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077858	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077858	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	29	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077859	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077859	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	30	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077860	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077860	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	31	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077861	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077861	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	32	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077862	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077862	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	33	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077863	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077863	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	34	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077864	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077864	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	35	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077865	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077865	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	36	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077866	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077866	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	37	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077867	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077867	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	38	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077868	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077868	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	39	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077869	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077869	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	40	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077870	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077870	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	41	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077871	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077871	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	42	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077872	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077872	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	43	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077873	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077873	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	44	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077874	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077874	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	45	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077875	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077875	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	46	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077876	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077876	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	47	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077877	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077877	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	48	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077878	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077878	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	49	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077879	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077879	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	50	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077880	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077880	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	51	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077881	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077881	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	52	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077882	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077882	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	53	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077883	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077883	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
90898	54	Ozren Bogdanovic	Single-base resolution methylomes of Xenopus laevis x Xenopus tropicalis embryos	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates. The most recent vertebrate genom	Ozren Bogdanovic, Ryan Lister	WGBS profiling of Xenopus tropicalis x Xenopus laevis st.10.5 embryos.	29065907	54195	SRP094579	SRR5077884	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004958/SRR5077884	GSM2417228	SRA500859	SRX2396569	Bisulfite-Seq	SINGLE	SRP094579	PRJNA356296
92366	1	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109836	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109836	GSM2428182	SRA503451	SRX2422228	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	2	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109837	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109837	GSM2428183	SRA503451	SRX2422229	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	3	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109838	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109838	GSM2428184	SRA503451	SRX2422230	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	4	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109839	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109839	GSM2428185	SRA503451	SRX2422231	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	5	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109840	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109840	GSM2428186	SRA503451	SRX2422232	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	6	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109841	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109841	GSM2428187	SRA503451	SRX2422233	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	7	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109842	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109842	GSM2428188	SRA503451	SRX2422234	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	8	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109843	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109843	GSM2428189	SRA503451	SRX2422235	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	9	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109844	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109844	GSM2428190	SRA503451	SRX2422236	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	10	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109845	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109845	GSM2428191	SRA503451	SRX2422237	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	11	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109846	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109846	GSM2428192	SRA503451	SRX2422238	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	12	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109847	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109847	GSM2428193	SRA503451	SRX2422239	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	13	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109848	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109848	GSM2428194	SRA503451	SRX2422240	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	14	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109849	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109849	GSM2428195	SRA503451	SRX2422241	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	15	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109850	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109850	GSM2428196	SRA503451	SRX2422242	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	16	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109851	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109851	GSM2428197	SRA503451	SRX2422243	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	17	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109852	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109852	GSM2428198	SRA503451	SRX2422244	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	18	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109853	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109853	GSM2428199	SRA503451	SRX2422245	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	19	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109854	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109854	GSM2428200	SRA503451	SRX2422246	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	20	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109855	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109855	GSM2428201	SRA503451	SRX2422247	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	21	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109856	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109856	GSM2428202	SRA503451	SRX2422248	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	22	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109857	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109857	GSM2428203	SRA503451	SRX2422249	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	23	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109858	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109858	GSM2428204	SRA503451	SRX2422250	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	24	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109859	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109859	GSM2428205	SRA503451	SRX2422251	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	25	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109860	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109860	GSM2428206	SRA503451	SRX2422252	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	26	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109861	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109861	GSM2428207	SRA503451	SRX2422253	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	27	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109862	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109862	GSM2428208	SRA503451	SRX2422254	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	28	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109863	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109863	GSM2428209	SRA503451	SRX2422255	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	29	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109864	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109864	GSM2428210	SRA503451	SRX2422256	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	30	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109865	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109865	GSM2428211	SRA503451	SRX2422257	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	31	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109866	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109866	GSM2428212	SRA503451	SRX2422258	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	32	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109867	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109867	GSM2428213	SRA503451	SRX2422259	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	33	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109868	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109868	GSM2428214	SRA503451	SRX2422260	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	34	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109869	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109869	GSM2428215	SRA503451	SRX2422261	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	35	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109870	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109870	GSM2428216	SRA503451	SRX2422262	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	36	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109871	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109871	GSM2428217	SRA503451	SRX2422263	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	37	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109872	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109872	GSM2428218	SRA503451	SRX2422264	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	38	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109873	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109873	GSM2428219	SRA503451	SRX2422265	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	39	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109874	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109874	GSM2428220	SRA503451	SRX2422266	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	40	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109875	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109875	GSM2428221	SRA503451	SRX2422267	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	41	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109876	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109876	GSM2428222	SRA503451	SRX2422268	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	42	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109877	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109877	GSM2428223	SRA503451	SRX2422269	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	43	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109878	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109878	GSM2428224	SRA503451	SRX2422270	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	44	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109879	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109879	GSM2428225	SRA503451	SRX2422271	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	45	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109880	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109880	GSM2428226	SRA503451	SRX2422272	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	46	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109881	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109881	GSM2428227	SRA503451	SRX2422273	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	47	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109882	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109882	GSM2428228	SRA503451	SRX2422274	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	48	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109883	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109883	GSM2428229	SRA503451	SRX2422275	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	49	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109884	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109884	GSM2428230	SRA503451	SRX2422276	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	50	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109885	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109885	GSM2428231	SRA503451	SRX2422277	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	51	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109886	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109886	GSM2428232	SRA503451	SRX2422278	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	52	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109887	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109887	GSM2428233	SRA503451	SRX2422279	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	53	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109888	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109888	GSM2428234	SRA503451	SRX2422280	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	54	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109889	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109889	GSM2428235	SRA503451	SRX2422281	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	55	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109890	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109890	GSM2428236	SRA503451	SRX2422282	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	56	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109891	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109891	GSM2428237	SRA503451	SRX2422283	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	57	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109892	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109892	GSM2428238	SRA503451	SRX2422284	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	58	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109893	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109893	GSM2428239	SRA503451	SRX2422285	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	59	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109894	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109894	GSM2428240	SRA503451	SRX2422286	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	60	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109895	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109895	GSM2428241	SRA503451	SRX2422287	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	61	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109896	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109896	GSM2428242	SRA503451	SRX2422288	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	62	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109897	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109897	GSM2428243	SRA503451	SRX2422289	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	63	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109898	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109898	GSM2428244	SRA503451	SRX2422290	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	64	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109899	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109899	GSM2428245	SRA503451	SRX2422291	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	65	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109900	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109900	GSM2428246	SRA503451	SRX2422292	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	66	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109901	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109901	GSM2428247	SRA503451	SRX2422293	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	67	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109902	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109902	GSM2428248	SRA503451	SRX2422294	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	68	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109903	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109903	GSM2428249	SRA503451	SRX2422295	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	69	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109904	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109904	GSM2428250	SRA503451	SRX2422296	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	70	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109905	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109905	GSM2428251	SRA503451	SRX2422297	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	71	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109906	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109906	GSM2428252	SRA503451	SRX2422298	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	72	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109907	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109907	GSM2428253	SRA503451	SRX2422299	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	73	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109908	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109908	GSM2428254	SRA503451	SRX2422300	RNA-Seq	SINGLE	SRP095083	PRJNA357356
92366	74	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109909	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109909	GSM2428255	SRA503451	SRX2422301	ChIP-Seq	SINGLE	SRP095083	PRJNA357356
92366	75	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109910	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109910	GSM2428256	SRA503451	SRX2422302	ChIP-Seq	SINGLE	SRP095083	PRJNA357356
92366	76	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109911	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109911	GSM2428257	SRA503451	SRX2422303	ChIP-Seq	SINGLE	SRP095083	PRJNA357356
92366	77	Angela Simeone	H3K4 Methylation-Mediated Memory of an Active Transcriptional State Impairs Nuclear Reprogramming	Xenopus eggs can induce the reversal of differentiation processes of somatic cells. Yet, the egg is not fully efficient in reprogramming a differentia	Angela Simeone, Eva Hörmanseder, George Allen, Charles Bradshaw, Magdalena Figlmüller, Jerome Jullien, John Gurdon	73 samples, single-ended RNA-seq libraries from neurula stage 18 or 21 endoderm and gastrula stage 11 ectoderm samples; 2 single-ended ChIP-seq libraries from endoderm cells of neurula (stage 21) embryos with antibody for H3K4me3, 2 replicates for each histone modification pull-down.	28366589	54691	SRP095083	SRR5109912	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5109912	GSM2428258	SRA503451	SRX2422304	ChIP-Seq	SINGLE	SRP095083	PRJNA357356
92382	1	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110206	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110206	GSM2428811	SRA503488	SRX2422594	OTHER	PAIRED	SRP095103	PRJNA357404
92382	2	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110207	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110207	GSM2428811	SRA503488	SRX2422594	OTHER	PAIRED	SRP095103	PRJNA357404
92382	3	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110208	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110208	GSM2428811	SRA503488	SRX2422594	OTHER	PAIRED	SRP095103	PRJNA357404
92382	4	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110209	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110209	GSM2428812	SRA503488	SRX2422595	OTHER	PAIRED	SRP095103	PRJNA357404
92382	5	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110210	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110210	GSM2428813	SRA503488	SRX2422596	RNA-Seq	SINGLE	SRP095103	PRJNA357404
92382	6	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110211	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110211	GSM2428814	SRA503488	SRX2422597	RNA-Seq	SINGLE	SRP095103	PRJNA357404
92382	7	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110212	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110212	GSM2428815	SRA503488	SRX2422598	ChIP-Seq	SINGLE	SRP095103	PRJNA357404
92382	8	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110213	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110213	GSM2428816	SRA503488	SRX2422599	ChIP-Seq	SINGLE	SRP095103	PRJNA357404
92382	9	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110214	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110214	GSM2428817	SRA503488	SRX2422600	ChIP-Seq	SINGLE	SRP095103	PRJNA357404
92382	10	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110215	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110215	GSM2428818	SRA503488	SRX2422601	ChIP-Seq	SINGLE	SRP095103	PRJNA357404
92382	11	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110216	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110216	GSM2428819	SRA503488	SRX2422602	ChIP-Seq	SINGLE	SRP095103	PRJNA357404
92382	12	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110217	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110217	GSM2428820	SRA503488	SRX2422603	ChIP-Seq	SINGLE	SRP095103	PRJNA357404
92382	13	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110218	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110218	GSM2428821	SRA503488	SRX2422604	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	14	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110219	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110219	GSM2428822	SRA503488	SRX2422605	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	15	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110220	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110220	GSM2428823	SRA503488	SRX2422606	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	16	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110221	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110221	GSM2428824	SRA503488	SRX2422607	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	17	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110222	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110222	GSM2428825	SRA503488	SRX2422608	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	18	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110223	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110223	GSM2428826	SRA503488	SRX2422609	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	19	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110224	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110224	GSM2428827	SRA503488	SRX2422610	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	20	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110225	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110225	GSM2428828	SRA503488	SRX2422611	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	21	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110226	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110226	GSM2428829	SRA503488	SRX2422612	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	22	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110227	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110227	GSM2428830	SRA503488	SRX2422613	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	23	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110228	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110228	GSM2428831	SRA503488	SRX2422614	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
92382	24	Simon van Heeringen	Regulatory remodeling in the allo-tetraploid frog Xenopus laevis	Genome duplication has played a pivotal role in the evolution of many eukaryotic lineages, including the vertebrates.The most recent vertebrate genome	Simon van Heeringen, Sarita Paranjpe, Georgios Georgiou, Ila van Kruijsbergen, Romain Gibeaux, Rebecca Heald, Simon van Heeringen, Gert Veenstra	Genomic DNA of Xenopus tropicalis and Xenopus laevis; RNA-seq (two replicates) in stage 10.5 Xenopus laevis embryos; ChIP-seq for H3K4me3 and p300 (each two replicates) in Xenopus laevis (LELS), Xenopus tropicalis (TETS) and Xenopus tropicals x laevis (hybrid; LETS) embryos.	29065907	54195	SRP095103	SRR5110229	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/004990/SRR5110229	GSM2428832	SRA503488	SRX2422615	ChIP-Seq	PAIRED	SRP095103	PRJNA357404
93195	1	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146641	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146641	GSM2446097	SRA520566	SRX2464697	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	2	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146642	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146642	GSM2446098	SRA520566	SRX2464698	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	3	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146643	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146643	GSM2446099	SRA520566	SRX2464699	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	4	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146644	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146644	GSM2446100	SRA520566	SRX2464700	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	5	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146645	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146645	GSM2446101	SRA520566	SRX2464701	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	6	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146646	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146646	GSM2446102	SRA520566	SRX2464702	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	7	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146647	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146647	GSM2446103	SRA520566	SRX2464703	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	8	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146648	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146648	GSM2446104	SRA520566	SRX2464704	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	9	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146649	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146649	GSM2446105	SRA520566	SRX2464705	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	10	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146650	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146650	GSM2446106	SRA520566	SRX2464706	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	11	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146651	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146651	GSM2446107	SRA520566	SRX2464707	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	12	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146652	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146652	GSM2446108	SRA520566	SRX2464708	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	13	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146653	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146653	GSM2446109	SRA520566	SRX2464709	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	14	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146654	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146654	GSM2446110	SRA520566	SRX2464710	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	15	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146655	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146655	GSM2446111	SRA520566	SRX2464711	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	16	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146656	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146656	GSM2446112	SRA520566	SRX2464712	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	17	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146657	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146657	GSM2446113	SRA520566	SRX2464713	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	18	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146658	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146658	GSM2446114	SRA520566	SRX2464714	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	19	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146659	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146659	GSM2446115	SRA520566	SRX2464715	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	20	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146660	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146660	GSM2446116	SRA520566	SRX2464716	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	21	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146661	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146661	GSM2446117	SRA520566	SRX2464717	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	22	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146662	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146662	GSM2446118	SRA520566	SRX2464718	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	23	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146663	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146663	GSM2446119	SRA520566	SRX2464719	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	24	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146664	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146664	GSM2446120	SRA520566	SRX2464720	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	25	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146665	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146665	GSM2446121	SRA520566	SRX2464721	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	26	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146666	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146666	GSM2446122	SRA520566	SRX2464722	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	27	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146667	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146667	GSM2446123	SRA520566	SRX2464723	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	28	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146668	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146668	GSM2446124	SRA520566	SRX2464724	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	29	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146669	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146669	GSM2446125	SRA520566	SRX2464725	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	30	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146670	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146670	GSM2446126	SRA520566	SRX2464726	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	31	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146671	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146671	GSM2446127	SRA520566	SRX2464727	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	32	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146672	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146672	GSM2446128	SRA520566	SRX2464728	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	33	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146673	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146673	GSM2446129	SRA520566	SRX2464729	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	34	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146674	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146674	GSM2446130	SRA520566	SRX2464730	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	35	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146675	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146675	GSM2446131	SRA520566	SRX2464731	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	36	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146676	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146676	GSM2446132	SRA520566	SRX2464732	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	37	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146677	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146677	GSM2446133	SRA520566	SRX2464733	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	38	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146678	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146678	GSM2446134	SRA520566	SRX2464734	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	39	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146679	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146679	GSM2446135	SRA520566	SRX2464735	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	40	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146680	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146680	GSM2446136	SRA520566	SRX2464736	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	41	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146681	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146681	GSM2446137	SRA520566	SRX2464737	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	42	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146682	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146682	GSM2446138	SRA520566	SRX2464738	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	43	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146683	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146683	GSM2446139	SRA520566	SRX2464739	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	44	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146684	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146684	GSM2446140	SRA520566	SRX2464740	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	45	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146685	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146685	GSM2446141	SRA520566	SRX2464741	RNA-Seq	SINGLE	SRP096124	PRJNA360282
93195	46	Edward De Robertis	Spemann organizer transcriptome induction by early β-Catenin, Wnt, Nodal and Siamois signals in Xenopus laevis	During Xenopus gastrulation, dorsal stabilization of β-Catenin at the earliest stage and subsequent target genes expression are critical for dorsal-v	Edward De Robertis, Yi Ding, Diego Ploper, Eric Sosa, Gabriele Colozza, Yuki Moriyama, Maria Benitez, Kelvin Zhang, Daria Merkurjev	A genome-wide study of the effects of depleting the early dorsal b-Catenin signal which is responsible for the induction of the body axis.	28348214	53589	SRP096124	SRR5146686	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/005026/SRR5146686	GSM2446142	SRA520566	SRX2464742	RNA-Seq	SINGLE	SRP096124	PRJNA360282
96655	1	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346041	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346041	GSM2537311	SRA546297	SRX2642672	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	2	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346042	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346042	GSM2537312	SRA546297	SRX2642673	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	3	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346043	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346043	GSM2537313	SRA546297	SRX2642674	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	4	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346044	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346044	GSM2537314	SRA546297	SRX2642675	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	5	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346045	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346045	GSM2537315	SRA546297	SRX2642676	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	6	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346046	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346046	GSM2537316	SRA546297	SRX2642677	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	7	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346047	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346047	GSM2537317	SRA546297	SRX2642678	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	8	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346048	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346048	GSM2537318	SRA546297	SRX2642679	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	9	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346049	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346049	GSM2537319	SRA546297	SRX2642680	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	10	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346050	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346050	GSM2537320	SRA546297	SRX2642681	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	11	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346051	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346051	GSM2537321	SRA546297	SRX2642682	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	12	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346052	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346052	GSM2537322	SRA546297	SRX2642683	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	13	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346053	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346053	GSM2537323	SRA546297	SRX2642684	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	14	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346054	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346054	GSM2537324	SRA546297	SRX2642685	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	15	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346055	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346055	GSM2537325	SRA546297	SRX2642686	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	16	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346056	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346056	GSM2537326	SRA546297	SRX2642687	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	17	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346057	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346057	GSM2537327	SRA546297	SRX2642688	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	18	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346058	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346058	GSM2537328	SRA546297	SRX2642689	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	19	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346059	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346059	GSM2537329	SRA546297	SRX2642690	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	20	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346060	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346060	GSM2537330	SRA546297	SRX2642691	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	21	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346061	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346061	GSM2537331	SRA546297	SRX2642692	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	22	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346062	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346062	GSM2537332	SRA546297	SRX2642693	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	23	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346063	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346063	GSM2537333	SRA546297	SRX2642694	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	24	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346064	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346064	GSM2537334	SRA546297	SRX2642695	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	25	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346065	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346065	GSM2537335	SRA546297	SRX2642696	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	26	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346066	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346066	GSM2537336	SRA546297	SRX2642697	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	27	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346067	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346067	GSM2537337	SRA546297	SRX2642698	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	28	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346068	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346068	GSM2537338	SRA546297	SRX2642699	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	29	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346069	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346069	GSM2537339	SRA546297	SRX2642700	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	30	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346070	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346070	GSM2537340	SRA546297	SRX2642701	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	31	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346071	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346071	GSM2537341	SRA546297	SRX2642702	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	32	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346072	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346072	GSM2537342	SRA546297	SRX2642703	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	33	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346073	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346073	GSM2537343	SRA546297	SRX2642704	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	34	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346074	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346074	GSM2537344	SRA546297	SRX2642705	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	35	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346075	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346075	GSM2537345	SRA546297	SRX2642706	RNA-Seq	PAIRED	SRP101960	PRJNA379304
96655	36	George Gentsch	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus	We report on the implications of genetic KO versus MO-mediated KD of the mesoderm-specifying Brachyury paralogues in the Western clawed frog Xenopus t	George Gentsch, George Gentsch, James Smith	Comparison of poly(A) transcriptome between Brachyury null mutants and morphants over two tailbud stages.	29478923	54637	SRP101960	SRR5346076	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/005220/SRR5346076	GSM2537346	SRA546297	SRX2642707	RNA-Seq	PAIRED	SRP101960	PRJNA379304
97367	1	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5508303	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5508303/SRR5508303.1	Anolis_Female_genome	SRA559581	SRX2783975	WGS	PAIRED	SRP102989	PRJNA381064
97367	2	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5508304	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5508304/SRR5508304.1	Anolis_Male_genome	SRA559581	SRX2783976	WGS	PAIRED	SRP102989	PRJNA381064
97367	3	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412266	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412266/SRR5412266.1	GSM2563127	SRA551247	SRX2704314	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	4	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412267	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412267/SRR5412267.1	GSM2563128	SRA551247	SRX2704315	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	5	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412268	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412268/SRR5412268.1	GSM2563129	SRA551247	SRX2704316	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	6	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412269	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412269/SRR5412269.1	GSM2563130	SRA551247	SRX2704317	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	7	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412270	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412270/SRR5412270.1	GSM2563131	SRA551247	SRX2704318	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	8	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412271	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412271/SRR5412271.1	GSM2563132	SRA551247	SRX2704319	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	9	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412272	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412272/SRR5412272.1	GSM2563133	SRA551247	SRX2704320	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	10	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412273	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412273/SRR5412273.1	GSM2563134	SRA551247	SRX2704321	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	11	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412274	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412274/SRR5412274.1	GSM2563135	SRA551247	SRX2704322	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	12	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412275	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412275/SRR5412275.1	GSM2563136	SRA551247	SRX2704323	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	13	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412276	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412276/SRR5412276.1	GSM2563137	SRA551247	SRX2704324	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	14	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412277	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412277/SRR5412277.1	GSM2563138	SRA551247	SRX2704325	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	15	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412278	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412278/SRR5412278.1	GSM2563139	SRA551247	SRX2704326	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	16	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412279	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412279/SRR5412279.1	GSM2563140	SRA551247	SRX2704327	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	17	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412280	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412280/SRR5412280.1	GSM2563141	SRA551247	SRX2704328	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	18	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514366	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514366/SRR5514366.1	GSM2601715	SRA551247	SRX2787757	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	19	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514367	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514367/SRR5514367.1	GSM2601716	SRA551247	SRX2787758	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	20	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514368	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514368/SRR5514368.1	GSM2601717	SRA551247	SRX2787759	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	21	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514369	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514369/SRR5514369.1	GSM2601718	SRA551247	SRX2787760	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	22	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514370	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514370/SRR5514370.1	GSM2601719	SRA551247	SRX2787761	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	23	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514371	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514371/SRR5514371.1	GSM2601720	SRA551247	SRX2787762	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	24	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514372	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514372/SRR5514372.1	GSM2601721	SRA551247	SRX2787763	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	25	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514373	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514373/SRR5514373.1	GSM2601722	SRA551247	SRX2787764	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	26	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514374	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514374/SRR5514374.1	GSM2601723	SRA551247	SRX2787765	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	27	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514375	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514375/SRR5514375.1	GSM2601724	SRA551247	SRX2787766	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	28	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514376	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514376/SRR5514376.1	GSM2601725	SRA551247	SRX2787767	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	29	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5514377	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5514377/SRR5514377.1	GSM2601726	SRA551247	SRX2787768	ChIP-Seq	PAIRED	SRP102989	PRJNA381064
97367	30	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5813770	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR5813770/SRR5813770.1	GSM2698413	SRA585166	SRX2992263	OTHER	PAIRED	SRP102989	PRJNA381064
97367	31	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5813771	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR5813771/SRR5813771.1	GSM2698414	SRA585166	SRX2992264	OTHER	PAIRED	SRP102989	PRJNA381064
97367	32	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5813772	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR5813772/SRR5813772.1	GSM2698415	SRA585166	SRX2992265	OTHER	PAIRED	SRP102989	PRJNA381064
97367	33	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5813773	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR5813773/SRR5813773.1	GSM2698416	SRA585166	SRX2992266	OTHER	PAIRED	SRP102989	PRJNA381064
97367	34	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5813774	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR5813774/SRR5813774.1	GSM2698417	SRA585166	SRX2992267	OTHER	PAIRED	SRP102989	PRJNA381064
97367	35	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5813775	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR5813775/SRR5813775.1	GSM2698418	SRA585166	SRX2992268	OTHER	PAIRED	SRP102989	PRJNA381064
97367	36	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5813776	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR5813776/SRR5813776.1	GSM2698419	SRA585166	SRX2992269	OTHER	PAIRED	SRP102989	PRJNA381064
97367	37	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261399	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261399/SRR6261399.1	GSM2843033	SRA551247	SRX3367730	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	38	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261400	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261400/SRR6261400.1	GSM2843034	SRA551247	SRX3367731	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	39	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261401	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261401/SRR6261401.1	GSM2843035	SRA551247	SRX3367732	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	40	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261402	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261402/SRR6261402.1	GSM2843036	SRA551247	SRX3367733	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	41	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261403	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261403/SRR6261403.1	GSM2843037	SRA551247	SRX3367734	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	42	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261404	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261404/SRR6261404.1	GSM2843038	SRA551247	SRX3367735	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	43	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261405	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261405/SRR6261405.1	GSM2843039	SRA551247	SRX3367736	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	44	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261406	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261406/SRR6261406.1	GSM2843040	SRA551247	SRX3367737	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	45	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261407	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261407/SRR6261407.1	GSM2843041	SRA551247	SRX3367738	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	46	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261408	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261408/SRR6261408.1	GSM2843042	SRA551247	SRX3367739	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	47	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261409	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261409/SRR6261409.1	GSM2843043	SRA551247	SRX3367740	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	48	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261410	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261410/SRR6261410.1	GSM2843044	SRA551247	SRX3367741	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	49	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261411	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261411/SRR6261411.1	GSM2843045	SRA551247	SRX3367742	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	50	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261412	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261412/SRR6261412.1	GSM2843046	SRA551247	SRX3367743	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	51	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261413	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261413/SRR6261413.1	GSM2843047	SRA551247	SRX3367744	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	52	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261414	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261414/SRR6261414.1	GSM2843048	SRA551247	SRX3367745	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	53	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261415	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261415/SRR6261415.1	GSM2843049	SRA551247	SRX3367746	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	54	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261416	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261416/SRR6261416.1	GSM2843050	SRA551247	SRX3367747	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	55	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261417	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261417/SRR6261417.1	GSM2843051	SRA551247	SRX3367748	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	56	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261418	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261418/SRR6261418.1	GSM2843052	SRA551247	SRX3367749	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	57	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261419	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261419/SRR6261419.1	GSM2843053	SRA551247	SRX3367750	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	58	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261420	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261420/SRR6261420.1	GSM2843054	SRA551247	SRX3367751	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	59	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261421	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261421/SRR6261421.1	GSM2843055	SRA551247	SRX3367752	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	60	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261422	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261422/SRR6261422.1	GSM2843056	SRA551247	SRX3367753	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	61	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261423	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261423/SRR6261423.1	GSM2843057	SRA551247	SRX3367754	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	62	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261424	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261424/SRR6261424.1	GSM2843058	SRA551247	SRX3367755	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	63	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261425	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261425/SRR6261425.1	GSM2843059	SRA551247	SRX3367756	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	64	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261426	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261426/SRR6261426.1	GSM2843060	SRA551247	SRX3367757	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	65	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261427	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261427/SRR6261427.1	GSM2843061	SRA551247	SRX3367758	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	66	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261428	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261428/SRR6261428.1	GSM2843062	SRA551247	SRX3367759	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	67	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261429	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261429/SRR6261429.1	GSM2843063	SRA551247	SRX3367760	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	68	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261430	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261430/SRR6261430.1	GSM2843064	SRA551247	SRX3367761	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	69	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261431	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261431/SRR6261431.1	GSM2843065	SRA551247	SRX3367762	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	70	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261432	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261432/SRR6261432.1	GSM2843066	SRA551247	SRX3367763	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	71	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261433	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261433/SRR6261433.1	GSM2843067	SRA551247	SRX3367764	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	72	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261434	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261434/SRR6261434.1	GSM2843068	SRA551247	SRX3367765	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	73	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261435	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261435/SRR6261435.1	GSM2843069	SRA551247	SRX3367766	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	74	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261436	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261436/SRR6261436.1	GSM2843070	SRA551247	SRX3367767	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	75	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261437	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261437/SRR6261437.1	GSM2843071	SRA551247	SRX3367768	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	76	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261438	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261438/SRR6261438.1	GSM2843072	SRA551247	SRX3367769	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	77	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261439	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261439/SRR6261439.1	GSM2843073	SRA551247	SRX3367770	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	78	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261440	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261440/SRR6261440.1	GSM2843074	SRA551247	SRX3367771	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	79	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261441	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261441/SRR6261441.1	GSM2843075	SRA551247	SRX3367772	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	80	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261442	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261442/SRR6261442.1	GSM2843076	SRA551247	SRX3367773	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	81	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261443	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261443/SRR6261443.1	GSM2843077	SRA551247	SRX3367774	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	82	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261444	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261444/SRR6261444.1	GSM2843078	SRA551247	SRX3367775	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	83	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261445	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261445/SRR6261445.1	GSM2843079	SRA551247	SRX3367776	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	84	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6261446	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR6261446/SRR6261446.1	GSM2843080	SRA551247	SRX3367777	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	85	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337910	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337910/SRR6337910.1	GSM2871941	SRA635532	SRX3436872	OTHER	PAIRED	SRP102989	PRJNA381064
97367	86	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337911	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337911/SRR6337911.1	GSM2871942	SRA635532	SRX3436873	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	87	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337912	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337912/SRR6337912.1	GSM2871943	SRA635532	SRX3436874	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	88	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337913	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337913/SRR6337913.1	GSM2871944	SRA635532	SRX3436875	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	89	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337914	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337914/SRR6337914.1	GSM2871945	SRA635532	SRX3436876	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	90	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337915	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337915/SRR6337915.1	GSM2871946	SRA635532	SRX3436877	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	91	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337916	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337916/SRR6337916.1	GSM2871947	SRA635532	SRX3436878	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	92	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337917	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337917/SRR6337917.1	GSM2871948	SRA635532	SRX3436879	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	93	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337918	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337918/SRR6337918.1	GSM2871949	SRA635532	SRX3436880	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	94	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337919	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337919/SRR6337919.1	GSM2871950	SRA635532	SRX3436881	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	95	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337920	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337920/SRR6337920.1	GSM2871951	SRA635532	SRX3436882	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	96	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337921	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337921/SRR6337921.1	GSM2871952	SRA635532	SRX3436883	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	97	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337922	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337922/SRR6337922.1	GSM2871953	SRA635532	SRX3436884	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	98	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337923	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337923/SRR6337923.1	GSM2871954	SRA635532	SRX3436885	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	99	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR6337924	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-11/SRR6337924/SRR6337924.1	GSM2871955	SRA635532	SRX3436886	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	100	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5508305	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5508305/SRR5508305.1	Iguana_Male_genome	SRA559581	SRX2783977	WGS	PAIRED	SRP102989	PRJNA381064
97367	101	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412166	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412166/SRR5412166.1	GSM2563027	SRA551247	SRX2704214	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	102	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412167	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412167/SRR5412167.1	GSM2563028	SRA551247	SRX2704215	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	103	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412168	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412168/SRR5412168.1	GSM2563029	SRA551247	SRX2704216	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	104	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412169	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412169/SRR5412169.1	GSM2563030	SRA551247	SRX2704217	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	105	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412170	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412170/SRR5412170.1	GSM2563031	SRA551247	SRX2704218	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	106	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412171	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412171/SRR5412171.1	GSM2563032	SRA551247	SRX2704219	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	107	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412172	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412172/SRR5412172.1	GSM2563033	SRA551247	SRX2704220	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	108	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412173	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412173/SRR5412173.1	GSM2563034	SRA551247	SRX2704221	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	109	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412174	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412174/SRR5412174.1	GSM2563035	SRA551247	SRX2704222	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	110	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412175	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412175/SRR5412175.1	GSM2563036	SRA551247	SRX2704223	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	111	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412176	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412176/SRR5412176.1	GSM2563037	SRA551247	SRX2704224	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	112	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412177	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412177/SRR5412177.1	GSM2563038	SRA551247	SRX2704225	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	113	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412178	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412178/SRR5412178.1	GSM2563039	SRA551247	SRX2704226	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	114	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412179	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412179/SRR5412179.1	GSM2563040	SRA551247	SRX2704227	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	115	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412180	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412180/SRR5412180.1	GSM2563041	SRA551247	SRX2704228	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	116	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412181	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412181/SRR5412181.1	GSM2563042	SRA551247	SRX2704229	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	117	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412182	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412182/SRR5412182.1	GSM2563043	SRA551247	SRX2704230	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	118	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412183	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412183/SRR5412183.1	GSM2563044	SRA551247	SRX2704231	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	119	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412184	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412184/SRR5412184.1	GSM2563045	SRA551247	SRX2704232	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	120	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412185	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412185/SRR5412185.1	GSM2563046	SRA551247	SRX2704233	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	121	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412186	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412186/SRR5412186.1	GSM2563047	SRA551247	SRX2704234	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	122	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412187	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412187/SRR5412187.1	GSM2563048	SRA551247	SRX2704235	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	123	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412188	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412188/SRR5412188.1	GSM2563049	SRA551247	SRX2704236	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	124	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412189	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412189/SRR5412189.1	GSM2563050	SRA551247	SRX2704237	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	125	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412190	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412190/SRR5412190.1	GSM2563051	SRA551247	SRX2704238	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	126	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412191	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412191/SRR5412191.1	GSM2563052	SRA551247	SRX2704239	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	127	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412192	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412192/SRR5412192.1	GSM2563053	SRA551247	SRX2704240	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	128	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412193	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412193/SRR5412193.1	GSM2563054	SRA551247	SRX2704241	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	129	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412194	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412194/SRR5412194.1	GSM2563055	SRA551247	SRX2704242	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	130	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412195	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412195/SRR5412195.1	GSM2563056	SRA551247	SRX2704243	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	131	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412196	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412196/SRR5412196.1	GSM2563057	SRA551247	SRX2704244	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	132	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412197	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412197/SRR5412197.1	GSM2563058	SRA551247	SRX2704245	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	133	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412198	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412198/SRR5412198.1	GSM2563059	SRA551247	SRX2704246	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	134	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412199	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412199/SRR5412199.1	GSM2563060	SRA551247	SRX2704247	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	135	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412200	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412200/SRR5412200.1	GSM2563061	SRA551247	SRX2704248	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	136	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412201	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412201/SRR5412201.1	GSM2563062	SRA551247	SRX2704249	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	137	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412202	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412202/SRR5412202.1	GSM2563063	SRA551247	SRX2704250	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	138	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412203	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412203/SRR5412203.1	GSM2563064	SRA551247	SRX2704251	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	139	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412204	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412204/SRR5412204.1	GSM2563065	SRA551247	SRX2704252	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	140	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412205	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412205/SRR5412205.1	GSM2563066	SRA551247	SRX2704253	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	141	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412206	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412206/SRR5412206.1	GSM2563067	SRA551247	SRX2704254	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	142	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412207	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412207/SRR5412207.1	GSM2563068	SRA551247	SRX2704255	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	143	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412208	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412208/SRR5412208.1	GSM2563069	SRA551247	SRX2704256	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	144	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412209	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412209/SRR5412209.1	GSM2563070	SRA551247	SRX2704257	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	145	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412210	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412210/SRR5412210.1	GSM2563071	SRA551247	SRX2704258	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	146	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412211	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412211/SRR5412211.1	GSM2563072	SRA551247	SRX2704259	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	147	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412212	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412212/SRR5412212.1	GSM2563073	SRA551247	SRX2704260	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	148	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412213	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412213/SRR5412213.1	GSM2563074	SRA551247	SRX2704261	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	149	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412214	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412214/SRR5412214.1	GSM2563075	SRA551247	SRX2704262	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	150	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412215	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412215/SRR5412215.1	GSM2563076	SRA551247	SRX2704263	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	151	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412216	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412216/SRR5412216.1	GSM2563077	SRA551247	SRX2704264	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	152	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412217	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412217/SRR5412217.1	GSM2563078	SRA551247	SRX2704265	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	153	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412218	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412218/SRR5412218.1	GSM2563079	SRA551247	SRX2704266	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	154	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412219	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412219/SRR5412219.1	GSM2563080	SRA551247	SRX2704267	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	155	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412220	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412220/SRR5412220.1	GSM2563081	SRA551247	SRX2704268	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	156	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412221	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412221/SRR5412221.1	GSM2563082	SRA551247	SRX2704269	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	157	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412222	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412222/SRR5412222.1	GSM2563083	SRA551247	SRX2704270	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	158	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412223	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412223/SRR5412223.1	GSM2563084	SRA551247	SRX2704271	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	159	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412224	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412224/SRR5412224.1	GSM2563085	SRA551247	SRX2704272	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	160	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412225	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412225/SRR5412225.1	GSM2563086	SRA551247	SRX2704273	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	161	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412226	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412226/SRR5412226.1	GSM2563087	SRA551247	SRX2704274	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	162	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412227	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412227/SRR5412227.1	GSM2563088	SRA551247	SRX2704275	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	163	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412228	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412228/SRR5412228.1	GSM2563089	SRA551247	SRX2704276	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	164	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412229	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412229/SRR5412229.1	GSM2563090	SRA551247	SRX2704277	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	165	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412230	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412230/SRR5412230.1	GSM2563091	SRA551247	SRX2704278	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	166	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412231	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412231/SRR5412231.1	GSM2563092	SRA551247	SRX2704279	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	167	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412232	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412232/SRR5412232.1	GSM2563093	SRA551247	SRX2704280	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	168	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412233	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412233/SRR5412233.1	GSM2563094	SRA551247	SRX2704281	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	169	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412234	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412234/SRR5412234.1	GSM2563095	SRA551247	SRX2704282	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	170	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412235	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412235/SRR5412235.1	GSM2563096	SRA551247	SRX2704283	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	171	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412236	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412236/SRR5412236.1	GSM2563097	SRA551247	SRX2704284	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	172	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412237	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412237/SRR5412237.1	GSM2563098	SRA551247	SRX2704285	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	173	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412238	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412238/SRR5412238.1	GSM2563099	SRA551247	SRX2704286	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	174	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412239	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412239/SRR5412239.1	GSM2563100	SRA551247	SRX2704287	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	175	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412240	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412240/SRR5412240.1	GSM2563101	SRA551247	SRX2704288	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	176	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412241	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412241/SRR5412241.1	GSM2563102	SRA551247	SRX2704289	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	177	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412242	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412242/SRR5412242.1	GSM2563103	SRA551247	SRX2704290	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	178	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412243	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412243/SRR5412243.1	GSM2563104	SRA551247	SRX2704291	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	179	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412244	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412244/SRR5412244.1	GSM2563105	SRA551247	SRX2704292	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	180	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412245	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412245/SRR5412245.1	GSM2563106	SRA551247	SRX2704293	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	181	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412246	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412246/SRR5412246.1	GSM2563107	SRA551247	SRX2704294	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	182	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412247	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412247/SRR5412247.1	GSM2563108	SRA551247	SRX2704295	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	183	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412248	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412248/SRR5412248.1	GSM2563109	SRA551247	SRX2704296	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	184	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412249	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412249/SRR5412249.1	GSM2563110	SRA551247	SRX2704297	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	185	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412250	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412250/SRR5412250.1	GSM2563111	SRA551247	SRX2704298	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	186	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412251	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412251/SRR5412251.1	GSM2563112	SRA551247	SRX2704299	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	187	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412252	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412252/SRR5412252.1	GSM2563113	SRA551247	SRX2704300	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	188	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412253	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412253/SRR5412253.1	GSM2563114	SRA551247	SRX2704301	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	189	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412254	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412254/SRR5412254.1	GSM2563115	SRA551247	SRX2704302	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	190	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412255	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412255/SRR5412255.1	GSM2563116	SRA551247	SRX2704303	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	191	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412256	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412256/SRR5412256.1	GSM2563117	SRA551247	SRX2704304	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	192	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412257	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412257/SRR5412257.1	GSM2563118	SRA551247	SRX2704305	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	193	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412258	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412258/SRR5412258.1	GSM2563119	SRA551247	SRX2704306	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	194	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412259	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412259/SRR5412259.1	GSM2563120	SRA551247	SRX2704307	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	195	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412260	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412260/SRR5412260.1	GSM2563121	SRA551247	SRX2704308	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	196	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412261	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412261/SRR5412261.1	GSM2563122	SRA551247	SRX2704309	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	197	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412262	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412262/SRR5412262.1	GSM2563123	SRA551247	SRX2704310	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	198	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412263	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412263/SRR5412263.1	GSM2563124	SRA551247	SRX2704311	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	199	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412264	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412264/SRR5412264.1	GSM2563125	SRA551247	SRX2704312	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	200	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412265	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412265/SRR5412265.1	GSM2563126	SRA551247	SRX2704313	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	201	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412144	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412144/SRR5412144.1	GSM2563005	SRA551247	SRX2704192	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	202	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412145	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412145/SRR5412145.1	GSM2563006	SRA551247	SRX2704193	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	203	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412146	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412146/SRR5412146.1	GSM2563007	SRA551247	SRX2704194	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	204	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412147	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412147/SRR5412147.1	GSM2563008	SRA551247	SRX2704195	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	205	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412148	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412148/SRR5412148.1	GSM2563009	SRA551247	SRX2704196	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	206	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412149	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412149/SRR5412149.1	GSM2563010	SRA551247	SRX2704197	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	207	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412150	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412150/SRR5412150.1	GSM2563011	SRA551247	SRX2704198	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	208	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412151	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412151/SRR5412151.1	GSM2563012	SRA551247	SRX2704199	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	209	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412152	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412152/SRR5412152.1	GSM2563013	SRA551247	SRX2704200	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	210	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412153	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412153/SRR5412153.1	GSM2563014	SRA551247	SRX2704201	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	211	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412154	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412154/SRR5412154.1	GSM2563015	SRA551247	SRX2704202	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	212	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412155	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412155/SRR5412155.1	GSM2563016	SRA551247	SRX2704203	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	213	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412156	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412156/SRR5412156.1	GSM2563017	SRA551247	SRX2704204	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	214	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412157	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412157/SRR5412157.1	GSM2563018	SRA551247	SRX2704205	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	215	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412158	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412158/SRR5412158.1	GSM2563019	SRA551247	SRX2704206	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	216	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412159	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412159/SRR5412159.1	GSM2563020	SRA551247	SRX2704207	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	217	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412160	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412160/SRR5412160.1	GSM2563021	SRA551247	SRX2704208	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	218	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412161	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412161/SRR5412161.1	GSM2563022	SRA551247	SRX2704209	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	219	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412162	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412162/SRR5412162.1	GSM2563023	SRA551247	SRX2704210	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	220	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412163	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412163/SRR5412163.1	GSM2563024	SRA551247	SRX2704211	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	221	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412164	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412164/SRR5412164.1	GSM2563025	SRA551247	SRX2704212	RNA-Seq	SINGLE	SRP102989	PRJNA381064
97367	222	Diego Cortez	BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage	In order to study the green anole dosage compensation mechanism we generated strand-specific RNA-seq libraries for a total of 186 samples from the gre	Diego Cortez, Henrik Kaessmann, Francesco Lamanna, Madapura Pradeepa	We generated strand-specific RNA-seq libraries using the Illumina TruSeq Stranded mRNA Library protocol. Sample size (minimum one male and one female for each species) was established to have a wide spectrum across amniotes and to capture general male/female sex-specific patterns. Each source RNA was of high quality, as assessed using a Fragment Analyzer machine from Advanced Analytical (RIN median = 9, RQN median = 8). Each library was sequenced on Illumina HiSeq 2500 platforms at the Lausanne Genomic Technologies Facility (https://www.unil.ch/gtf/en/home.html). At least 17 million sequencing reads (100 nt, single-end) were produced for each library (median: 34 million reads). Examination of H4K16ac enrichment between males and females in liver and brain. Two biological replicates, four genomic DNA input libraries. Y-linked transcripts of Anolis carolinensis were obtained using a male/female subtraction approach. The sequences were validated using re-sequenced male and female genomes.	0	56019	SRP102989	SRR5412165	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-7/SRR5412165/SRR5412165.1	GSM2563026	SRA551247	SRX2704213	RNA-Seq	SINGLE	SRP102989	PRJNA381064
100434	1	Neil Hukriede	Regulation of kidney field specification by transcriptional regulation of microRNAs	The transcriptional events driving specification of the kidney field have been well characterized.  However, it remains unknown how the initial field 	Neil Hukriede, Neil Hukriede, M Cirio	miRNA Deep sequencing of 3 Xenopus laevis samples	30375416	55420	SRP110298	SRR5753209	https://sra-download.ncbi.nlm.nih.gov/traces/sra49/SRR/005618/SRR5753209	GSM2683080	SRA580653	SRX2953428	miRNA-Seq	SINGLE	SRP110298	PRJNA391724
100434	2	Neil Hukriede	Regulation of kidney field specification by transcriptional regulation of microRNAs	The transcriptional events driving specification of the kidney field have been well characterized.  However, it remains unknown how the initial field 	Neil Hukriede, Neil Hukriede, M Cirio	miRNA Deep sequencing of 3 Xenopus laevis samples	30375416	55420	SRP110298	SRR5753210	https://sra-download.ncbi.nlm.nih.gov/traces/sra49/SRR/005618/SRR5753210	GSM2683081	SRA580653	SRX2953429	miRNA-Seq	SINGLE	SRP110298	PRJNA391724
100434	3	Neil Hukriede	Regulation of kidney field specification by transcriptional regulation of microRNAs	The transcriptional events driving specification of the kidney field have been well characterized.  However, it remains unknown how the initial field 	Neil Hukriede, Neil Hukriede, M Cirio	miRNA Deep sequencing of 3 Xenopus laevis samples	30375416	55420	SRP110298	SRR5753211	https://sra-download.ncbi.nlm.nih.gov/traces/sra49/SRR/005618/SRR5753211	GSM2683082	SRA580653	SRX2953430	miRNA-Seq	SINGLE	SRP110298	PRJNA391724
102047	1	Mary Lou King	The Xenopus Primordial Germ Cell Transcriptome: Unexpected Role for sox7 in Early PGC Development	Xenopus primordial germ cells (PGCs) are determined by the presence of maternally derived germ plasm. Germ plasm components both protect PGCs from so	Mary Lou King, Amanda Butler, Dawn Owens, Lingyu Wang, Mary King	Examination of X. laevis primordial germ cell (PGC) and neighboring endoderm cell (Endo) RNAs after lineage segregation to determine PGC-enriched transcripts that may contribute to germline development.	29158442	54309	SRP114372	SRR5883382	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/005745/SRR5883382	GSM2722410	SRA594757	SRX3049471	RNA-Seq	PAIRED	SRP114372	PRJNA396491
102047	2	Mary Lou King	The Xenopus Primordial Germ Cell Transcriptome: Unexpected Role for sox7 in Early PGC Development	Xenopus primordial germ cells (PGCs) are determined by the presence of maternally derived germ plasm. Germ plasm components both protect PGCs from so	Mary Lou King, Amanda Butler, Dawn Owens, Lingyu Wang, Mary King	Examination of X. laevis primordial germ cell (PGC) and neighboring endoderm cell (Endo) RNAs after lineage segregation to determine PGC-enriched transcripts that may contribute to germline development.	29158442	54309	SRP114372	SRR5883383	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/005745/SRR5883383	GSM2722411	SRA594757	SRX3049472	RNA-Seq	PAIRED	SRP114372	PRJNA396491
102047	3	Mary Lou King	The Xenopus Primordial Germ Cell Transcriptome: Unexpected Role for sox7 in Early PGC Development	Xenopus primordial germ cells (PGCs) are determined by the presence of maternally derived germ plasm. Germ plasm components both protect PGCs from so	Mary Lou King, Amanda Butler, Dawn Owens, Lingyu Wang, Mary King	Examination of X. laevis primordial germ cell (PGC) and neighboring endoderm cell (Endo) RNAs after lineage segregation to determine PGC-enriched transcripts that may contribute to germline development.	29158442	54309	SRP114372	SRR5883384	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/005745/SRR5883384	GSM2722412	SRA594757	SRX3049473	RNA-Seq	PAIRED	SRP114372	PRJNA396491
102047	4	Mary Lou King	The Xenopus Primordial Germ Cell Transcriptome: Unexpected Role for sox7 in Early PGC Development	Xenopus primordial germ cells (PGCs) are determined by the presence of maternally derived germ plasm. Germ plasm components both protect PGCs from so	Mary Lou King, Amanda Butler, Dawn Owens, Lingyu Wang, Mary King	Examination of X. laevis primordial germ cell (PGC) and neighboring endoderm cell (Endo) RNAs after lineage segregation to determine PGC-enriched transcripts that may contribute to germline development.	29158442	54309	SRP114372	SRR5883385	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/005745/SRR5883385	GSM2722413	SRA594757	SRX3049474	RNA-Seq	PAIRED	SRP114372	PRJNA396491
102047	5	Mary Lou King	The Xenopus Primordial Germ Cell Transcriptome: Unexpected Role for sox7 in Early PGC Development	Xenopus primordial germ cells (PGCs) are determined by the presence of maternally derived germ plasm. Germ plasm components both protect PGCs from so	Mary Lou King, Amanda Butler, Dawn Owens, Lingyu Wang, Mary King	Examination of X. laevis primordial germ cell (PGC) and neighboring endoderm cell (Endo) RNAs after lineage segregation to determine PGC-enriched transcripts that may contribute to germline development.	29158442	54309	SRP114372	SRR5883386	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/005745/SRR5883386	GSM2722414	SRA594757	SRX3049475	RNA-Seq	PAIRED	SRP114372	PRJNA396491
102047	6	Mary Lou King	The Xenopus Primordial Germ Cell Transcriptome: Unexpected Role for sox7 in Early PGC Development	Xenopus primordial germ cells (PGCs) are determined by the presence of maternally derived germ plasm. Germ plasm components both protect PGCs from so	Mary Lou King, Amanda Butler, Dawn Owens, Lingyu Wang, Mary King	Examination of X. laevis primordial germ cell (PGC) and neighboring endoderm cell (Endo) RNAs after lineage segregation to determine PGC-enriched transcripts that may contribute to germline development.	29158442	54309	SRP114372	SRR5883387	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/005745/SRR5883387	GSM2722415	SRA594757	SRX3049476	RNA-Seq	PAIRED	SRP114372	PRJNA396491
103240	1	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988444	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988444	GSM2758809	SRA603666	SRX3144219	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	2	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988445	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988445	GSM2758810	SRA603666	SRX3144220	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	3	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988446	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988446	GSM2758811	SRA603666	SRX3144221	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	4	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988447	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988447	GSM2758812	SRA603666	SRX3144222	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	5	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988448	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988448	GSM2758813	SRA603666	SRX3144223	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	6	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988449	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988449	GSM2758814	SRA603666	SRX3144224	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	7	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988450	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988450	GSM2758815	SRA603666	SRX3144225	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	8	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988451	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988451	GSM2758816	SRA603666	SRX3144226	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	9	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988452	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988452	GSM2758817	SRA603666	SRX3144227	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	10	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988453	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988453	GSM2758818	SRA603666	SRX3144228	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	11	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988454	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988454	GSM2758819	SRA603666	SRX3144229	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	12	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988455	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988455	GSM2758820	SRA603666	SRX3144230	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	13	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988456	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988456	GSM2758821	SRA603666	SRX3144231	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	14	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988457	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988457	GSM2758822	SRA603666	SRX3144232	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	15	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988458	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988458	GSM2758823	SRA603666	SRX3144233	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	16	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988459	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988459	GSM2758824	SRA603666	SRX3144234	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	17	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988460	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988460	GSM2758825	SRA603666	SRX3144235	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	18	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988461	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988461	GSM2758826	SRA603666	SRX3144236	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	19	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988462	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988462	GSM2758827	SRA603666	SRX3144237	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	20	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988463	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988463	GSM2758828	SRA603666	SRX3144238	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	21	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988464	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988464	GSM2758829	SRA603666	SRX3144239	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	22	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988465	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988465	GSM2758830	SRA603666	SRX3144240	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	23	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988466	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988466	GSM2758831	SRA603666	SRX3144241	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	24	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988467	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988467	GSM2758832	SRA603666	SRX3144242	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	25	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988468	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988468	GSM2758833	SRA603666	SRX3144243	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	26	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988469	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988469	GSM2758834	SRA603666	SRX3144244	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	27	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988470	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988470	GSM2758835	SRA603666	SRX3144245	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	28	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988471	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988471	GSM2758836	SRA603666	SRX3144246	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	29	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988472	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988472	GSM2758837	SRA603666	SRX3144247	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	30	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988473	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988473	GSM2758838	SRA603666	SRX3144248	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	31	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988474	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988474	GSM2758839	SRA603666	SRX3144249	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	32	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988475	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988475	GSM2758840	SRA603666	SRX3144250	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	33	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988476	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988476	GSM2758841	SRA603666	SRX3144251	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	34	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988477	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988477	GSM2758842	SRA603666	SRX3144252	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	35	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988478	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988478	GSM2758843	SRA603666	SRX3144253	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	36	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988479	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988479	GSM2758844	SRA603666	SRX3144254	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	37	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988480	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988480	GSM2758845	SRA603666	SRX3144255	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	38	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988481	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988481	GSM2758846	SRA603666	SRX3144256	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	39	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988482	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988482	GSM2758847	SRA603666	SRX3144257	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	40	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988483	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988483	GSM2758848	SRA603666	SRX3144258	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	41	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988484	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988484	GSM2758849	SRA603666	SRX3144259	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	42	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988485	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988485	GSM2758850	SRA603666	SRX3144260	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	43	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988486	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988486	GSM2758851	SRA603666	SRX3144261	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	44	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988487	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988487	GSM2758852	SRA603666	SRX3144262	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	45	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988488	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988488	GSM2758853	SRA603666	SRX3144263	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	46	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988489	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988489	GSM2758854	SRA603666	SRX3144264	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	47	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988490	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988490	GSM2758855	SRA603666	SRX3144265	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	48	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988491	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988491	GSM2758856	SRA603666	SRX3144266	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	49	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988492	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988492	GSM2758857	SRA603666	SRX3144267	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	50	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988493	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988493	GSM2758858	SRA603666	SRX3144268	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	51	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988494	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988494	GSM2758859	SRA603666	SRX3144269	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	52	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988495	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988495	GSM2758860	SRA603666	SRX3144270	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	53	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988496	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988496	GSM2758861	SRA603666	SRX3144271	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	54	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988497	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988497	GSM2758862	SRA603666	SRX3144272	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	55	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988498	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988498	GSM2758863	SRA603666	SRX3144273	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	56	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988499	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988499	GSM2758864	SRA603666	SRX3144274	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	57	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988500	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988500	GSM2758865	SRA603666	SRX3144275	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	58	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988501	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988501	GSM2758866	SRA603666	SRX3144276	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	59	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988502	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988502	GSM2758867	SRA603666	SRX3144277	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	60	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988503	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988503	GSM2758868	SRA603666	SRX3144278	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	61	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988504	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988504	GSM2758869	SRA603666	SRX3144279	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	62	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988505	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988505	GSM2758870	SRA603666	SRX3144280	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	63	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988506	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988506	GSM2758871	SRA603666	SRX3144281	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	64	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988507	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988507	GSM2758872	SRA603666	SRX3144282	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	65	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988508	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988508	GSM2758873	SRA603666	SRX3144283	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	66	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988509	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988509	GSM2758874	SRA603666	SRX3144284	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	67	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988510	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988510	GSM2758875	SRA603666	SRX3144285	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	68	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988511	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988511	GSM2758876	SRA603666	SRX3144286	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	69	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988512	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988512	GSM2758877	SRA603666	SRX3144287	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	70	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988513	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988513	GSM2758878	SRA603666	SRX3144288	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	71	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988514	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988514	GSM2758879	SRA603666	SRX3144289	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	72	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988515	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988515	GSM2758880	SRA603666	SRX3144290	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	73	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988516	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988516	GSM2758881	SRA603666	SRX3144291	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	74	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988517	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988517	GSM2758882	SRA603666	SRX3144292	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	75	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988518	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988518	GSM2758883	SRA603666	SRX3144293	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	76	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988519	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988519	GSM2758884	SRA603666	SRX3144294	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	77	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988520	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988520	GSM2758885	SRA603666	SRX3144295	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	78	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988521	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988521	GSM2758886	SRA603666	SRX3144296	RNA-Seq	PAIRED	SRP116397	PRJNA400602
103240	79	Anne-Helene Monsoro-Burq	A Molecular Atlas of the Developing Ectoderm Defines Neural, Neural Crest, Placode and Non-Neural Progenitor Identity in Vertebrates.	During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. He	Anne-Helene Monsoro-Burq, Jean-Louis Plouhinec, Sofía Medina-Ruiz, Caroline Borday, Elsa Bernard, Jean-Philippe Vert, Michael Eisen, Richard Harland, Anne Monsoro-Burq	Xenopus laevis ectodermal sample were dissected at embryonic stages 12.5, 14, and 17 and mRNA profiles were generated by deep sequencing using an Illumina HiSeq 2000	29049289	54144	SRP116397	SRR5988522	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/005848/SRR5988522	GSM2758887	SRA603666	SRX3144297	RNA-Seq	PAIRED	SRP116397	PRJNA400602
104848	1	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160922	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160922	GSM2808768	SRA618931	SRX3272460	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	2	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160923	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160923	GSM2808769	SRA618931	SRX3272461	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	3	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160924	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160924	GSM2808770	SRA618931	SRX3272462	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	4	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160925	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160925	GSM2808771	SRA618931	SRX3272463	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	5	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160926	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160926	GSM2808772	SRA618931	SRX3272464	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	6	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160927	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160927	GSM2808773	SRA618931	SRX3272465	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	7	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160928	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160928	GSM2808774	SRA618931	SRX3272466	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	8	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160929	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160929	GSM2808775	SRA618931	SRX3272467	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	9	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160930	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160930	GSM2808776	SRA618931	SRX3272468	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	10	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160931	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160931	GSM2808777	SRA618931	SRX3272469	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	11	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160932	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160932	GSM2808778	SRA618931	SRX3272470	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	12	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160933	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160933	GSM2808779	SRA618931	SRX3272471	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	13	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160934	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160934	GSM2808780	SRA618931	SRX3272472	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	14	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160935	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160935	GSM2808781	SRA618931	SRX3272473	RNA-Seq	PAIRED	SRP119791	PRJNA413987
104848	15	Radek Šindelka	RNA-Seq analysis of localization along animal-vegetal axis of Xenopus laevis	We combined cryosectining of oocytes along the animal-vegetal axis (first developmental axis) and RNA-Seq to determine localization profiles of coding	Radek Šindelka, Radek Sindelka, Pavel Abaffy	RNA profiles (mRNA, lncRNA, other RNA) were generated by deep sequencing, in biological triplicates (each oocyte divided into five segments), using Illumina HiSeq.	29844480	54969	SRP119791	SRR6160936	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006016/SRR6160936	GSM2808782	SRA618931	SRX3272474	RNA-Seq	PAIRED	SRP119791	PRJNA413987
106157	1	Taejoon Kwon	Paternal chromosome loss and metabolic crisis contribute to hybrid inviability in Xenopus	Hybridization of eggs and sperm from closely related species can give rise to genetic diversity, or can lead to embryo inviability due to incompatibil	Taejoon Kwon, Romain Gibeaux, Rachael Acker, Maiko Kitaoka, Georgios Georgiou, Ilavan Kruijsbergen, Breanna Ford, Edward Marcotte, Daniel Nomura, GertJan Veenstra, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	29320479	54448	SRP121460	SRR6216948	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006071/SRR6216948	GSM2830578	SRA624598	SRX3325611	RNA-Seq	PAIRED	SRP121460	PRJNA415788
106157	2	Taejoon Kwon	Paternal chromosome loss and metabolic crisis contribute to hybrid inviability in Xenopus	Hybridization of eggs and sperm from closely related species can give rise to genetic diversity, or can lead to embryo inviability due to incompatibil	Taejoon Kwon, Romain Gibeaux, Rachael Acker, Maiko Kitaoka, Georgios Georgiou, Ilavan Kruijsbergen, Breanna Ford, Edward Marcotte, Daniel Nomura, GertJan Veenstra, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	29320479	54448	SRP121460	SRR6216949	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006071/SRR6216949	GSM2830579	SRA624598	SRX3325612	RNA-Seq	PAIRED	SRP121460	PRJNA415788
106157	3	Taejoon Kwon	Paternal chromosome loss and metabolic crisis contribute to hybrid inviability in Xenopus	Hybridization of eggs and sperm from closely related species can give rise to genetic diversity, or can lead to embryo inviability due to incompatibil	Taejoon Kwon, Romain Gibeaux, Rachael Acker, Maiko Kitaoka, Georgios Georgiou, Ilavan Kruijsbergen, Breanna Ford, Edward Marcotte, Daniel Nomura, GertJan Veenstra, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	29320479	54448	SRP121460	SRR6216950	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006071/SRR6216950	GSM2830580	SRA624598	SRX3325613	RNA-Seq	PAIRED	SRP121460	PRJNA415788
106157	4	Taejoon Kwon	Paternal chromosome loss and metabolic crisis contribute to hybrid inviability in Xenopus	Hybridization of eggs and sperm from closely related species can give rise to genetic diversity, or can lead to embryo inviability due to incompatibil	Taejoon Kwon, Romain Gibeaux, Rachael Acker, Maiko Kitaoka, Georgios Georgiou, Ilavan Kruijsbergen, Breanna Ford, Edward Marcotte, Daniel Nomura, GertJan Veenstra, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	29320479	54448	SRP121460	SRR6216951	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006071/SRR6216951	GSM2830581	SRA624598	SRX3325614	RNA-Seq	PAIRED	SRP121460	PRJNA415788
106157	5	Taejoon Kwon	Paternal chromosome loss and metabolic crisis contribute to hybrid inviability in Xenopus	Hybridization of eggs and sperm from closely related species can give rise to genetic diversity, or can lead to embryo inviability due to incompatibil	Taejoon Kwon, Romain Gibeaux, Rachael Acker, Maiko Kitaoka, Georgios Georgiou, Ilavan Kruijsbergen, Breanna Ford, Edward Marcotte, Daniel Nomura, GertJan Veenstra, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	29320479	54448	SRP121460	SRR6216952	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006071/SRR6216952	GSM2830582	SRA624598	SRX3325615	RNA-Seq	PAIRED	SRP121460	PRJNA415788
106157	6	Taejoon Kwon	Paternal chromosome loss and metabolic crisis contribute to hybrid inviability in Xenopus	Hybridization of eggs and sperm from closely related species can give rise to genetic diversity, or can lead to embryo inviability due to incompatibil	Taejoon Kwon, Romain Gibeaux, Rachael Acker, Maiko Kitaoka, Georgios Georgiou, Ilavan Kruijsbergen, Breanna Ford, Edward Marcotte, Daniel Nomura, GertJan Veenstra, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	29320479	54448	SRP121460	SRR6216953	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006071/SRR6216953	GSM2830583	SRA624598	SRX3325616	RNA-Seq	PAIRED	SRP121460	PRJNA415788
106320	1	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234315	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234315	GSM2835917	SRA626226	SRX3342727	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	2	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234316	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234316	GSM2835918	SRA626226	SRX3342728	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	3	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234317	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234317	GSM2835919	SRA626226	SRX3342729	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	4	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234318	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234318	GSM2835920	SRA626226	SRX3342730	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	5	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234319	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234319	GSM2835921	SRA626226	SRX3342731	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	6	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234320	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234320	GSM2835922	SRA626226	SRX3342732	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	7	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234321	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234321	GSM2835923	SRA626226	SRX3342733	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	8	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234322	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234322	GSM2835924	SRA626226	SRX3342734	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	9	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234323	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234323	GSM2835925	SRA626226	SRX3342735	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	10	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234324	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234324	GSM2835926	SRA626226	SRX3342736	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	11	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234325	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234325	GSM2835927	SRA626226	SRX3342737	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	12	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234326	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234326	GSM2835928	SRA626226	SRX3342738	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	13	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234327	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234327	GSM2835929	SRA626226	SRX3342739	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	14	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234328	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234328	GSM2835930	SRA626226	SRX3342740	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	15	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234329	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234329	GSM2835931	SRA626226	SRX3342741	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106320	16	Edward De Robertis	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis	The Xenopus laevis embryo has been subjected to almost saturating screens for molecules specifically expressed in dorsal Spemann organizer tissue. In 	Edward De Robertis, Yi Ding, Gabriele Colozza, Eric Sosa, Yuki Moriyama, Samantha Rundle, Lukasz Salwinski	A genome-wide study of the effects of vavious growth factors and dissociation on animal caps of Xenopus laevis	30209221	55302	SRP122914	SRR6234330	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/006088/SRR6234330	GSM2835932	SRA626226	SRX3342742	RNA-Seq	SINGLE	SRP122914	PRJNA416291
106877	1	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289332	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289332	GSM2856492	SRA630478	SRX3390648	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	2	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289333	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289333	GSM2856493	SRA630478	SRX3390649	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	3	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289334	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289334	GSM2856494	SRA630478	SRX3390650	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	4	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289335	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289335	GSM2856495	SRA630478	SRX3390651	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	5	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289336	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289336	GSM2856496	SRA630478	SRX3390652	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	6	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289337	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289337	GSM2856497	SRA630478	SRX3390653	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	7	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289338	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289338	GSM2856498	SRA630478	SRX3390654	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	8	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289339	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289339	GSM2856499	SRA630478	SRX3390655	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	9	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289340	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289340	GSM2856500	SRA630478	SRX3390656	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	10	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289341	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289341	GSM2856501	SRA630478	SRX3390657	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	11	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289342	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289342	GSM2856502	SRA630478	SRX3390658	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	12	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289343	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289343	GSM2856503	SRA630478	SRX3390659	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	13	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289344	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289344	GSM2856504	SRA630478	SRX3390660	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	14	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289345	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289345	GSM2856505	SRA630478	SRX3390661	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	15	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289346	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289346	GSM2856506	SRA630478	SRX3390662	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	16	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289347	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289347	GSM2856507	SRA630478	SRX3390663	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	17	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289348	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289348	GSM2856508	SRA630478	SRX3390664	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	18	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289349	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289349	GSM2856509	SRA630478	SRX3390665	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	19	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289350	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289350	GSM2856510	SRA630478	SRX3390666	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	20	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289351	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289351	GSM2856511	SRA630478	SRX3390667	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	21	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289352	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289352	GSM2856512	SRA630478	SRX3390668	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	22	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289353	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289353	GSM2856513	SRA630478	SRX3390669	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	23	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289354	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289354	GSM2856514	SRA630478	SRX3390670	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	24	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289355	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289355	GSM2856515	SRA630478	SRX3390671	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	25	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289356	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289356	GSM2856516	SRA630478	SRX3390672	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	26	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289357	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289357	GSM2856517	SRA630478	SRX3390673	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	27	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289358	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289358	GSM2856518	SRA630478	SRX3390674	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	28	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289359	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289359	GSM2856519	SRA630478	SRX3390675	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	29	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289360	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289360	GSM2856520	SRA630478	SRX3390676	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	30	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289361	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289361	GSM2856521	SRA630478	SRX3390677	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	31	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289362	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289362	GSM2856522	SRA630478	SRX3390678	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	32	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289363	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289363	GSM2856523	SRA630478	SRX3390679	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	33	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289364	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289364	GSM2856524	SRA630478	SRX3390680	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	34	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289365	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289365	GSM2856525	SRA630478	SRX3390681	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	35	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289366	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289366	GSM2856526	SRA630478	SRX3390682	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	36	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289367	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289367	GSM2856527	SRA630478	SRX3390683	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	37	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289368	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289368	GSM2856528	SRA630478	SRX3390684	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	38	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289369	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289369	GSM2856529	SRA630478	SRX3390685	RNA-Seq	PAIRED	SRP124956	PRJNA418305
106877	39	Carsten Lueder	Changes in the gene expression in the olfactory organ of Xenopus laevis	We report changes of the olfactory receptor gene expression and other important gene over the timecourse of metamorphosis                             	Carsten Lueder, Katarina Dittrich	Comparison of larval and adult stages under normal conditions and after an injury	0	57683	SRP124956	SRR6289370	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006141/SRR6289370	GSM2856530	SRA630478	SRX3390686	RNA-Seq	PAIRED	SRP124956	PRJNA418305
107424	1	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326658	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006178/SRR6326658	GSM2866830	SRA634412	SRX3426351	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	2	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326659	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006178/SRR6326659	GSM2866831	SRA634412	SRX3426352	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	3	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326660	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326660	GSM2866832	SRA634412	SRX3426353	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	4	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326661	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326661	GSM2866833	SRA634412	SRX3426354	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	5	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326662	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326662	GSM2866834	SRA634412	SRX3426355	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	6	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326663	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326663	GSM2866835	SRA634412	SRX3426356	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	7	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326664	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326664	GSM2866836	SRA634412	SRX3426357	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	8	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326665	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326665	GSM2866837	SRA634412	SRX3426358	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	9	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326666	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326666	GSM2866838	SRA634412	SRX3426359	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	10	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326667	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326667	GSM2866839	SRA634412	SRX3426360	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	11	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326668	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326668	GSM2866840	SRA634412	SRX3426361	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	12	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326669	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326669	GSM2866841	SRA634412	SRX3426362	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	13	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326670	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/006178/SRR6326670	GSM2866842	SRA634412	SRX3426363	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	14	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326671	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326671	GSM2866843	SRA634412	SRX3426364	RNA-Seq	PAIRED	SRP125755	PRJNA420057
107424	15	Rita Monteiro	Transcriptomics of Dorso-Ventral axis determination in Xenopus tropicalis	We studied the transcriptomic differences between ventralised and dorsalised Xenopus tropicalisembryos as a result of UV irradiation and LiCl treatmen	Rita Monteiro, Rita Monteiro, James Smith, George Gentsch	Comparison of poly(A) transcriptome between Xenopus tropicalis LiCl-, UV-treated and untreated gastrulae embryos. For each condition there are five biological replicates that were used for the analyses.	29709598	54855	SRP125755	SRR6326672	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/006178/SRR6326672	GSM2866844	SRA634412	SRX3426365	RNA-Seq	PAIRED	SRP125755	PRJNA420057
110063	1	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666795	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666795/SRR6666795.1	GSM2977205	SRA655102	SRX3643656	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	2	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666796	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666796/SRR6666796.1	GSM2977206	SRA655102	SRX3643657	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	3	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666797	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666797/SRR6666797.1	GSM2977207	SRA655102	SRX3643658	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	4	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666798	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666798/SRR6666798.1	GSM2977208	SRA655102	SRX3643659	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	5	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666799	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666799/SRR6666799.1	GSM2977209	SRA655102	SRX3643660	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	6	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666800	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666800/SRR6666800.1	GSM2977210	SRA655102	SRX3643661	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	7	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666801	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666801/SRR6666801.1	GSM2977211	SRA655102	SRX3643662	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	8	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666802	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666802/SRR6666802.1	GSM2977212	SRA655102	SRX3643663	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	9	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666803	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666803/SRR6666803.1	GSM2977213	SRA655102	SRX3643664	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	10	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666804	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666804/SRR6666804.1	GSM2977214	SRA655102	SRX3643665	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	11	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666805	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666805/SRR6666805.1	GSM2977215	SRA655102	SRX3643666	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	12	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666806	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666806/SRR6666806.1	GSM2977216	SRA655102	SRX3643667	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	13	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666807	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666807/SRR6666807.1	GSM2977217	SRA655102	SRX3643668	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	14	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666808	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666808/SRR6666808.1	GSM2977218	SRA655102	SRX3643669	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	15	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666809	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666809/SRR6666809.1	GSM2977219	SRA655102	SRX3643670	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	16	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666810	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666810/SRR6666810.1	GSM2977220	SRA655102	SRX3643671	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	17	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666811	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666811/SRR6666811.1	GSM2977221	SRA655102	SRX3643672	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	18	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666812	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666812/SRR6666812.1	GSM2977222	SRA655102	SRX3643673	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	19	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666813	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666813/SRR6666813.1	GSM2977223	SRA655102	SRX3643674	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	20	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666814	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666814/SRR6666814.1	GSM2977224	SRA655102	SRX3643675	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	21	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666815	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666815/SRR6666815.1	GSM2977225	SRA655102	SRX3643676	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	22	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666816	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666816/SRR6666816.1	GSM2977226	SRA655102	SRX3643677	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	23	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666817	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666817/SRR6666817.1	GSM2977227	SRA655102	SRX3643678	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	24	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666818	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666818/SRR6666818.1	GSM2977228	SRA655102	SRX3643679	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	25	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666819	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666819/SRR6666819.1	GSM2977229	SRA655102	SRX3643680	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	26	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666820	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666820/SRR6666820.1	GSM2977230	SRA655102	SRX3643681	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	27	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666821	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666821/SRR6666821.1	GSM2977231	SRA655102	SRX3643682	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	28	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666822	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666822/SRR6666822.1	GSM2977232	SRA655102	SRX3643683	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	29	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666823	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666823/SRR6666823.1	GSM2977233	SRA655102	SRX3643684	RNA-Seq	SINGLE	SRP132061	PRJNA432702
110063	30	Zhihua Jiang	Profiling of alternative transcription start sites and alternative polyadenylation sites in Xenopus tropicalis	We have developed both WTSS-seq (whole transcriptome start site sequencing) and WTTS-seq (whole transcriptome termini site sequencing) methods to capt	Zhihua Jiang, Xiang Zhou, Yangzi Zhang, Jennifer Michal, Lujiang Qu	A total of 14 WTSS-seq libraries were constructed using six individual adult males, six individual adult females and an RNA pool with three adult females (repeated twice). One CAGE-seq library was prepared with the three adult female pool using service provided by DNAFORM Precision Gene Technologies, Yokohama, Japan. The same three-female pool was used to develop one HATT-seq library. The same six individual males and six individual females were also used to profile 3’-ends of transcripts using WTTS-seq for a total of 12 libraries.  One embryo pool was formed using total RNA collected from two families at stage 6, 8, 11, 15 and 28. As well, an adult pool was prepared from three male and three female adults.  The embryo and adult pools were used to construct a total of one Iso-seq libraries.  In brief, this submission involved 30 libraries in total.	0	57141	SRP132061	SRR6666824	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR6666824/SRR6666824.1	GSM2977234	SRA655102	SRX3643685	RNA-Seq	SINGLE	SRP132061	PRJNA432702
111171	1	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786715	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786715	GSM3024606	SRA662540	SRX3746139	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	2	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786716	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786716	GSM3024606	SRA662540	SRX3746139	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	3	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786717	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786717	GSM3024606	SRA662540	SRX3746139	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	4	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786718	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786718	GSM3024607	SRA662540	SRX3746140	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	5	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786719	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786719	GSM3024607	SRA662540	SRX3746140	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	6	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786720	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786720	GSM3024607	SRA662540	SRX3746140	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	7	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786721	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786721	GSM3024608	SRA662540	SRX3746141	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	8	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786722	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786722	GSM3024608	SRA662540	SRX3746141	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111171	9	Pawel Smialowski	The Xenopus animal cap transcriptome: building a mucociliary epithelium.	Here we investigate dynamics of the RNA landscape during formation of the Xenopus tropicalis larval epidermis.  To obtain RNA expression data, we used	Pawel Smialowski, Alessandro Angerilli, Ralph Rupp	Transcriptomic analysis of 3 developmental stages of embryonic epidermis development in Xenopus tropicalis. We looked at gene´s  expression and splicing isoforms expression	30165493	55254	SRP133568	SRR6786723	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006627/SRR6786723	GSM3024608	SRA662540	SRX3746141	RNA-Seq	PAIRED	SRP133568	PRJNA436118
111454	1	Ye Jin	RNA Sequencing facilitates the identification of transcriptional targets of Pitx1 in Xenopus laevis	The cement gland in Xenopus laevis has long been used as a model to study the interplay of cell signaling and transcription factors during embryogenes	Ye Jin, Daniel Weinstein	mRNA profile of pitx1-injected or control animal cap explants at neurula stages were generated by deep sequencing, in duplicate, using Illumina HiSeq2500 by Genewiz.	29530451	54672	SRP134011	SRR6809320	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006649/SRR6809320	GSM3031399	SRA664463	SRX3767534	RNA-Seq	PAIRED	SRP134011	PRJNA437084
111454	2	Ye Jin	RNA Sequencing facilitates the identification of transcriptional targets of Pitx1 in Xenopus laevis	The cement gland in Xenopus laevis has long been used as a model to study the interplay of cell signaling and transcription factors during embryogenes	Ye Jin, Daniel Weinstein	mRNA profile of pitx1-injected or control animal cap explants at neurula stages were generated by deep sequencing, in duplicate, using Illumina HiSeq2500 by Genewiz.	29530451	54672	SRP134011	SRR6809321	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006649/SRR6809321	GSM3031400	SRA664463	SRX3767535	RNA-Seq	PAIRED	SRP134011	PRJNA437084
111454	3	Ye Jin	RNA Sequencing facilitates the identification of transcriptional targets of Pitx1 in Xenopus laevis	The cement gland in Xenopus laevis has long been used as a model to study the interplay of cell signaling and transcription factors during embryogenes	Ye Jin, Daniel Weinstein	mRNA profile of pitx1-injected or control animal cap explants at neurula stages were generated by deep sequencing, in duplicate, using Illumina HiSeq2500 by Genewiz.	29530451	54672	SRP134011	SRR6809322	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006649/SRR6809322	GSM3031401	SRA664463	SRX3767536	RNA-Seq	PAIRED	SRP134011	PRJNA437084
111454	4	Ye Jin	RNA Sequencing facilitates the identification of transcriptional targets of Pitx1 in Xenopus laevis	The cement gland in Xenopus laevis has long been used as a model to study the interplay of cell signaling and transcription factors during embryogenes	Ye Jin, Daniel Weinstein	mRNA profile of pitx1-injected or control animal cap explants at neurula stages were generated by deep sequencing, in duplicate, using Illumina HiSeq2500 by Genewiz.	29530451	54672	SRP134011	SRR6809323	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006649/SRR6809323	GSM3031402	SRA664463	SRX3767537	RNA-Seq	PAIRED	SRP134011	PRJNA437084
111639	1	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821881	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006661/SRR6821881	GSM3036206	SRA665478	SRX3778722	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	2	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821882	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006661/SRR6821882	GSM3036207	SRA665478	SRX3778723	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	3	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821883	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006661/SRR6821883	GSM3036208	SRA665478	SRX3778724	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	4	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821884	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006661/SRR6821884	GSM3036209	SRA665478	SRX3778725	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	5	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821885	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006661/SRR6821885	GSM3036210	SRA665478	SRX3778726	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	6	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821886	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006661/SRR6821886	GSM3036211	SRA665478	SRX3778727	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	7	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821887	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006661/SRR6821887	GSM3036212	SRA665478	SRX3778728	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	8	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821888	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006662/SRR6821888	GSM3036213	SRA665478	SRX3778729	RNA-Seq	PAIRED	SRP134281	PRJNA437641
111639	9	Margaret Saha	Xenopus andrei RNA-Seq	The Xenopus genus is well known for the high degree of polyploidy observed in its constituent species, but there is minimal information about transcri	Margaret Saha, Mark Pownall, Ronald Cutler, Margaret Saha	Embryos were obtained from one mating of two adult X. andrei frogs. Nine samples are analyzed, each from a different developmental stage.	29900348	55017	SRP134281	SRR6821889	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/006662/SRR6821889	GSM3036214	SRA665478	SRX3778730	RNA-Seq	PAIRED	SRP134281	PRJNA437641
112249	1	Richard Harland	Genome-wide map of ETS2 binding in gastrula stage Xenopus.laevis embryos	We examined the location of ETS2 biding in gastrula stage Xenopus embryos to identify direct transcriptional targets of the FGF signaling pathway.    	Richard Harland, Rachel Kjolby	Examination of tripple-FLAG tagged ETS2 binding in whole Xenopus embryos	0	57686	SRP136318	SRR6884606	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006723/SRR6884606	GSM3062917	SRA672001	SRX3836834	ChIP-Seq	SINGLE	SRP136318	PRJNA445381
112249	2	Richard Harland	Genome-wide map of ETS2 binding in gastrula stage Xenopus.laevis embryos	We examined the location of ETS2 biding in gastrula stage Xenopus embryos to identify direct transcriptional targets of the FGF signaling pathway.    	Richard Harland, Rachel Kjolby	Examination of tripple-FLAG tagged ETS2 binding in whole Xenopus embryos	0	57686	SRP136318	SRR6884607	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006723/SRR6884607	GSM3062918	SRA672001	SRX3836835	ChIP-Seq	SINGLE	SRP136318	PRJNA445381
112249	3	Richard Harland	Genome-wide map of ETS2 binding in gastrula stage Xenopus.laevis embryos	We examined the location of ETS2 biding in gastrula stage Xenopus embryos to identify direct transcriptional targets of the FGF signaling pathway.    	Richard Harland, Rachel Kjolby	Examination of tripple-FLAG tagged ETS2 binding in whole Xenopus embryos	0	57686	SRP136318	SRR6884608	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006723/SRR6884608	GSM3062919	SRA672001	SRX3836836	ChIP-Seq	SINGLE	SRP136318	PRJNA445381
112249	4	Richard Harland	Genome-wide map of ETS2 binding in gastrula stage Xenopus.laevis embryos	We examined the location of ETS2 biding in gastrula stage Xenopus embryos to identify direct transcriptional targets of the FGF signaling pathway.    	Richard Harland, Rachel Kjolby	Examination of tripple-FLAG tagged ETS2 binding in whole Xenopus embryos	0	57686	SRP136318	SRR6884609	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006723/SRR6884609	GSM3062920	SRA672001	SRX3836837	ChIP-Seq	SINGLE	SRP136318	PRJNA445381
112364	1	Chris Kintner	RNAseq profiliing of Xenopus laevis animal caps expressing Xnr2 at st14	To determine if Xnr2 induces mesodermal genes expression in ectodermal tissues                                                                        	Chris Kintner, Yuan-Hung Chien	We force the ectodermal tissues to express xnr2 by injecting xnr2 RNA at the 2-4cell stage. The animal caps were excised at st10, the blastula stage. Tissues are cultured at DFA and harvested at stage 14 for RNA extraction.	29738711	54874	SRP136530	SRR6902663	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006740/SRR6902663	GSM3068398	SRA675067	SRX3851506	RNA-Seq	SINGLE	SRP136530	PRJNA445807
112364	2	Chris Kintner	RNAseq profiliing of Xenopus laevis animal caps expressing Xnr2 at st14	To determine if Xnr2 induces mesodermal genes expression in ectodermal tissues                                                                        	Chris Kintner, Yuan-Hung Chien	We force the ectodermal tissues to express xnr2 by injecting xnr2 RNA at the 2-4cell stage. The animal caps were excised at st10, the blastula stage. Tissues are cultured at DFA and harvested at stage 14 for RNA extraction.	29738711	54874	SRP136530	SRR6902664	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006740/SRR6902664	GSM3068399	SRA675067	SRX3851507	RNA-Seq	SINGLE	SRP136530	PRJNA445807
112718	1	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941643	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941643	GSM3082043	SRA681856	SRX3885766	RNA-Seq	SINGLE	SRP137258	PRJNA448780
112718	2	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941644	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941644	GSM3082044	SRA681856	SRX3885767	RNA-Seq	SINGLE	SRP137258	PRJNA448780
112718	3	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941645	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941645	GSM3082045	SRA681856	SRX3885768	RNA-Seq	SINGLE	SRP137258	PRJNA448780
112718	4	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941646	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941646	GSM3082046	SRA681856	SRX3885769	RNA-Seq	SINGLE	SRP137258	PRJNA448780
112718	5	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941647	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941647	GSM3082047	SRA681856	SRX3885770	RNA-Seq	SINGLE	SRP137258	PRJNA448780
112718	6	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941648	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941648	GSM3082048	SRA681856	SRX3885771	RNA-Seq	SINGLE	SRP137258	PRJNA448780
112718	7	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941649	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941649	GSM3082049	SRA681856	SRX3885772	RNA-Seq	SINGLE	SRP137258	PRJNA448780
112718	8	Gabriela Salinas-Riester	Retinoic acid induced expression of Hnf1β and Fzd4 is required for pancreas development in Xenopus laevis	Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA-s	Gabriela Salinas-Riester, Tomas Pieler, Maja Gere, Claudia Pommerenke, Thomas Lingner	VegT/Noggin/Cyp26a1 programmed animal cap explants from Xenopus laevis, untreated and treated with RA/CHX and collected  2 hours after RA addition at the equivalent of gastrula stage 11; two replicates A and B for each condition	29769220	54918	SRP137258	SRR6941650	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/006778/SRR6941650	GSM3082050	SRA681856	SRX3885773	RNA-Seq	SINGLE	SRP137258	PRJNA448780
113074	1	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061415	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061415	GSM3095780	SRA694978	SRX3992347	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	2	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061416	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061416	GSM3095781	SRA694978	SRX3992348	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	3	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061417	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061417	GSM3095782	SRA694978	SRX3992349	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	4	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061418	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061418	GSM3095783	SRA694978	SRX3992350	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	5	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061419	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061419	GSM3095784	SRA694978	SRX3992351	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	6	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061420	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061420	GSM3095785	SRA694978	SRX3992352	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	7	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061421	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061421	GSM3095786	SRA694978	SRX3992353	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	8	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061422	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061422	GSM3095787	SRA694978	SRX3992354	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	9	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061423	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061423	GSM3095788	SRA694978	SRX3992355	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	10	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061424	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061424	GSM3095789	SRA694978	SRX3992356	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	11	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061425	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061425	GSM3095790	SRA694978	SRX3992357	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	12	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061426	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061426	GSM3095791	SRA694978	SRX3992358	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	13	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061427	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061427	GSM3095792	SRA694978	SRX3992359	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	14	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061428	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061428	GSM3095793	SRA694978	SRX3992360	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	15	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061429	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061429	GSM3095794	SRA694978	SRX3992361	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	16	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061430	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061430	GSM3095795	SRA694978	SRX3992362	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	17	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061431	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061431	GSM3095796	SRA694978	SRX3992363	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	18	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061432	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061432	GSM3095797	SRA694978	SRX3992364	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	19	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061433	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061433	GSM3095798	SRA694978	SRX3992365	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	20	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061434	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061434	GSM3095799	SRA694978	SRX3992366	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	21	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061435	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061435	GSM3095800	SRA694978	SRX3992367	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	22	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061437	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061437	GSM3095802	SRA694978	SRX3992369	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	23	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061438	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061438	GSM3095803	SRA694978	SRX3992370	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	24	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061439	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061439	GSM3095804	SRA694978	SRX3992371	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	25	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061440	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061440	GSM3095805	SRA694978	SRX3992372	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	26	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061441	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061441	GSM3095806	SRA694978	SRX3992373	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	27	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061442	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061442	GSM3095807	SRA694978	SRX3992374	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	28	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061443	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061443	GSM3095808	SRA694978	SRX3992375	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	29	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061444	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061444	GSM3095809	SRA694978	SRX3992376	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	30	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061445	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061445	GSM3095810	SRA694978	SRX3992377	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	31	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061446	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061446	GSM3095811	SRA694978	SRX3992378	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	32	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061447	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061447	GSM3095812	SRA694978	SRX3992379	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	33	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061448	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061448	GSM3095813	SRA694978	SRX3992380	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	34	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061449	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061449	GSM3095814	SRA694978	SRX3992381	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	35	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061450	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061450	GSM3095815	SRA694978	SRX3992382	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	36	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061451	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061451	GSM3095816	SRA694978	SRX3992383	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	37	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061452	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061452	GSM3095817	SRA694978	SRX3992384	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	38	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061453	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061453	GSM3095818	SRA694978	SRX3992385	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	39	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061454	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061454	GSM3095819	SRA694978	SRX3992386	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	40	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061455	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061455	GSM3095820	SRA694978	SRX3992387	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	41	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061456	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061456	GSM3095821	SRA694978	SRX3992388	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	42	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061457	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061457	GSM3095822	SRA694978	SRX3992389	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	43	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061458	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061458	GSM3095823	SRA694978	SRX3992390	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	44	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061459	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061459	GSM3095824	SRA694978	SRX3992391	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	45	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061460	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061460	GSM3095825	SRA694978	SRX3992392	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	46	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061461	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061461	GSM3095826	SRA694978	SRX3992393	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	47	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061462	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061462	GSM3095827	SRA694978	SRX3992394	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	48	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061463	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061463	GSM3095828	SRA694978	SRX3992395	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	49	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061464	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061464	GSM3095829	SRA694978	SRX3992396	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	50	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061465	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061465	GSM3095830	SRA694978	SRX3992397	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	51	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061466	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061466	GSM3095831	SRA694978	SRX3992398	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	52	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061467	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061467	GSM3095832	SRA694978	SRX3992399	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	53	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061468	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061468	GSM3095833	SRA694978	SRX3992400	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	54	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061469	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061469	GSM3095834	SRA694978	SRX3992401	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	55	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061470	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061470	GSM3095835	SRA694978	SRX3992402	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	56	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061471	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061471	GSM3095836	SRA694978	SRX3992403	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	57	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061472	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061472	GSM3095837	SRA694978	SRX3992404	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	58	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061473	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061473	GSM3095838	SRA694978	SRX3992405	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	59	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061474	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061474	GSM3095839	SRA694978	SRX3992406	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	60	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061475	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061475	GSM3095840	SRA694978	SRX3992407	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	61	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061476	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061476	GSM3095841	SRA694978	SRX3992408	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	62	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061477	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061477	GSM3095842	SRA694978	SRX3992409	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	63	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061478	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061478	GSM3095843	SRA694978	SRX3992410	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	64	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061479	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061479	GSM3095844	SRA694978	SRX3992411	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	65	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061480	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061480	GSM3095845	SRA694978	SRX3992412	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	66	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061481	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061481	GSM3095846	SRA694978	SRX3992413	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	67	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061482	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061482	GSM3095847	SRA694978	SRX3992414	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	68	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061483	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061483	GSM3095848	SRA694978	SRX3992415	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	69	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061484	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061484	GSM3095849	SRA694978	SRX3992416	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	70	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061485	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061485	GSM3095850	SRA694978	SRX3992417	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	71	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061486	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061486	GSM3095851	SRA694978	SRX3992418	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	72	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061487	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061487	GSM3095852	SRA694978	SRX3992419	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	73	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061488	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061488	GSM3095853	SRA694978	SRX3992420	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113074	74	James Briggs	The dynamics of gene expression in vertebrate embryogenesis at single cell resolution	Time series of single cell transcriptome measurements can reveal dynamic features of cell differentiation pathways. From measurements of whole frog em	James Briggs, James Briggs, Caleb Weinreb, Daniel Wagner, Sean Megason, Leonid Peshkin, Marc Kirschner, Allon Klein	136,966 single cell transcriptomes were profiled from whole Xenopus tropicalis embryos at ten timepoints during the first 24 hours of its embryonic development. The data includes 75 total single cell RNA sequencing libraries, collected in 2 replicate timeseries. 4 of the 75 libraries focussed on dissected neural plate border tissue. The counts data for all pass filter cells are available in a single matrix (see "Corrected_combined.annotated_counts.tsv.gz" and "Raw_combined.annotated_counts.tsv.gz"). Alternatively, raw FASTQ or unfiltered counts files are also available for each individual library.	29700227	54862	SRP142544	SRR7061489	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006895/SRR7061489	GSM3095854	SRA694978	SRX3992421	RNA-Seq	PAIRED	SRP142544	PRJNA449931
113186	1	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010183	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010183	GSM3099554	SRA691345	SRX3942662	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	2	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010184	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010184	GSM3099555	SRA691345	SRX3942663	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	3	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010185	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010185	GSM3099556	SRA691345	SRX3942664	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	4	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010186	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010186	GSM3099557	SRA691345	SRX3942665	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	5	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010187	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010187	GSM3099558	SRA691345	SRX3942666	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	6	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010188	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010188	GSM3099559	SRA691345	SRX3942667	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	7	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010189	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010189	GSM3099560	SRA691345	SRX3942668	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	8	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010190	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010190	GSM3099561	SRA691345	SRX3942669	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	9	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010191	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010191	GSM3099562	SRA691345	SRX3942670	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	10	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010192	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010192	GSM3099563	SRA691345	SRX3942671	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	11	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010193	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010193	GSM3099564	SRA691345	SRX3942672	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	12	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010194	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010194	GSM3099565	SRA691345	SRX3942673	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	13	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010195	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010195	GSM3099566	SRA691345	SRX3942674	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	14	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010196	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010196	GSM3099567	SRA691345	SRX3942675	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	15	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010197	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010197	GSM3099568	SRA691345	SRX3942676	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	16	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010198	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010198	GSM3099569	SRA691345	SRX3942677	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	17	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010199	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010199	GSM3099570	SRA691345	SRX3942678	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	18	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010200	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010200	GSM3099571	SRA691345	SRX3942679	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	19	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010201	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010201	GSM3099572	SRA691345	SRX3942680	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	20	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010202	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010202	GSM3099573	SRA691345	SRX3942681	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	21	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010203	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010203	GSM3099574	SRA691345	SRX3942682	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	22	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010204	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010204	GSM3099575	SRA691345	SRX3942683	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	23	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010205	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010205	GSM3099576	SRA691345	SRX3942684	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	24	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010206	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010206	GSM3099577	SRA691345	SRX3942685	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	25	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010207	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010207	GSM3099578	SRA691345	SRX3942686	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	26	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010208	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010208	GSM3099579	SRA691345	SRX3942687	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	27	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010209	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010209	GSM3099580	SRA691345	SRX3942688	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	28	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010210	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010210	GSM3099581	SRA691345	SRX3942689	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	29	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010211	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010211	GSM3099582	SRA691345	SRX3942690	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	30	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010212	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010212	GSM3099583	SRA691345	SRX3942691	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	31	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010213	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010213	GSM3099584	SRA691345	SRX3942692	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	32	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010214	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010214	GSM3099585	SRA691345	SRX3942693	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	33	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010215	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010215	GSM3099586	SRA691345	SRX3942694	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	34	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010216	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010216	GSM3099587	SRA691345	SRX3942695	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	35	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010217	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010217	GSM3099588	SRA691345	SRX3942696	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	36	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010218	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010218	GSM3099589	SRA691345	SRX3942697	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	37	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010219	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010219	GSM3099590	SRA691345	SRX3942698	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	38	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010220	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010220	GSM3099591	SRA691345	SRX3942699	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	39	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010221	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010221	GSM3099592	SRA691345	SRX3942700	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	40	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010222	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010222	GSM3099593	SRA691345	SRX3942701	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	41	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010223	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010223	GSM3099594	SRA691345	SRX3942702	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	42	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010224	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010224	GSM3099595	SRA691345	SRX3942703	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	43	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010225	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010225	GSM3099596	SRA691345	SRX3942704	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	44	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010226	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010226	GSM3099597	SRA691345	SRX3942705	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	45	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010227	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010227	GSM3099598	SRA691345	SRX3942706	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	46	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010228	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010228	GSM3099599	SRA691345	SRX3942707	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	47	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010229	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010229	GSM3099600	SRA691345	SRX3942708	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	48	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010230	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010230	GSM3099601	SRA691345	SRX3942709	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	49	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010231	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010231	GSM3099602	SRA691345	SRX3942710	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	50	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010232	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010232	GSM3099603	SRA691345	SRX3942711	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	51	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010233	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010233	GSM3099604	SRA691345	SRX3942712	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	52	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010234	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010234	GSM3099605	SRA691345	SRX3942713	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	53	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010235	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010235	GSM3099606	SRA691345	SRX3942714	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	54	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010236	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010236	GSM3099607	SRA691345	SRX3942715	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	55	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010237	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010237	GSM3099608	SRA691345	SRX3942716	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	56	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010238	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010238	GSM3099609	SRA691345	SRX3942717	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	57	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010239	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010239	GSM3099610	SRA691345	SRX3942718	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	58	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010240	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010240	GSM3099611	SRA691345	SRX3942719	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	59	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010241	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010241	GSM3099612	SRA691345	SRX3942720	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	60	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010242	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010242	GSM3099613	SRA691345	SRX3942721	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	61	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010243	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010243	GSM3099614	SRA691345	SRX3942722	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	62	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010244	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010244	GSM3099615	SRA691345	SRX3942723	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	63	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010245	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010245	GSM3099616	SRA691345	SRX3942724	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	64	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010246	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010246	GSM3099617	SRA691345	SRX3942725	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	65	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010247	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010247	GSM3099618	SRA691345	SRX3942726	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	66	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010248	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010248	GSM3099619	SRA691345	SRX3942727	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	67	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010249	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010249	GSM3099620	SRA691345	SRX3942728	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	68	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010250	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010250	GSM3099621	SRA691345	SRX3942729	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	69	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010251	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010251	GSM3099622	SRA691345	SRX3942730	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	70	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010252	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010252	GSM3099623	SRA691345	SRX3942731	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	71	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010253	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010253	GSM3099624	SRA691345	SRX3942732	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	72	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010254	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010254	GSM3099625	SRA691345	SRX3942733	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	73	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010255	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010255	GSM3099626	SRA691345	SRX3942734	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	74	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010256	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010256	GSM3099627	SRA691345	SRX3942735	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	75	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010257	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010257	GSM3099628	SRA691345	SRX3942736	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	76	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010258	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010258	GSM3099629	SRA691345	SRX3942737	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	77	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010259	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010259	GSM3099630	SRA691345	SRX3942738	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	78	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010260	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010260	GSM3099631	SRA691345	SRX3942739	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	79	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010261	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010261	GSM3099632	SRA691345	SRX3942740	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	80	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010262	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010262	GSM3099633	SRA691345	SRX3942741	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	81	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010263	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010263	GSM3099634	SRA691345	SRX3942742	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	82	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010264	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010264	GSM3099635	SRA691345	SRX3942743	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	83	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010265	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010265	GSM3099636	SRA691345	SRX3942744	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	84	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010266	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010266	GSM3099637	SRA691345	SRX3942745	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	85	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010267	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010267	GSM3099638	SRA691345	SRX3942746	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	86	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010268	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010268	GSM3099639	SRA691345	SRX3942747	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	87	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010269	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010269	GSM3099640	SRA691345	SRX3942748	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	88	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010270	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010270	GSM3099641	SRA691345	SRX3942749	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	89	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010271	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010271	GSM3099642	SRA691345	SRX3942750	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	90	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010272	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010272	GSM3099643	SRA691345	SRX3942751	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	91	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010273	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010273	GSM3099644	SRA691345	SRX3942752	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	92	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010274	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010274	GSM3099645	SRA691345	SRX3942753	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	93	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010275	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010275	GSM3099646	SRA691345	SRX3942754	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	94	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010276	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010276	GSM3099647	SRA691345	SRX3942755	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	95	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010277	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010277	GSM3099648	SRA691345	SRX3942756	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	96	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010278	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010278	GSM3099649	SRA691345	SRX3942757	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	97	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010279	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010279	GSM3099650	SRA691345	SRX3942758	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	98	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010280	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010280	GSM3099651	SRA691345	SRX3942759	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	99	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010281	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010281	GSM3099652	SRA691345	SRX3942760	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	100	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010282	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010282	GSM3099653	SRA691345	SRX3942761	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	101	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010083	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010083	GSM3099454	SRA691345	SRX3942562	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	102	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010084	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010084	GSM3099455	SRA691345	SRX3942563	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	103	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010085	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010085	GSM3099456	SRA691345	SRX3942564	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	104	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010086	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010086	GSM3099457	SRA691345	SRX3942565	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	105	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010087	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010087	GSM3099458	SRA691345	SRX3942566	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	106	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010088	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010088	GSM3099459	SRA691345	SRX3942567	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	107	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010089	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010089	GSM3099460	SRA691345	SRX3942568	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	108	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010090	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010090	GSM3099461	SRA691345	SRX3942569	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	109	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010091	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010091	GSM3099462	SRA691345	SRX3942570	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	110	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010092	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010092	GSM3099463	SRA691345	SRX3942571	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	111	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010093	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010093	GSM3099464	SRA691345	SRX3942572	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	112	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010094	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010094	GSM3099465	SRA691345	SRX3942573	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	113	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010095	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010095	GSM3099466	SRA691345	SRX3942574	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	114	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010096	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010096	GSM3099467	SRA691345	SRX3942575	ChIP-Seq	PAIRED	SRP140517	PRJNA450396
113186	115	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010097	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010097	GSM3099468	SRA691345	SRX3942576	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	116	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010098	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010098	GSM3099469	SRA691345	SRX3942577	ChIP-Seq	PAIRED	SRP140517	PRJNA450396
113186	117	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010099	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010099	GSM3099470	SRA691345	SRX3942578	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	118	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010100	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010100	GSM3099471	SRA691345	SRX3942579	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	119	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010101	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010101	GSM3099472	SRA691345	SRX3942580	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	120	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010102	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010102	GSM3099473	SRA691345	SRX3942581	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	121	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010103	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010103	GSM3099474	SRA691345	SRX3942582	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	122	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010104	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010104	GSM3099475	SRA691345	SRX3942583	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	123	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010105	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010105	GSM3099476	SRA691345	SRX3942584	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	124	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010106	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010106	GSM3099477	SRA691345	SRX3942585	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	125	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010107	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010107	GSM3099478	SRA691345	SRX3942586	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	126	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010108	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010108	GSM3099479	SRA691345	SRX3942587	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	127	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010109	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010109	GSM3099480	SRA691345	SRX3942588	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	128	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010110	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010110	GSM3099481	SRA691345	SRX3942589	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	129	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010111	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010111	GSM3099482	SRA691345	SRX3942590	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	130	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010112	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010112	GSM3099483	SRA691345	SRX3942591	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	131	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010113	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010113	GSM3099484	SRA691345	SRX3942592	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	132	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010114	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010114	GSM3099485	SRA691345	SRX3942593	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	133	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010115	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010115	GSM3099486	SRA691345	SRX3942594	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	134	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010116	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010116	GSM3099487	SRA691345	SRX3942595	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	135	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010117	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010117	GSM3099488	SRA691345	SRX3942596	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	136	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010118	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010118	GSM3099489	SRA691345	SRX3942597	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	137	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010119	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010119	GSM3099490	SRA691345	SRX3942598	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	138	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010120	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010120	GSM3099491	SRA691345	SRX3942599	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	139	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010121	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010121	GSM3099492	SRA691345	SRX3942600	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	140	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010122	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010122	GSM3099493	SRA691345	SRX3942601	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	141	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010123	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010123	GSM3099494	SRA691345	SRX3942602	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	142	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010124	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010124	GSM3099495	SRA691345	SRX3942603	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	143	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010125	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010125	GSM3099496	SRA691345	SRX3942604	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	144	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010126	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010126	GSM3099497	SRA691345	SRX3942605	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	145	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010127	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010127	GSM3099498	SRA691345	SRX3942606	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	146	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010128	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010128	GSM3099499	SRA691345	SRX3942607	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	147	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010129	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010129	GSM3099500	SRA691345	SRX3942608	ChIP-Seq	PAIRED	SRP140517	PRJNA450396
113186	148	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010130	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010130	GSM3099501	SRA691345	SRX3942609	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	149	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010131	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010131	GSM3099502	SRA691345	SRX3942610	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	150	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010132	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010132	GSM3099503	SRA691345	SRX3942611	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	151	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010133	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010133	GSM3099504	SRA691345	SRX3942612	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	152	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010134	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010134	GSM3099505	SRA691345	SRX3942613	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	153	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010135	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010135	GSM3099506	SRA691345	SRX3942614	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	154	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010136	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010136	GSM3099507	SRA691345	SRX3942615	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	155	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010137	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010137	GSM3099508	SRA691345	SRX3942616	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	156	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010138	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010138	GSM3099509	SRA691345	SRX3942617	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	157	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010139	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010139	GSM3099510	SRA691345	SRX3942618	ChIP-Seq	PAIRED	SRP140517	PRJNA450396
113186	158	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010140	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010140	GSM3099511	SRA691345	SRX3942619	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	159	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010141	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010141	GSM3099512	SRA691345	SRX3942620	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	160	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010142	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010142	GSM3099513	SRA691345	SRX3942621	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	161	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010143	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010143	GSM3099514	SRA691345	SRX3942622	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	162	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010144	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010144	GSM3099515	SRA691345	SRX3942623	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	163	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010145	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010145	GSM3099516	SRA691345	SRX3942624	DNase-Hypersensitivity	SINGLE	SRP140517	PRJNA450396
113186	164	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010146	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010146	GSM3099517	SRA691345	SRX3942625	DNase-Hypersensitivity	PAIRED	SRP140517	PRJNA450396
113186	165	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010147	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010147	GSM3099518	SRA691345	SRX3942626	DNase-Hypersensitivity	SINGLE	SRP140517	PRJNA450396
113186	166	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010148	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010148	GSM3099519	SRA691345	SRX3942627	DNase-Hypersensitivity	PAIRED	SRP140517	PRJNA450396
113186	167	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010149	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010149	GSM3099520	SRA691345	SRX3942628	DNase-Hypersensitivity	SINGLE	SRP140517	PRJNA450396
113186	168	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010150	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010150	GSM3099521	SRA691345	SRX3942629	DNase-Hypersensitivity	PAIRED	SRP140517	PRJNA450396
113186	169	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010151	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010151	GSM3099522	SRA691345	SRX3942630	OTHER	PAIRED	SRP140517	PRJNA450396
113186	170	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010152	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010152	GSM3099523	SRA691345	SRX3942631	OTHER	PAIRED	SRP140517	PRJNA450396
113186	171	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010153	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010153	GSM3099524	SRA691345	SRX3942632	OTHER	PAIRED	SRP140517	PRJNA450396
113186	172	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010154	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010154	GSM3099525	SRA691345	SRX3942633	OTHER	PAIRED	SRP140517	PRJNA450396
113186	173	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010155	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010155	GSM3099526	SRA691345	SRX3942634	OTHER	PAIRED	SRP140517	PRJNA450396
113186	174	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010156	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010156	GSM3099527	SRA691345	SRX3942635	OTHER	PAIRED	SRP140517	PRJNA450396
113186	175	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010157	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010157	GSM3099528	SRA691345	SRX3942636	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	176	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010158	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010158	GSM3099529	SRA691345	SRX3942637	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	177	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010159	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010159	GSM3099530	SRA691345	SRX3942638	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	178	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010160	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010160	GSM3099531	SRA691345	SRX3942639	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	179	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010161	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010161	GSM3099532	SRA691345	SRX3942640	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	180	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010162	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010162	GSM3099533	SRA691345	SRX3942641	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	181	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010163	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010163	GSM3099534	SRA691345	SRX3942642	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	182	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010164	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010164	GSM3099535	SRA691345	SRX3942643	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	183	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010165	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010165	GSM3099536	SRA691345	SRX3942644	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	184	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010166	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010166	GSM3099537	SRA691345	SRX3942645	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	185	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010167	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010167	GSM3099538	SRA691345	SRX3942646	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	186	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010168	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010168	GSM3099539	SRA691345	SRX3942647	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	187	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010169	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010169	GSM3099540	SRA691345	SRX3942648	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	188	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010170	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010170	GSM3099541	SRA691345	SRX3942649	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	189	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010171	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010171	GSM3099542	SRA691345	SRX3942650	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	190	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010172	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010172	GSM3099543	SRA691345	SRX3942651	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	191	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010173	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010173	GSM3099544	SRA691345	SRX3942652	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	192	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010174	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010174	GSM3099545	SRA691345	SRX3942653	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	193	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010175	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010175	GSM3099546	SRA691345	SRX3942654	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	194	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010176	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010176	GSM3099547	SRA691345	SRX3942655	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	195	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010177	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010177	GSM3099548	SRA691345	SRX3942656	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	196	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010178	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010178	GSM3099549	SRA691345	SRX3942657	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	197	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010179	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010179	GSM3099550	SRA691345	SRX3942658	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	198	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010180	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010180	GSM3099551	SRA691345	SRX3942659	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	199	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010181	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010181	GSM3099552	SRA691345	SRX3942660	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	200	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010182	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010182	GSM3099553	SRA691345	SRX3942661	RNA-Seq	PAIRED	SRP140517	PRJNA450396
113186	201	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010081	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010081	GSM3099452	SRA691345	SRX3942560	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
113186	202	George Gentsch	The role of maternal pioneer factors in predefining first zygotic responses to inductive signals	Embryonic development yields many different cell types in response to just a few families of inductive signals. The property of a signal-receiving cel	George Gentsch, George Gentsch, James Smith	This study generated 202 samples of different applications of high-throughput sequencing inluding ChIP-Seq, DNase-Seq, next-generation capture-C and RNA-Seq.	31537794	56302	SRP140517	SRR7010082	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/006845/SRR7010082	GSM3099453	SRA691345	SRX3942561	ChIP-Seq	SINGLE	SRP140517	PRJNA450396
115220	1	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248465	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248465	GSM3171642	SRA713922	SRX4153291	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	2	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248466	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248466	GSM3171642	SRA713922	SRX4153291	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	3	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248467	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248467	GSM3171642	SRA713922	SRX4153291	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	4	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248468	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248468	GSM3171642	SRA713922	SRX4153291	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	5	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248469	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248469	GSM3171643	SRA713922	SRX4153292	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	6	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248470	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248470	GSM3171643	SRA713922	SRX4153292	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	7	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248471	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248471	GSM3171643	SRA713922	SRX4153292	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	8	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248472	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248472	GSM3171643	SRA713922	SRX4153292	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	9	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248473	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248473	GSM3171644	SRA713922	SRX4153293	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	10	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248474	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248474	GSM3171644	SRA713922	SRX4153293	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	11	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248475	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248475	GSM3171644	SRA713922	SRX4153293	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	12	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248476	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248476	GSM3171644	SRA713922	SRX4153293	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	13	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248477	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248477	GSM3171645	SRA713922	SRX4153294	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	14	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248478	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248478	GSM3171645	SRA713922	SRX4153294	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	15	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248479	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248479	GSM3171645	SRA713922	SRX4153294	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	16	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248480	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248480	GSM3171645	SRA713922	SRX4153294	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	17	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248481	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248481	GSM3171646	SRA713922	SRX4153295	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	18	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248482	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248482	GSM3171646	SRA713922	SRX4153295	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	19	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248483	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248483	GSM3171646	SRA713922	SRX4153295	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	20	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248484	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248484	GSM3171646	SRA713922	SRX4153295	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	21	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248485	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248485	GSM3171647	SRA713922	SRX4153296	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	22	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248486	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248486	GSM3171647	SRA713922	SRX4153296	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	23	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248487	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248487	GSM3171647	SRA713922	SRX4153296	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115220	24	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [RNA-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	RNA-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) or etv6 morpholino injected stage 22 embryos. Indexed libraries were then generated, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149548	SRR7248488	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248488	GSM3171647	SRA713922	SRX4153296	RNA-Seq	PAIRED	SRP149548	PRJNA474192
115224	1	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248713	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248713	GSM3171680	SRA713924	SRX4153521	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	2	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248714	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248714	GSM3171680	SRA713924	SRX4153521	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	3	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248715	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248715	GSM3171680	SRA713924	SRX4153521	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	4	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248716	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248716	GSM3171680	SRA713924	SRX4153521	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	5	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248717	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248717	GSM3171681	SRA713924	SRX4153522	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	6	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248718	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248718	GSM3171681	SRA713924	SRX4153522	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	7	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248719	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248719	GSM3171681	SRA713924	SRX4153522	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	8	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248720	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248720	GSM3171681	SRA713924	SRX4153522	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	9	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248721	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248721	GSM3171682	SRA713924	SRX4153523	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	10	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248722	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248722	GSM3171682	SRA713924	SRX4153523	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	11	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248723	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248723	GSM3171682	SRA713924	SRX4153523	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	12	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248724	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248724	GSM3171682	SRA713924	SRX4153523	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	13	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248725	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248725	GSM3171683	SRA713924	SRX4153524	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	14	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248726	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248726	GSM3171683	SRA713924	SRX4153524	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	15	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248727	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248727	GSM3171683	SRA713924	SRX4153524	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	16	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248728	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248728	GSM3171683	SRA713924	SRX4153524	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	17	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248729	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248729	GSM3171684	SRA713924	SRX4153525	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	18	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248730	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248730	GSM3171684	SRA713924	SRX4153525	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	19	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248731	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248731	GSM3171684	SRA713924	SRX4153525	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	20	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248732	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248732	GSM3171684	SRA713924	SRX4153525	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	21	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248733	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248733	GSM3171685	SRA713924	SRX4153526	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	22	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248734	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248734	GSM3171685	SRA713924	SRX4153526	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	23	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248735	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248735	GSM3171685	SRA713924	SRX4153526	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
115224	24	Lei Li	Etv6-dependent positive and negative gene regulatory network controls vegfa expression in vivo [ChIP-seq]	VEGFA signaling is crucial for physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent signaling pathways downs	Lei Li, Rossella Rispoli, Roger Patient, Aldo Ciau-Uitz, Catherine Porcher	Etv6 ChIP-seq was performed on three independent biological samples obtained from the somites of wild-type (WT) stage 22 embryos. Indexed libraries were then generated from immunoprecipited DNA and control input samples, pooled and sequenced using a NextSeq 500 sequencer.	30842454	55761	SRP149552	SRR7248736	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/007078/SRR7248736	GSM3171685	SRA713924	SRX4153526	ChIP-Seq	PAIRED	SRP149552	PRJNA474199
116819	1	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500842	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/007325/SRR7500842	GSM3262255	SRA736036	SRX4370238	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	2	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500843	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500843	GSM3262255	SRA736036	SRX4370238	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	3	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500844	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500844	GSM3262256	SRA736036	SRX4370239	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	4	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500845	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500845	GSM3262256	SRA736036	SRX4370239	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	5	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500846	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500846	GSM3262257	SRA736036	SRX4370240	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	6	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500847	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500847	GSM3262257	SRA736036	SRX4370240	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	7	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500848	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500848	GSM3262258	SRA736036	SRX4370241	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	8	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500849	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/007325/SRR7500849	GSM3262258	SRA736036	SRX4370241	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	9	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500850	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/007325/SRR7500850	GSM3262259	SRA736036	SRX4370242	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	10	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500851	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500851	GSM3262259	SRA736036	SRX4370242	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	11	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500852	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/007325/SRR7500852	GSM3262260	SRA736036	SRX4370243	RNA-Seq	SINGLE	SRP152872	PRJNA480292
116819	12	Stacey Wahl	Transcriptome analysis of wild type and RAR deficient frog faces during development	We utilized RNASeq to investigate the changes in mRNA expression when retinoic acid signaling is inhibited by treatment with an RAR inhibitor, BMS453.	Stacey Wahl, Stephen Turner, Amanda Dickinson	Embryos were treated with RAR inhibtior during the latter stage of facial development, 35-66 hours post fertilzation, facial region was dissection and global changes in gene expression were assessed. Further analyses to determine funcitonal networks that were affected was performed.	30390632	55440	SRP152872	SRR7500853	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/007325/SRR7500853	GSM3262260	SRA736036	SRX4370243	RNA-Seq	SINGLE	SRP152872	PRJNA480292
117754	1	Taejoon Kwon	Critical roles of lysine demethylase Kdm3a in craniofacial and neural development during Xenopus embryogenesis	The epigenetic modifier lysine-specific histone demethylase 3a (kdm3a) is specific for demethylation of mono- and di-methylated 9th lysine of histone 	Taejoon Kwon, Hyun-Kyung Lee, Tayaba Ismail, Chowon Kim, Youni Kim, Jeen-Woo Park, Oh-Shin Kwon, Beom-Sik Kang, Dong-Seok Lee, Tae Park, Hyun-Shik Lee	Collect mRNA from whole embryos; two biological replicates were analyzed	30522514	55525	SRP155436	SRR7609575	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007431/SRR7609575	GSM3308290	SRA745502	SRX4474418	RNA-Seq	PAIRED	SRP155436	PRJNA483070
117754	2	Taejoon Kwon	Critical roles of lysine demethylase Kdm3a in craniofacial and neural development during Xenopus embryogenesis	The epigenetic modifier lysine-specific histone demethylase 3a (kdm3a) is specific for demethylation of mono- and di-methylated 9th lysine of histone 	Taejoon Kwon, Hyun-Kyung Lee, Tayaba Ismail, Chowon Kim, Youni Kim, Jeen-Woo Park, Oh-Shin Kwon, Beom-Sik Kang, Dong-Seok Lee, Tae Park, Hyun-Shik Lee	Collect mRNA from whole embryos; two biological replicates were analyzed	30522514	55525	SRP155436	SRR7609576	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007431/SRR7609576	GSM3308291	SRA745502	SRX4474419	RNA-Seq	PAIRED	SRP155436	PRJNA483070
117754	3	Taejoon Kwon	Critical roles of lysine demethylase Kdm3a in craniofacial and neural development during Xenopus embryogenesis	The epigenetic modifier lysine-specific histone demethylase 3a (kdm3a) is specific for demethylation of mono- and di-methylated 9th lysine of histone 	Taejoon Kwon, Hyun-Kyung Lee, Tayaba Ismail, Chowon Kim, Youni Kim, Jeen-Woo Park, Oh-Shin Kwon, Beom-Sik Kang, Dong-Seok Lee, Tae Park, Hyun-Shik Lee	Collect mRNA from whole embryos; two biological replicates were analyzed	30522514	55525	SRP155436	SRR7609577	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007431/SRR7609577	GSM3308292	SRA745502	SRX4474420	RNA-Seq	PAIRED	SRP155436	PRJNA483070
117754	4	Taejoon Kwon	Critical roles of lysine demethylase Kdm3a in craniofacial and neural development during Xenopus embryogenesis	The epigenetic modifier lysine-specific histone demethylase 3a (kdm3a) is specific for demethylation of mono- and di-methylated 9th lysine of histone 	Taejoon Kwon, Hyun-Kyung Lee, Tayaba Ismail, Chowon Kim, Youni Kim, Jeen-Woo Park, Oh-Shin Kwon, Beom-Sik Kang, Dong-Seok Lee, Tae Park, Hyun-Shik Lee	Collect mRNA from whole embryos; two biological replicates were analyzed	30522514	55525	SRP155436	SRR7609578	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007431/SRR7609578	GSM3308293	SRA745502	SRX4474421	RNA-Seq	PAIRED	SRP155436	PRJNA483070
117754	5	Taejoon Kwon	Critical roles of lysine demethylase Kdm3a in craniofacial and neural development during Xenopus embryogenesis	The epigenetic modifier lysine-specific histone demethylase 3a (kdm3a) is specific for demethylation of mono- and di-methylated 9th lysine of histone 	Taejoon Kwon, Hyun-Kyung Lee, Tayaba Ismail, Chowon Kim, Youni Kim, Jeen-Woo Park, Oh-Shin Kwon, Beom-Sik Kang, Dong-Seok Lee, Tae Park, Hyun-Shik Lee	Collect mRNA from whole embryos; two biological replicates were analyzed	30522514	55525	SRP155436	SRR7609579	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007431/SRR7609579	GSM3308294	SRA745502	SRX4474422	RNA-Seq	PAIRED	SRP155436	PRJNA483070
117754	6	Taejoon Kwon	Critical roles of lysine demethylase Kdm3a in craniofacial and neural development during Xenopus embryogenesis	The epigenetic modifier lysine-specific histone demethylase 3a (kdm3a) is specific for demethylation of mono- and di-methylated 9th lysine of histone 	Taejoon Kwon, Hyun-Kyung Lee, Tayaba Ismail, Chowon Kim, Youni Kim, Jeen-Woo Park, Oh-Shin Kwon, Beom-Sik Kang, Dong-Seok Lee, Tae Park, Hyun-Shik Lee	Collect mRNA from whole embryos; two biological replicates were analyzed	30522514	55525	SRP155436	SRR7609580	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007431/SRR7609580	GSM3308295	SRA745502	SRX4474423	RNA-Seq	PAIRED	SRP155436	PRJNA483070
118024	1	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637649	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637649	GSM3317414	SRA750217	SRX4501193	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	2	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637650	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637650	GSM3317415	SRA750217	SRX4501194	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	3	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637651	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637651	GSM3317416	SRA750217	SRX4501195	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	4	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637652	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637652	GSM3317417	SRA750217	SRX4501196	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	5	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637653	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637653	GSM3317418	SRA750217	SRX4501197	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	6	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637654	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637654	GSM3317419	SRA750217	SRX4501198	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	7	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637655	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637655	GSM3317420	SRA750217	SRX4501199	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	8	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637656	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007458/SRR7637656	GSM3317421	SRA750217	SRX4501200	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	9	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637657	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637657	GSM3317422	SRA750217	SRX4501201	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	10	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637658	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637658	GSM3317423	SRA750217	SRX4501202	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	11	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637659	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637659	GSM3317424	SRA750217	SRX4501203	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	12	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637660	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637660	GSM3317425	SRA750217	SRX4501204	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	13	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637661	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637661	GSM3317426	SRA750217	SRX4501205	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	14	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637662	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637662	GSM3317427	SRA750217	SRX4501206	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	15	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637663	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637663	GSM3317428	SRA750217	SRX4501207	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	16	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637664	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637664	GSM3317429	SRA750217	SRX4501208	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	17	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637665	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637665	GSM3317430	SRA750217	SRX4501209	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	18	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637666	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637666	GSM3317431	SRA750217	SRX4501210	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	19	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637667	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637667	GSM3317432	SRA750217	SRX4501211	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	20	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637668	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637668	GSM3317433	SRA750217	SRX4501212	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	21	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637669	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007458/SRR7637669	GSM3317434	SRA750217	SRX4501213	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	22	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637670	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637670	GSM3317435	SRA750217	SRX4501214	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	23	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637671	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637671	GSM3317436	SRA750217	SRX4501215	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	24	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637672	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637672	GSM3317437	SRA750217	SRX4501216	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	25	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637673	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637673	GSM3317438	SRA750217	SRX4501217	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	26	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637674	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007458/SRR7637674	GSM3317439	SRA750217	SRX4501218	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	27	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637675	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637675	GSM3317440	SRA750217	SRX4501219	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	28	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637676	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637676	GSM3317441	SRA750217	SRX4501220	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	29	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637677	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007458/SRR7637677	GSM3317442	SRA750217	SRX4501221	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	30	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637678	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637678	GSM3317443	SRA750217	SRX4501222	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	31	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637679	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637679	GSM3317444	SRA750217	SRX4501223	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	32	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637680	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637680	GSM3317445	SRA750217	SRX4501224	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	33	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637681	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637681	GSM3317446	SRA750217	SRX4501225	RNA-Seq	SINGLE	SRP156130	PRJNA484112
118024	34	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637682	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637682	GSM3317447	SRA750217	SRX4501226	ChIP-Seq	SINGLE	SRP156130	PRJNA484112
118024	35	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637683	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007458/SRR7637683	GSM3317448	SRA750217	SRX4501227	ChIP-Seq	SINGLE	SRP156130	PRJNA484112
118024	36	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637684	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/007458/SRR7637684	GSM3317449	SRA750217	SRX4501228	ChIP-Seq	SINGLE	SRP156130	PRJNA484112
118024	37	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR7637685	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007458/SRR7637685	GSM3317450	SRA750217	SRX4501229	ChIP-Seq	SINGLE	SRP156130	PRJNA484112
118024	38	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR8661030	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/008458/SRR8661030	GSM3638163	SRA750217	SRX5458167	ChIP-Seq	PAIRED	SRP156130	PRJNA484112
118024	39	Kitt Paraiso	Endodermal maternal transcription factors establish super enhancers during zygotic genome activation	We examined the combinatorial function of the Xenopus tropicalis maternal transcription factors Foxh1, Vegt and Otx1. The study involved combinatorial	Kitt Paraiso, Kitt Paraiso, Ken Cho	Screen for animally and vegetally expressed transcription factors: In biological triplicates, the animal and vegetal blastomeres of 8-cell stage embryos were separated. Subsequently, RNA was harvested from both set of blastomeres and whole embryos at the same stage and prepared for RNA sequencing. Combinatorial ectopic expression experiment: In biological duplicates, titrating levels of vegt and otx1 RNA were combinatorially microinjected into 1-cell stage embryos. Animal caps (putative ectoderm) were microdissected at stage 9 (6 hpf) from uninjected and injected samples, and RNA was harvested at stage 10.5 (7 hpf) for RNA sequencing. Double morpholino experiment: In biological duplicates, Vegt and Otx1 morpholinos were injected in 1-cell stage embryos independently or together. Vegetal masses (putative endoderm) were microdissected at stage 9 (6 hpf) and RNA was harvested from uninjected and injected samples at stage 10.5 (7 hpf) for RNA sequencing. Vegt and Otx1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 8 (prior to zygotic gene activation) and fixed with formaldehyde in biological duplicates. Chromatin immunoprecipitation as performed using anti-Vegt or anti-Otx1 antibody and DNA was purified for sequencing. H3K4me1 ChIP-seq analysis: Developmentally synchronized embryos were harvested at stage 10.5 and fixed with formaldehyde in biological duplicates. The vegetal tissue was disssected from the fixed embryos, and ChIP-seq was performed using anti-H3K4me1 antibody.

Previously published Foxh1 ChIP-seq from GSE85273 was re-analyzed along with this study.

GSM2263590 and GSM2263598 used to generate:
GSE118024_foxh1_IDR_optimal_peaks.bed.gz

GSM2263598 used to generate:
GSE118024_otx1_IDR_optimal_peaks.bed.gz, GSE118024_vegt_IDR_optimal_peaks.bed.gz	31167141	55999	SRP156130	SRR8661031	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/008458/SRR8661031	GSM3638164	SRA750217	SRX5458168	ChIP-Seq	PAIRED	SRP156130	PRJNA484112
118382	1	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665341	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665341	GSM3326039	SRA756671	SRX4525909	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118382	2	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665342	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665342	GSM3326040	SRA756671	SRX4525910	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118382	3	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665343	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665343	GSM3326041	SRA756671	SRX4525911	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118382	4	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665344	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665344	GSM3326042	SRA756671	SRX4525912	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118382	5	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665345	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665345	GSM3326043	SRA756671	SRX4525913	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118382	6	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665346	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665346	GSM3326044	SRA756671	SRX4525914	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118382	7	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665347	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665347	GSM3326045	SRA756671	SRX4525915	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118382	8	Taejoon Kwon	Xenopus hybrids provide insight into cell and organism size control	Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. 	Taejoon Kwon, Romain Gibeaux, Kelly Miller, Rachael Acker, Rebecca Heald	Collect mRNA from whole embryos; three biological replicates were analyzed	30564147	55549	SRP156967	SRR7665348	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007485/SRR7665348	GSM3326046	SRA756671	SRX4525916	RNA-Seq	PAIRED	SRP156967	PRJNA485371
118454	1	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687956	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687956	GSM3330437	SRA757532	SRX4548331	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	2	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687957	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687957	GSM3330438	SRA757532	SRX4548332	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	3	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687958	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687958	GSM3330439	SRA757532	SRX4548333	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	4	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687959	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687959	GSM3330440	SRA757532	SRX4548334	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	5	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687960	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687960	GSM3330441	SRA757532	SRX4548335	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	6	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687961	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687961	GSM3330442	SRA757532	SRX4548336	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	7	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687962	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687962	GSM3330443	SRA757532	SRX4548337	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	8	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687963	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687963	GSM3330444	SRA757532	SRX4548338	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	9	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687964	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687964	GSM3330445	SRA757532	SRX4548339	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	10	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687965	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687965	GSM3330446	SRA757532	SRX4548340	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	11	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687966	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687966	GSM3330447	SRA757532	SRX4548341	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	12	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687967	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687967	GSM3330448	SRA757532	SRX4548342	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	13	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687968	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687968	GSM3330449	SRA757532	SRX4548343	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	14	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687969	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687969	GSM3330450	SRA757532	SRX4548344	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	15	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687970	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687970	GSM3330451	SRA757532	SRX4548345	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	16	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687971	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687971	GSM3330452	SRA757532	SRX4548346	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	17	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687972	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687972	GSM3330453	SRA757532	SRX4548347	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	18	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687973	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687973	GSM3330454	SRA757532	SRX4548348	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	19	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687974	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687974	GSM3330455	SRA757532	SRX4548349	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	20	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687975	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687975	GSM3330456	SRA757532	SRX4548350	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	21	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687976	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687976	GSM3330457	SRA757532	SRX4548351	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	22	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687977	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687977	GSM3330458	SRA757532	SRX4548352	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	23	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687978	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687978	GSM3330459	SRA757532	SRX4548353	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	24	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687979	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687979	GSM3330461	SRA757532	SRX4548354	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	25	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687980	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687980	GSM3330462	SRA757532	SRX4548355	RNA-Seq	SINGLE	SRP157614	PRJNA485703
118454	26	Christopher Martyniuk	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb	The induction of limb repair depends on signals that initiate regeneration and the successful transmission of those signals in vivo. Here, we characte	Christopher Martyniuk, Celia Herrera-Rincon, Christopher Martyniuk, Mike Levin	Samples from 3 treatment groups were RNA sequenced (Control, Sham or Silk, and Prog) via NGS, n= 9 per group, n=3 for three tissues (brain, stump, and blastema)	30404012	55432	SRP157614	SRR7687981	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/007507/SRR7687981	GSM3330463	SRA757532	SRX4548356	RNA-Seq	SINGLE	SRP157614	PRJNA485703
119124	1	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761189	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761189	GSM3358737	SRA763838	SRX4616812	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	2	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761190	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761190	GSM3358738	SRA763838	SRX4616813	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	3	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761191	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761191	GSM3358739	SRA763838	SRX4616814	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	4	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761192	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761192	GSM3358740	SRA763838	SRX4616815	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	5	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761193	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761193	GSM3358741	SRA763838	SRX4616816	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	6	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761194	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761194	GSM3358742	SRA763838	SRX4616817	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	7	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761195	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761195	GSM3358743	SRA763838	SRX4616818	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	8	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761196	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761196	GSM3358744	SRA763838	SRX4616819	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	9	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761197	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761197	GSM3358745	SRA763838	SRX4616820	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	10	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761198	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761198	GSM3358746	SRA763838	SRX4616821	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	11	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761199	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761199	GSM3358747	SRA763838	SRX4616822	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	12	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761200	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761200	GSM3358748	SRA763838	SRX4616823	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	13	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761201	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761201	GSM3358749	SRA763838	SRX4616824	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	14	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761202	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761202	GSM3358750	SRA763838	SRX4616825	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	15	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761203	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761203	GSM3358751	SRA763838	SRX4616826	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	16	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761204	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761204	GSM3358752	SRA763838	SRX4616827	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	17	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761205	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761205	GSM3358753	SRA763838	SRX4616828	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	18	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761206	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761206	GSM3358754	SRA763838	SRX4616829	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	19	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761207	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761207	GSM3358755	SRA763838	SRX4616830	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	20	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761208	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761208	GSM3358756	SRA763838	SRX4616831	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	21	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761209	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761209	GSM3358757	SRA763838	SRX4616832	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	22	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761210	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761210	GSM3358758	SRA763838	SRX4616833	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	23	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761211	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761211	GSM3358759	SRA763838	SRX4616834	RNA-Seq	SINGLE	SRP159000	PRJNA488225
119124	24	Toshi Shioda	RARγ is required for mesodermal gene expression prior to gastrulation	The developing vertebrate embryo is exquisitely sensitive to retinoic acid (RA) concentration, particularly during anteroposterior patterning. In cont	Toshi Shioda, Amanda Jenesick, Weiyi Tang, Bruce Blumberg	RNA-sequencing of gastrula stage embryos treated with RAR agonist TTNPB or RAR antagonist AGN193109	30111657	55309	SRP159000	SRR7761212	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/007579/SRR7761212	GSM3358760	SRA763838	SRX4616835	RNA-Seq	SINGLE	SRP159000	PRJNA488225
122551	1	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189090	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189090	GSM3473720	SRA809630	SRX5008749	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	2	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189091	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189091	GSM3473721	SRA809630	SRX5008750	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	3	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189092	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189092	GSM3473722	SRA809630	SRX5008751	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	4	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189093	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189093	GSM3473723	SRA809630	SRX5008752	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	5	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189094	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189094	GSM3473724	SRA809630	SRX5008753	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	6	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189095	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189095	GSM3473725	SRA809630	SRX5008754	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	7	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189096	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189096	GSM3473726	SRA809630	SRX5008755	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	8	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189097	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189097	GSM3473727	SRA809630	SRX5008756	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	9	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189098	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189098	GSM3473728	SRA809630	SRX5008757	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	10	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189099	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189099	GSM3473729	SRA809630	SRX5008758	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	11	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189100	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189100	GSM3473730	SRA809630	SRX5008759	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	12	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189101	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189101	GSM3473731	SRA809630	SRX5008760	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	13	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189102	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189102	GSM3473732	SRA809630	SRX5008761	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	14	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189103	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189103	GSM3473733	SRA809630	SRX5008762	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	15	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189104	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189104	GSM3473734	SRA809630	SRX5008763	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	16	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189105	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189105	GSM3473735	SRA809630	SRX5008764	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	17	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189106	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189106	GSM3473736	SRA809630	SRX5008765	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	18	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189107	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189107	GSM3473737	SRA809630	SRX5008766	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	19	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189108	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189108	GSM3473738	SRA809630	SRX5008767	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	20	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189109	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189109	GSM3473739	SRA809630	SRX5008768	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	21	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189110	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189110	GSM3473740	SRA809630	SRX5008769	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	22	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189111	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189111	GSM3473741	SRA809630	SRX5008770	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	23	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189112	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189112	GSM3473742	SRA809630	SRX5008771	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	24	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189113	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189113	GSM3473743	SRA809630	SRX5008772	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	25	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189114	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189114	GSM3473744	SRA809630	SRX5008773	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	26	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189115	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189115	GSM3473745	SRA809630	SRX5008774	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	27	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189116	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189116	GSM3473746	SRA809630	SRX5008775	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	28	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189117	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189117	GSM3473747	SRA809630	SRX5008776	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	29	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189118	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189118	GSM3473748	SRA809630	SRX5008777	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	30	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189119	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189119	GSM3473749	SRA809630	SRX5008778	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	31	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189120	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189120	GSM3473750	SRA809630	SRX5008779	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	32	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189121	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189121	GSM3473751	SRA809630	SRX5008780	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	33	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189122	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189122	GSM3473752	SRA809630	SRX5008781	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	34	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189123	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189123	GSM3473753	SRA809630	SRX5008782	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	35	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189124	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189124	GSM3473754	SRA809630	SRX5008783	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	36	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189125	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189125	GSM3473755	SRA809630	SRX5008784	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	37	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189126	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189126	GSM3473756	SRA809630	SRX5008785	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	38	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189127	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189127	GSM3473757	SRA809630	SRX5008786	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	39	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189128	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189128	GSM3473758	SRA809630	SRX5008787	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	40	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189129	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189129	GSM3473759	SRA809630	SRX5008788	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	41	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189130	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189130	GSM3473760	SRA809630	SRX5008789	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	42	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189131	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189131	GSM3473761	SRA809630	SRX5008790	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	43	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189132	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189132	GSM3473762	SRA809630	SRX5008791	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	44	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189133	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189133	GSM3473763	SRA809630	SRX5008792	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	45	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189134	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189134	GSM3473764	SRA809630	SRX5008793	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	46	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189135	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189135	GSM3473765	SRA809630	SRX5008794	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	47	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189136	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189136	GSM3473766	SRA809630	SRX5008795	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	48	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189137	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189137	GSM3473767	SRA809630	SRX5008796	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	49	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189138	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189138	GSM3473768	SRA809630	SRX5008797	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	50	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189139	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189139	GSM3473769	SRA809630	SRX5008798	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	51	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189140	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189140	GSM3473770	SRA809630	SRX5008799	RNA-Seq	PAIRED	SRP168643	PRJNA505537
122551	52	George Gentsch	The Spatio-Temporal Control of Zygotic Genome Activation	One of the earliest and most significant events in embryonic development is zygotic genome activation (ZGA). In several species, bulk transcription be	George Gentsch, George Gentsch, James Smith	This study generated four 4sU-Seq samples and 48 RNA-Seq samples.	31229896	56693	SRP168643	SRR8189141	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/007997/SRR8189141	GSM3473771	SRA809630	SRX5008800	RNA-Seq	PAIRED	SRP168643	PRJNA505537
124168	1	Cei Abreu-Goodger	Axonal precursor miRNAs hitchhike on endosomes and locally regulate the development of neural circuits	Various species of non-coding RNAs (ncRNAs) are enriched in subcellular compartments but the mechanisms orchestrating their localization and their loc	Cei Abreu-Goodger, Eloina Corradi, Irene Dalla Costa, Antoneta Gavoci, Archana Iyer, Michela Roccuzzo, Tegan Otto, Eleonora Oliani, Simone Bridi, Stephanie Strohbuecker, Gabriela Santos-Rodriguez, Donatella Valdembri, Guido Serini, Marie-Laure Baudet	Total RNA profile were obtained from isolated retinal ganglion cell axons from Xenopus laevis retinal eye cultures using RNA-sequencing	32073171	57123	SRP174009	SRR8358349	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008162/SRR8358349	GSM3523319	SRA825551	SRX5169111	RNA-Seq	PAIRED	SRP174009	PRJNA510932
124563	1	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384741	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008188/SRR8384741	GSM3536579	SRA829329	SRX5194600	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	2	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384742	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384742/SRR8384742.1	GSM3536580	SRA829329	SRX5194601	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	3	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384743	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008188/SRR8384743	GSM3536581	SRA829329	SRX5194602	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	4	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384744	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008188/SRR8384744	GSM3536582	SRA829329	SRX5194603	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	5	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384745	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384745/SRR8384745.1	GSM3536583	SRA829329	SRX5194604	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	6	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384746	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384746/SRR8384746.1	GSM3536584	SRA829329	SRX5194605	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	7	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384747	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384747/SRR8384747.1	GSM3536585	SRA829329	SRX5194606	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	8	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384748	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384748/SRR8384748.1	GSM3536586	SRA829329	SRX5194607	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	9	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384749	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384749/SRR8384749.1	GSM3536587	SRA829329	SRX5194608	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	10	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384750	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384750/SRR8384750.1	GSM3536588	SRA829329	SRX5194609	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	11	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384751	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384751/SRR8384751.1	GSM3536589	SRA829329	SRX5194610	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	12	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384752	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008188/SRR8384752	GSM3536590	SRA829329	SRX5194611	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	13	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384753	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384753/SRR8384753.1	GSM3536591	SRA829329	SRX5194612	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	14	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384754	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384754/SRR8384754.1	GSM3536592	SRA829329	SRX5194613	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	15	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384755	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384755/SRR8384755.1	GSM3536593	SRA829329	SRX5194614	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	16	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384756	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008188/SRR8384756	GSM3536594	SRA829329	SRX5194615	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	17	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384757	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384757/SRR8384757.1	GSM3536595	SRA829329	SRX5194616	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	18	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384758	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384758/SRR8384758.1	GSM3536596	SRA829329	SRX5194617	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	19	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384759	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384759/SRR8384759.1	GSM3536597	SRA829329	SRX5194618	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	20	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384760	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008188/SRR8384760	GSM3536598	SRA829329	SRX5194619	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	21	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384761	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384761/SRR8384761.1	GSM3536599	SRA829329	SRX5194620	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	22	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384762	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008188/SRR8384762	GSM3536600	SRA829329	SRX5194621	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	23	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384763	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384763/SRR8384763.1	GSM3536601	SRA829329	SRX5194622	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	24	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384764	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384764/SRR8384764.1	GSM3536602	SRA829329	SRX5194623	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	25	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384765	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384765/SRR8384765.1	GSM3536603	SRA829329	SRX5194624	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	26	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384766	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384766/SRR8384766.1	GSM3536604	SRA829329	SRX5194625	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	27	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384767	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384767/SRR8384767.1	GSM3536605	SRA829329	SRX5194627	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	28	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384768	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384768/SRR8384768.1	GSM3536606	SRA829329	SRX5194628	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	29	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384769	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384769/SRR8384769.1	GSM3536607	SRA829329	SRX5194629	RNA-Seq	SINGLE	SRP175030	PRJNA512511
124563	30	Edward De Robertis	Transcriptome analysis of regeneration in Xenopus laevis twin embryos	Animal embryos have the remarkable property of self-organization. Over 125 years ago Hans Driesch separated the two blastomeres of sea urchin embryos 	Edward De Robertis, Yuki Moriyama, Eric Sosa, Yi Ding	A genome-wide study of genes that regulate regeneration of twin embryos in Xenopus laevis	31250914	56074	SRP175030	SRR8384770	https://sra-download.ncbi.nlm.nih.gov/sos/sra-pub-run-2/SRR8384770/SRR8384770.1	GSM3536608	SRA829329	SRX5194630	RNA-Seq	SINGLE	SRP175030	PRJNA512511
125982	1	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515029	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515029	GSM3587279	SRA842485	SRX5318616	ChIP-Seq	PAIRED	SRP183098	PRJNA518148
125982	2	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515030	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515030	GSM3587280	SRA842485	SRX5318617	ChIP-Seq	PAIRED	SRP183098	PRJNA518148
125982	3	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515031	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515031	GSM3587281	SRA842485	SRX5318618	ChIP-Seq	PAIRED	SRP183098	PRJNA518148
125982	4	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515032	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515032	GSM3587282	SRA842485	SRX5318619	ChIP-Seq	PAIRED	SRP183098	PRJNA518148
125982	5	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515033	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515033	GSM3587283	SRA842485	SRX5318620	ChIP-Seq	PAIRED	SRP183098	PRJNA518148
125982	6	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515034	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515034	GSM3587284	SRA842485	SRX5318621	ChIP-Seq	PAIRED	SRP183098	PRJNA518148
125982	7	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515035	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515035	GSM3587285	SRA842485	SRX5318622	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	8	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515036	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515036	GSM3587286	SRA842485	SRX5318623	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	9	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515037	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515037	GSM3587287	SRA842485	SRX5318624	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	10	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515038	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515038	GSM3587288	SRA842485	SRX5318625	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	11	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515039	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515039	GSM3587289	SRA842485	SRX5318626	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	12	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515040	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515040	GSM3587290	SRA842485	SRX5318627	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	13	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515041	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515041	GSM3587291	SRA842485	SRX5318628	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	14	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515042	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515042	GSM3587292	SRA842485	SRX5318629	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	15	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515043	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515043	GSM3587293	SRA842485	SRX5318630	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	16	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515044	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515044	GSM3587294	SRA842485	SRX5318631	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	17	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515045	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515045	GSM3587295	SRA842485	SRX5318632	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	18	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515046	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515046	GSM3587296	SRA842485	SRX5318633	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	19	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515047	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515047	GSM3587297	SRA842485	SRX5318634	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	20	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515048	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515048	GSM3587298	SRA842485	SRX5318635	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	21	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515049	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515049	GSM3587299	SRA842485	SRX5318636	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	22	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515050	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515050	GSM3587300	SRA842485	SRX5318637	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	23	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515051	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515051	GSM3587301	SRA842485	SRX5318638	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	24	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515052	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515052	GSM3587302	SRA842485	SRX5318639	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	25	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515053	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515053	GSM3587303	SRA842485	SRX5318640	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	26	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515054	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515054	GSM3587304	SRA842485	SRX5318641	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	27	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515055	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515055	GSM3587305	SRA842485	SRX5318642	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	28	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515056	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515056	GSM3587306	SRA842485	SRX5318643	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	29	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515057	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515057	GSM3587307	SRA842485	SRX5318644	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	30	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8515058	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008315/SRR8515058	GSM3587308	SRA842485	SRX5318645	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	31	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8730286	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/008525/SRR8730286	GSM3671366	SRA842485	SRX5523278	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	32	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8730287	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/008525/SRR8730287	GSM3671367	SRA842485	SRX5523279	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	33	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8730288	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008525/SRR8730288	GSM3671368	SRA842485	SRX5523280	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
125982	34	Angela Simeone	Epigenetic homogeneity underlies sperm programming for embryonic transcription	Epigenetic homogeneity underlies sperm programming for embryonic transcriptionsingle-ended ChIP-Seq libraries from sperm, egg extract (-geminin) trea	Angela Simeone, Mami Oikawa, Eva Hormanseder, Marta Teperek, Clive D’Santos, Charles Bradshaw, Alan O’Doherthy, T Freour, L David, Adrian Grzybowski, Alexander Ruthenburg, John Gurdon, Jerome Jullien	30 samples, paired-ended and single-ended ChIP-Seq libraries from sperm, egg extract (-geminin) treated sperm, egg extract (+geminin) treated sperm, and St 7 embryos with antibody for H3Kme3, H3K27me3, 3 replicates for each histone modification pull-down.
-------------------------------------------------
*The authors state the following regarding the human raw data: "We don't have the required patient consents to deposit them".  Thus, this submission is incomplete.	0	57326	SRP183098	SRR8730289	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008525/SRR8730289	GSM3671369	SRA842485	SRX5523281	ChIP-Seq	SINGLE	SRP183098	PRJNA518148
126058	1	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527274	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527274	GSM3589901	SRA843840	SRX5330019	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	2	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527275	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527275	GSM3589902	SRA843840	SRX5330020	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	3	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527276	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527276	GSM3589903	SRA843840	SRX5330021	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	4	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527277	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527277	GSM3589904	SRA843840	SRX5330022	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	5	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527278	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527278	GSM3589905	SRA843840	SRX5330023	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	6	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527279	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527279	GSM3589906	SRA843840	SRX5330024	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	7	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527280	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527280	GSM3589907	SRA843840	SRX5330025	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	8	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527281	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527281	GSM3589908	SRA843840	SRX5330026	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	9	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527282	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527282	GSM3589909	SRA843840	SRX5330027	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	10	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527283	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527283	GSM3589910	SRA843840	SRX5330028	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	11	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527284	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527284	GSM3589911	SRA843840	SRX5330029	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	12	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527285	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527285	GSM3589912	SRA843840	SRX5330030	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	13	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527286	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527286	GSM3589913	SRA843840	SRX5330031	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	14	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527287	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527287	GSM3589914	SRA843840	SRX5330032	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	15	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527288	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527288	GSM3589915	SRA843840	SRX5330033	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	16	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527289	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527289	GSM3589916	SRA843840	SRX5330034	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	17	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527290	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527290	GSM3589917	SRA843840	SRX5330035	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	18	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527291	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527291	GSM3589918	SRA843840	SRX5330036	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	19	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527292	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527292	GSM3589919	SRA843840	SRX5330037	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	20	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527293	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527293	GSM3589920	SRA843840	SRX5330038	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	21	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527294	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527294	GSM3589921	SRA843840	SRX5330039	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	22	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527295	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527295	GSM3589922	SRA843840	SRX5330040	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	23	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527296	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527296	GSM3589923	SRA843840	SRX5330041	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	24	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527297	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527297	GSM3589924	SRA843840	SRX5330042	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	25	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527298	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527298	GSM3589925	SRA843840	SRX5330043	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	26	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527299	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527299	GSM3589926	SRA843840	SRX5330044	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	27	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527300	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527300	GSM3589927	SRA843840	SRX5330045	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	28	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527301	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527301	GSM3589928	SRA843840	SRX5330046	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	29	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527302	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527302	GSM3589929	SRA843840	SRX5330047	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	30	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527303	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527303	GSM3589930	SRA843840	SRX5330048	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	31	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527304	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527304	GSM3589931	SRA843840	SRX5330049	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	32	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527305	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527305	GSM3589932	SRA843840	SRX5330050	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	33	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527306	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527306	GSM3589933	SRA843840	SRX5330051	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	34	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527307	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527307	GSM3589934	SRA843840	SRX5330052	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	35	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527308	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527308	GSM3589935	SRA843840	SRX5330053	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	36	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527309	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527309	GSM3589936	SRA843840	SRX5330054	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	37	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527310	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527310	GSM3589937	SRA843840	SRX5330055	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	38	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527311	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527311	GSM3589938	SRA843840	SRX5330056	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	39	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527312	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527312	GSM3589939	SRA843840	SRX5330057	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	40	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527313	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527313	GSM3589940	SRA843840	SRX5330058	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	41	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527314	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527314	GSM3589941	SRA843840	SRX5330059	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	42	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527315	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527315	GSM3589942	SRA843840	SRX5330060	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	43	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527316	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527316	GSM3589943	SRA843840	SRX5330061	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	44	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527317	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527317	GSM3589944	SRA843840	SRX5330062	RNA-Seq	SINGLE	SRP183483	PRJNA520892
126058	45	Gabriela Salinas	Identification of genes regulated by Erythroferrone (ERFE)  in Xenopus embryos at tadpole stages.	RNA-seq was employed to analyze differential gene expression upon ERFE knockdown in Xenopus laevis embryos at three different developmental stages usi	Gabriela Salinas, Tomas Pieler, Juliane Melchert, Thomas Lingner	Xenopus eight-cell stage embryos were injected with 10 ng ERFE-MO1 or 20 ng ERFE-MO2 into the four vegetal blastomeres and cultivated until stage 35/36, stage 37/38 or stage 41.
Uninjected embryos as well as embryos injected with equal amounts of standard control morpholino (cMO) served as controls.	31846624	56559	SRP183483	SRR8527318	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/008327/SRR8527318	GSM3589945	SRA843840	SRX5330063	RNA-Seq	SINGLE	SRP183483	PRJNA520892
130448	1	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986263	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008775/SRR8986263	GSM3738794	SRA880624	SRX5765493	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	2	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986264	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008775/SRR8986264	GSM3738794	SRA880624	SRX5765493	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	3	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986265	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008775/SRR8986265	GSM3738795	SRA880624	SRX5765494	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	4	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986266	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/008775/SRR8986266	GSM3738795	SRA880624	SRX5765494	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	5	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986267	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008775/SRR8986267	GSM3738796	SRA880624	SRX5765495	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	6	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986268	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008775/SRR8986268	GSM3738796	SRA880624	SRX5765495	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	7	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986269	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/008775/SRR8986269	GSM3738797	SRA880624	SRX5765496	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	8	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986270	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/008775/SRR8986270	GSM3738797	SRA880624	SRX5765496	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	9	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986271	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008775/SRR8986271	GSM3738798	SRA880624	SRX5765497	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	10	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986272	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008775/SRR8986272	GSM3738798	SRA880624	SRX5765497	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	11	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986273	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/008775/SRR8986273	GSM3738799	SRA880624	SRX5765498	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	12	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986274	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008775/SRR8986274	GSM3738799	SRA880624	SRX5765498	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	13	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986275	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008775/SRR8986275	GSM3738800	SRA880624	SRX5765499	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	14	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986276	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008775/SRR8986276	GSM3738800	SRA880624	SRX5765499	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	15	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986277	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/008775/SRR8986277	GSM3738801	SRA880624	SRX5765500	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	16	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986278	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008775/SRR8986278	GSM3738801	SRA880624	SRX5765500	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	17	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986279	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/008775/SRR8986279	GSM3738802	SRA880624	SRX5765501	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	18	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986280	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008775/SRR8986280	GSM3738802	SRA880624	SRX5765501	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	19	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986281	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/008775/SRR8986281	GSM3738803	SRA880624	SRX5765502	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	20	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986282	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/008775/SRR8986282	GSM3738803	SRA880624	SRX5765502	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	21	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986283	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/008775/SRR8986283	GSM3738804	SRA880624	SRX5765503	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	22	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986284	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008775/SRR8986284	GSM3738804	SRA880624	SRX5765503	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	23	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986285	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008775/SRR8986285	GSM3738805	SRA880624	SRX5765504	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	24	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986286	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/008775/SRR8986286	GSM3738805	SRA880624	SRX5765504	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	25	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986287	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/008775/SRR8986287	GSM3738806	SRA880624	SRX5765505	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	26	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986288	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008775/SRR8986288	GSM3738806	SRA880624	SRX5765505	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	27	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986289	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/008775/SRR8986289	GSM3738807	SRA880624	SRX5765506	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	28	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986290	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/008775/SRR8986290	GSM3738807	SRA880624	SRX5765506	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	29	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986291	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008775/SRR8986291	GSM3738808	SRA880624	SRX5765507	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	30	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986292	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/008775/SRR8986292	GSM3738808	SRA880624	SRX5765507	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	31	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986293	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/008775/SRR8986293	GSM3738809	SRA880624	SRX5765508	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	32	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986294	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/008775/SRR8986294	GSM3738809	SRA880624	SRX5765508	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	33	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986295	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008775/SRR8986295	GSM3738810	SRA880624	SRX5765509	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	34	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986296	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008775/SRR8986296	GSM3738810	SRA880624	SRX5765509	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	35	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986297	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/008775/SRR8986297	GSM3738811	SRA880624	SRX5765510	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130448	36	Peter Walentek	Mucociliary epidermis RNA-seq data from comparison of controls and DN-tp63 morpholino knockdown in Xenopus animal cap explants.	This study was conducted to investigate the effects of DN-tp63 loss-of-function on mucociliary basal stem cells in Xenopus laevis. Uninjected control 	Peter Walentek	The experiment was conducted in three biological replicates (embryos were derived from three different females and fertilizations). Control samples remained uninjected, DN-tp63 morphant samples were injected with morpholino oligonucleotides targeting the start condon of DN-tp63 and resulted in protein knockdown (loss-of-function). Sequencing was performed in two seperate paired-end runs to increase sequencing dpth, with each run containing all samples.	31553905	56304	SRP194164	SRR8986298	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/008775/SRR8986298	GSM3738811	SRA880624	SRX5765510	RNA-Seq	PAIRED	SRP194164	PRJNA540273
130816	1	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046652	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/008834/SRR9046652	GSM3754697	SRA885609	SRX5823191	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	2	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046653	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008834/SRR9046653	GSM3754698	SRA885609	SRX5823192	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	3	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046654	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/008834/SRR9046654	GSM3754699	SRA885609	SRX5823193	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	4	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046655	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008834/SRR9046655	GSM3754700	SRA885609	SRX5823194	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	5	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046656	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008834/SRR9046656	GSM3754701	SRA885609	SRX5823195	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	6	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046657	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008834/SRR9046657	GSM3754702	SRA885609	SRX5823196	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	7	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046658	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008834/SRR9046658	GSM3754703	SRA885609	SRX5823197	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	8	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046659	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008834/SRR9046659	GSM3754704	SRA885609	SRX5823198	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	9	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046660	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008834/SRR9046660	GSM3754705	SRA885609	SRX5823199	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	10	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046661	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008834/SRR9046661	GSM3754706	SRA885609	SRX5823200	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	11	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046662	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008834/SRR9046662	GSM3754707	SRA885609	SRX5823201	RNA-Seq	SINGLE	SRP198181	PRJNA542536
130816	12	Robert Denver	Thyroid hormone receptor alpha is required for thyroid hormone-dependent neural cell proliferation during tadpole metamorphosis	Using tadpoles mutant for thyroid hormone receptor alpha (thra), we show that TRa is required for thyroid hormone (T3) induction of cell proliferation	Robert Denver, Luan Wen	Wild type and thra mutant tadpoles were treated with vehicle (DMSO) or T3 (5 nM) added to the aquarium water for 16 hr before sacrifice and tissue harvest. The region of the brain containing the preoptic area/hypothalamus/thalamus was microdissected, RNA isolated and RNA sequencing conducted.	31316462	56139	SRP198181	SRR9046663	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008834/SRR9046663	GSM3754708	SRA885609	SRX5823202	RNA-Seq	SINGLE	SRP198181	PRJNA542536
131962	1	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160380	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008945/SRR9160380	GSM3832849	SRA892086	SRX5933458	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	2	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160381	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008945/SRR9160381	GSM3832849	SRA892086	SRX5933458	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	3	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160382	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008945/SRR9160382	GSM3832849	SRA892086	SRX5933458	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	4	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160383	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008945/SRR9160383	GSM3832849	SRA892086	SRX5933458	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	5	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160384	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008945/SRR9160384	GSM3832850	SRA892086	SRX5933459	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	6	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160385	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/008945/SRR9160385	GSM3832850	SRA892086	SRX5933459	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	7	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160386	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008945/SRR9160386	GSM3832850	SRA892086	SRX5933459	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	8	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160387	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008945/SRR9160387	GSM3832850	SRA892086	SRX5933459	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	9	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160388	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008945/SRR9160388	GSM3832851	SRA892086	SRX5933460	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	10	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160389	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008945/SRR9160389	GSM3832851	SRA892086	SRX5933460	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	11	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160390	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008945/SRR9160390	GSM3832851	SRA892086	SRX5933460	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	12	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160391	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008945/SRR9160391	GSM3832851	SRA892086	SRX5933460	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	13	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160392	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008945/SRR9160392	GSM3832852	SRA892086	SRX5933461	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	14	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160393	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008945/SRR9160393	GSM3832852	SRA892086	SRX5933461	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	15	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160394	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008945/SRR9160394	GSM3832852	SRA892086	SRX5933461	RNA-Seq	PAIRED	SRP199866	PRJNA545469
131962	16	Matthew Good	Nascent transcriptome of Xenopus laevis embryos at mid-blastula transition (MBT) stages	To validate that EU-RNA imaging provides a direct readout of wide-spread zygotic transcription, we sought to identify the nascent transcriptome using 	Matthew Good, Hui Chen, Matthew Good	Duplicates for nascent EU-RNA from EU-injected embryos and total RNA from normal embryos, respectively	31211992	56041	SRP199866	SRR9160395	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008945/SRR9160395	GSM3832852	SRA892086	SRX5933461	RNA-Seq	PAIRED	SRP199866	PRJNA545469
132116	1	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186334	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/008971/SRR9186334	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	2	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186335	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/008971/SRR9186335	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	3	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186336	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/008971/SRR9186336	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	4	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186337	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/008971/SRR9186337	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	5	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186338	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/008971/SRR9186338	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	6	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186339	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/008971/SRR9186339	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	7	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186340	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/008971/SRR9186340	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	8	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186341	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186341	GSM3844820	SRA893482	SRX5958820	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	9	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186342	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186342	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	10	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186343	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/008971/SRR9186343	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	11	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186344	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008971/SRR9186344	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	12	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186345	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186345	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	13	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186346	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/008971/SRR9186346	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	14	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186347	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/008971/SRR9186347	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	15	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186348	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008971/SRR9186348	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	16	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186349	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008971/SRR9186349	GSM3844821	SRA893482	SRX5958821	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	17	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186350	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/008971/SRR9186350	GSM3844822	SRA893482	SRX5958822	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	18	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186351	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/008971/SRR9186351	GSM3844822	SRA893482	SRX5958822	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	19	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186352	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/008971/SRR9186352	GSM3844822	SRA893482	SRX5958822	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	20	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186353	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186353	GSM3844822	SRA893482	SRX5958822	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	21	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186354	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/008971/SRR9186354	GSM3844822	SRA893482	SRX5958822	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	22	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186355	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/008971/SRR9186355	GSM3844822	SRA893482	SRX5958822	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	23	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186356	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/008971/SRR9186356	GSM3844823	SRA893482	SRX5958823	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	24	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186357	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/008971/SRR9186357	GSM3844823	SRA893482	SRX5958823	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	25	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186358	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/008971/SRR9186358	GSM3844823	SRA893482	SRX5958823	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	26	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186359	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/008971/SRR9186359	GSM3844823	SRA893482	SRX5958823	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	27	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186360	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/008971/SRR9186360	GSM3844823	SRA893482	SRX5958823	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	28	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186361	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008971/SRR9186361	GSM3844823	SRA893482	SRX5958823	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	29	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186362	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008971/SRR9186362	GSM3844824	SRA893482	SRX5958824	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	30	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186363	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186363	GSM3844824	SRA893482	SRX5958824	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	31	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186364	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/008971/SRR9186364	GSM3844824	SRA893482	SRX5958824	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	32	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186365	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186365	GSM3844824	SRA893482	SRX5958824	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	33	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186366	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186366	GSM3844824	SRA893482	SRX5958824	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	34	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186367	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186367	GSM3844824	SRA893482	SRX5958824	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	35	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186368	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186368	GSM3844824	SRA893482	SRX5958824	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	36	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186369	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186369	GSM3844825	SRA893482	SRX5958825	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	37	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186370	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008971/SRR9186370	GSM3844825	SRA893482	SRX5958825	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	38	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186371	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186371	GSM3844825	SRA893482	SRX5958825	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	39	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186372	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/008971/SRR9186372	GSM3844825	SRA893482	SRX5958825	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	40	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186373	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186373	GSM3844825	SRA893482	SRX5958825	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	41	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186374	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/008971/SRR9186374	GSM3844825	SRA893482	SRX5958825	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	42	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186375	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/008971/SRR9186375	GSM3844825	SRA893482	SRX5958825	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	43	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186376	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008971/SRR9186376	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	44	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186377	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186377	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	45	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186378	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/008971/SRR9186378	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	46	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186379	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/008971/SRR9186379	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	47	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186380	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/008971/SRR9186380	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	48	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186381	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008971/SRR9186381	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	49	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186382	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/008971/SRR9186382	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	50	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186383	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186383	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	51	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186384	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/008971/SRR9186384	GSM3844826	SRA893482	SRX5958826	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	52	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186385	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/008971/SRR9186385	GSM3844827	SRA893482	SRX5958827	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	53	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186386	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/008971/SRR9186386	GSM3844827	SRA893482	SRX5958827	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	54	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186387	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008971/SRR9186387	GSM3844827	SRA893482	SRX5958827	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	55	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186388	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/008971/SRR9186388	GSM3844827	SRA893482	SRX5958827	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	56	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186389	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/008971/SRR9186389	GSM3844827	SRA893482	SRX5958827	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	57	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186390	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186390	GSM3844827	SRA893482	SRX5958827	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	58	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186391	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/008971/SRR9186391	GSM3844827	SRA893482	SRX5958827	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	59	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186392	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008971/SRR9186392	GSM3844828	SRA893482	SRX5958828	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	60	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186393	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186393	GSM3844828	SRA893482	SRX5958828	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	61	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186394	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/008971/SRR9186394	GSM3844828	SRA893482	SRX5958828	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	62	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186395	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/008971/SRR9186395	GSM3844828	SRA893482	SRX5958828	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	63	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186396	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008971/SRR9186396	GSM3844828	SRA893482	SRX5958828	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	64	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186397	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008971/SRR9186397	GSM3844828	SRA893482	SRX5958828	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	65	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186398	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186398	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	66	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186399	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008971/SRR9186399	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	67	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186400	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/008971/SRR9186400	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	68	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186401	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008971/SRR9186401	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	69	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186402	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008971/SRR9186402	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	70	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186403	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008971/SRR9186403	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	71	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186404	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008971/SRR9186404	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	72	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186405	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/008971/SRR9186405	GSM3844829	SRA893482	SRX5958829	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	73	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186406	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/008971/SRR9186406	GSM3844830	SRA893482	SRX5958830	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	74	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186407	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186407	GSM3844830	SRA893482	SRX5958830	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	75	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186408	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008971/SRR9186408	GSM3844830	SRA893482	SRX5958830	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	76	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186409	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008971/SRR9186409	GSM3844830	SRA893482	SRX5958830	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	77	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186410	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/008971/SRR9186410	GSM3844830	SRA893482	SRX5958830	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	78	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186411	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/008971/SRR9186411	GSM3844831	SRA893482	SRX5958831	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	79	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186412	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/008971/SRR9186412	GSM3844831	SRA893482	SRX5958831	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	80	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186413	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/008971/SRR9186413	GSM3844831	SRA893482	SRX5958831	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	81	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186414	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186414	GSM3844831	SRA893482	SRX5958831	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	82	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186415	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/008971/SRR9186415	GSM3844831	SRA893482	SRX5958831	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	83	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186416	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008971/SRR9186416	GSM3844831	SRA893482	SRX5958831	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	84	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186417	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/008971/SRR9186417	GSM3844831	SRA893482	SRX5958831	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	85	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186418	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008971/SRR9186418	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	86	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186419	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186419	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	87	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186420	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/008971/SRR9186420	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	88	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186421	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/008971/SRR9186421	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	89	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186422	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/008971/SRR9186422	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	90	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186423	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186423	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	91	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186424	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008971/SRR9186424	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	92	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186425	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/008971/SRR9186425	GSM3844832	SRA893482	SRX5958832	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	93	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186426	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186426	GSM3844833	SRA893482	SRX5958833	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	94	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186427	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/008971/SRR9186427	GSM3844833	SRA893482	SRX5958833	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	95	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186428	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186428	GSM3844833	SRA893482	SRX5958833	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	96	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186429	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186429	GSM3844833	SRA893482	SRX5958833	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	97	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186430	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186430	GSM3844833	SRA893482	SRX5958833	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	98	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186431	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008971/SRR9186431	GSM3844833	SRA893482	SRX5958833	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	99	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186432	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008971/SRR9186432	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	100	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186433	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186433	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	101	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186434	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186434	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	102	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186435	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/008971/SRR9186435	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	103	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186436	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/008971/SRR9186436	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	104	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186437	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008971/SRR9186437	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	105	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186438	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186438	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	106	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186439	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008971/SRR9186439	GSM3844834	SRA893482	SRX5958834	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	107	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186440	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008971/SRR9186440	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	108	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186441	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008971/SRR9186441	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	109	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186442	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186442	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	110	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186443	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186443	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	111	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186444	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008971/SRR9186444	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	112	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186445	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/008971/SRR9186445	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	113	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186446	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186446	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	114	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186447	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186447	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	115	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186448	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008971/SRR9186448	GSM3844835	SRA893482	SRX5958835	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	116	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186449	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186449	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	117	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186450	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/008971/SRR9186450	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	118	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186451	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186451	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	119	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186452	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186452	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	120	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186453	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008971/SRR9186453	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	121	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186454	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/008971/SRR9186454	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	122	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186455	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186455	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	123	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186456	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/008971/SRR9186456	GSM3844836	SRA893482	SRX5958836	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	124	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186457	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/008971/SRR9186457	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	125	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186458	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/008971/SRR9186458	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	126	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186459	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/008971/SRR9186459	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	127	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186460	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/008971/SRR9186460	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	128	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186461	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/008971/SRR9186461	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	129	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186462	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/008971/SRR9186462	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	130	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186463	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186463	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	131	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186464	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/008971/SRR9186464	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	132	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186465	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008971/SRR9186465	GSM3844837	SRA893482	SRX5958837	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	133	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186466	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186466	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	134	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186467	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/008971/SRR9186467	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	135	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186468	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/008971/SRR9186468	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	136	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186469	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/008971/SRR9186469	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	137	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186470	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008971/SRR9186470	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	138	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186471	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/008971/SRR9186471	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	139	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186472	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/008971/SRR9186472	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	140	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186473	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/008971/SRR9186473	GSM3844838	SRA893482	SRX5958838	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	141	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186474	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/008971/SRR9186474	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	142	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186475	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/008971/SRR9186475	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	143	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186476	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/008971/SRR9186476	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	144	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186477	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/008971/SRR9186477	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	145	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186478	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/008971/SRR9186478	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	146	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186479	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008971/SRR9186479	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	147	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186480	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/008971/SRR9186480	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	148	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186481	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/008971/SRR9186481	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	149	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186482	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/008971/SRR9186482	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	150	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186483	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186483	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	151	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186484	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/008971/SRR9186484	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	152	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186485	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/008971/SRR9186485	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	153	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186486	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/008971/SRR9186486	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	154	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186487	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186487	GSM3844839	SRA893482	SRX5958839	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	155	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186488	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008971/SRR9186488	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	156	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186489	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/008971/SRR9186489	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	157	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186490	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/008971/SRR9186490	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	158	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186491	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186491	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	159	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186492	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/008971/SRR9186492	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	160	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186493	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/008971/SRR9186493	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	161	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186494	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/008971/SRR9186494	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	162	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186495	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/008971/SRR9186495	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	163	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186496	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/008971/SRR9186496	GSM3844840	SRA893482	SRX5958840	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	164	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186497	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/008971/SRR9186497	GSM3844841	SRA893482	SRX5958841	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	165	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186498	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/008971/SRR9186498	GSM3844841	SRA893482	SRX5958841	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	166	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186499	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/008971/SRR9186499	GSM3844841	SRA893482	SRX5958841	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	167	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186500	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/008971/SRR9186500	GSM3844841	SRA893482	SRX5958841	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	168	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186501	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/008971/SRR9186501	GSM3844841	SRA893482	SRX5958841	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	169	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186502	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/008971/SRR9186502	GSM3844841	SRA893482	SRX5958841	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	170	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186503	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/008971/SRR9186503	GSM3844841	SRA893482	SRX5958841	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	171	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186504	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/008971/SRR9186504	GSM3844842	SRA893482	SRX5958842	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	172	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186505	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/008971/SRR9186505	GSM3844842	SRA893482	SRX5958842	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	173	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186506	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/008971/SRR9186506	GSM3844842	SRA893482	SRX5958842	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	174	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186507	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/008971/SRR9186507	GSM3844842	SRA893482	SRX5958842	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	175	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186508	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/008971/SRR9186508	GSM3844842	SRA893482	SRX5958842	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	176	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186509	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/008971/SRR9186509	GSM3844842	SRA893482	SRX5958842	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	177	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186510	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/008971/SRR9186510	GSM3844842	SRA893482	SRX5958842	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	178	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186511	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186511	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	179	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186512	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008971/SRR9186512	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	180	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186513	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/008971/SRR9186513	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	181	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186514	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/008971/SRR9186514	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	182	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186515	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/008971/SRR9186515	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	183	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186516	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186516	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	184	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186517	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/008971/SRR9186517	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	185	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186518	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/008971/SRR9186518	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	186	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186519	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/008971/SRR9186519	GSM3844843	SRA893482	SRX5958843	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	187	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186520	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/008971/SRR9186520	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	188	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186521	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/008971/SRR9186521	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	189	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186522	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/008971/SRR9186522	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	190	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186523	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/008971/SRR9186523	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	191	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186524	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/008971/SRR9186524	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	192	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186525	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/008971/SRR9186525	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	193	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186526	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/008971/SRR9186526	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
132116	194	Martina Brueckner	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility [RNA-Seq]	Genomic analyses of patients with congenital heart disease (CHD) have identified significant contribution from mutations affecting cilia genes and chr	Martina Brueckner, Mustafa Khokha	Xenopus embryo mRNA profiling in wt (in duplicate) and RNF20 morpholino (in triplicate) at 12 hpf, 13 hpf, 14 hpf, 15 hpf, and 16 hpf	31235600	56064	SRP200236	SRR9186527	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/008971/SRR9186527	GSM3844844	SRA893482	SRX5958844	RNA-Seq	SINGLE	SRP200236	PRJNA545973
134537	1	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715854	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/009488/SRR9715854	GSM3955306	SRA923235	SRX6473708	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	2	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715855	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/009488/SRR9715855	GSM3955307	SRA923235	SRX6473709	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	3	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715856	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/009488/SRR9715856	GSM3955308	SRA923235	SRX6473710	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	4	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715857	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/009488/SRR9715857	GSM3955309	SRA923235	SRX6473711	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	5	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715858	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/009488/SRR9715858	GSM3955310	SRA923235	SRX6473712	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	6	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715859	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/009488/SRR9715859	GSM3955311	SRA923235	SRX6473713	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	7	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715860	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/009488/SRR9715860	GSM3955312	SRA923235	SRX6473714	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	8	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715861	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/009488/SRR9715861	GSM3955313	SRA923235	SRX6473715	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	9	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715862	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/009488/SRR9715862	GSM3955314	SRA923235	SRX6473716	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	10	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715863	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/009488/SRR9715863	GSM3955315	SRA923235	SRX6473717	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	11	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715864	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/009488/SRR9715864	GSM3955316	SRA923235	SRX6473718	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	12	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715865	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/009488/SRR9715865	GSM3955317	SRA923235	SRX6473719	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	13	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715866	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/009488/SRR9715866	GSM3955318	SRA923235	SRX6473720	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	14	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715867	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/009488/SRR9715867	GSM3955319	SRA923235	SRX6473721	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	15	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715868	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/009488/SRR9715868	GSM3955320	SRA923235	SRX6473722	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	16	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715869	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/009488/SRR9715869	GSM3955321	SRA923235	SRX6473723	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	17	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715870	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/009488/SRR9715870	GSM3955322	SRA923235	SRX6473724	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	18	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715871	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/009488/SRR9715871	GSM3955323	SRA923235	SRX6473725	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	19	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715872	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/009488/SRR9715872	GSM3955324	SRA923235	SRX6473726	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	20	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715873	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/009488/SRR9715873	GSM3955325	SRA923235	SRX6473727	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	21	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715874	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/009488/SRR9715874	GSM3955326	SRA923235	SRX6473728	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	22	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715875	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/009488/SRR9715875	GSM3955327	SRA923235	SRX6473729	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	23	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715876	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/009488/SRR9715876	GSM3955328	SRA923235	SRX6473730	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	24	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715877	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/009488/SRR9715877	GSM3955329	SRA923235	SRX6473731	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	25	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715878	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/009488/SRR9715878	GSM3955330	SRA923235	SRX6473732	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	26	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715879	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/009488/SRR9715879	GSM3955331	SRA923235	SRX6473733	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	27	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715880	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/009488/SRR9715880	GSM3955332	SRA923235	SRX6473734	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	28	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715881	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/009488/SRR9715881	GSM3955333	SRA923235	SRX6473735	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	29	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715882	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/009488/SRR9715882	GSM3955334	SRA923235	SRX6473736	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	30	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715883	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/009488/SRR9715883	GSM3955335	SRA923235	SRX6473737	RNA-Seq	SINGLE	SRP215429	PRJNA555524
134537	31	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715884	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/009488/SRR9715884	GSM3955336	SRA923235	SRX6473738	OTHER	SINGLE	SRP215429	PRJNA555524
134537	32	Michael Blower	Genome-wide analysis of mRNA polyadenylation and translation during vertebrate oocyte maturation	Changes in gene expression are required to orchestrate changes in cell state during development. Most cells change patterns of gene expression through	Michael Blower, Michael Blower	poly-A tail lengths and polysome fractions were measured for genome-wide during oocyte maturation in Xenopus laevis	31896558	56611	SRP215429	SRR9715885	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/009488/SRR9715885	GSM3955337	SRA923235	SRX6473739	OTHER	SINGLE	SRP215429	PRJNA555524
137844	1	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163172	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/009924/SRR10163172	GSM4089657	SRA966374	SRX6888561	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	2	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163173	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/009924/SRR10163173	GSM4089658	SRA966374	SRX6888562	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	3	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163174	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/009924/SRR10163174	GSM4089659	SRA966374	SRX6888563	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	4	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163175	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/009924/SRR10163175	GSM4089660	SRA966374	SRX6888564	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	5	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163176	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/009924/SRR10163176	GSM4089661	SRA966374	SRX6888565	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	6	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163177	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/009924/SRR10163177	GSM4089662	SRA966374	SRX6888566	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	7	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163178	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/009924/SRR10163178	GSM4089663	SRA966374	SRX6888567	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	8	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163179	https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/009924/SRR10163179	GSM4089664	SRA966374	SRX6888568	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	9	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163180	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/009924/SRR10163180	GSM4089665	SRA966374	SRX6888569	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	10	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163181	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/009924/SRR10163181	GSM4089666	SRA966374	SRX6888570	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	11	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163182	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/009924/SRR10163182	GSM4089667	SRA966374	SRX6888571	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	12	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163183	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/009924/SRR10163183	GSM4089668	SRA966374	SRX6888572	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	13	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163184	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/009924/SRR10163184	GSM4089669	SRA966374	SRX6888573	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	14	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163185	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/009924/SRR10163185	GSM4089670	SRA966374	SRX6888574	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	15	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163186	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/009924/SRR10163186	GSM4089671	SRA966374	SRX6888575	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	16	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163187	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/009924/SRR10163187	GSM4089672	SRA966374	SRX6888576	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	17	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163188	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/009924/SRR10163188	GSM4089673	SRA966374	SRX6888577	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	18	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163189	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/009924/SRR10163189	GSM4089674	SRA966374	SRX6888578	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	19	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163190	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/009924/SRR10163190	GSM4089675	SRA966374	SRX6888579	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	20	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163191	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/009924/SRR10163191	GSM4089676	SRA966374	SRX6888580	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	21	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163192	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/009924/SRR10163192	GSM4089677	SRA966374	SRX6888581	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	22	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163193	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/009924/SRR10163193	GSM4089678	SRA966374	SRX6888582	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	23	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163194	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/009924/SRR10163194	GSM4089679	SRA966374	SRX6888583	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	24	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163195	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/009924/SRR10163195	GSM4089680	SRA966374	SRX6888584	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	25	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163196	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/009924/SRR10163196	GSM4089681	SRA966374	SRX6888585	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	26	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163197	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/009924/SRR10163197	GSM4089682	SRA966374	SRX6888586	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	27	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163198	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/009924/SRR10163198	GSM4089683	SRA966374	SRX6888587	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	28	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163199	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/009924/SRR10163199	GSM4089684	SRA966374	SRX6888588	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	29	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163200	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/009925/SRR10163200	GSM4089685	SRA966374	SRX6888589	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	30	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163201	https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/009925/SRR10163201	GSM4089686	SRA966374	SRX6888590	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	31	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163202	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/009925/SRR10163202	GSM4089687	SRA966374	SRX6888591	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	32	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163203	https://sra-download.ncbi.nlm.nih.gov/traces/sra72/SRR/009925/SRR10163203	GSM4089688	SRA966374	SRX6888592	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	33	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163204	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/009925/SRR10163204	GSM4089689	SRA966374	SRX6888593	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	34	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163205	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/009925/SRR10163205	GSM4089690	SRA966374	SRX6888594	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	35	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163206	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/009925/SRR10163206	GSM4089691	SRA966374	SRX6888595	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	36	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163207	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/009925/SRR10163207	GSM4089692	SRA966374	SRX6888596	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	37	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163208	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/009925/SRR10163208	GSM4089693	SRA966374	SRX6888597	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	38	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163209	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/009925/SRR10163209	GSM4089694	SRA966374	SRX6888598	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	39	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163210	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/009925/SRR10163210	GSM4089695	SRA966374	SRX6888599	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	40	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163211	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/009925/SRR10163211	GSM4089696	SRA966374	SRX6888600	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	41	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163212	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/009925/SRR10163212	GSM4089697	SRA966374	SRX6888601	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	42	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163213	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/009925/SRR10163213	GSM4089698	SRA966374	SRX6888602	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	43	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163214	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/009925/SRR10163214	GSM4089699	SRA966374	SRX6888603	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	44	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163215	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/009925/SRR10163215	GSM4089700	SRA966374	SRX6888604	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	45	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163216	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/009925/SRR10163216	GSM4089701	SRA966374	SRX6888605	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	46	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163217	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/009925/SRR10163217	GSM4089702	SRA966374	SRX6888606	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	47	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163218	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/009925/SRR10163218	GSM4089703	SRA966374	SRX6888607	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	48	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163219	https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/009925/SRR10163219	GSM4089704	SRA966374	SRX6888608	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	49	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163220	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/009925/SRR10163220	GSM4089705	SRA966374	SRX6888609	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	50	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163221	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/009925/SRR10163221	GSM4089706	SRA966374	SRX6888610	RNA-Seq	SINGLE	SRP222957	PRJNA573657
137844	51	Ben Szaro	Comparative Gene Expression Profiling between Xenopus Optic Nerve and Spinal Cord Injury to Identify Genes Involved in Successful Regeneration of Vertebrate CNS Axons	Xenopus is uniquely suited for addressing the question of whether a core gene expression program for successful CNS axon regeneration exists, because 	Ben Szaro, Ben Szaro, Kurt Gibbs, Jamie Belrose	RNA-seq (30 million nominal reads per sample) was performed on 51 samples: operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at three different timepoints (3 days, 11 days, 3 weeks), plus surgiically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at three timepoints (3 days, 7 days, 3 weeks), with 5 pooled hindbrains for each sample; juvenile frog hindbrain after spinal cord transection at 3 timepoints (3 days, 7 days, 3 weeks), plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	32758133	57252	SRP222957	SRR10163222	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/009925/SRR10163222	GSM4089707	SRA966374	SRX6888611	RNA-Seq	SINGLE	SRP222957	PRJNA573657
138303	1	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215912	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/009976/SRR10215912	GSM4105018	SRA971336	SRX6935589	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	2	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215913	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/009976/SRR10215913	GSM4105019	SRA971336	SRX6935590	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	3	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215914	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/009976/SRR10215914	GSM4105020	SRA971336	SRX6935573	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	4	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215915	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/009976/SRR10215915	GSM4105021	SRA971336	SRX6935574	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	5	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215916	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/009976/SRR10215916	GSM4105022	SRA971336	SRX6935575	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	6	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215917	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/009976/SRR10215917	GSM4105023	SRA971336	SRX6935576	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	7	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215918	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/009976/SRR10215918	GSM4105024	SRA971336	SRX6935577	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	8	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215919	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/009976/SRR10215919	GSM4105025	SRA971336	SRX6935578	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	9	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215920	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/009976/SRR10215920	GSM4105026	SRA971336	SRX6935579	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	10	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215921	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/009976/SRR10215921	GSM4105027	SRA971336	SRX6935580	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	11	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215922	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/009976/SRR10215922	GSM4105028	SRA971336	SRX6935581	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	12	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215923	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/009976/SRR10215923	GSM4105029	SRA971336	SRX6935582	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	13	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215924	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/009976/SRR10215924	GSM4105030	SRA971336	SRX6935583	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	14	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215925	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/009976/SRR10215925	GSM4105031	SRA971336	SRX6935584	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	15	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215926	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/009976/SRR10215926	GSM4105032	SRA971336	SRX6935585	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	16	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215927	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/009976/SRR10215927	GSM4105033	SRA971336	SRX6935586	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	17	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215928	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/009976/SRR10215928	GSM4105034	SRA971336	SRX6935587	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138303	18	Jessica Chang	ATAC-Seq of Xenopus tail regeneration	Mammals possess limited regeneration capabilities, where the few examples of scarless healing tend to be restricted to early development. In light of 	Jessica Chang, Jessica Chang, Andrea Wills, Julie Baker	Profiling of chromatin accessibility across nine time points in tadpole tail regeneration; sequenced in duplicate via Illumina HiSeq and NextSeq.

Please note that each *combined_reps.bw file was generated from both replicates and is linked to the corresponding 'rep1' sample records.	0	57142	SRP223949	SRR10215929	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/009976/SRR10215929	GSM4105035	SRA971336	SRX6935588	ATAC-seq	PAIRED	SRP223949	PRJNA575367
138905	1	Peter Klein	ATAC-seq identifies accessible chromatin domains in gastrula stage Xenopus laevis	In the embryo, inductive cues are interpreted by competent tissues in a spatially and temporally restricted manner, and the mechanisms for the loss of	Peter Klein, Jing Yang, Kai Zhang, Melody Esmaeili, Peter Klein	ATAC-seq performed on ectodermal explants from stage 10 (early gastrula) and stage 12 (late gastrula).	0	56750	SRP225796	SRR10285468	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/010044/SRR10285468	GSM4121478	SRA979583	SRX6998460	ATAC-seq	PAIRED	SRP225796	PRJNA577715
138905	2	Peter Klein	ATAC-seq identifies accessible chromatin domains in gastrula stage Xenopus laevis	In the embryo, inductive cues are interpreted by competent tissues in a spatially and temporally restricted manner, and the mechanisms for the loss of	Peter Klein, Jing Yang, Kai Zhang, Melody Esmaeili, Peter Klein	ATAC-seq performed on ectodermal explants from stage 10 (early gastrula) and stage 12 (late gastrula).	0	56750	SRP225796	SRR10285469	https://sra-download.ncbi.nlm.nih.gov/traces/sra30/SRR/010044/SRR10285469	GSM4121479	SRA979583	SRX6998461	ATAC-seq	PAIRED	SRP225796	PRJNA577715
138905	3	Peter Klein	ATAC-seq identifies accessible chromatin domains in gastrula stage Xenopus laevis	In the embryo, inductive cues are interpreted by competent tissues in a spatially and temporally restricted manner, and the mechanisms for the loss of	Peter Klein, Jing Yang, Kai Zhang, Melody Esmaeili, Peter Klein	ATAC-seq performed on ectodermal explants from stage 10 (early gastrula) and stage 12 (late gastrula).	0	56750	SRP225796	SRR10285470	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/010044/SRR10285470	GSM4121480	SRA979583	SRX6998462	ATAC-seq	PAIRED	SRP225796	PRJNA577715
138905	4	Peter Klein	ATAC-seq identifies accessible chromatin domains in gastrula stage Xenopus laevis	In the embryo, inductive cues are interpreted by competent tissues in a spatially and temporally restricted manner, and the mechanisms for the loss of	Peter Klein, Jing Yang, Kai Zhang, Melody Esmaeili, Peter Klein	ATAC-seq performed on ectodermal explants from stage 10 (early gastrula) and stage 12 (late gastrula).	0	56750	SRP225796	SRR10285471	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/010044/SRR10285471	GSM4121481	SRA979583	SRX6998463	ATAC-seq	PAIRED	SRP225796	PRJNA577715
138905	5	Peter Klein	ATAC-seq identifies accessible chromatin domains in gastrula stage Xenopus laevis	In the embryo, inductive cues are interpreted by competent tissues in a spatially and temporally restricted manner, and the mechanisms for the loss of	Peter Klein, Jing Yang, Kai Zhang, Melody Esmaeili, Peter Klein	ATAC-seq performed on ectodermal explants from stage 10 (early gastrula) and stage 12 (late gastrula).	0	56750	SRP225796	SRR10285472	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/010044/SRR10285472	GSM4121482	SRA979583	SRX6998464	ATAC-seq	PAIRED	SRP225796	PRJNA577715
138905	6	Peter Klein	ATAC-seq identifies accessible chromatin domains in gastrula stage Xenopus laevis	In the embryo, inductive cues are interpreted by competent tissues in a spatially and temporally restricted manner, and the mechanisms for the loss of	Peter Klein, Jing Yang, Kai Zhang, Melody Esmaeili, Peter Klein	ATAC-seq performed on ectodermal explants from stage 10 (early gastrula) and stage 12 (late gastrula).	0	56750	SRP225796	SRR10285473	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/010044/SRR10285473	GSM4121483	SRA979583	SRX6998465	ATAC-seq	PAIRED	SRP225796	PRJNA577715
139267	1	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327373	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/010085/SRR10327373	GSM4135833	SRA983503	SRX7037557	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	2	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327374	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/010085/SRR10327374	GSM4135834	SRA983503	SRX7037558	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	3	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327375	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/010085/SRR10327375	GSM4135835	SRA983503	SRX7037559	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	4	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327376	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/010085/SRR10327376	GSM4135836	SRA983503	SRX7037560	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	5	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327377	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/010085/SRR10327377	GSM4135837	SRA983503	SRX7037561	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	6	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327378	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/010085/SRR10327378	GSM4135838	SRA983503	SRX7037562	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	7	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327379	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/010085/SRR10327379	GSM4135839	SRA983503	SRX7037563	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	8	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327380	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/010085/SRR10327380	GSM4135840	SRA983503	SRX7037564	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	9	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327381	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/010085/SRR10327381	GSM4135841	SRA983503	SRX7037565	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	10	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327382	https://sra-download.ncbi.nlm.nih.gov/traces/sra30/SRR/010085/SRR10327382	GSM4135842	SRA983503	SRX7037566	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	11	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327383	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/010085/SRR10327383	GSM4135843	SRA983503	SRX7037567	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	12	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327384	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/010085/SRR10327384	GSM4135844	SRA983503	SRX7037568	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	13	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327385	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/010085/SRR10327385	GSM4135845	SRA983503	SRX7037569	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	14	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327386	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/010085/SRR10327386	GSM4135846	SRA983503	SRX7037570	MBD-Seq	SINGLE	SRP226648	PRJNA578937
139267	15	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain	Changes in DNA methylation in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using Methylated DNA Capture sequen	Robert Denver, Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, conducted Methylated DNA Capture using the Diogenode kit, generated libraries and did deep sequencing.	32240642	56853	SRP226648	SRR10327387	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/010085/SRR10327387	GSM4135847	SRA983503	SRX7037571	MBD-Seq	SINGLE	SRP226648	PRJNA578937
140120	1	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417502	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/010173/SRR10417502	GSM4154616	SRA992784	SRX7115530	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	2	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417503	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/010173/SRR10417503	GSM4154617	SRA992784	SRX7115531	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	3	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417504	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/010173/SRR10417504	GSM4154618	SRA992784	SRX7115532	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	4	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417505	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/010173/SRR10417505	GSM4154619	SRA992784	SRX7115533	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	5	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417506	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/010173/SRR10417506	GSM4154620	SRA992784	SRX7115534	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	6	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417507	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/010173/SRR10417507	GSM4154621	SRA992784	SRX7115535	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	7	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417508	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/010173/SRR10417508	GSM4154622	SRA992784	SRX7115536	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	8	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417509	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/010173/SRR10417509	GSM4154623	SRA992784	SRX7115537	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	9	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417510	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/010173/SRR10417510	GSM4154624	SRA992784	SRX7115538	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	10	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417511	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/010173/SRR10417511	GSM4154625	SRA992784	SRX7115539	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	11	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417512	https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/010173/SRR10417512	GSM4154626	SRA992784	SRX7115540	RNA-Seq	SINGLE	SRP229123	PRJNA588299
140120	12	Robert Denver	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain [RNA-seq]	Changes in gene expression in the preoptic area/hypothalamus/thalamus of Xenopus tropicalis tadpoles were analyzed using RNAseq at four stages of meta	Robert Denver, Christopher Sifuentes, Yasuhiro Kyono, Samhitha Raj, Nicolas Buisine, Laurent Sachs	The middle brain region containing preoptic area/hypothalamus/thalamus was microdissected from Xenopus tropicalis tadpoles at four stages of metamorphosis: Nieuwkoop-Faber (NF) stage 50 (pre-metamorphosis), NF56 (pro-metamorphosis), NF62 (metamorphic climax), and NF66 (completion of metamorphosis). We isolated genomic DNA from tadpole brain to generate 3 biological replicates per developmental stage, isolated total RNA, generated libraries and did deep sequencing.	32240642	56853	SRP229123	SRR10417513	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/010173/SRR10417513	GSM4154627	SRA992784	SRX7115541	RNA-Seq	SINGLE	SRP229123	PRJNA588299
143395	1	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859344	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/010604/SRR10859344	GSM4258351	SRA1023079	SRX7529421	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	2	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859345	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/010604/SRR10859345	GSM4258352	SRA1023079	SRX7529422	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	3	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859346	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/010604/SRR10859346	GSM4258353	SRA1023079	SRX7529423	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	4	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859347	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/010604/SRR10859347	GSM4258354	SRA1023079	SRX7529424	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	5	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859348	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010604/SRR10859348	GSM4258355	SRA1023079	SRX7529425	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	6	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859349	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/010604/SRR10859349	GSM4258356	SRA1023079	SRX7529426	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	7	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859350	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010604/SRR10859350	GSM4258357	SRA1023079	SRX7529427	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	8	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859351	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/010604/SRR10859351	GSM4258358	SRA1023079	SRX7529428	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	9	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859352	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/010604/SRR10859352	GSM4258359	SRA1023079	SRX7529429	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	10	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859353	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/010604/SRR10859353	GSM4258360	SRA1023079	SRX7529430	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	11	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859354	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/010604/SRR10859354	GSM4258361	SRA1023079	SRX7529431	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	12	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859355	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/010604/SRR10859355	GSM4258362	SRA1023079	SRX7529432	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	13	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859356	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/010604/SRR10859356	GSM4258363	SRA1023079	SRX7529433	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	14	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859357	https://sra-download.ncbi.nlm.nih.gov/traces/sra40/SRR/010604/SRR10859357	GSM4258364	SRA1023079	SRX7529434	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	15	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859358	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/010604/SRR10859358	GSM4258365	SRA1023079	SRX7529435	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	16	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859359	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010604/SRR10859359	GSM4258366	SRA1023079	SRX7529436	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	17	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859360	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/010604/SRR10859360	GSM4258367	SRA1023079	SRX7529437	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	18	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859361	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/010604/SRR10859361	GSM4258368	SRA1023079	SRX7529438	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	19	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859362	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/010604/SRR10859362	GSM4258369	SRA1023079	SRX7529439	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	20	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859363	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/010604/SRR10859363	GSM4258370	SRA1023079	SRX7529440	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	21	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859364	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/010604/SRR10859364	GSM4258371	SRA1023079	SRX7529441	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	22	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859365	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/010604/SRR10859365	GSM4258372	SRA1023079	SRX7529442	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	23	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859366	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/010604/SRR10859366	GSM4258373	SRA1023079	SRX7529443	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	24	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859367	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/010604/SRR10859367	GSM4258374	SRA1023079	SRX7529444	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	25	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859368	https://sra-download.ncbi.nlm.nih.gov/traces/sra14/SRR/010604/SRR10859368	GSM4258375	SRA1023079	SRX7529445	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	26	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859369	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/010604/SRR10859369	GSM4258376	SRA1023079	SRX7529446	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	27	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859370	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/010604/SRR10859370	GSM4258377	SRA1023079	SRX7529447	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	28	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859371	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/010604/SRR10859371	GSM4258378	SRA1023079	SRX7529448	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	29	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859372	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/010604/SRR10859372	GSM4258379	SRA1023079	SRX7529449	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143395	30	Varshini Vasudevaraja	Targets of Sf3b4 during neural crest development	Mutations in Sf3b4, a component of the spliceosome, have been linked to craniofacial dismorphology known as Nager syndrome. To understand the role Sf3	Varshini Vasudevaraja, Jean-Pierre Saint-Jeannet, Santosh Maharana	Xenopus laevis embryos were injected at the 2-cell stage with mRNAs encoding noggin and wnt8 to induce neural crest progenitors. A subset of these embryos were co-injected with Sf3b4MO antisense oligonucleotides to interfere with  Sf3b4 fonction during neural crest forrmation. At the blastula stage (stage 8/9), animal cap explants were dissected and cultured for 8 hours in a defined medium. Either two or three biological replicates were performed for each condition.	0	57146	SRP240958	SRR10859373	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/010604/SRR10859373	GSM4258380	SRA1023079	SRX7529450	RNA-Seq	PAIRED	SRP240958	PRJNA600273
143795	1	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903013	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/010647/SRR10903013	GSM4274726	SRA1027270	SRX7571183	RNA-Seq	PAIRED	SRP242211	PRJNA601731
143795	2	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903014	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/010647/SRR10903014	GSM4274727	SRA1027270	SRX7571184	RNA-Seq	PAIRED	SRP242211	PRJNA601731
143795	3	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903015	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/010647/SRR10903015	GSM4274728	SRA1027270	SRX7571185	RNA-Seq	PAIRED	SRP242211	PRJNA601731
143795	4	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903016	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/010647/SRR10903016	GSM4274729	SRA1027270	SRX7571186	RNA-Seq	PAIRED	SRP242211	PRJNA601731
143795	5	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903017	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/010647/SRR10903017	GSM4274730	SRA1027270	SRX7571187	RNA-Seq	PAIRED	SRP242211	PRJNA601731
143795	6	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903018	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/010647/SRR10903018	GSM4274731	SRA1027270	SRX7571188	RNA-Seq	PAIRED	SRP242211	PRJNA601731
143795	7	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903019	https://sra-download.ncbi.nlm.nih.gov/traces/sra5/SRR/010647/SRR10903019	GSM4274732	SRA1027270	SRX7571189	RNA-Seq	PAIRED	SRP242211	PRJNA601731
143795	8	Olga Ossipova	Specification of embryonic mesoderm by Pinhead signaling	Among the three embryonic germ layers, mesoderm plays a central role in the establishment of the vertebrate body plan.  Mesoderm is specified by secre	Olga Ossipova, Keiji Itoh, Aurelian Radu, Ezan Jerome, Sergei Sokol	Gain of function and loss of function study of Pinhead, a novel growth factor. Duplicate samples for control ectoderm explants (Cocaps1, Cocaps2) and Flag-Pinhead-expressing caps (FlagPin1, FlagPin2) at stage 11, gastrula were analyzed for Pinhead gain-of-function by RNAseq. For Pinhead loss-of-function, duplicate samples for control marginal zone explants (Co1, Co2) and Pinhead-depleted (Pinhead SpMo) marginal zone explants  (PhSpMo1, PhSpMo2) were studied at st.11 by RNAseq.	32859582	57304	SRP242211	SRR10903020	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/010647/SRR10903020	GSM4274733	SRA1027270	SRX7571190	RNA-Seq	PAIRED	SRP242211	PRJNA601731
145619	1	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122354	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122354	GSM4322303	SRA1045163	SRX7759414	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	2	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122355	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122355	GSM4322304	SRA1045163	SRX7759415	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	3	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122356	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122356	GSM4322305	SRA1045163	SRX7759416	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	4	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122357	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/010861/SRR11122357	GSM4322306	SRA1045163	SRX7759417	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	5	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122358	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122358	GSM4322307	SRA1045163	SRX7759418	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	6	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122359	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122359	GSM4322308	SRA1045163	SRX7759419	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	7	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122360	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122360	GSM4322309	SRA1045163	SRX7759420	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	8	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122361	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122361	GSM4322310	SRA1045163	SRX7759421	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	9	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122362	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122362	GSM4322311	SRA1045163	SRX7759422	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	10	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122363	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122363	GSM4322312	SRA1045163	SRX7759423	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	11	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122364	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122364	GSM4322313	SRA1045163	SRX7759424	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	12	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122365	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122365	GSM4322314	SRA1045163	SRX7759425	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	13	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122366	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122366	GSM4322315	SRA1045163	SRX7759426	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	14	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122367	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122367	GSM4322316	SRA1045163	SRX7759427	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	15	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122368	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122368	GSM4322317	SRA1045163	SRX7759428	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	16	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122369	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122369	GSM4322318	SRA1045163	SRX7759429	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	17	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122370	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/010861/SRR11122370	GSM4322319	SRA1045163	SRX7759430	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	18	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122371	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122371	GSM4322320	SRA1045163	SRX7759431	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	19	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122372	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122372	GSM4322321	SRA1045163	SRX7759432	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	20	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122373	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122373	GSM4322322	SRA1045163	SRX7759433	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	21	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122374	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122374	GSM4322323	SRA1045163	SRX7759434	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	22	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122375	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122375	GSM4322324	SRA1045163	SRX7759435	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	23	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122376	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122376	GSM4322325	SRA1045163	SRX7759436	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	24	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122377	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122377	GSM4322326	SRA1045163	SRX7759437	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	25	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122378	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122378	GSM4322327	SRA1045163	SRX7759438	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	26	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122380	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122380	GSM4322328	SRA1045163	SRX7759439	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	27	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122381	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122381	GSM4322329	SRA1045163	SRX7759440	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	28	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122382	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122382	GSM4322330	SRA1045163	SRX7759441	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	29	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122383	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122383	GSM4322331	SRA1045163	SRX7759442	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	30	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122384	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122384	GSM4322332	SRA1045163	SRX7759443	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	31	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122385	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122385	GSM4322333	SRA1045163	SRX7759444	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	32	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122386	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122386	GSM4322334	SRA1045163	SRX7759445	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	33	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122387	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122387	GSM4322335	SRA1045163	SRX7759446	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	34	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122388	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122388	GSM4322336	SRA1045163	SRX7759447	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	35	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122389	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122389	GSM4322337	SRA1045163	SRX7759448	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	36	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122390	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122390	GSM4322338	SRA1045163	SRX7759449	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	37	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122391	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122391	GSM4322339	SRA1045163	SRX7759450	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	38	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122392	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122392	GSM4322340	SRA1045163	SRX7759451	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	39	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122393	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122393	GSM4322341	SRA1045163	SRX7759452	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	40	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122394	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122394	GSM4322342	SRA1045163	SRX7759453	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	41	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122395	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122395	GSM4322343	SRA1045163	SRX7759454	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	42	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122396	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122396	GSM4322344	SRA1045163	SRX7759455	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	43	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122397	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122397	GSM4322345	SRA1045163	SRX7759456	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	44	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122398	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122398	GSM4322346	SRA1045163	SRX7759457	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	45	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122399	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122399	GSM4322347	SRA1045163	SRX7759458	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	46	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122400	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122400	GSM4322348	SRA1045163	SRX7759459	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	47	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122401	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122401	GSM4322349	SRA1045163	SRX7759460	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	48	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122402	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122402	GSM4322350	SRA1045163	SRX7759461	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	49	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122411	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122411	GSM4322359	SRA1045163	SRX7759361	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	50	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122412	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122412	GSM4322360	SRA1045163	SRX7759362	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	51	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122413	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122413	GSM4322361	SRA1045163	SRX7759363	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	52	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122414	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122414	GSM4322362	SRA1045163	SRX7759364	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	53	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122415	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122415	GSM4322363	SRA1045163	SRX7759365	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	54	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122416	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122416	GSM4322364	SRA1045163	SRX7759366	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	55	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122417	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122417	GSM4322365	SRA1045163	SRX7759367	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	56	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122418	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122418	GSM4322366	SRA1045163	SRX7759368	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	57	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122419	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122419	GSM4322367	SRA1045163	SRX7759369	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	58	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122420	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122420	GSM4322368	SRA1045163	SRX7759370	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	59	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122421	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122421	GSM4322369	SRA1045163	SRX7759371	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	60	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122422	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122422	GSM4322370	SRA1045163	SRX7759372	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	61	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122423	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122423	GSM4322371	SRA1045163	SRX7759373	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	62	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122424	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122424	GSM4322372	SRA1045163	SRX7759374	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	63	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122425	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122425	GSM4322373	SRA1045163	SRX7759375	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	64	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122426	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122426	GSM4322374	SRA1045163	SRX7759376	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	65	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122427	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122427	GSM4322375	SRA1045163	SRX7759377	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	66	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122428	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122428	GSM4322376	SRA1045163	SRX7759378	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	67	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122429	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122429	GSM4322377	SRA1045163	SRX7759379	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	68	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122430	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122430	GSM4322378	SRA1045163	SRX7759380	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	69	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122431	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122431	GSM4322379	SRA1045163	SRX7759381	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	70	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122432	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122432	GSM4322380	SRA1045163	SRX7759382	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	71	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122433	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122433	GSM4322381	SRA1045163	SRX7759383	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	72	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122434	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122434	GSM4322382	SRA1045163	SRX7759384	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	73	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122435	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122435	GSM4322383	SRA1045163	SRX7759385	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	74	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122436	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122436	GSM4322384	SRA1045163	SRX7759386	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	75	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122437	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122437	GSM4322385	SRA1045163	SRX7759387	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	76	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122438	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122438	GSM4322386	SRA1045163	SRX7759388	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	77	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122439	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122439	GSM4322387	SRA1045163	SRX7759389	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	78	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122440	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122440	GSM4322388	SRA1045163	SRX7759390	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	79	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122441	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122441	GSM4322389	SRA1045163	SRX7759391	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	80	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122442	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122442	GSM4322390	SRA1045163	SRX7759392	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	81	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122443	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122443	GSM4322391	SRA1045163	SRX7759393	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	82	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122444	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/010861/SRR11122444	GSM4322392	SRA1045163	SRX7759394	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	83	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122445	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122445	GSM4322393	SRA1045163	SRX7759395	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	84	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122446	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/010861/SRR11122446	GSM4322394	SRA1045163	SRX7759396	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	85	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122447	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122447	GSM4322395	SRA1045163	SRX7759397	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	86	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122448	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122448	GSM4322396	SRA1045163	SRX7759398	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	87	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122449	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122449	GSM4322397	SRA1045163	SRX7759399	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	88	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122450	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122450	GSM4322398	SRA1045163	SRX7759400	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	89	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122451	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122451	GSM4322399	SRA1045163	SRX7759401	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	90	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122452	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122452	GSM4322400	SRA1045163	SRX7759402	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	91	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122453	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122453	GSM4322401	SRA1045163	SRX7759404	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	92	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122454	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122454	GSM4322402	SRA1045163	SRX7759405	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	93	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122455	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122455	GSM4322403	SRA1045163	SRX7759406	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	94	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122456	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122456	GSM4322404	SRA1045163	SRX7759407	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	95	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122457	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122457	GSM4322405	SRA1045163	SRX7759408	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	96	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122458	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122458	GSM4322406	SRA1045163	SRX7759409	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	97	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122459	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122459	GSM4322407	SRA1045163	SRX7759410	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	98	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122460	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/010861/SRR11122460	GSM4322408	SRA1045163	SRX7759411	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	99	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122461	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122461	GSM4322409	SRA1045163	SRX7759412	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	100	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122462	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122462	GSM4322410	SRA1045163	SRX7759413	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	101	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122334	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122334	GSM4322283	SRA1045163	SRX7759333	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	102	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122335	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122335	GSM4322284	SRA1045163	SRX7759334	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	103	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122336	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122336	GSM4322285	SRA1045163	SRX7759335	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	104	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122337	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122337	GSM4322286	SRA1045163	SRX7759336	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	105	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122338	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122338	GSM4322287	SRA1045163	SRX7759337	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	106	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122339	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122339	GSM4322288	SRA1045163	SRX7759338	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	107	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122340	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122340	GSM4322289	SRA1045163	SRX7759339	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	108	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122341	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122341	GSM4322290	SRA1045163	SRX7759340	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	109	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122342	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122342	GSM4322291	SRA1045163	SRX7759341	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	110	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122343	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122343	GSM4322292	SRA1045163	SRX7759342	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	111	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122344	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122344	GSM4322293	SRA1045163	SRX7759343	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	112	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122345	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122345	GSM4322294	SRA1045163	SRX7759344	ATAC-seq	PAIRED	SRP250335	PRJNA607864
145619	113	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122346	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122346	GSM4322295	SRA1045163	SRX7759345	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	114	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122347	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122347	GSM4322296	SRA1045163	SRX7759346	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	115	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122348	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122348	GSM4322297	SRA1045163	SRX7759347	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	116	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122349	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122349	GSM4322298	SRA1045163	SRX7759348	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	117	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122350	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010861/SRR11122350	GSM4322299	SRA1045163	SRX7759349	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	118	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122351	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122351	GSM4322300	SRA1045163	SRX7759350	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	119	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122352	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122352	GSM4322301	SRA1045163	SRX7759351	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	120	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122353	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122353	GSM4322302	SRA1045163	SRX7759352	RNA-Seq	PAIRED	SRP250335	PRJNA607864
145619	121	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122403	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122403	GSM4322351	SRA1045163	SRX7759353	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	122	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122404	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122404	GSM4322352	SRA1045163	SRX7759354	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	123	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122405	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122405	GSM4322353	SRA1045163	SRX7759355	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	124	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122406	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/010861/SRR11122406	GSM4322354	SRA1045163	SRX7759356	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	125	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122407	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122407	GSM4322355	SRA1045163	SRX7759357	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	126	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122408	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122408	GSM4322356	SRA1045163	SRX7759358	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	127	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122409	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010861/SRR11122409	GSM4322357	SRA1045163	SRX7759359	RNA-Seq	SINGLE	SRP250335	PRJNA607864
145619	128	Ann Bright	Combinatorial action of transcription factors in open chromatin contributes to early cellular heterogeneity and organizer mesendoderm specification	We applied chromatin accessibility and single cell transcriptome analyses to explore the emergence of heterogeneity and underlying gene-regulatory mec	Ann Bright, Ann Bright, Siebe van Genesen, Qingqing Li, Alexia Grasso, Gert Veenstra	ATAC-seq on Xenopus embryos (stage 9, 10.5, 12 and 16) and gastrula stage embryo explants (Animal cap and Dorsal marginal zone). RNA-seq on animal caps overexpressed with Foxb1, Foxb1 + Eomes, Eomes, Irx3, Irx3 + Otx2 and Lhx8 mRNA. ScRNA-seq on Animal cap and Dorsal marginal zone explants	0	57688	SRP250335	SRR11122410	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/010861/SRR11122410	GSM4322358	SRA1045163	SRX7759360	RNA-Seq	SINGLE	SRP250335	PRJNA607864
146830	1	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292378	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/011027/SRR11292378	GSM4407619	SRA1054068	SRX7897943	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	2	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292379	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011027/SRR11292379	GSM4407620	SRA1054068	SRX7897944	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	3	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292380	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/011027/SRR11292380	GSM4407621	SRA1054068	SRX7897945	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	4	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292381	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/011027/SRR11292381	GSM4407622	SRA1054068	SRX7897946	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	5	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292382	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011027/SRR11292382	GSM4407623	SRA1054068	SRX7897947	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	6	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292383	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/011027/SRR11292383	GSM4407624	SRA1054068	SRX7897948	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	7	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292384	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/011027/SRR11292384	GSM4407625	SRA1054068	SRX7897949	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	8	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292385	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/011027/SRR11292385	GSM4407626	SRA1054068	SRX7897950	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	9	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292386	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/011027/SRR11292386	GSM4407627	SRA1054068	SRX7897951	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	10	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292387	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011027/SRR11292387	GSM4407628	SRA1054068	SRX7897952	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	11	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292388	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/011027/SRR11292388	GSM4407629	SRA1054068	SRX7897953	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	12	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292389	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/011027/SRR11292389	GSM4407630	SRA1054068	SRX7897954	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	13	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292390	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011027/SRR11292390	GSM4407631	SRA1054068	SRX7897955	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	14	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292391	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/011027/SRR11292391	GSM4407632	SRA1054068	SRX7897956	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	15	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292392	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/011027/SRR11292392	GSM4407633	SRA1054068	SRX7897957	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	16	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292393	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/011027/SRR11292393	GSM4407634	SRA1054068	SRX7897958	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	17	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292394	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/011027/SRR11292394	GSM4407635	SRA1054068	SRX7897959	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	18	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292395	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/011027/SRR11292395	GSM4407636	SRA1054068	SRX7897960	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	19	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292396	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/011027/SRR11292396	GSM4407637	SRA1054068	SRX7897961	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	20	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292397	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/011027/SRR11292397	GSM4407638	SRA1054068	SRX7897962	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	21	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292398	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/011027/SRR11292398	GSM4407639	SRA1054068	SRX7897963	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	22	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292399	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011027/SRR11292399	GSM4407640	SRA1054068	SRX7897964	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	23	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292400	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011027/SRR11292400	GSM4407641	SRA1054068	SRX7897965	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	24	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292401	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/011027/SRR11292401	GSM4407642	SRA1054068	SRX7897966	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	25	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292402	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011027/SRR11292402	GSM4407643	SRA1054068	SRX7897967	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	26	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292403	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011027/SRR11292403	GSM4407644	SRA1054068	SRX7897968	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	27	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292404	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011027/SRR11292404	GSM4407645	SRA1054068	SRX7897969	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	28	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292405	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/011027/SRR11292405	GSM4407646	SRA1054068	SRX7897970	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	29	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292406	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/011027/SRR11292406	GSM4407647	SRA1054068	SRX7897971	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	30	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292407	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/011027/SRR11292407	GSM4407648	SRA1054068	SRX7897972	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146830	31	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, Kakebeen Anneke, Chitsazan Alex	Investigation of chromatin accessiblity dynamics in neural progenitor cells over the course of tadpole tail regeneration	0	56933	SRP252458	SRR11292408	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/011027/SRR11292408	GSM4407649	SRA1054068	SRX7897973	ATAC-seq	PAIRED	SRP252458	PRJNA612063
146836	1	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, A Kakebeen, A Wills	Single-cell RNA-seq experiments were performed on the 10X Genom+D:Dics platform from FAC sorted, pax6:GFP positive cells from uninjured stage 41 Xenopus tropicalis tadpoles and 24 hours post amputation regenerated tail tissue.	0	56933	SRP252466	SRR11292562	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/011027/SRR11292562	GSM4407688	SRA1054090	SRX7898127	RNA-Seq	PAIRED	SRP252466	PRJNA612070
146836	2	Anneke Kakebeen	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors	Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation 	Anneke Kakebeen, A Kakebeen, A Wills	Single-cell RNA-seq experiments were performed on the 10X Genom+D:Dics platform from FAC sorted, pax6:GFP positive cells from uninjured stage 41 Xenopus tropicalis tadpoles and 24 hours post amputation regenerated tail tissue.	0	56933	SRP252466	SRR11292563	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011027/SRR11292563	GSM4407689	SRA1054090	SRX7898128	RNA-Seq	PAIRED	SRP252466	PRJNA612070
147621	1	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432510	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011164/SRR11432510	GSM4435518	SRA1059860	SRX8010722	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	2	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432511	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432511	GSM4435519	SRA1059860	SRX8010723	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	3	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432512	https://sra-download.ncbi.nlm.nih.gov/traces/sra79/SRR/011164/SRR11432512	GSM4435520	SRA1059860	SRX8010724	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	4	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432513	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432513	GSM4435521	SRA1059860	SRX8010725	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	5	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432514	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011164/SRR11432514	GSM4435522	SRA1059860	SRX8010726	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	6	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432515	https://sra-download.ncbi.nlm.nih.gov/traces/sra79/SRR/011164/SRR11432515	GSM4435523	SRA1059860	SRX8010727	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	7	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432516	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432516	GSM4435524	SRA1059860	SRX8010728	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	8	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432517	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432517	GSM4435525	SRA1059860	SRX8010729	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	9	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432518	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432518	GSM4435526	SRA1059860	SRX8010730	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	10	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432519	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011164/SRR11432519	GSM4435527	SRA1059860	SRX8010731	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	11	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432520	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/011164/SRR11432520	GSM4435528	SRA1059860	SRX8010732	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	12	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432521	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432521	GSM4435529	SRA1059860	SRX8010733	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	13	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432522	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432522	GSM4435530	SRA1059860	SRX8010734	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	14	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432523	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432523	GSM4435531	SRA1059860	SRX8010735	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	15	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432524	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432524	GSM4435532	SRA1059860	SRX8010736	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	16	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432525	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432525	GSM4435533	SRA1059860	SRX8010737	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	17	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432526	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432526	GSM4435534	SRA1059860	SRX8010738	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	18	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432527	https://sra-download.ncbi.nlm.nih.gov/traces/sra79/SRR/011164/SRR11432527	GSM4435535	SRA1059860	SRX8010739	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	19	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432528	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432528	GSM4435536	SRA1059860	SRX8010740	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	20	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432529	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/011164/SRR11432529	GSM4435537	SRA1059860	SRX8010741	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	21	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432530	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432530	GSM4435538	SRA1059860	SRX8010742	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	22	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432531	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432531	GSM4435539	SRA1059860	SRX8010743	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	23	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432532	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011164/SRR11432532	GSM4435540	SRA1059860	SRX8010744	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	24	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432533	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432533	GSM4435541	SRA1059860	SRX8010745	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	25	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432534	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432534	GSM4435542	SRA1059860	SRX8010746	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	26	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432535	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/011164/SRR11432535	GSM4435543	SRA1059860	SRX8010747	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	27	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432536	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432536	GSM4435544	SRA1059860	SRX8010748	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	28	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432537	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432537	GSM4435545	SRA1059860	SRX8010749	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	29	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432538	https://sra-download.ncbi.nlm.nih.gov/traces/sra30/SRR/011164/SRR11432538	GSM4435546	SRA1059860	SRX8010750	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	30	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432539	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011164/SRR11432539	GSM4435547	SRA1059860	SRX8010751	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	31	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432540	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/011164/SRR11432540	GSM4435548	SRA1059860	SRX8010752	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	32	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432541	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432541	GSM4435549	SRA1059860	SRX8010753	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	33	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432542	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432542	GSM4435550	SRA1059860	SRX8010754	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	34	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432543	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432543	GSM4435551	SRA1059860	SRX8010755	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	35	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432544	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432544	GSM4435552	SRA1059860	SRX8010756	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	36	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432545	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432545	GSM4435553	SRA1059860	SRX8010757	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	37	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432546	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432546	GSM4435554	SRA1059860	SRX8010758	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	38	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432547	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011164/SRR11432547	GSM4435555	SRA1059860	SRX8010759	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	39	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432548	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432548	GSM4435556	SRA1059860	SRX8010760	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	40	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432549	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011164/SRR11432549	GSM4435557	SRA1059860	SRX8010761	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	41	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432550	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011164/SRR11432550	GSM4435558	SRA1059860	SRX8010762	RNA-Seq	PAIRED	SRP254296	PRJNA615819
147621	42	Paul Huber	Proteomic and Transcriptomic Analysis of Neural Cell Fate in Developing Xenopus laevis Embryos and Explants	Purpose: Study the developing neural cell fate of the D1 blastomere in the 8-cell embryo. Determine what transcripts are dependant on cell/cell signal	Paul Huber, Kyle Dubiak, Paul Huber	Dissect tissue or explant mRNA profiles at 7 critical developmental timepoints, in triplicate, using Illumina NextSeq.	0	60223	SRP254296	SRR11432551	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011164/SRR11432551	GSM4435559	SRA1059860	SRX8010763	RNA-Seq	PAIRED	SRP254296	PRJNA615819
148726	1	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549523	https://sra-download.ncbi.nlm.nih.gov/traces/sra80/SRR/011278/SRR11549523	GSM4477737	SRA1065608	SRX8119313	ChIP-Seq	SINGLE	SRP256469	PRJNA625510
148726	2	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549524	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011278/SRR11549524	GSM4477738	SRA1065608	SRX8119314	ChIP-Seq	SINGLE	SRP256469	PRJNA625510
148726	3	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549525	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/011278/SRR11549525	GSM4477739	SRA1065608	SRX8119315	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	4	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549526	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/011278/SRR11549526	GSM4477740	SRA1065608	SRX8119316	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	5	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549527	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/011278/SRR11549527	GSM4477741	SRA1065608	SRX8119317	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	6	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549528	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/011278/SRR11549528	GSM4477742	SRA1065608	SRX8119318	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	7	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549529	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/011278/SRR11549529	GSM4477743	SRA1065608	SRX8119319	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	8	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549530	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/011278/SRR11549530	GSM4477744	SRA1065608	SRX8119320	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	9	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549531	https://sra-download.ncbi.nlm.nih.gov/traces/sra72/SRR/011278/SRR11549531	GSM4477745	SRA1065608	SRX8119321	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	10	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549532	https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/011278/SRR11549532	GSM4477746	SRA1065608	SRX8119322	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	11	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549533	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/011278/SRR11549533	GSM4477747	SRA1065608	SRX8119323	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	12	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549534	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/011278/SRR11549534	GSM4477748	SRA1065608	SRX8119324	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	13	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549535	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/011278/SRR11549535	GSM4477749	SRA1065608	SRX8119325	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	14	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549536	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/011278/SRR11549536	GSM4477750	SRA1065608	SRX8119326	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	15	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549537	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/011278/SRR11549537	GSM4477751	SRA1065608	SRX8119327	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	16	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549538	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011278/SRR11549538	GSM4477752	SRA1065608	SRX8119328	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	17	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549539	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/011278/SRR11549539	GSM4477753	SRA1065608	SRX8119329	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	18	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549540	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/011278/SRR11549540	GSM4477754	SRA1065608	SRX8119330	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	19	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549541	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/011278/SRR11549541	GSM4477755	SRA1065608	SRX8119331	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	20	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549542	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/011278/SRR11549542	GSM4477756	SRA1065608	SRX8119332	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	21	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549543	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/011278/SRR11549543	GSM4477757	SRA1065608	SRX8119333	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	22	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549544	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/011278/SRR11549544	GSM4477758	SRA1065608	SRX8119334	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	23	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549545	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/011278/SRR11549545	GSM4477759	SRA1065608	SRX8119335	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	24	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549546	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011278/SRR11549546	GSM4477760	SRA1065608	SRX8119336	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	25	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549547	https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/011278/SRR11549547	GSM4477761	SRA1065608	SRX8119337	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	26	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549548	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/011278/SRR11549548	GSM4477762	SRA1065608	SRX8119338	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	27	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549549	https://sra-download.ncbi.nlm.nih.gov/traces/sra61/SRR/011278/SRR11549549	GSM4477763	SRA1065608	SRX8119339	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	28	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549550	https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/011278/SRR11549550	GSM4477764	SRA1065608	SRX8119340	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	29	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549551	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/011278/SRR11549551	GSM4477765	SRA1065608	SRX8119341	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	30	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549552	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/011278/SRR11549552	GSM4477766	SRA1065608	SRX8119342	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	31	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549553	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/011278/SRR11549553	GSM4477767	SRA1065608	SRX8119343	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	32	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549554	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011278/SRR11549554	GSM4477768	SRA1065608	SRX8119344	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	33	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549555	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/011278/SRR11549555	GSM4477769	SRA1065608	SRX8119345	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	34	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549556	https://sra-download.ncbi.nlm.nih.gov/traces/sra16/SRR/011278/SRR11549556	GSM4477770	SRA1065608	SRX8119346	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	35	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549557	https://sra-download.ncbi.nlm.nih.gov/traces/sra80/SRR/011278/SRR11549557	GSM4477771	SRA1065608	SRX8119347	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	36	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549558	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/011278/SRR11549558	GSM4477772	SRA1065608	SRX8119348	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	37	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549559	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/011278/SRR11549559	GSM4477773	SRA1065608	SRX8119349	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	38	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549560	https://sra-download.ncbi.nlm.nih.gov/traces/sra80/SRR/011278/SRR11549560	GSM4477774	SRA1065608	SRX8119350	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	39	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549561	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/011278/SRR11549561	GSM4477775	SRA1065608	SRX8119351	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	40	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549562	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/011278/SRR11549562	GSM4477776	SRA1065608	SRX8119352	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	41	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549563	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/011278/SRR11549563	GSM4477777	SRA1065608	SRX8119353	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	42	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549564	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/011278/SRR11549564	GSM4477778	SRA1065608	SRX8119354	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	43	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549565	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/011278/SRR11549565	GSM4477779	SRA1065608	SRX8119355	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	44	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549566	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011278/SRR11549566	GSM4477780	SRA1065608	SRX8119356	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	45	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549567	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/011278/SRR11549567	GSM4477781	SRA1065608	SRX8119357	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	46	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549568	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/011278/SRR11549568	GSM4477782	SRA1065608	SRX8119358	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	47	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549569	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/011278/SRR11549569	GSM4477783	SRA1065608	SRX8119359	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	48	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549570	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/011278/SRR11549570	GSM4477784	SRA1065608	SRX8119360	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	49	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549571	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/011278/SRR11549571	GSM4477785	SRA1065608	SRX8119361	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	50	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549572	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/011278/SRR11549572	GSM4477786	SRA1065608	SRX8119362	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	51	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549573	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/011278/SRR11549573	GSM4477787	SRA1065608	SRX8119363	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	52	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549574	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/011278/SRR11549574	GSM4477788	SRA1065608	SRX8119364	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	53	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549575	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/011278/SRR11549575	GSM4477789	SRA1065608	SRX8119365	RNA-Seq	SINGLE	SRP256469	PRJNA625510
148726	54	Kitt Paraiso	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endodermal gene regulatory network	We report the ChIP-seq analysis of Sox17 genome-wide binding and its loss-of-function transcriptomic analysis of both Sox17 and Ctnnb1 (beta-catenin) 	Kitt Paraiso, Kitt Paraiso, Aaron Zorn, Shreyasi Mukherjee	ChIP-seq was performed to detect endogenous Sox17 binding (N&F stage 10.5) and RNA-seq was used to assess gene expression changes in Sox17 (N&F stages 9, 9.5, 10, 10.5, 11, 12) or Ctnnb1 (N&F stages 7, 8, 9, 9.5, 10, 10.5, 11, 12) in morpholino antisense oligo injected versus uninjected control embryos	32894225	57340	SRP256469	SRR11549576	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/011278/SRR11549576	GSM4477790	SRA1065608	SRX8119366	RNA-Seq	SINGLE	SRP256469	PRJNA625510
149538	1	Arthur Willsey	Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos	DYRK1A (dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A) is a high confidence autism risk gene that encodes a conserved kinase. In 	Arthur Willsey, Helen Willsey, A Willsey	3 replicates each of 3 pooled dissected stage 46 X. tropicalis brains, either uninjected or bilaterally injected with CRISPR reagents targeting dyrk1a at the 2 cell stage. Trizol extracted RNA, low yield library preparation, and Illumina sequencing.	32467234	57038	SRP258988	SRR11635832	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/011363/SRR11635832	GSM4504552	SRA1070177	SRX8199916	RNA-Seq	PAIRED	SRP258988	PRJNA628999
149538	2	Arthur Willsey	Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos	DYRK1A (dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A) is a high confidence autism risk gene that encodes a conserved kinase. In 	Arthur Willsey, Helen Willsey, A Willsey	3 replicates each of 3 pooled dissected stage 46 X. tropicalis brains, either uninjected or bilaterally injected with CRISPR reagents targeting dyrk1a at the 2 cell stage. Trizol extracted RNA, low yield library preparation, and Illumina sequencing.	32467234	57038	SRP258988	SRR11635833	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/011363/SRR11635833	GSM4504553	SRA1070177	SRX8199917	RNA-Seq	PAIRED	SRP258988	PRJNA628999
149538	3	Arthur Willsey	Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos	DYRK1A (dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A) is a high confidence autism risk gene that encodes a conserved kinase. In 	Arthur Willsey, Helen Willsey, A Willsey	3 replicates each of 3 pooled dissected stage 46 X. tropicalis brains, either uninjected or bilaterally injected with CRISPR reagents targeting dyrk1a at the 2 cell stage. Trizol extracted RNA, low yield library preparation, and Illumina sequencing.	32467234	57038	SRP258988	SRR11635834	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/011363/SRR11635834	GSM4504554	SRA1070177	SRX8199918	RNA-Seq	PAIRED	SRP258988	PRJNA628999
149538	4	Arthur Willsey	Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos	DYRK1A (dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A) is a high confidence autism risk gene that encodes a conserved kinase. In 	Arthur Willsey, Helen Willsey, A Willsey	3 replicates each of 3 pooled dissected stage 46 X. tropicalis brains, either uninjected or bilaterally injected with CRISPR reagents targeting dyrk1a at the 2 cell stage. Trizol extracted RNA, low yield library preparation, and Illumina sequencing.	32467234	57038	SRP258988	SRR11635835	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/011363/SRR11635835	GSM4504555	SRA1070177	SRX8199919	RNA-Seq	PAIRED	SRP258988	PRJNA628999
149538	5	Arthur Willsey	Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos	DYRK1A (dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A) is a high confidence autism risk gene that encodes a conserved kinase. In 	Arthur Willsey, Helen Willsey, A Willsey	3 replicates each of 3 pooled dissected stage 46 X. tropicalis brains, either uninjected or bilaterally injected with CRISPR reagents targeting dyrk1a at the 2 cell stage. Trizol extracted RNA, low yield library preparation, and Illumina sequencing.	32467234	57038	SRP258988	SRR11635836	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/011363/SRR11635836	GSM4504556	SRA1070177	SRX8199914	RNA-Seq	PAIRED	SRP258988	PRJNA628999
149538	6	Arthur Willsey	Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos	DYRK1A (dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A) is a high confidence autism risk gene that encodes a conserved kinase. In 	Arthur Willsey, Helen Willsey, A Willsey	3 replicates each of 3 pooled dissected stage 46 X. tropicalis brains, either uninjected or bilaterally injected with CRISPR reagents targeting dyrk1a at the 2 cell stage. Trizol extracted RNA, low yield library preparation, and Illumina sequencing.	32467234	57038	SRP258988	SRR11635837	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/011363/SRR11635837	GSM4504557	SRA1070177	SRX8199915	RNA-Seq	PAIRED	SRP258988	PRJNA628999
150911	1	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816742	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/011539/SRR11816742	GSM4560793	SRA1077321	SRX8367761	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	2	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816743	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/011539/SRR11816743	GSM4560794	SRA1077321	SRX8367762	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	3	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816744	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/011539/SRR11816744	GSM4560795	SRA1077321	SRX8367763	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	4	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816745	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/011539/SRR11816745	GSM4560796	SRA1077321	SRX8367743	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	5	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816746	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/011539/SRR11816746	GSM4560797	SRA1077321	SRX8367744	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	6	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816747	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/011539/SRR11816747	GSM4560798	SRA1077321	SRX8367745	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	7	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816748	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/011539/SRR11816748	GSM4560799	SRA1077321	SRX8367746	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	8	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816749	https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRR/011539/SRR11816749	GSM4560800	SRA1077321	SRX8367747	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	9	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816750	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/011539/SRR11816750	GSM4560801	SRA1077321	SRX8367748	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	10	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816751	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011539/SRR11816751	GSM4560802	SRA1077321	SRX8367749	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	11	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816752	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/011539/SRR11816752	GSM4560803	SRA1077321	SRX8367750	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	12	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816753	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011539/SRR11816753	GSM4560804	SRA1077321	SRX8367751	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	13	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816754	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/011539/SRR11816754	GSM4560805	SRA1077321	SRX8367752	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	14	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816755	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/011539/SRR11816755	GSM4560806	SRA1077321	SRX8367753	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	15	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816756	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/011539/SRR11816756	GSM4560807	SRA1077321	SRX8367754	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	16	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816757	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011539/SRR11816757	GSM4560808	SRA1077321	SRX8367755	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	17	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816758	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/011539/SRR11816758	GSM4560809	SRA1077321	SRX8367756	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	18	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816738	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/011539/SRR11816738	GSM4560810	SRA1077321	SRX8367757	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	19	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816739	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/011539/SRR11816739	GSM4560811	SRA1077321	SRX8367758	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	20	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816740	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/011539/SRR11816740	GSM4560812	SRA1077321	SRX8367759	RNA-Seq	SINGLE	SRP262433	PRJNA634073
150911	21	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene exposure (F0 generation) in Xenopus tropicalis	We investigated the multi- and transgenerational impact of BaP on Xenopus females following F0 generation exposure from the tadpole to the mature adul	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females.	33234375	57563	SRP262433	SRR11816741	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/011539/SRR11816741	GSM4560813	SRA1077321	SRX8367760	RNA-Seq	SINGLE	SRP262433	PRJNA634073
152902	1	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060513	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/011777/SRR12060513	GSM4629156	SRA1089346	SRX8588692	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	2	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060514	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/011777/SRR12060514	GSM4629157	SRA1089346	SRX8588693	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	3	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060515	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/011777/SRR12060515	GSM4629158	SRA1089346	SRX8588694	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	4	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060516	https://sra-download.ncbi.nlm.nih.gov/traces/sra56/SRR/011777/SRR12060516	GSM4629159	SRA1089346	SRX8588695	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	5	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060517	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/011777/SRR12060517	GSM4629160	SRA1089346	SRX8588696	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	6	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060518	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/011777/SRR12060518	GSM4629161	SRA1089346	SRX8588697	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	7	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060519	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/011777/SRR12060519	GSM4629162	SRA1089346	SRX8588698	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	8	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060520	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/011777/SRR12060520	GSM4629163	SRA1089346	SRX8588699	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	9	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060521	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/011777/SRR12060521	GSM4629164	SRA1089346	SRX8588700	RNA-Seq	PAIRED	SRP268142	PRJNA640808
152902	10	Miler Lee	Optimized design of antisense oligomers for targeted RNA depletion	RNA sequencing (RNA-seq) has become a standard method for quantifying gene expression transcriptome-wide. Due to the extremely high proportion of ribo	Miler Lee, Wesley Phelps	RNA-seq with different mRNA enrichment methods	33221877	57554	SRP268142	SRR12060522	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/011777/SRR12060522	GSM4629165	SRA1089346	SRX8588701	RNA-Seq	PAIRED	SRP268142	PRJNA640808
153058	1	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075263	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/011792/SRR12075263	GSM4633643	SRA1090230	SRX8602695	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	2	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075264	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/011792/SRR12075264	GSM4633644	SRA1090230	SRX8602696	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	3	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075265	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/011792/SRR12075265	GSM4633645	SRA1090230	SRX8602697	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	4	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075266	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/011792/SRR12075266	GSM4633646	SRA1090230	SRX8602698	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	5	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075267	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/011792/SRR12075267	GSM4633647	SRA1090230	SRX8602699	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	6	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075268	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/011792/SRR12075268	GSM4633648	SRA1090230	SRX8602700	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	7	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075269	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/011792/SRR12075269	GSM4633649	SRA1090230	SRX8602701	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	8	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075270	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/011792/SRR12075270	GSM4633650	SRA1090230	SRX8602702	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	9	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075271	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/011792/SRR12075271	GSM4633651	SRA1090230	SRX8602703	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	10	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075272	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/011792/SRR12075272	GSM4633652	SRA1090230	SRX8602704	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	11	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075273	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/011792/SRR12075273	GSM4633653	SRA1090230	SRX8602705	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	12	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075274	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/011792/SRR12075274	GSM4633654	SRA1090230	SRX8602706	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	13	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075275	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/011792/SRR12075275	GSM4633655	SRA1090230	SRX8602707	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	14	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075276	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/011792/SRR12075276	GSM4633656	SRA1090230	SRX8602708	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153058	15	Owen Smith	Identification and characterization of centromeric sequences in Xenopus laevis	Centromeres play an essential role in cell division by specifying the site of kinetochore formation on each chromosome so that chromosomes can attach 	Owen Smith, Owen Smith, Charles Limouse, Kelsey Fryer, Nikki Teran, Kousik Sundararajan, Rebecca Heals, Aaron Straight	four replicates each of native Mnase ChIP-seq from CENP-A and H4 Ips, along with input seqeuncing libraries were sequenced on Illumina MiSeq. One replicate of each was further sequenced on Illumina HiSeq	0	57139	SRP268455	SRR12075277	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/011792/SRR12075277	GSM4633657	SRA1090230	SRX8602709	ChIP-Seq	SINGLE	SRP268455	PRJNA641345
153925	1	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162974	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162974/SRR12162974.1	GSM4658472	SRA1095739	SRX8678465	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	2	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162975	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162975/SRR12162975.1	GSM4658473	SRA1095739	SRX8678466	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	3	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162976	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162976/SRR12162976.1	GSM4658474	SRA1095739	SRX8678467	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	4	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162977	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162977/SRR12162977.1	GSM4658475	SRA1095739	SRX8678468	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	5	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162978	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162978/SRR12162978.1	GSM4658476	SRA1095739	SRX8678469	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	6	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162979	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162979/SRR12162979.1	GSM4658477	SRA1095739	SRX8678470	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	7	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162980	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162980/SRR12162980.1	GSM4658478	SRA1095739	SRX8678471	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	8	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162981	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162981/SRR12162981.1	GSM4658479	SRA1095739	SRX8678472	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	9	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162982	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162982/SRR12162982.1	GSM4658480	SRA1095739	SRX8678473	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	10	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162983	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162983/SRR12162983.1	GSM4658481	SRA1095739	SRX8678474	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	11	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162984	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162984/SRR12162984.1	GSM4658482	SRA1095739	SRX8678475	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	12	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162985	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162985/SRR12162985.1	GSM4658483	SRA1095739	SRX8678476	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	13	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162986	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162986/SRR12162986.1	GSM4658484	SRA1095739	SRX8678477	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	14	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162987	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162987/SRR12162987.1	GSM4658485	SRA1095739	SRX8678478	RNA-Seq	PAIRED	SRP270638	PRJNA644555
153925	15	Jun-Dal Kim	Comprehensive expression profile reveals dynamic changes in Xenopus gene expression depending on the duration of activin A treatment.	In amphibian embryo, the animal cap explants treated with activin A, which is a member of TGF-β family protein, have a potent of Spemann-Mangold orga	Jun-Dal Kim, Yumeko Kobayashi, Makoto Asashima, Akiyoshi Fukamizu	Time-course RNA expression data from Xenopus animal cap treated with activin A. mRNA profiles of animal caps were generated by RNA sequencing using the NextSeq 500 (Illumina).	34267234	58287	SRP270638	SRR12162988	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR12162988/SRR12162988.1	GSM4658486	SRA1095739	SRX8678479	RNA-Seq	PAIRED	SRP270638	PRJNA644555
154399	1	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224382	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224382/SRR10224382.1	A_0.5%_ETOH_t_0hr	SRA972085	SRX6943936	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	2	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224338	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224338/SRR10224338.1	A_0.5%_ETOH_t_1.5hr	SRA972085	SRX6943980	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	3	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224402	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224402/SRR10224402.1	A_0.5%_ETOH_t_3hr	SRA972085	SRX6943916	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	4	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224398	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224398/SRR10224398.1	A_0.5%_ETOH_t_4.5hr	SRA972085	SRX6943920	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	5	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224404	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224404/SRR10224404.1	A_10nM_RA_t_0hr	SRA972085	SRX6943914	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	6	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224360	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224360/SRR10224360.1	A_10nM_RA_t_1.5hr	SRA972085	SRX6943958	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	7	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224316	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224316/SRR10224316.1	A_10nM_RA_t_3hr	SRA972085	SRX6944002	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	8	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224400	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224400/SRR10224400.1	A_10nM_RA_t_4.5hr	SRA972085	SRX6943918	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	9	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224393	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224393/SRR10224393.1	A_50uM_DEAB_t_0hr	SRA972085	SRX6943925	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	10	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224349	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224349/SRR10224349.1	A_50uM_DEAB_t_1.5hr	SRA972085	SRX6943969	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	11	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224403	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224403/SRR10224403.1	A_50uM_DEAB_t_3hr	SRA972085	SRX6943915	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	12	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224399	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224399/SRR10224399.1	A_50uM_DEAB_t_4.5hr	SRA972085	SRX6943919	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	13	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224405	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224405/SRR10224405.1	A_control_t_0hr	SRA972085	SRX6943913	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	14	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224371	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224371/SRR10224371.1	A_control_t_1.5hr	SRA972085	SRX6943947	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	15	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224327	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224327/SRR10224327.1	A_control_t_3hr	SRA972085	SRX6943991	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	16	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224401	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224401/SRR10224401.1	A_control_t_4.5hr	SRA972085	SRX6943917	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	17	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224394	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224394/SRR10224394.1	B_0.5%_ETOH_t_0hr	SRA972085	SRX6943924	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	18	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224389	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224389/SRR10224389.1	B_0.5%_ETOH_t_1.5hr	SRA972085	SRX6943929	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	19	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224385	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224385/SRR10224385.1	B_0.5%_ETOH_t_3hr	SRA972085	SRX6943933	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	20	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224380	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224380/SRR10224380.1	B_0.5%_ETOH_t_4.5hr	SRA972085	SRX6943938	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	21	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224396	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224396/SRR10224396.1	B_10nM_RA_t_0hr	SRA972085	SRX6943922	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	22	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224391	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224391/SRR10224391.1	B_10nM_RA_t_1.5hr	SRA972085	SRX6943927	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	23	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224387	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224387/SRR10224387.1	B_10nM_RA_t_3hr	SRA972085	SRX6943931	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	24	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224383	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224383/SRR10224383.1	B_10nM_RA_t_4.5hr	SRA972085	SRX6943935	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	25	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224395	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224395/SRR10224395.1	B_50uM_DEAB_t_0hr	SRA972085	SRX6943923	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	26	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224390	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224390/SRR10224390.1	B_50uM_DEAB_t_1.5hr	SRA972085	SRX6943928	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	27	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224386	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224386/SRR10224386.1	B_50uM_DEAB_t_3hr	SRA972085	SRX6943932	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	28	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224381	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224381/SRR10224381.1	B_50uM_DEAB_t_4.5hr	SRA972085	SRX6943937	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	29	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224397	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224397/SRR10224397.1	B_control_t_0hr	SRA972085	SRX6943921	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	30	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224392	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224392/SRR10224392.1	B_control_t_1.5hr	SRA972085	SRX6943926	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	31	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224388	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224388/SRR10224388.1	B_control_t_3hr	SRA972085	SRX6943930	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	32	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224384	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224384/SRR10224384.1	B_control_t_4.5hr	SRA972085	SRX6943934	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	33	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224376	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224376/SRR10224376.1	C_0.5%_ETOH_t_0hr	SRA972085	SRX6943942	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	34	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224372	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224372/SRR10224372.1	C_0.5%_ETOH_t_1.5hr	SRA972085	SRX6943946	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	35	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224367	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224367/SRR10224367.1	C_0.5%_ETOH_t_3hr	SRA972085	SRX6943951	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	36	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224363	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224363/SRR10224363.1	C_0.5%_ETOH_t_4.5hr	SRA972085	SRX6943955	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	37	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224378	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224378/SRR10224378.1	C_10nM_RA_t_0hr	SRA972085	SRX6943940	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	38	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224374	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224374/SRR10224374.1	C_10nM_RA_t_1.5hr	SRA972085	SRX6943944	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	39	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224369	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224369/SRR10224369.1	C_10nM_RA_t_3hr	SRA972085	SRX6943949	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	40	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224365	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224365/SRR10224365.1	C_10nM_RA_t_4.5hr	SRA972085	SRX6943953	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	41	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224377	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224377/SRR10224377.1	C_50uM_DEAB_t_0hr	SRA972085	SRX6943941	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	42	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224373	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224373/SRR10224373.1	C_50uM_DEAB_t_1.5hr	SRA972085	SRX6943945	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	43	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224368	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224368/SRR10224368.1	C_50uM_DEAB_t_3hr	SRA972085	SRX6943950	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	44	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224364	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224364/SRR10224364.1	C_50uM_DEAB_t_4.5hr	SRA972085	SRX6943954	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	45	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224379	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224379/SRR10224379.1	C_control_t_0hr	SRA972085	SRX6943939	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	46	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224375	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224375/SRR10224375.1	C_control_t_1.5hr	SRA972085	SRX6943943	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	47	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224370	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224370/SRR10224370.1	C_control_t_3hr	SRA972085	SRX6943948	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	48	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224366	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224366/SRR10224366.1	C_control_t_4.5hr	SRA972085	SRX6943952	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	49	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224358	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224358/SRR10224358.1	D_0.5%_ETOH_t_0hr	SRA972085	SRX6943960	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	50	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224354	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224354/SRR10224354.1	D_0.5%_ETOH_t_1.5hr	SRA972085	SRX6943964	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	51	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224350	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224350/SRR10224350.1	D_0.5%_ETOH_t_3hr	SRA972085	SRX6943968	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	52	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224345	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224345/SRR10224345.1	D_0.5%_ETOH_t_4.5hr	SRA972085	SRX6943973	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	53	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224361	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224361/SRR10224361.1	D_10nM_RA_t_0hr	SRA972085	SRX6943957	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	54	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224356	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224356/SRR10224356.1	D_10nM_RA_t_1.5hr	SRA972085	SRX6943962	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	55	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224352	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224352/SRR10224352.1	D_10nM_RA_t_3hr	SRA972085	SRX6943966	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	56	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224347	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224347/SRR10224347.1	D_10nM_RA_t_4.5hr	SRA972085	SRX6943971	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	57	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224359	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224359/SRR10224359.1	D_50uM_DEAB_t_0hr	SRA972085	SRX6943959	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	58	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224355	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224355/SRR10224355.1	D_50uM_DEAB_t_1.5hr	SRA972085	SRX6943963	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	59	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224351	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224351/SRR10224351.1	D_50uM_DEAB_t_3hr	SRA972085	SRX6943967	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	60	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224346	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224346/SRR10224346.1	D_50uM_DEAB_t_4.5hr	SRA972085	SRX6943972	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	61	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224362	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224362/SRR10224362.1	D_control_t_0hr	SRA972085	SRX6943956	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	62	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224357	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224357/SRR10224357.1	D_control_t_1.5hr	SRA972085	SRX6943961	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	63	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224353	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224353/SRR10224353.1	D_control_t_3hr	SRA972085	SRX6943965	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	64	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224348	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224348/SRR10224348.1	D_control_t_4.5hr	SRA972085	SRX6943970	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	65	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224341	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224341/SRR10224341.1	E_0.5%_ETOH_t_0hr	SRA972085	SRX6943977	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	66	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224336	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224336/SRR10224336.1	E_0.5%_ETOH_t_1.5hr	SRA972085	SRX6943982	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	67	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224332	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224332/SRR10224332.1	E_0.5%_ETOH_t_3hr	SRA972085	SRX6943986	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	68	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224328	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224328/SRR10224328.1	E_0.5%_ETOH_t_4.5hr	SRA972085	SRX6943990	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	69	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224343	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224343/SRR10224343.1	E_10nM_RA_t_0hr	SRA972085	SRX6943975	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	70	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224339	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224339/SRR10224339.1	E_10nM_RA_t_1.5hr	SRA972085	SRX6943979	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	71	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224334	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224334/SRR10224334.1	E_10nM_RA_t_3hr	SRA972085	SRX6943984	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	72	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224330	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224330/SRR10224330.1	E_10nM_RA_t_4.5hr	SRA972085	SRX6943988	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	73	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224342	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224342/SRR10224342.1	E_50uM_DEAB_t_0hr	SRA972085	SRX6943976	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	74	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224337	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224337/SRR10224337.1	E_50uM_DEAB_t_1.5hr	SRA972085	SRX6943981	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	75	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224333	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224333/SRR10224333.1	E_50uM_DEAB_t_3hr	SRA972085	SRX6943985	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	76	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224329	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224329/SRR10224329.1	E_50uM_DEAB_t_4.5hr	SRA972085	SRX6943989	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	77	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224344	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224344/SRR10224344.1	E_control_t_0hr	SRA972085	SRX6943974	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	78	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224340	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224340/SRR10224340.1	E_control_t_1.5hr	SRA972085	SRX6943978	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	79	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224335	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224335/SRR10224335.1	E_control_t_3hr	SRA972085	SRX6943983	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	80	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224331	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224331/SRR10224331.1	E_control_t_4.5hr	SRA972085	SRX6943987	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	81	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224323	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224323/SRR10224323.1	F_0.5%_ETOH_t_0hr	SRA972085	SRX6943995	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	82	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224319	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224319/SRR10224319.1	F_0.5%_ETOH_t_1.5hr	SRA972085	SRX6943999	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	83	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224314	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224314/SRR10224314.1	F_0.5%_ETOH_t_3hr	SRA972085	SRX6944004	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	84	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224310	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224310/SRR10224310.1	F_0.5%_ETOH_t_4.5hr	SRA972085	SRX6944008	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	85	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224325	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224325/SRR10224325.1	F_10nM_RA_t_0hr	SRA972085	SRX6943993	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	86	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224321	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224321/SRR10224321.1	F_10nM_RA_t_1.5hr	SRA972085	SRX6943997	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	87	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224317	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224317/SRR10224317.1	F_10nM_RA_t_3hr	SRA972085	SRX6944001	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	88	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224312	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224312/SRR10224312.1	F_10nM_RA_t_4.5hr	SRA972085	SRX6944006	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	89	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224324	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224324/SRR10224324.1	F_50uM_DEAB_t_0hr	SRA972085	SRX6943994	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	90	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224320	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224320/SRR10224320.1	F_50uM_DEAB_t_1.5hr	SRA972085	SRX6943998	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	91	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224315	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224315/SRR10224315.1	F_50uM_DEAB_t_3hr	SRA972085	SRX6944003	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	92	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224311	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224311/SRR10224311.1	F_50uM_DEAB_t_4.5hr	SRA972085	SRX6944007	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	93	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224326	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224326/SRR10224326.1	F_control_t_0hr	SRA972085	SRX6943992	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	94	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224322	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-19/SRR10224322/SRR10224322.1	F_control_t_1.5hr	SRA972085	SRX6943996	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	95	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224318	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-21/SRR10224318/SRR10224318.1	F_control_t_3hr	SRA972085	SRX6944000	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154399	96	Rajanikanth Vadigepalli	Robustness of retinoic acid regulatory homeostasis during early development (RNA-seq)	Retinoic acid (RA) is a central developmental signal whose perturbation results in teratogenic outcomes. RA are tightly regulated during early embryon	Rajanikanth Vadigepalli, Madhur Parihar, Liat Bendelac-Kapon, Michal Gur, Abha Belorkar, Keren Kinberg, Abraham Fainsod	We considered multiple experimental perturbations including exogenous addition of 10 nM RA, inhibition of RA production by 50 uM DEAB (an inhibitor of RALDH2 enzyme), 0.5% ethanol exposure, and no exposure control. We obtained data from six independent clutches for each experimental condition. The embryos were isolated at multiple time points (t=0, 1.5, 3, and 4.5 hours) following two hours of perturbation and a wash.	34746144	58611	SRP224065	SRR10224313	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos3/sra-pub-run-20/SRR10224313/SRR10224313.1	F_control_t_4.5hr	SRA972085	SRX6944005	RNA-Seq	PAIRED	SRP224065	PRJNA575640
154766	1	Chao Yang	Detection of RNAs binding to Vg1 RNP	We report the application of NGS for high-throughput profiling of transcripts assoicated with the ribonuleoprotein (RNP) formed on Vg1 mRNA  in oocyte	Chao Yang, Paul Huber	Biriefly, Biotinylated-Vg1 RNA was microinjected into Xenopus  oocyte to allow formation of RNP complex in vivo. Next, streptavidin beads were added to the oocyte extract to specificly pull down the biotin-Vg1 RNP. After extensive washes, biotin-Vg1 RNP were eluted off by incubating the beads with free biotin and the associted RNAs were extracted by phenol and precipitated by ethanol.For RNA sequencing strategy, a single RNA library was prepared and sequenced on an Illumina MiSeq nano 300 cycle reagent kit.	0	57689	SRP272643	SRR12271074	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/011983/SRR12271074	GSM4679353	SRA1100974	SRX8776133	RNA-Seq	PAIRED	SRP272643	PRJNA647395
154896	1	Sushant Bangru	Single-cell transcriptomic analysis reveals unique cell types and patterns of gene expression in the frog corneal epithelium.	Here, we use scRNA-seq to expand our understanding of the vertebrate corneal epithelium in an amphibian model, having undertaken a comprehensive chara	Sushant Bangru, Surabhi Sonam, John Henry	Adult Xenopus laevis were obtained from Nasco (Fort Atkinson, WI). Fertilized eggs were collected, and larvae were raised to Stage 49-51 based on developmental staging by Nieuwkoop and Faber (1956). The corneal epithelial tissue was dissected using very fine microscissors (Henry et al., 2019), taking care not to include any surrounding skin. Corneal tissue was dissociated and processed through the 10X pipeline, and we identified 5173 cells using Cellranger.	36049533	59307	SRP273066	SRR12287402	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/011999/SRR12287402	GSM4681962	SRA1102343	SRX8790735	RNA-Seq	PAIRED	SRP273066	PRJNA647844
155553	1	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368249	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/012078/SRR12368249	GSM4706047	SRA1106960	SRX8867433	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	2	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368250	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/012078/SRR12368250	GSM4706048	SRA1106960	SRX8867434	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	3	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368251	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/012078/SRR12368251	GSM4706049	SRA1106960	SRX8867435	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	4	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368252	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/012078/SRR12368252	GSM4706050	SRA1106960	SRX8867436	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	5	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368253	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/012078/SRR12368253	GSM4706051	SRA1106960	SRX8867437	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	6	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368254	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/012078/SRR12368254	GSM4706052	SRA1106960	SRX8867438	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	7	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368255	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/012078/SRR12368255	GSM4706053	SRA1106960	SRX8867439	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	8	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368256	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/012078/SRR12368256	GSM4706054	SRA1106960	SRX8867440	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	9	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368257	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/012078/SRR12368257	GSM4706055	SRA1106960	SRX8867441	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	10	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368258	https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/012078/SRR12368258	GSM4706056	SRA1106960	SRX8867442	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	11	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368259	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/012078/SRR12368259	GSM4706057	SRA1106960	SRX8867443	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	12	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368260	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/012078/SRR12368260	GSM4706058	SRA1106960	SRX8867444	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	13	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368261	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/012078/SRR12368261	GSM4706059	SRA1106960	SRX8867445	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	14	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368262	https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/012078/SRR12368262	GSM4706060	SRA1106960	SRX8867446	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	15	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368263	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/012078/SRR12368263	GSM4706061	SRA1106960	SRX8867447	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	16	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368264	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/012078/SRR12368264	GSM4706062	SRA1106960	SRX8867448	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	17	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368265	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/012078/SRR12368265	GSM4706063	SRA1106960	SRX8867449	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	18	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368266	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/012078/SRR12368266	GSM4706064	SRA1106960	SRX8867450	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	19	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368267	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/012078/SRR12368267	GSM4706065	SRA1106960	SRX8867451	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	20	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368268	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/012078/SRR12368268	GSM4706066	SRA1106960	SRX8867452	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	21	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368269	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/012078/SRR12368269	GSM4706067	SRA1106960	SRX8867453	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	22	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368270	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/012078/SRR12368270	GSM4706068	SRA1106960	SRX8867454	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	23	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368271	https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRR/012078/SRR12368271	GSM4706069	SRA1106960	SRX8867455	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	24	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368272	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/012078/SRR12368272	GSM4706070	SRA1106960	SRX8867456	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	25	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368273	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/012078/SRR12368273	GSM4706071	SRA1106960	SRX8867457	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	26	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368274	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/012078/SRR12368274	GSM4706072	SRA1106960	SRX8867458	RNA-Seq	PAIRED	SRP275563	PRJNA650290
155553	27	Arthur Willsey	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience [Xenopus]	Gene Ontology analyses of autism spectrum disorders (ASD) risk genes have repeatedly highlighted synaptic function and transcriptional regulation as k	Arthur Willsey, Helen Willsey, A Willsey	3 pooled stage 46 brains in triplicate. DMSO-treated samples are the controls.	33497602	57754	SRP275563	SRR12368275	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/012078/SRR12368275	GSM4706073	SRA1106960	SRX8867459	RNA-Seq	PAIRED	SRP275563	PRJNA650290
157915	1	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12638133	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/012341/SRR12638133	GSM4780720	SRA1125264	SRX9120190	RNA-Seq	PAIRED	SRP282347	PRJNA663331
157915	2	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12638134	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/012341/SRR12638134	GSM4780721	SRA1125264	SRX9120191	RNA-Seq	PAIRED	SRP282347	PRJNA663331
157915	3	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12992319	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/012687/SRR12992319	GSM4780722	SRA1125264	SRX9120192	RNA-Seq	PAIRED	SRP282347	PRJNA663331
157915	4	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12992320	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/012687/SRR12992320	GSM4780723	SRA1125264	SRX9120193	RNA-Seq	PAIRED	SRP282347	PRJNA663331
157915	5	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12638137	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/012341/SRR12638137	GSM4780724	SRA1125264	SRX9120194	RNA-Seq	PAIRED	SRP282347	PRJNA663331
157915	6	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12638138	https://sra-download.ncbi.nlm.nih.gov/traces/sra79/SRR/012341/SRR12638138	GSM4780725	SRA1125264	SRX9120195	RNA-Seq	PAIRED	SRP282347	PRJNA663331
157915	7	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12638139	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/012341/SRR12638139	GSM4780726	SRA1125264	SRX9120196	RNA-Seq	PAIRED	SRP282347	PRJNA663331
157915	8	Valerie Ducret	Transcriptomic analysis of the trade-off between endurance and burst-performance in the frog Xenopus allofraseri	Background: Variation in locomotor capacity among animals often reflects adaptations to different environments. Despite evidence that physical perform	Valerie Ducret, Adam Richards, Mathieu Videlier, Thibault Scalvenzi, Karen Moore, Konrad Paszkiewicz, Camille Bonneaud, Nicolas Pollet, Anthony Herrel	Differential expression analysis between four endurant and four burst-performant males	33757428	57943	SRP282347	SRR12638140	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/012341/SRR12638140	GSM4780727	SRA1125264	SRX9120197	RNA-Seq	PAIRED	SRP282347	PRJNA663331
158246	1	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676663	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/012379/SRR12676663	GSM4795812	SRA1128294	SRX9156828	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	2	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676664	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/012379/SRR12676664	GSM4795813	SRA1128294	SRX9156829	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	3	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676665	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/012379/SRR12676665	GSM4795814	SRA1128294	SRX9156830	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	4	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676666	https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/012379/SRR12676666	GSM4795815	SRA1128294	SRX9156831	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	5	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676667	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/012379/SRR12676667	GSM4795816	SRA1128294	SRX9156832	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	6	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676668	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/012379/SRR12676668	GSM4795817	SRA1128294	SRX9156833	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	7	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676669	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/012379/SRR12676669	GSM4795818	SRA1128294	SRX9156834	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	8	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676670	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/012379/SRR12676670	GSM4795819	SRA1128294	SRX9156835	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	9	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676671	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/012379/SRR12676671	GSM4795820	SRA1128294	SRX9156836	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	10	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676672	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/012379/SRR12676672	GSM4795821	SRA1128294	SRX9156837	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	11	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676673	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/012379/SRR12676673	GSM4795822	SRA1128294	SRX9156838	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158246	12	Kimberly Mowry	L-bodies are novel RNA-protein condensates driving RNA transport in Xenopus oocytes	RNP granules are membrane-less compartments within cells, formed by phase separation, that function as regulatory hubs for diverse biological processe	Kimberly Mowry, Christopher Neil, Samantha Jeschonek, Sarah Cabral, Liam O'Connell, Jessica Otis, Erin Powrie, Timothy Wood, Kimberly Mowry	4 replicates of 3 conditions were analyzed, the conditions being RNA collected after immunoprecipitating Xenopus oocyte lysates with different antibodies. The experimental conditions were precipitated with Staufen and hnRNPab antibodies and the control condition precipitated with IgG.	0	57691	SRP284001	SRR12676674	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/012379/SRR12676674	GSM4795823	SRA1128294	SRX9156839	RNA-Seq	PAIRED	SRP284001	PRJNA664513
158331	1	Anneke Kakebeen	Tissue disaggregation and isolation of specific cell types from transgenic Xenopus appendages for transcriptional analysis by FACS	Xenopus embryos and tadpoles are versatile models for embryological, cell biological, and regenerative studies. Genomic and transcriptomic approaches 	Anneke Kakebeen, Anneke Kakebeen, Alex Chitsazan	The posterior third of an anestitized tadpole tail was amputated at NF stage 41. Tadpoles were replaced in media without anesthetiz and allowed to regenerated until desired collection timepoint. The regenerated tail was isolated from the tadpole and cells were dissociated into single cell suspension using Liberase, washed in PBS and sorted for fluoresence through an Aria III cell sorter.	33137227	57511	SRP284834	SRR12691427	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/012393/SRR12691427	GSM4797960	SRA1129693	SRX9171385	ATAC-seq	PAIRED	SRP284834	PRJNA664919
158331	2	Anneke Kakebeen	Tissue disaggregation and isolation of specific cell types from transgenic Xenopus appendages for transcriptional analysis by FACS	Xenopus embryos and tadpoles are versatile models for embryological, cell biological, and regenerative studies. Genomic and transcriptomic approaches 	Anneke Kakebeen, Anneke Kakebeen, Alex Chitsazan	The posterior third of an anestitized tadpole tail was amputated at NF stage 41. Tadpoles were replaced in media without anesthetiz and allowed to regenerated until desired collection timepoint. The regenerated tail was isolated from the tadpole and cells were dissociated into single cell suspension using Liberase, washed in PBS and sorted for fluoresence through an Aria III cell sorter.	33137227	57511	SRP284834	SRR12691428	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/012393/SRR12691428	GSM4797961	SRA1129693	SRX9171386	ATAC-seq	PAIRED	SRP284834	PRJNA664919
158664	1	Evgeny Orlov	Identification of genes with different expression in wild- and half-size Xenopus laevis embryos by transcriptome comparison	To identify genes with different expression levels in Xenopus laevis embryos of different sizes, RNAseq of middle gastrula RNA of the wild-size and ar	Evgeny Orlov, Eugeny Orlov, Andrey Zaraisky	Three biological replicates were analyzed for 2 conditions (intact embryos vs their siblings divided at two-blastomere stage)	0	57685	SRP285632	SRR12730396	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/012432/SRR12730396	GSM4805183	SRA1133787	SRX9203751	RNA-Seq	SINGLE	SRP285632	PRJNA666158
158664	2	Evgeny Orlov	Identification of genes with different expression in wild- and half-size Xenopus laevis embryos by transcriptome comparison	To identify genes with different expression levels in Xenopus laevis embryos of different sizes, RNAseq of middle gastrula RNA of the wild-size and ar	Evgeny Orlov, Eugeny Orlov, Andrey Zaraisky	Three biological replicates were analyzed for 2 conditions (intact embryos vs their siblings divided at two-blastomere stage)	0	57685	SRP285632	SRR12730397	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/012432/SRR12730397	GSM4805184	SRA1133787	SRX9203752	RNA-Seq	SINGLE	SRP285632	PRJNA666158
158664	3	Evgeny Orlov	Identification of genes with different expression in wild- and half-size Xenopus laevis embryos by transcriptome comparison	To identify genes with different expression levels in Xenopus laevis embryos of different sizes, RNAseq of middle gastrula RNA of the wild-size and ar	Evgeny Orlov, Eugeny Orlov, Andrey Zaraisky	Three biological replicates were analyzed for 2 conditions (intact embryos vs their siblings divided at two-blastomere stage)	0	57685	SRP285632	SRR12730398	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/012432/SRR12730398	GSM4805185	SRA1133787	SRX9203753	RNA-Seq	SINGLE	SRP285632	PRJNA666158
158664	4	Evgeny Orlov	Identification of genes with different expression in wild- and half-size Xenopus laevis embryos by transcriptome comparison	To identify genes with different expression levels in Xenopus laevis embryos of different sizes, RNAseq of middle gastrula RNA of the wild-size and ar	Evgeny Orlov, Eugeny Orlov, Andrey Zaraisky	Three biological replicates were analyzed for 2 conditions (intact embryos vs their siblings divided at two-blastomere stage)	0	57685	SRP285632	SRR12730399	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/012432/SRR12730399	GSM4805186	SRA1133787	SRX9203754	RNA-Seq	SINGLE	SRP285632	PRJNA666158
158664	5	Evgeny Orlov	Identification of genes with different expression in wild- and half-size Xenopus laevis embryos by transcriptome comparison	To identify genes with different expression levels in Xenopus laevis embryos of different sizes, RNAseq of middle gastrula RNA of the wild-size and ar	Evgeny Orlov, Eugeny Orlov, Andrey Zaraisky	Three biological replicates were analyzed for 2 conditions (intact embryos vs their siblings divided at two-blastomere stage)	0	57685	SRP285632	SRR12730400	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/012432/SRR12730400	GSM4805187	SRA1133787	SRX9203755	RNA-Seq	SINGLE	SRP285632	PRJNA666158
158664	6	Evgeny Orlov	Identification of genes with different expression in wild- and half-size Xenopus laevis embryos by transcriptome comparison	To identify genes with different expression levels in Xenopus laevis embryos of different sizes, RNAseq of middle gastrula RNA of the wild-size and ar	Evgeny Orlov, Eugeny Orlov, Andrey Zaraisky	Three biological replicates were analyzed for 2 conditions (intact embryos vs their siblings divided at two-blastomere stage)	0	57685	SRP285632	SRR12730401	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/012432/SRR12730401	GSM4805188	SRA1133787	SRX9203756	RNA-Seq	SINGLE	SRP285632	PRJNA666158
158849	1	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749591	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/012450/SRR12749591	GSM4812175	SRA1136461	SRX9221548	RNA-Seq	PAIRED	SRP285948	PRJNA666689
158849	2	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749592	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/012450/SRR12749592	GSM4812176	SRA1136461	SRX9221549	RNA-Seq	PAIRED	SRP285948	PRJNA666689
158849	3	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749593	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/012450/SRR12749593	GSM4812177	SRA1136461	SRX9221550	RNA-Seq	PAIRED	SRP285948	PRJNA666689
158849	4	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749594	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/012450/SRR12749594	GSM4812178	SRA1136461	SRX9221551	RNA-Seq	PAIRED	SRP285948	PRJNA666689
158849	5	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749595	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/012450/SRR12749595	GSM4812179	SRA1136461	SRX9221552	RNA-Seq	PAIRED	SRP285948	PRJNA666689
158849	6	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749596	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/012450/SRR12749596	GSM4812180	SRA1136461	SRX9221553	RNA-Seq	PAIRED	SRP285948	PRJNA666689
158849	7	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749597	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/012450/SRR12749597	GSM4812181	SRA1136461	SRX9221554	RNA-Seq	PAIRED	SRP285948	PRJNA666689
158849	8	Jan Philipp Junker	Subcellular analysis of transcriptome localization in the early zebrafish embryo	We performed spatially resolved transcriptomics with sub-single-cell resolution in zebrafish embryos at the one-cell stage, which allowed us to identi	Jan Philipp Junker, Karoline Holler, Anika Neuschulz, Philipp Boß, Janita Mintcheva, Roberto Arsiè, Uwe Ohler, Markus Landthaler, Jan Junker	Spatial transcriptomic data (tomo-seq) from zebrafish one-cell stage embroys, mature X. laevis and X. tropicalis oocytes. Single-cell metabolic labeling (scSLAM-seq) of zebrafish embryos at 6 hpf.	0		SRP285948	SRR12749598	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/012450/SRR12749598	GSM4812182	SRA1136461	SRX9221555	RNA-Seq	PAIRED	SRP285948	PRJNA666689
160777	1	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975534	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/012671/SRR12975534	GSM4879075	SRA1153583	SRX9427727	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	2	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975535	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/012671/SRR12975535	GSM4879076	SRA1153583	SRX9427728	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	3	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975536	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/012671/SRR12975536	GSM4879077	SRA1153583	SRX9427729	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	4	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975537	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/012671/SRR12975537	GSM4879078	SRA1153583	SRX9427730	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	5	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975538	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/012671/SRR12975538	GSM4879079	SRA1153583	SRX9427731	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	6	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975539	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/012671/SRR12975539	GSM4879080	SRA1153583	SRX9427732	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	7	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975540	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/012671/SRR12975540	GSM4879081	SRA1153583	SRX9427733	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	8	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975541	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/012671/SRR12975541	GSM4879082	SRA1153583	SRX9427734	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	9	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975542	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/012671/SRR12975542	GSM4879083	SRA1153583	SRX9427735	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	10	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975543	https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRR/012671/SRR12975543	GSM4879084	SRA1153583	SRX9427736	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	11	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975544	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/012671/SRR12975544	GSM4879085	SRA1153583	SRX9427737	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	12	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975545	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/012671/SRR12975545	GSM4879086	SRA1153583	SRX9427738	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	13	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975546	https://sra-download.ncbi.nlm.nih.gov/traces/sra79/SRR/012671/SRR12975546	GSM4879087	SRA1153583	SRX9427739	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	14	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975547	https://sra-download.ncbi.nlm.nih.gov/traces/sra12/SRR/012671/SRR12975547	GSM4879088	SRA1153583	SRX9427740	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	15	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975548	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/012671/SRR12975548	GSM4879089	SRA1153583	SRX9427741	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	16	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975549	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/012671/SRR12975549	GSM4879090	SRA1153583	SRX9427742	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	17	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975550	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/012671/SRR12975550	GSM4879091	SRA1153583	SRX9427743	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	18	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975551	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/012671/SRR12975551	GSM4879092	SRA1153583	SRX9427744	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	19	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975552	https://sra-download.ncbi.nlm.nih.gov/traces/sra2/SRR/012671/SRR12975552	GSM4879093	SRA1153583	SRX9427745	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	20	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975553	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/012671/SRR12975553	GSM4879094	SRA1153583	SRX9427746	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	21	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975554	https://sra-download.ncbi.nlm.nih.gov/traces/sra65/SRR/012671/SRR12975554	GSM4879095	SRA1153583	SRX9427747	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	22	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975555	https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/012671/SRR12975555	GSM4879096	SRA1153583	SRX9427748	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	23	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975556	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/012671/SRR12975556	GSM4879097	SRA1153583	SRX9427749	RNA-Seq	PAIRED	SRP291031	PRJNA674389
160777	24	Anneke Kakebeen	A temporally resolved transcriptome for developing “Keller” explants of the Xenopus laevis dorsal marginal zone	Explanted tissues from vertebrate embryos reliably develop in culture and have provided essential paradigms for understanding embryogenesis, from earl	Anneke Kakebeen, Anneke Kakebeenm, Robert Huebner, Asako Shindo, Kujin Kwon, Taejoon Kwon, Andrea Wills, John Wallingford	RNA-Seq analysis of a timecourse of dorsal marginal zone explants from Xenopus embryos from stage 11 to stage 18.	0	57664	SRP291031	SRR12975557	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/012671/SRR12975557	GSM4879098	SRA1153583	SRX9427750	RNA-Seq	PAIRED	SRP291031	PRJNA674389
161247	1	Tamas Schauer	Genome wide analysis of Suv4-20h1/2 depleted animal caps [dataset1]	Suv4-20h1/2 are histone methyltransferases that write the H4K20me2 and H4K20me3 marks. We knocked down these enzymes using translation blocking morph	Tamas Schauer, Alessandro Angerilli, Janet Tait, Pawel Smialowski, Ralph Rupp	RNA-seq experiment of Suv4-20H1/2 and Control morpholino knock down in 2 biological replicates.	37116939	59747	SRP292400	SRR13023967	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/012718/SRR13023967	GSM4903938	SRA1157610	SRX9474201	RNA-Seq	PAIRED	SRP292400	PRJNA677830
161249	1	Tamas Schauer	Genome wide analysis of Suv4-20h1/2 depleted animal caps [dataset3]	Suv4-20h1/2 are histone methyltransferases that write the H4K20me2 and H4K20me3 marks. We knocked down these enzymes using translation blocking morph	Tamas Schauer, Alessandro Angerilli, Janet Tait, Irina Shcherbakova, Ralph Rupp	RNA-seq experiment of human Phf8 mRNA injection in Suv4-20H1/2 knock down or control conditions (i.e. control morpholino, LacZ mRNA) in 3 biological replicates.	37116939	59747	SRP292402	SRR13023975	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/012718/SRR13023975	GSM4903946	SRA1157612	SRX9474209	RNA-Seq	SINGLE	SRP292402	PRJNA677828
161250	1	Tamas Schauer	Genome wide analysis of Suv4-20h1/2 depleted animal caps [dataset4]	Suv4-20h1/2 are histone methyltransferases that write the H4K20me2 and H4K20me3 marks. We knocked down these enzymes using translation blocking morph	Tamas Schauer, Alessandro Angerilli, Janet Tait, Pawel Smialowski, Ralph Rupp	RNA-seq experiment of Suv4-20H1/2 and Control morpholino knock down in 3 developmental stages and in 2 or 3 biological replicates.	37116939	59747	SRP292404	SRR13023987	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/012718/SRR13023987	GSM4903958	SRA1157613	SRX9474221	RNA-Seq	PAIRED	SRP292404	PRJNA677827
161714	1	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080669	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/012774/SRR13080669	GSM4913144	SRA1160944	SRX9527433	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	2	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080670	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/012774/SRR13080670	GSM4913145	SRA1160944	SRX9527434	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	3	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080671	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/012774/SRR13080671	GSM4913146	SRA1160944	SRX9527435	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	4	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080672	https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/012774/SRR13080672	GSM4913147	SRA1160944	SRX9527437	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	5	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080673	https://sra-download.ncbi.nlm.nih.gov/traces/sra21/SRR/012774/SRR13080673	GSM4913148	SRA1160944	SRX9527438	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	6	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080674	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/012774/SRR13080674	GSM4913149	SRA1160944	SRX9527439	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	7	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080675	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/012774/SRR13080675	GSM4913150	SRA1160944	SRX9527440	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	8	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080676	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/012774/SRR13080676	GSM4913151	SRA1160944	SRX9527441	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	9	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080677	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/012774/SRR13080677	GSM4913152	SRA1160944	SRX9527442	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	10	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080678	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/012774/SRR13080678	GSM4913153	SRA1160944	SRX9527443	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	11	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080679	https://sra-download.ncbi.nlm.nih.gov/traces/sra52/SRR/012774/SRR13080679	GSM4913154	SRA1160944	SRX9527444	RNA-Seq	PAIRED	SRP293086	PRJNA679241
161714	12	Henry Zhang	Thyroid hormone receptor is essential for larval eptiehlial apoptosis and adult epithelial stem cell development	Our experiment revealed that TR double knockout completely blocks intestinal length shortening, larval cell death, and adult stem cell development, de	Henry Zhang, Yuki Shibata, Yun-Bo Shi, Hongen Zhang	Compare the thyroid hormone target gene expression with or without thyroid hormone receptor in the intestine during metamorphosis climax of Xenopus tropicalis	33802526	57996	SRP293086	SRR13080680	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/012774/SRR13080680	GSM4913155	SRA1160944	SRX9527445	RNA-Seq	PAIRED	SRP293086	PRJNA679241
163875	1	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308360	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/012996/SRR13308360	GSM4988988	SRA1177934	SRX9736366	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	2	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308361	https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/012996/SRR13308361	GSM4988989	SRA1177934	SRX9736367	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	3	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308362	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/012996/SRR13308362	GSM4988990	SRA1177934	SRX9736368	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	4	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308363	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/012996/SRR13308363	GSM4988991	SRA1177934	SRX9736353	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	5	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308364	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/012996/SRR13308364	GSM4988992	SRA1177934	SRX9736354	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	6	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308365	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/012996/SRR13308365	GSM4988993	SRA1177934	SRX9736355	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	7	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308366	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/012996/SRR13308366	GSM4988994	SRA1177934	SRX9736356	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	8	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308367	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/012996/SRR13308367	GSM4988995	SRA1177934	SRX9736357	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	9	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308368	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/012996/SRR13308368	GSM4988996	SRA1177934	SRX9736358	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	10	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308369	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/012996/SRR13308369	GSM4988997	SRA1177934	SRX9736359	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	11	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308370	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/012996/SRR13308370	GSM4988998	SRA1177934	SRX9736360	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	12	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308371	https://sra-download.ncbi.nlm.nih.gov/traces/sra72/SRR/012996/SRR13308371	GSM4988999	SRA1177934	SRX9736361	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	13	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308372	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/012996/SRR13308372	GSM4989000	SRA1177934	SRX9736362	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	14	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308373	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/012996/SRR13308373	GSM4989001	SRA1177934	SRX9736363	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	15	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308374	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/012996/SRR13308374	GSM4989002	SRA1177934	SRX9736364	RNA-Seq	PAIRED	SRP299616	PRJNA687987
163875	16	Taejoon Kwon	Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells	Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is 	Taejoon Kwon, Hee-Sun Yang, Hyo Sim, Hanna Cho, Woo Bang, Ha Kim, Taeg Kwon, Tae Park	For each species (X. laevis and B. orientalis), we treated 100 ug/mL of the particulate matters (PM) to whole embryo. For each condition, we used duplicated biological replicates. To evaluate the transcriptonal response among time, we sampled at two time points: 3 hours after PM treatment, and 9 hours after the treatment.	0	60224	SRP299616	SRR13308375	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/012996/SRR13308375	GSM4989003	SRA1177934	SRX9736365	RNA-Seq	PAIRED	SRP299616	PRJNA687987
164204	1	Juan Larraín	Cellular response to spinal cord injury in regenerative and non-regenerative stages in Xenopus laevis.	Background: The efficient regenerative abilities at larvae stages followed by a non-regenerative response after metamorphosis in froglets makes Xenopu	Juan Larraín, Gabriela Edwards-Faret, Karina González-Pinto, Arantxa Cebrián-Silla, Johany Peñailillo, José García-Verdugo	Characterization of cell population GFAP::EGFP from the transgenic line Xla.Tg(Dre.gfap:EGFP)Larra in regenerative stages of Xenopus laevis	33526076	57773	SRP300206	SRR13348911	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/013036/SRR13348911	GSM5003918	SRA1179899	SRX9774935	RNA-Seq	PAIRED	SRP300206	PRJNA689548
164204	2	Juan Larraín	Cellular response to spinal cord injury in regenerative and non-regenerative stages in Xenopus laevis.	Background: The efficient regenerative abilities at larvae stages followed by a non-regenerative response after metamorphosis in froglets makes Xenopu	Juan Larraín, Gabriela Edwards-Faret, Karina González-Pinto, Arantxa Cebrián-Silla, Johany Peñailillo, José García-Verdugo	Characterization of cell population GFAP::EGFP from the transgenic line Xla.Tg(Dre.gfap:EGFP)Larra in regenerative stages of Xenopus laevis	33526076	57773	SRP300206	SRR13348912	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/013036/SRR13348912	GSM5003919	SRA1179899	SRX9774936	RNA-Seq	PAIRED	SRP300206	PRJNA689548
164434	1	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386548	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386548/SRR13386548.1	GSM5009568	SRA1181562	SRX9805835	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	2	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386549	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386549/SRR13386549.1	GSM5009569	SRA1181562	SRX9805836	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	3	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386550	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386550/SRR13386550.1	GSM5009570	SRA1181562	SRX9805837	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	4	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386551	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386551/SRR13386551.1	GSM5009571	SRA1181562	SRX9805838	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	5	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386552	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386552/SRR13386552.1	GSM5009572	SRA1181562	SRX9805839	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	6	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386553	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386553/SRR13386553.1	GSM5009573	SRA1181562	SRX9805840	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	7	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386554	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386554/SRR13386554.1	GSM5009574	SRA1181562	SRX9805841	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	8	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386555	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386555/SRR13386555.1	GSM5009575	SRA1181562	SRX9805842	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	9	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386556	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386556/SRR13386556.1	GSM5009576	SRA1181562	SRX9805843	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	10	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386557	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386557/SRR13386557.1	GSM5009577	SRA1181562	SRX9805844	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	11	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386558	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386558/SRR13386558.1	GSM5009578	SRA1181562	SRX9805845	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	12	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386559	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386559/SRR13386559.1	GSM5009579	SRA1181562	SRX9805846	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	13	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386560	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386560/SRR13386560.1	GSM5009580	SRA1181562	SRX9805847	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	14	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386561	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386561/SRR13386561.1	GSM5009581	SRA1181562	SRX9805848	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	15	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386562	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386562/SRR13386562.1	GSM5009582	SRA1181562	SRX9805849	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	16	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386563	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386563/SRR13386563.1	GSM5009583	SRA1181562	SRX9805850	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	17	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386564	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386564/SRR13386564.1	GSM5009584	SRA1181562	SRX9805851	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	18	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386565	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386565/SRR13386565.1	GSM5009585	SRA1181562	SRX9805852	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	19	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386566	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386566/SRR13386566.1	GSM5009586	SRA1181562	SRX9805853	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	20	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386567	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386567/SRR13386567.1	GSM5009587	SRA1181562	SRX9805854	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	21	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR13386568	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13386568/SRR13386568.1	GSM5009588	SRA1181562	SRX9805855	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	22	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR14135959	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR14135959/SRR14135959.1	GSM5224854	SRA1181562	SRX10505594	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	23	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR14135960	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR14135960/SRR14135960.1	GSM5224855	SRA1181562	SRX10505595	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	24	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR14135961	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR14135961/SRR14135961.1	GSM5224856	SRA1181562	SRX10505596	Hi-C	PAIRED	SRP300874	PRJNA690708
164434	25	Bastiaan Dekker	Linker histone H1.8 inhibits chromatin-binding of condensins and DNA topoisomerase II to tune chromosome compaction and individualization	Hi-C on reconstituted mitotic chromosomes in Xenopus system in IGG or specific depleted egg extracts to study to role of condensin and linker histone 	Bastiaan Dekker, Pavan Choppakatla, Erin  Cutts, Alessandro Vannini, Job Dekker, Hironori Funabiki	Hi-C on reconstituted mitotic chromosomes in Xenopus system	34406118	58313	SRP300874	SRR14135962	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR14135962/SRR14135962.1	GSM5224857	SRA1181562	SRX10505597	Hi-C	PAIRED	SRP300874	PRJNA690708
165343	1	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509509	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/013192/SRR13509509	GSM5031797	SRA1186851	SRX9920972	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	2	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509510	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/013192/SRR13509510	GSM5031798	SRA1186851	SRX9920973	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	3	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509511	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/013192/SRR13509511	GSM5031799	SRA1186851	SRX9920974	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	4	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509512	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/013192/SRR13509512	GSM5031800	SRA1186851	SRX9920975	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	5	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509513	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/013192/SRR13509513	GSM5031801	SRA1186851	SRX9920976	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	6	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509514	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/013192/SRR13509514	GSM5031802	SRA1186851	SRX9920977	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	7	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509515	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/013192/SRR13509515	GSM5031803	SRA1186851	SRX9920978	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	8	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509516	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/013192/SRR13509516	GSM5031804	SRA1186851	SRX9920979	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	9	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509517	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/013192/SRR13509517	GSM5031805	SRA1186851	SRX9920980	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165343	10	Juan Larraín	High expression profiling analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling	Xenopus laevis are able to regenerate the spinal cord during larvae stages through the activation of neural stem progenitor cells (NSPC). Here, we use	Juan Larraín, Johany Peñailillo, Miriam Palacios, Constanza Mounieres, Elena De Domenico, Ilya Patrushev, Mike Gilchrist	Time-series analysis of the early transcriptional changes deployed in response to spinal cord injury in regenerative stage of Xenopus laevis.	34686684	58545	SRP302901	SRR13509518	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/013192/SRR13509518	GSM5031806	SRA1186851	SRX9920981	RNA-Seq	PAIRED	SRP302901	PRJNA694138
165763	1	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576990	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/013258/SRR13576990	GSM5049608	SRA1189308	SRX9975066	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	2	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576991	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/013258/SRR13576991	GSM5049609	SRA1189308	SRX9975067	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	3	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576992	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/013258/SRR13576992	GSM5049610	SRA1189308	SRX9975068	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	4	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576993	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/013258/SRR13576993	GSM5049611	SRA1189308	SRX9975069	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	5	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576994	https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/013258/SRR13576994	GSM5049612	SRA1189308	SRX9975070	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	6	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576995	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/013258/SRR13576995	GSM5049613	SRA1189308	SRX9975071	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	7	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576996	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/013258/SRR13576996	GSM5049614	SRA1189308	SRX9975072	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	8	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576997	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/013258/SRR13576997	GSM5049615	SRA1189308	SRX9975073	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	9	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576998	https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/013258/SRR13576998	GSM5049616	SRA1189308	SRX9975074	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	10	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13576999	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/013258/SRR13576999	GSM5049617	SRA1189308	SRX9975075	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	11	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577000	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/013258/SRR13577000	GSM5049618	SRA1189308	SRX9975076	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	12	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577001	https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/013258/SRR13577001	GSM5049619	SRA1189308	SRX9975077	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	13	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577002	https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/013258/SRR13577002	GSM5049620	SRA1189308	SRX9975078	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	14	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577003	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/013258/SRR13577003	GSM5049621	SRA1189308	SRX9975079	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	15	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577004	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/013258/SRR13577004	GSM5049622	SRA1189308	SRX9975080	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	16	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577005	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/013258/SRR13577005	GSM5049623	SRA1189308	SRX9975081	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	17	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577006	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/013258/SRR13577006	GSM5049624	SRA1189308	SRX9975082	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	18	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577007	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/013258/SRR13577007	GSM5049625	SRA1189308	SRX9975083	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	19	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577008	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/013258/SRR13577008	GSM5049626	SRA1189308	SRX9975084	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	20	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577009	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/013258/SRR13577009	GSM5049627	SRA1189308	SRX9975085	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	21	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577010	https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/013258/SRR13577010	GSM5049628	SRA1189308	SRX9975086	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	22	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577011	https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/013258/SRR13577011	GSM5049629	SRA1189308	SRX9975087	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	23	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577012	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/013258/SRR13577012	GSM5049630	SRA1189308	SRX9975088	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	24	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577013	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/013258/SRR13577013	GSM5049631	SRA1189308	SRX9975089	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	25	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577014	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/013258/SRR13577014	GSM5049632	SRA1189308	SRX9975090	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	26	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577015	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/013258/SRR13577015	GSM5049633	SRA1189308	SRX9975091	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	27	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577016	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/013258/SRR13577016	GSM5049634	SRA1189308	SRX9975092	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	28	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577017	https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRR/013258/SRR13577017	GSM5049635	SRA1189308	SRX9975093	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	29	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577018	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/013258/SRR13577018	GSM5049636	SRA1189308	SRX9975094	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	30	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577019	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/013258/SRR13577019	GSM5049637	SRA1189308	SRX9975095	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	31	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577020	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/013258/SRR13577020	GSM5049638	SRA1189308	SRX9975096	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	32	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577021	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/013258/SRR13577021	GSM5049639	SRA1189308	SRX9975097	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	33	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577022	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/013258/SRR13577022	GSM5049640	SRA1189308	SRX9975098	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	34	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577023	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/013258/SRR13577023	GSM5049641	SRA1189308	SRX9975099	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	35	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577024	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/013258/SRR13577024	GSM5049642	SRA1189308	SRX9975100	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	36	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577025	https://sra-download.ncbi.nlm.nih.gov/traces/sra33/SRR/013258/SRR13577025	GSM5049643	SRA1189308	SRX9975101	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	37	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577026	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/013258/SRR13577026	GSM5049644	SRA1189308	SRX9975102	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	38	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577027	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/013258/SRR13577027	GSM5049645	SRA1189308	SRX9975103	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	39	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577028	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/013258/SRR13577028	GSM5049646	SRA1189308	SRX9975104	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	40	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577029	https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRR/013258/SRR13577029	GSM5049647	SRA1189308	SRX9975105	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	41	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577030	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/013258/SRR13577030	GSM5049648	SRA1189308	SRX9975106	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	42	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577031	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/013258/SRR13577031	GSM5049649	SRA1189308	SRX9975107	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	43	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577032	https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/013258/SRR13577032	GSM5049650	SRA1189308	SRX9975108	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	44	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577033	https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/013258/SRR13577033	GSM5049651	SRA1189308	SRX9975109	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	45	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577034	https://sra-download.ncbi.nlm.nih.gov/traces/sra11/SRR/013258/SRR13577034	GSM5049652	SRA1189308	SRX9975110	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	46	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577035	https://sra-download.ncbi.nlm.nih.gov/traces/sra27/SRR/013258/SRR13577035	GSM5049653	SRA1189308	SRX9975111	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	47	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577036	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/013258/SRR13577036	GSM5049654	SRA1189308	SRX9975112	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	48	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577037	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/013258/SRR13577037	GSM5049655	SRA1189308	SRX9975113	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	49	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577038	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/013258/SRR13577038	GSM5049656	SRA1189308	SRX9975114	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	50	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577039	https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRR/013258/SRR13577039	GSM5049657	SRA1189308	SRX9975115	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	51	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577040	https://sra-download.ncbi.nlm.nih.gov/traces/sra72/SRR/013258/SRR13577040	GSM5049658	SRA1189308	SRX9975116	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	52	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577041	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/013258/SRR13577041	GSM5049659	SRA1189308	SRX9975117	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	53	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577042	https://sra-download.ncbi.nlm.nih.gov/traces/sra30/SRR/013258/SRR13577042	GSM5049660	SRA1189308	SRX9975118	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	54	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577043	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/013258/SRR13577043	GSM5049661	SRA1189308	SRX9975119	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	55	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577044	https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/013258/SRR13577044	GSM5049662	SRA1189308	SRX9975120	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	56	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577045	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/013258/SRR13577045	GSM5049663	SRA1189308	SRX9975121	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	57	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577046	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/013258/SRR13577046	GSM5049664	SRA1189308	SRX9975122	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	58	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577047	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/013258/SRR13577047	GSM5049665	SRA1189308	SRX9975123	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	59	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577048	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/013258/SRR13577048	GSM5049666	SRA1189308	SRX9975124	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	60	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577049	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/013258/SRR13577049	GSM5049667	SRA1189308	SRX9975125	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	61	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577050	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/013258/SRR13577050	GSM5049668	SRA1189308	SRX9975126	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	62	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577051	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/013258/SRR13577051	GSM5049669	SRA1189308	SRX9975127	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	63	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577052	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/013258/SRR13577052	GSM5049670	SRA1189308	SRX9975128	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	64	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577053	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/013258/SRR13577053	GSM5049671	SRA1189308	SRX9975129	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	65	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577054	https://sra-download.ncbi.nlm.nih.gov/traces/sra68/SRR/013258/SRR13577054	GSM5049672	SRA1189308	SRX9975130	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	66	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577055	https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/013258/SRR13577055	GSM5049673	SRA1189308	SRX9975131	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	67	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577056	https://sra-download.ncbi.nlm.nih.gov/traces/sra7/SRR/013258/SRR13577056	GSM5049674	SRA1189308	SRX9975132	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	68	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577057	https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/013258/SRR13577057	GSM5049675	SRA1189308	SRX9975133	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	69	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577058	https://sra-download.ncbi.nlm.nih.gov/traces/sra35/SRR/013258/SRR13577058	GSM5049676	SRA1189308	SRX9975134	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	70	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577059	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/013258/SRR13577059	GSM5049677	SRA1189308	SRX9975135	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	71	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577060	https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/013258/SRR13577060	GSM5049678	SRA1189308	SRX9975136	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	72	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577061	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/013258/SRR13577061	GSM5049679	SRA1189308	SRX9975137	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	73	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577062	https://sra-download.ncbi.nlm.nih.gov/traces/sra4/SRR/013258/SRR13577062	GSM5049680	SRA1189308	SRX9975138	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165763	74	Margaret Saha	Anterior-Posterior Rotation Transcriptome RNA-Sequencing Analysis of X. laevis	To analyze the limits of embryo robustness, several different types of surgeries were performed on the anterior-posterior neural axis of Xenopus laevi	Margaret Saha, Margaret Saha, LeAnn Lo, Bryan Weselman	RNA-Seq data of sequenced X.laevis embryos with varying surgeries and an accompanying sibling control	0	60222	SRP303801	SRR13577063	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/013258/SRR13577063	GSM5049681	SRA1189308	SRX9975139	RNA-Seq	PAIRED	SRP303801	PRJNA697849
165901	1	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600548	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600548/SRR13600548.1	GSM5057655	SRA1189998	SRX9994960	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	2	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600549	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600549/SRR13600549.1	GSM5057656	SRA1189998	SRX9994961	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	3	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600550	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600550/SRR13600550.1	GSM5057657	SRA1189998	SRX9994962	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	4	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600551	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600551/SRR13600551.1	GSM5057658	SRA1189998	SRX9994963	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	5	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600552	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600552/SRR13600552.1	GSM5057659	SRA1189998	SRX9994964	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	6	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600553	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600553/SRR13600553.1	GSM5057660	SRA1189998	SRX9994965	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	7	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600554	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600554/SRR13600554.1	GSM5057661	SRA1189998	SRX9994966	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	8	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600555	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600555/SRR13600555.1	GSM5057662	SRA1189998	SRX9994967	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	9	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600557	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600557/SRR13600557.1	GSM5057663	SRA1189998	SRX9994968	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	10	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600558	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600558/SRR13600558.1	GSM5057664	SRA1189998	SRX9994969	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	11	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600560	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600560/SRR13600560.1	GSM5057665	SRA1189998	SRX9994970	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	12	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600561	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600561/SRR13600561.1	GSM5057666	SRA1189998	SRX9994971	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	13	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600563	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600563/SRR13600563.1	GSM5057667	SRA1189998	SRX9994972	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	14	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600564	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600564/SRR13600564.1	GSM5057668	SRA1189998	SRX9994973	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	15	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600565	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600565/SRR13600565.1	GSM5057669	SRA1189998	SRX9994974	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	16	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600566	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600566/SRR13600566.1	GSM5057670	SRA1189998	SRX9994975	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	17	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600567	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600567/SRR13600567.1	GSM5057671	SRA1189998	SRX9994976	RNA-Seq	PAIRED	SRP304111	PRJNA698552
165901	18	Tobias Gerber	Fibroblast Dedifferentiation as a Determinant of Successful Regeneration	Limb regeneration, while observed lifelong in salamanders, is restricted to pre-metamorphic stages in Xenopus laevis frogs. After amputation, post-met	Tobias Gerber, Barbara Treutlein	Tissue grafting, single-cell transcriptomics, reporter lineage tracking and cell transplantions were used to deconstruct cell compositions and to reconstruct lineage relationships aiming to find determinants of the successful regeneration in axolotl compared to the incomplete regenration in frogs.	34004152	58108	SRP304111	SRR13600568	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13600568/SRR13600568.1	GSM5057672	SRA1189998	SRX9994977	RNA-Seq	PAIRED	SRP304111	PRJNA698552
166455	1	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13667998	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13667998/SRR13667998.1	GSM5071357	SRA1194004	SRX10059503	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	2	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13667999	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13667999/SRR13667999.1	GSM5071358	SRA1194004	SRX10059504	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	3	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668000	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-23/SRR13668000/SRR13668000.1	GSM5071359	SRA1194004	SRX10059505	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	4	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668001	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-24/SRR13668001/SRR13668001.1	GSM5071360	SRA1194004	SRX10059506	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	5	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668002	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13668002/SRR13668002.1	GSM5071361	SRA1194004	SRX10059507	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	6	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668003	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-22/SRR13668003/SRR13668003.1	GSM5071362	SRA1194004	SRX10059508	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	7	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668004	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-22/SRR13668004/SRR13668004.1	GSM5071363	SRA1194004	SRX10059509	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	8	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668005	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-23/SRR13668005/SRR13668005.1	GSM5071364	SRA1194004	SRX10059510	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	9	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668006	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-22/SRR13668006/SRR13668006.1	GSM5071365	SRA1194004	SRX10059511	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	10	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668007	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-23/SRR13668007/SRR13668007.1	GSM5071366	SRA1194004	SRX10059512	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	11	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668008	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-23/SRR13668008/SRR13668008.1	GSM5071367	SRA1194004	SRX10059513	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166455	12	Ian Boys	Poly(I:C) transfection time course in Xenopus laevis A6 cells	This study was designed to identify Xenopus laevis genes that respond to stimulation with an immune agonist, poly(I:C).                               	Ian Boys, Ian Boys, John Schoggins	12 samples in 4 groups with 3 biological replicates each. Treatment time course of 6 12 and 24 hours of poly(I:C) transfection, with a mock-transfected reference.	34014925	58124	SRP305512	SRR13668009	https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos3/sra-pub-run-24/SRR13668009/SRR13668009.1	GSM5071368	SRA1194004	SRX10059514	RNA-Seq	PAIRED	SRP305512	PRJNA700989
166544	1	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679779	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679779/SRR13679779.1	GSM5074337	SRA1194491	SRX10069179	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	2	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679780	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679780/SRR13679780.1	GSM5074338	SRA1194491	SRX10069171	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	3	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679781	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679781/SRR13679781.1	GSM5074339	SRA1194491	SRX10069172	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	4	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679782	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679782/SRR13679782.1	GSM5074340	SRA1194491	SRX10069173	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	5	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679783	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679783/SRR13679783.1	GSM5074341	SRA1194491	SRX10069174	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	6	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679784	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679784/SRR13679784.1	GSM5074341	SRA1194491	SRX10069174	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	7	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679785	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679785/SRR13679785.1	GSM5074342	SRA1194491	SRX10069175	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	8	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679786	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679786/SRR13679786.1	GSM5074342	SRA1194491	SRX10069175	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	9	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679787	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679787/SRR13679787.1	GSM5074343	SRA1194491	SRX10069176	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	10	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679788	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679788/SRR13679788.1	GSM5074344	SRA1194491	SRX10069177	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	11	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679789	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679789/SRR13679789.1	GSM5074345	SRA1194491	SRX10069178	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	12	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679790	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679790/SRR13679790.1	GSM5074346	SRA1194491	SRX10069180	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	13	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679791	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679791/SRR13679791.1	GSM5074347	SRA1194491	SRX10069181	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	14	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679792	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679792/SRR13679792.1	GSM5074348	SRA1194491	SRX10069182	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	15	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679793	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679793/SRR13679793.1	GSM5074349	SRA1194491	SRX10069183	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	16	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679794	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679794/SRR13679794.1	GSM5074350	SRA1194491	SRX10069184	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	17	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679795	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679795/SRR13679795.1	GSM5074351	SRA1194491	SRX10069185	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	18	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679796	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679796/SRR13679796.1	GSM5074352	SRA1194491	SRX10069186	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	19	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679797	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679797/SRR13679797.1	GSM5074353	SRA1194491	SRX10069187	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	20	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679798	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679798/SRR13679798.1	GSM5074354	SRA1194491	SRX10069188	OTHER	SINGLE	SRP305686	PRJNA701262
166544	21	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679799	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679799/SRR13679799.1	GSM5074355	SRA1194491	SRX10069189	OTHER	SINGLE	SRP305686	PRJNA701262
166544	22	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679800	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679800/SRR13679800.1	GSM5074356	SRA1194491	SRX10069190	OTHER	SINGLE	SRP305686	PRJNA701262
166544	23	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679801	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679801/SRR13679801.1	GSM5074357	SRA1194491	SRX10069191	OTHER	SINGLE	SRP305686	PRJNA701262
166544	24	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679802	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679802/SRR13679802.1	GSM5074358	SRA1194491	SRX10069192	OTHER	SINGLE	SRP305686	PRJNA701262
166544	25	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679803	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679803/SRR13679803.1	GSM5074358	SRA1194491	SRX10069192	OTHER	SINGLE	SRP305686	PRJNA701262
166544	26	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679804	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679804/SRR13679804.1	GSM5074359	SRA1194491	SRX10069193	OTHER	SINGLE	SRP305686	PRJNA701262
166544	27	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679805	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679805/SRR13679805.1	GSM5074359	SRA1194491	SRX10069193	OTHER	SINGLE	SRP305686	PRJNA701262
166544	28	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679806	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679806/SRR13679806.1	GSM5074360	SRA1194491	SRX10069194	OTHER	SINGLE	SRP305686	PRJNA701262
166544	29	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679807	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679807/SRR13679807.1	GSM5074361	SRA1194491	SRX10069195	OTHER	SINGLE	SRP305686	PRJNA701262
166544	30	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679808	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679808/SRR13679808.1	GSM5074362	SRA1194491	SRX10069196	OTHER	SINGLE	SRP305686	PRJNA701262
166544	31	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679809	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679809/SRR13679809.1	GSM5074363	SRA1194491	SRX10069197	OTHER	SINGLE	SRP305686	PRJNA701262
166544	32	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679810	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679810/SRR13679810.1	GSM5074364	SRA1194491	SRX10069198	OTHER	SINGLE	SRP305686	PRJNA701262
166544	33	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679811	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679811/SRR13679811.1	GSM5074365	SRA1194491	SRX10069199	OTHER	SINGLE	SRP305686	PRJNA701262
166544	34	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679812	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679812/SRR13679812.1	GSM5074366	SRA1194491	SRX10069200	OTHER	SINGLE	SRP305686	PRJNA701262
166544	35	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679813	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679813/SRR13679813.1	GSM5074367	SRA1194491	SRX10069201	OTHER	SINGLE	SRP305686	PRJNA701262
166544	36	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679814	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679814/SRR13679814.1	GSM5074368	SRA1194491	SRX10069202	OTHER	SINGLE	SRP305686	PRJNA701262
166544	37	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679815	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679815/SRR13679815.1	GSM5074369	SRA1194491	SRX10069203	OTHER	SINGLE	SRP305686	PRJNA701262
166544	38	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679816	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679816/SRR13679816.1	GSM5074370	SRA1194491	SRX10069204	OTHER	PAIRED	SRP305686	PRJNA701262
166544	39	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679817	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679817/SRR13679817.1	GSM5074371	SRA1194491	SRX10069205	OTHER	PAIRED	SRP305686	PRJNA701262
166544	40	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679818	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679818/SRR13679818.1	GSM5074372	SRA1194491	SRX10069206	OTHER	PAIRED	SRP305686	PRJNA701262
166544	41	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679819	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679819/SRR13679819.1	GSM5074373	SRA1194491	SRX10069207	OTHER	PAIRED	SRP305686	PRJNA701262
166544	42	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679820	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679820/SRR13679820.1	GSM5074374	SRA1194491	SRX10069208	OTHER	PAIRED	SRP305686	PRJNA701262
166544	43	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679821	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679821/SRR13679821.1	GSM5074374	SRA1194491	SRX10069208	OTHER	PAIRED	SRP305686	PRJNA701262
166544	44	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679822	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679822/SRR13679822.1	GSM5074375	SRA1194491	SRX10069209	OTHER	PAIRED	SRP305686	PRJNA701262
166544	45	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679823	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679823/SRR13679823.1	GSM5074376	SRA1194491	SRX10069210	OTHER	PAIRED	SRP305686	PRJNA701262
166544	46	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679824	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679824/SRR13679824.1	GSM5074376	SRA1194491	SRX10069210	OTHER	PAIRED	SRP305686	PRJNA701262
166544	47	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679825	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679825/SRR13679825.1	GSM5074377	SRA1194491	SRX10069211	OTHER	PAIRED	SRP305686	PRJNA701262
166544	48	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679826	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679826/SRR13679826.1	GSM5074377	SRA1194491	SRX10069211	OTHER	PAIRED	SRP305686	PRJNA701262
166544	49	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679827	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679827/SRR13679827.1	GSM5074378	SRA1194491	SRX10069212	OTHER	PAIRED	SRP305686	PRJNA701262
166544	50	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679828	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679828/SRR13679828.1	GSM5074379	SRA1194491	SRX10069213	OTHER	PAIRED	SRP305686	PRJNA701262
166544	51	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679829	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679829/SRR13679829.1	GSM5074379	SRA1194491	SRX10069213	OTHER	PAIRED	SRP305686	PRJNA701262
166544	52	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679830	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679830/SRR13679830.1	GSM5074380	SRA1194491	SRX10069214	OTHER	PAIRED	SRP305686	PRJNA701262
166544	53	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679831	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679831/SRR13679831.1	GSM5074381	SRA1194491	SRX10069215	OTHER	PAIRED	SRP305686	PRJNA701262
166544	54	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679832	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679832/SRR13679832.1	GSM5074382	SRA1194491	SRX10069216	OTHER	PAIRED	SRP305686	PRJNA701262
166544	55	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679833	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679833/SRR13679833.1	GSM5074383	SRA1194491	SRX10069217	OTHER	PAIRED	SRP305686	PRJNA701262
166544	56	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679834	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679834/SRR13679834.1	GSM5074384	SRA1194491	SRX10069218	OTHER	PAIRED	SRP305686	PRJNA701262
166544	57	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679835	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679835/SRR13679835.1	GSM5074385	SRA1194491	SRX10069219	OTHER	PAIRED	SRP305686	PRJNA701262
166544	58	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679836	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679836/SRR13679836.1	GSM5074386	SRA1194491	SRX10069220	OTHER	PAIRED	SRP305686	PRJNA701262
166544	59	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679837	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679837/SRR13679837.1	GSM5074387	SRA1194491	SRX10069221	OTHER	PAIRED	SRP305686	PRJNA701262
166544	60	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679838	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679838/SRR13679838.1	GSM5074388	SRA1194491	SRX10069222	OTHER	PAIRED	SRP305686	PRJNA701262
166544	61	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679839	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679839/SRR13679839.1	GSM5074389	SRA1194491	SRX10069223	OTHER	PAIRED	SRP305686	PRJNA701262
166544	62	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679840	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679840/SRR13679840.1	GSM5074390	SRA1194491	SRX10069224	OTHER	PAIRED	SRP305686	PRJNA701262
166544	63	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679841	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679841/SRR13679841.1	GSM5074391	SRA1194491	SRX10069225	OTHER	PAIRED	SRP305686	PRJNA701262
166544	64	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679842	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679842/SRR13679842.1	GSM5074392	SRA1194491	SRX10069226	OTHER	PAIRED	SRP305686	PRJNA701262
166544	65	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679843	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679843/SRR13679843.1	GSM5074393	SRA1194491	SRX10069227	OTHER	PAIRED	SRP305686	PRJNA701262
166544	66	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679844	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679844/SRR13679844.1	GSM5074394	SRA1194491	SRX10069228	OTHER	PAIRED	SRP305686	PRJNA701262
166544	67	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679845	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679845/SRR13679845.1	GSM5074395	SRA1194491	SRX10069229	OTHER	PAIRED	SRP305686	PRJNA701262
166544	68	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679846	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679846/SRR13679846.1	GSM5074396	SRA1194491	SRX10069230	OTHER	PAIRED	SRP305686	PRJNA701262
166544	69	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679847	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679847/SRR13679847.1	GSM5074397	SRA1194491	SRX10069231	OTHER	PAIRED	SRP305686	PRJNA701262
166544	70	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679848	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679848/SRR13679848.1	GSM5074398	SRA1194491	SRX10069232	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	71	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679849	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679849/SRR13679849.1	GSM5074399	SRA1194491	SRX10069233	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	72	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679850	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679850/SRR13679850.1	GSM5074400	SRA1194491	SRX10069234	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	73	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679851	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679851/SRR13679851.1	GSM5074401	SRA1194491	SRX10069235	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	74	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679852	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679852/SRR13679852.1	GSM5074402	SRA1194491	SRX10069236	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	75	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679853	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679853/SRR13679853.1	GSM5074403	SRA1194491	SRX10069237	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	76	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679854	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679854/SRR13679854.1	GSM5074404	SRA1194491	SRX10069238	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	77	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679855	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679855/SRR13679855.1	GSM5074405	SRA1194491	SRX10069239	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	78	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679856	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679856/SRR13679856.1	GSM5074406	SRA1194491	SRX10069240	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	79	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679857	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679857/SRR13679857.1	GSM5074407	SRA1194491	SRX10069241	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	80	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679858	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679858/SRR13679858.1	GSM5074408	SRA1194491	SRX10069242	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	81	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679859	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679859/SRR13679859.1	GSM5074409	SRA1194491	SRX10069243	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	82	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679860	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679860/SRR13679860.1	GSM5074410	SRA1194491	SRX10069244	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	83	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679861	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679861/SRR13679861.1	GSM5074411	SRA1194491	SRX10069245	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	84	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679862	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679862/SRR13679862.1	GSM5074412	SRA1194491	SRX10069246	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	85	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679863	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679863/SRR13679863.1	GSM5074413	SRA1194491	SRX10069247	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	86	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679864	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679864/SRR13679864.1	GSM5074414	SRA1194491	SRX10069248	RNA-Seq	SINGLE	SRP305686	PRJNA701262
166544	87	David Bartel	The molecular basis of coupling between poly(A)-tail length and translational efficiency	In animal oocytes and early embryos, mRNA poly(A)-tail length strongly influences translational efficiency (TE), but later in development this couplin	David Bartel, Kehui Xiang	RNA-seq, Ribo-seq TAIL-seq, PAL-seq	34213414	58243	SRP305686	SRR13679865	https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos4/sra-pub-run-25/SRR13679865/SRR13679865.1	GSM5074415	SRA1194491	SRX10069249	RNA-Seq	SINGLE	SRP305686	PRJNA701262
167139	1	Young-suk Lee	Identification of the FTO-FOXJ1 axis as a conserved regulatory module of embryonic and homeostatic motile ciliogenesis	Adenosine N6-methylation (m6A) is one of the most pervasive mRNA modifications, and yet the physiological significance of m6A removal (demethylation) 	Young-suk Lee, Hyunjoon Kim, V Kim	m6A-seq in Xenopus animal cap tissues	33761320	57939	SRP307184	SRR13753019	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/013430/SRR13753019	GSM5097940	SRA1198251	SRX10139790	OTHER	SINGLE	SRP307184	PRJNA703058
167139	2	Young-suk Lee	Identification of the FTO-FOXJ1 axis as a conserved regulatory module of embryonic and homeostatic motile ciliogenesis	Adenosine N6-methylation (m6A) is one of the most pervasive mRNA modifications, and yet the physiological significance of m6A removal (demethylation) 	Young-suk Lee, Hyunjoon Kim, V Kim	m6A-seq in Xenopus animal cap tissues	33761320	57939	SRP307184	SRR13753020	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/013430/SRR13753020	GSM5097941	SRA1198251	SRX10139791	OTHER	SINGLE	SRP307184	PRJNA703058
167139	3	Young-suk Lee	Identification of the FTO-FOXJ1 axis as a conserved regulatory module of embryonic and homeostatic motile ciliogenesis	Adenosine N6-methylation (m6A) is one of the most pervasive mRNA modifications, and yet the physiological significance of m6A removal (demethylation) 	Young-suk Lee, Hyunjoon Kim, V Kim	m6A-seq in Xenopus animal cap tissues	33761320	57939	SRP307184	SRR13753021	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/013430/SRR13753021	GSM5097942	SRA1198251	SRX10139792	OTHER	SINGLE	SRP307184	PRJNA703058
167139	4	Young-suk Lee	Identification of the FTO-FOXJ1 axis as a conserved regulatory module of embryonic and homeostatic motile ciliogenesis	Adenosine N6-methylation (m6A) is one of the most pervasive mRNA modifications, and yet the physiological significance of m6A removal (demethylation) 	Young-suk Lee, Hyunjoon Kim, V Kim	m6A-seq in Xenopus animal cap tissues	33761320	57939	SRP307184	SRR13753022	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/013430/SRR13753022	GSM5097943	SRA1198251	SRX10139793	OTHER	SINGLE	SRP307184	PRJNA703058
168370	1	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866614	https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRR/013541/SRR13866614	GSM5137445	SRA1203437	SRX10247126	RNA-Seq	PAIRED	SRP309498	PRJNA707043
168370	2	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866615	https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/013541/SRR13866615	GSM5137446	SRA1203437	SRX10247127	RNA-Seq	PAIRED	SRP309498	PRJNA707043
168370	3	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866616	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/013541/SRR13866616	GSM5137447	SRA1203437	SRX10247128	RNA-Seq	PAIRED	SRP309498	PRJNA707043
168370	4	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866617	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/013541/SRR13866617	GSM5137448	SRA1203437	SRX10247129	RNA-Seq	PAIRED	SRP309498	PRJNA707043
168370	5	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866618	https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRR/013541/SRR13866618	GSM5137449	SRA1203437	SRX10247130	RNA-Seq	PAIRED	SRP309498	PRJNA707043
168370	6	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866619	https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/013541/SRR13866619	GSM5137450	SRA1203437	SRX10247131	RNA-Seq	PAIRED	SRP309498	PRJNA707043
168370	7	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866620	https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/013541/SRR13866620	GSM5137451	SRA1203437	SRX10247132	RNA-Seq	PAIRED	SRP309498	PRJNA707043
168370	8	Keiji Itoh	Induction of dorsal mesodermal genes by pinhead and chordin	Xenopus embryonic ectodermal cells are responsive to various inducing factors.  Mesoderm is specified and patterned by extracellular factors including	Keiji Itoh, Olga Ossipova, Sergei Sokol	Eight samples are collected for RNAseq from four groups with duplicates. One group is control ectodermal explants (Co), the second is Flag-Pnhd expressing explants (Fpinh), the third is Chordin expressing explants (Chor) and the fourth is Pinhd and chordin expressing explants (Chor-Pinh).	0	58208	SRP309498	SRR13866621	https://sra-download.ncbi.nlm.nih.gov/traces/sra42/SRR/013541/SRR13866621	GSM5137452	SRA1203437	SRX10247133	RNA-Seq	PAIRED	SRP309498	PRJNA707043
169088	1	Olga Dudchenko	3D genomics across the tree of life reveals condensin II as a determinant of architecture type	We investigated genome folding across the eukaryotic tree of life. We find four general manifestations of genome organization at chromosome-scale that	Olga Dudchenko, Erez Lieberman Aiden	26 species across the tree of life were included in the analysis, representing all subphyla of chordates, all 7 extant vertebrate classes, and 7 out of 9 major animal phyla, as well as plants and fungi.	34045355	60217	SRP175152	SRR16086864	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/015709/SRR16086864	Sample0016	SRA1300830	SRX12373245	Hi-C	PAIRED	SRP175152	PRJNA512907
169088	2	Olga Dudchenko	3D genomics across the tree of life reveals condensin II as a determinant of architecture type	We investigated genome folding across the eukaryotic tree of life. We find four general manifestations of genome organization at chromosome-scale that	Olga Dudchenko, Erez Lieberman Aiden	26 species across the tree of life were included in the analysis, representing all subphyla of chordates, all 7 extant vertebrate classes, and 7 out of 9 major animal phyla, as well as plants and fungi.	34045355	60217	SRP175152	SRR16086865	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/015709/SRR16086865	Sample0016	SRA1300830	SRX12373244	Hi-C	PAIRED	SRP175152	PRJNA512907
169088	3	Olga Dudchenko	3D genomics across the tree of life reveals condensin II as a determinant of architecture type	We investigated genome folding across the eukaryotic tree of life. We find four general manifestations of genome organization at chromosome-scale that	Olga Dudchenko, Erez Lieberman Aiden	26 species across the tree of life were included in the analysis, representing all subphyla of chordates, all 7 extant vertebrate classes, and 7 out of 9 major animal phyla, as well as plants and fungi.	34045355	60217	SRP175152	SRR16086866	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/015709/SRR16086866	Sample0016	SRA1300830	SRX12373243	Hi-C	PAIRED	SRP175152	PRJNA512907
169088	4	Olga Dudchenko	3D genomics across the tree of life reveals condensin II as a determinant of architecture type	We investigated genome folding across the eukaryotic tree of life. We find four general manifestations of genome organization at chromosome-scale that	Olga Dudchenko, Erez Lieberman Aiden	26 species across the tree of life were included in the analysis, representing all subphyla of chordates, all 7 extant vertebrate classes, and 7 out of 9 major animal phyla, as well as plants and fungi.	34045355	60217	SRP175152	SRR16086867	https://sra-download.ncbi.nlm.nih.gov/traces/sra63/SRR/015709/SRR16086867	Sample0016	SRA1300830	SRX12373242	Hi-C	PAIRED	SRP175152	PRJNA512907
169088	5	Olga Dudchenko	3D genomics across the tree of life reveals condensin II as a determinant of architecture type	We investigated genome folding across the eukaryotic tree of life. We find four general manifestations of genome organization at chromosome-scale that	Olga Dudchenko, Erez Lieberman Aiden	26 species across the tree of life were included in the analysis, representing all subphyla of chordates, all 7 extant vertebrate classes, and 7 out of 9 major animal phyla, as well as plants and fungi.	34045355	60217	SRP175152	SRR16086868	https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/015709/SRR16086868	Sample0016	SRA1300830	SRX12373241	WGS	PAIRED	SRP175152	PRJNA512907
169088	6	Olga Dudchenko	3D genomics across the tree of life reveals condensin II as a determinant of architecture type	We investigated genome folding across the eukaryotic tree of life. We find four general manifestations of genome organization at chromosome-scale that	Olga Dudchenko, Erez Lieberman Aiden	26 species across the tree of life were included in the analysis, representing all subphyla of chordates, all 7 extant vertebrate classes, and 7 out of 9 major animal phyla, as well as plants and fungi.	34045355	60217	SRP175152	SRR16086824	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/015709/SRR16086824	Sample0054	SRA1300830	SRX12373284	Hi-C	PAIRED	SRP175152	PRJNA512907
169088	7	Olga Dudchenko	3D genomics across the tree of life reveals condensin II as a determinant of architecture type	We investigated genome folding across the eukaryotic tree of life. We find four general manifestations of genome organization at chromosome-scale that	Olga Dudchenko, Erez Lieberman Aiden	26 species across the tree of life were included in the analysis, representing all subphyla of chordates, all 7 extant vertebrate classes, and 7 out of 9 major animal phyla, as well as plants and fungi.	34045355	60217	SRP175152	SRR16086807	https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/015709/SRR16086807	Sample0155	SRA1300830	SRX12373301	Hi-C	PAIRED	SRP175152	PRJNA512907
179257	1	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014444	https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/014662/SRR15014444	GSM5412628	SRA1253486	SRX11326453	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	2	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014445	https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/014662/SRR15014445	GSM5412629	SRA1253486	SRX11326454	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	3	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014446	https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/014662/SRR15014446	GSM5412630	SRA1253486	SRX11326455	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	4	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014447	https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/014662/SRR15014447	GSM5412631	SRA1253486	SRX11326456	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	5	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014448	https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/014662/SRR15014448	GSM5412632	SRA1253486	SRX11326457	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	6	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014449	https://sra-download.ncbi.nlm.nih.gov/traces/sra62/SRR/014662/SRR15014449	GSM5412633	SRA1253486	SRX11326458	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	7	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014450	https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/014662/SRR15014450	GSM5412634	SRA1253486	SRX11326459	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	8	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014451	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/014662/SRR15014451	GSM5412635	SRA1253486	SRX11326460	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	9	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014452	https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/014662/SRR15014452	GSM5412636	SRA1253486	SRX11326461	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	10	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014453	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/014662/SRR15014453	GSM5412637	SRA1253486	SRX11326462	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	11	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014454	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/014662/SRR15014454	GSM5412638	SRA1253486	SRX11326463	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	12	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014455	https://sra-download.ncbi.nlm.nih.gov/traces/sra65/SRR/014662/SRR15014455	GSM5412639	SRA1253486	SRX11326464	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	13	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014456	https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/014662/SRR15014456	GSM5412640	SRA1253486	SRX11326465	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	14	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014457	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/014662/SRR15014457	GSM5412641	SRA1253486	SRX11326466	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	15	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014458	https://sra-download.ncbi.nlm.nih.gov/traces/sra74/SRR/014662/SRR15014458	GSM5412642	SRA1253486	SRX11326467	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	16	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014459	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/014662/SRR15014459	GSM5412643	SRA1253486	SRX11326468	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	17	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014460	https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/014662/SRR15014460	GSM5412644	SRA1253486	SRX11326469	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	18	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014461	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/014662/SRR15014461	GSM5412645	SRA1253486	SRX11326470	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	19	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014462	https://sra-download.ncbi.nlm.nih.gov/traces/sra60/SRR/014662/SRR15014462	GSM5412646	SRA1253486	SRX11326471	RNA-Seq	SINGLE	SRP326481	PRJNA743018
179257	20	Stéphane REYNAUD	Using RNAseq for identifying hepatic genes involved in  multi- (F1 generation) and transgenerational (F2 generation) responses to chronic benzo[a]pyrene  (BaP) and triclosan (TCS) mixture exposure (F0 generation) in Xenopus tropicalis.	We investigated the multi- and transgenerational impact of BaP and TCS mixture on Xenopus females following F0 generation exposure from the tadpole to	Stéphane REYNAUD	mRNAseq from liver of mature F1 and F2 females exposed to BaP and TCS mixture. Processed data file (Cuffdiff) have been performed by using RNAseq sequence from control mRNAseq data deposited on NCBI Gene Expression Omnibus (GEO) (accession no GSE150911)	0	60225	SRP326481	SRR15014463	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/014662/SRR15014463	GSM5412647	SRA1253486	SRX11326472	RNA-Seq	SINGLE	SRP326481	PRJNA743018
180671	1	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217956	https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRR/014861/SRR15217956	GSM5467454	SRA1263338	SRX11523907	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	2	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217957	https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/014861/SRR15217957	GSM5467455	SRA1263338	SRX11523908	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	3	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217958	https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/014861/SRR15217958	GSM5467456	SRA1263338	SRX11523909	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	4	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217959	https://sra-download.ncbi.nlm.nih.gov/traces/sra76/SRR/014861/SRR15217959	GSM5467457	SRA1263338	SRX11523910	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	5	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217960	https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/014861/SRR15217960	GSM5467458	SRA1263338	SRX11523911	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	6	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217961	https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/014861/SRR15217961	GSM5467459	SRA1263338	SRX11523912	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	7	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217962	https://sra-download.ncbi.nlm.nih.gov/traces/sra23/SRR/014861/SRR15217962	GSM5467460	SRA1263338	SRX11523913	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	8	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217963	https://sra-download.ncbi.nlm.nih.gov/traces/sra39/SRR/014861/SRR15217963	GSM5467461	SRA1263338	SRX11523914	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	9	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217964	https://sra-download.ncbi.nlm.nih.gov/traces/sra37/SRR/014861/SRR15217964	GSM5467462	SRA1263338	SRX11523915	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	10	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217965	https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/014861/SRR15217965	GSM5467463	SRA1263338	SRX11523916	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	11	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217966	https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRR/014861/SRR15217966	GSM5467464	SRA1263338	SRX11523917	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	12	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217967	https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRR/014861/SRR15217967	GSM5467465	SRA1263338	SRX11523918	RNA-Seq	PAIRED	SRP329511	PRJNA749055
180671	13	Richard Harland	Whole embryo depletion of Taf15 in gastrula and neurula stage Xenopus tropicalis embryos	We examined the role of Taf15 in in gastrula and neurula stage Xenopus tropicalis embryos.                                                            	Richard Harland, Caitlin DeJong, Darwin Dichmann, Cameron Exner, Yuxiao Xu, Richard Harland	To determine the role of Taf15 in early Xenopus development, we used RNA-sequencing (RNA-seq) from single embryos depleted of M- and Z-Taf15, using reagents that targeted either all mRNA by inhibiting translation with Morpholino antisense and mismatch oligonucleotides (MOs) or only zygotic function using splice-blocking MOs or CRISPR-mediated mutagenesis.	0	60230	SRP329511	SRR15217968	https://sra-download.ncbi.nlm.nih.gov/traces/sra45/SRR/014861/SRR15217968	GSM5467466	SRA1263338	SRX11523919	RNA-Seq	PAIRED	SRP329511	PRJNA749055
183350	1	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System assayed by 5hmC MeDIP and by ChIP-seq for Histone Markers	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Histone ChIP seq: Two biological replicates for each of the tissues and conditions used previously for WGBS (6 pooled eyes after optic nerve crush, from the operated side and contralateral unoperated side, plus 6 pooled eyes from unoperated animals; 5 pooled hindbrains from tadpoles and 5 from frogs subject to spinal cord injury (SCI) plus 5 pooled hindbrains from age-matched, uninjured tadpoles and frogs each. 5hmC DIP seq: performed on eye samples only, otherwise collected as for WGBS and histone ChIP-seq, with replicates (2) pooled for sequencing.	34979916	58796	SRP335528	SRR15712079	https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/015343/SRR15712079	GSM5555985	SRA1288414	SRX12007731	ChIP-Seq	SINGLE	SRP335528	PRJNA760351
183350	2	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System assayed by 5hmC MeDIP and by ChIP-seq for Histone Markers	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Histone ChIP seq: Two biological replicates for each of the tissues and conditions used previously for WGBS (6 pooled eyes after optic nerve crush, from the operated side and contralateral unoperated side, plus 6 pooled eyes from unoperated animals; 5 pooled hindbrains from tadpoles and 5 from frogs subject to spinal cord injury (SCI) plus 5 pooled hindbrains from age-matched, uninjured tadpoles and frogs each. 5hmC DIP seq: performed on eye samples only, otherwise collected as for WGBS and histone ChIP-seq, with replicates (2) pooled for sequencing.	34979916	58796	SRP335528	SRR15712080	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/015343/SRR15712080	GSM5555986	SRA1288414	SRX12007732	ChIP-Seq	SINGLE	SRP335528	PRJNA760351
183350	3	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System assayed by 5hmC MeDIP and by ChIP-seq for Histone Markers	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Histone ChIP seq: Two biological replicates for each of the tissues and conditions used previously for WGBS (6 pooled eyes after optic nerve crush, from the operated side and contralateral unoperated side, plus 6 pooled eyes from unoperated animals; 5 pooled hindbrains from tadpoles and 5 from frogs subject to spinal cord injury (SCI) plus 5 pooled hindbrains from age-matched, uninjured tadpoles and frogs each. 5hmC DIP seq: performed on eye samples only, otherwise collected as for WGBS and histone ChIP-seq, with replicates (2) pooled for sequencing.	34979916	58796	SRP335528	SRR15712081	https://sra-download.ncbi.nlm.nih.gov/traces/sra32/SRR/015343/SRR15712081	GSM5555987	SRA1288414	SRX12007733	ChIP-Seq	SINGLE	SRP335528	PRJNA760351
183355	1	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System Characterized by Whole Genome Bisulfite Sequencing (WGBS)	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Whole Genome Bisulfite Sequencing (WGBS: 15XGenome coverage per sample) was performed on 21 samples (3 biological replicates; 7 tissues/conditions): operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at 11 days post optic nerve crush, plus surgically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at 7 days post spinal cord transection, with 5 pooled hindbrains for each sample; juvenile frog hindbrain at 7 days after spinal cord transection, plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	34979916	58796	SRP335531	SRR15712136	https://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15712136/SRR15712136	GSM5556097	SRA1288417	SRX12007843	Bisulfite-Seq	PAIRED	SRP335531	PRJNA760352
183355	2	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System Characterized by Whole Genome Bisulfite Sequencing (WGBS)	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Whole Genome Bisulfite Sequencing (WGBS: 15XGenome coverage per sample) was performed on 21 samples (3 biological replicates; 7 tissues/conditions): operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at 11 days post optic nerve crush, plus surgically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at 7 days post spinal cord transection, with 5 pooled hindbrains for each sample; juvenile frog hindbrain at 7 days after spinal cord transection, plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	34979916	58796	SRP335531	SRR15712137	https://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15712137/SRR15712137	GSM5556098	SRA1288417	SRX12007844	Bisulfite-Seq	PAIRED	SRP335531	PRJNA760352
183355	3	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System Characterized by Whole Genome Bisulfite Sequencing (WGBS)	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Whole Genome Bisulfite Sequencing (WGBS: 15XGenome coverage per sample) was performed on 21 samples (3 biological replicates; 7 tissues/conditions): operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at 11 days post optic nerve crush, plus surgically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at 7 days post spinal cord transection, with 5 pooled hindbrains for each sample; juvenile frog hindbrain at 7 days after spinal cord transection, plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	34979916	58796	SRP335531	SRR15712138	https://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15712138/SRR15712138	GSM5556099	SRA1288417	SRX12007845	Bisulfite-Seq	PAIRED	SRP335531	PRJNA760352
183355	4	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System Characterized by Whole Genome Bisulfite Sequencing (WGBS)	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Whole Genome Bisulfite Sequencing (WGBS: 15XGenome coverage per sample) was performed on 21 samples (3 biological replicates; 7 tissues/conditions): operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at 11 days post optic nerve crush, plus surgically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at 7 days post spinal cord transection, with 5 pooled hindbrains for each sample; juvenile frog hindbrain at 7 days after spinal cord transection, plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	34979916	58796	SRP335531	SRR15712139	https://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15712139/SRR15712139	GSM5556100	SRA1288417	SRX12007846	Bisulfite-Seq	PAIRED	SRP335531	PRJNA760352
183355	5	Ben Szaro	Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate (Xenopus laevis) Central Nervous System Characterized by Whole Genome Bisulfite Sequencing (WGBS)	Xenopus is uniquely suited for identifying core features of successful CNS axon regeneration, because parts of its CNS (e.g., eye), regenerate axons t	Ben Szaro, Ben Szaro, Sergei Reverdatto, Xiang Zhang, Morgan Sammons, Kurt Gibbs	Whole Genome Bisulfite Sequencing (WGBS: 15XGenome coverage per sample) was performed on 21 samples (3 biological replicates; 7 tissues/conditions): operated juvenile frog eye and contralateral unoperated eye after optic nerve injury at 11 days post optic nerve crush, plus surgically naïve frog eyes, with 6 pooled eyes for each sample; tadpole hindbrain after spinal cord transection plus age-matched unoperated controls at 7 days post spinal cord transection, with 5 pooled hindbrains for each sample; juvenile frog hindbrain at 7 days after spinal cord transection, plus unoperated hindbrain control, with 5 pooled hindbrains for each sample.	34979916	58796	SRP335531	SRR15712140	https://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15712140/SRR15712140	GSM5556101	SRA1288417	SRX12007847	Bisulfite-Seq	PAIRED	SRP335531	PRJNA760352