rowid,run.accession,experiment.accession,sample.accession,study.accession,bioproject,study.title,study.alias,study.type,study.abstract,study.attributes,study.PMIDs,sample.description,sample.title,sample.alias,sample.centername,sample.attributes,GEOsample.title,GEOsample.dataprocessing,GEOsample.source,GEOsample.treatmentprotocol,GEOsample.extractprotocol,GEOsample.growthprotocol,GEOsample.characteristics,GEOsample.accession,experiment.title,experiment.alias,experiment.library_name,experiment.design_description,experiment.library_construction_protocol,experiment.attributes,experiment.library_strategy,experiment.library_source,experiment.library_selection,experiment.library_layout,experiment.platform,experiment.instrument_model,experiment.spot_descriptor,experiment.study_ref,run.title,run.attributes,run.filename,run.semantic_name,run.total_bases,run.total_spots,run.alias,run.read_lengths,run.base_counts,run.r1_length,run.r2_length,run.r3_length,run.r4_length,run.Acount,run.Ccount,run.Gcount,run.Tcount,run.Ncount,run.experiment,run.pool_member,submission.accession,submission.srasource,submission.bioprojectsource,seqdetective.n_mates,seqdetective.mapping_rate.mate1,seqdetective.mapping_rate.mate2,seqdetective.nofeature_rate.mate1,seqdetective.nofeature_rate.mate2,seqdetective.sparsity.mate1,seqdetective.sparsity.mate2,seqdetective.pos_strand_rate.mate1,seqdetective.pos_strand_rate.mate2,seqdetective.readlen.mate1,seqdetective.readlen.mate2,seqdetective.judgement.mate1,seqdetective.judgement.mate2,seqdetective.judgement.reason,platform_family,instrument_generation,read_bias,selection_class,prep_kit,sc_or_bulk,tech_class,technology,tech_variant,submission.bioprojectsource.country,earliest_date,devstage_curation,devstage_curation_coarse,tissue_curation,tissue_curation_coarse 39686,SRR2047225,SRX1045363,SRS950607,SRP058956,PRJNA285515,Danio rerio shield stage transcriptome,PRJNA285515,Transcriptome Analysis,Matched RNA seq to ribosome profiling,,,Matched to ribosome profiling experiments in SAMN02087561,Danio rerio Shield Stage Embryos RNA Seq,Shield Stage Embryos,,strain:TLAB|dev stage:Shield|sex:not determined|tissue:whole embryos|BioSampleModel:Model organism or animal,,,,,,,,,Shield Stage Embryos matched to Ribosome Profiling,Shield Stage Embryos,1,Standard multiplexed paired end RNA Seq on the Broad Institute platform.,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,Illumina HiSeq 2000,1520Application ReadForward11Application ReadReverse77,SRP058956,,,RPF-RNASeq_Shield_1_L.fastq.gz RPF-RNASeq_Shield_3_R.fastq.gz RPF-RNASeq_Shield_3_L.fastq.gz RPF-RNASeq_Shield_2_R.fastq.gz RPF-RNASeq_Shield_2_L.fastq.gz RPF-RNASeq_Shield_1_R.fastq.gz,fastq fastq fastq fastq fastq fastq,7345884728.0,48328189.0,Shield Stage Embryos,0:76 1:76,A:1932619942;C:1748899064;G:1767113490;T:1895258511;N:1993721,76,76,,,1932619942,1748899064,1767113490,1895258511,1993721,SRX1045363,SRS950607,SRA270772,Harvard University|Schier,Harvard University,2,0.94974,0.95573,0.08627,0.08599,0.76536,0.76812,0.4916,0.4943,76,76,B,B,biological fallback assumption,illumina,hiseq_era,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2015-06-03,Gastrula,Embryo,Whole Organism,All anatomical structures 49337,SRR7891983,SRX4729615,SRS3812053,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 24hpf whole embryo sample1 Lane1,3.I1 24 wy 1 Lane1,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 24hpf whole embryo sample1 Lane1|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 24hpf whole embryo sample1 Lane1,3.I1 24 wy 1 Lane1,3.I1 24 wy 1 Lane1,mH2A1 24hpf whole embryo sample1 Lane1,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,3.I1-24-wy-1-Lane1-R1.fastq 3.I1-24-wy-1-Lane1-R2.fastq,fastq fastq,509730568.0,3380092.0,3.I1 24 wy 1 Lane1 R1.fastq,0:75.48 1:75.33,A:125795631;C:125405901;G:134009974;T:124231387;N:287675,75,75,,,125795631,125405901,134009974,124231387,287675,SRX4729615,SRS3812053,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96512,0.96416,0.03453,0.0333,0.72328,0.7301,0.45116,0.46056,76,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2018-09-22,Gastrula,Embryo,Whole Organism,All anatomical structures 49341,SRR7891987,SRX4729611,SRS3812049,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo sample1 Lane1,1.I1 ep wy 1 Lane1,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo sample1 Lane1|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo sample1 Lane1,1.I1 ep wy 1 Lane1,1.I1 ep wy 1 Lane1,mH2A1 75% epiboly whole embryo sample1 Lane1,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,1.I1-ep-wy-1-Lane1-R1.fastq 1.I1-ep-wy-1-Lane1-R2.fastq,fastq fastq,456184111.0,3022885.0,1.I1 ep wy 1 Lane1 R2.fastq,0:75.49 1:75.42,A:124801154;C:101476348;G:105797177;T:123852606;N:256826,75,75,,,124801154,101476348,105797177,123852606,256826,SRX4729611,SRS3812049,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.86441,0.86837,0.12005,0.11911,0.78301,0.7848,0.53529,0.53799,76,74,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49342,SRR7891988,SRX4729610,SRS3812048,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo sample1 Lane2,1.I1 ep wy 1 Lane2,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo sample1 Lane2|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo sample1 Lane2,1.I1 ep wy 1 Lane2,1.I1 ep wy 1 Lane2,mH2A1 75% epiboly whole embryo sample1 Lane2,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,1.I1-ep-wy-1-Lane2-R1.fastq 1.I1-ep-wy-1-Lane2-R2.fastq,fastq fastq,444073291.0,2942645.0,1.I1 ep wy 1 Lane2 R2.fastq,0:75.49 1:75.42,A:121583905;C:98843982;G:102905490;T:120494449;N:245465,75,75,,,121583905,98843982,102905490,120494449,245465,SRX4729610,SRS3812048,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.86283,0.86631,0.12072,0.11849,0.78397,0.78516,0.53735,0.5281,74,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2018-09-22,Gastrula,Embryo,Whole Organism,All anatomical structures 49343,SRR7891989,SRX4729609,SRS3812047,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample1 Lane3,9.I2 epi gfp 1 Lane3,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample1 Lane3|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample1 Lane3,9.I2 epi gfp 1 Lane3,9.I2 epi gfp 1 Lane3,mH2A2 75% epiboly GFP sample1 Lane3,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,9.I2-epi-gfp-1-Lane3-R1.fastq 9.I2-epi-gfp-1-Lane3-R2.fastq,fastq fastq,502199133.0,3328291.0,9.I2 epi gfp 1 Lane3 R1.fastq,0:75.51 1:75.38,A:129406575;C:119580810;G:123955765;T:128950548;N:305435,75,75,,,129406575,119580810,123955765,128950548,305435,SRX4729609,SRS3812047,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96374,0.96625,0.06525,0.06451,0.76315,0.76532,0.50665,0.50497,76,35,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49345,SRR7891991,SRX4729607,SRS3812045,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo without xxx sample1 Lane1,2.I1 ep woy 1 Lane1,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo whitout yolk|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo without xxx sample1 Lane1|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo without xxx sample1 Lane1,2.I1 ep woy 1 Lane1,2.I1 ep woy 1 Lane1,mH2A1 75% epiboly whole embryo without xxx sample1 Lane1,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,2.I1-ep-woy-1-Lane1-R1.fastq 2.I1-ep-woy-1-Lane1-R2.fastq,fastq fastq,495265704.0,3281045.0,2.I1 ep woy 1 Lane1 R2.fastq,0:75.51 1:75.44,A:140352102;C:107215423;G:109240908;T:138188537;N:268734,75,75,,,140352102,107215423,109240908,138188537,268734,SRX4729607,SRS3812045,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.93815,0.94258,0.09194,0.08757,0.78843,0.78764,0.50789,0.50592,76,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49346,SRR7891992,SRX4729606,SRS3812044,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo without xxx sample1 Lane2,2.I1 ep woy 1 Lane2,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo whitout yolk|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo without xxx sample1 Lane2|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo without xxx sample1 Lane2,2.I1 ep woy 1 Lane2,2.I1 ep woy 1 Lane2,mH2A1 75% epiboly whole embryo without xxx sample1 Lane2,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,2.I1-ep-woy-1-Lane2-R1.fastq 2.I1-ep-woy-1-Lane2-R2.fastq,fastq fastq,482046254.0,3193445.0,2.I1 ep woy 1 Lane2 R1.fastq,0:75.51 1:75.44,A:136696224;C:104395317;G:106243276;T:134451171;N:260266,75,75,,,136696224,104395317,106243276,134451171,260266,SRX4729606,SRS3812044,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.93845,0.94352,0.09271,0.08933,0.78644,0.78614,0.50588,0.50714,76,75,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49347,SRR7891993,SRX4729605,SRS3812043,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample1 Lane4,9.I2 epi gfp 1 Lane4,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample1 Lane4|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample1 Lane4,9.I2 epi gfp 1 Lane4,9.I2 epi gfp 1 Lane4,mH2A2 75% epiboly GFP sample1 Lane4,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,9.I2-epi-gfp-1-Lane4-R1.fastq 9.I2-epi-gfp-1-Lane4-R2.fastq,fastq fastq,486218126.0,3222419.0,9.I2 epi gfp 1 Lane4 R1.fastq,0:75.51 1:75.38,A:125547722;C:115764880;G:119631877;T:124996326;N:277321,75,75,,,125547722,115764880,119631877,124996326,277321,SRX4729605,SRS3812043,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96348,0.96647,0.06552,0.06421,0.76295,0.76522,0.50657,0.50703,76,35,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49348,SRR7891994,SRX4729604,SRS3812042,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 24hpf whole embryo sample1 Lane2,3.I1 24 wy 1 Lane2,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 24hpf whole embryo sample1 Lane2|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 24hpf whole embryo sample1 Lane2,3.I1 24 wy 1 Lane2,3.I1 24 wy 1 Lane2,mH2A1 24hpf whole embryo sample1 Lane2,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,3.I1-24-wy-1-Lane2-R1.fastq 3.I1-24-wy-1-Lane2-R2.fastq,fastq fastq,500221294.0,3317079.0,3.I1 24 wy 1 Lane2 R2.fastq,0:75.48 1:75.33,A:123749555;C:123078893;G:131273530;T:121835014;N:284302,75,75,,,123749555,123078893,131273530,121835014,284302,SRX4729604,SRS3812042,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.9659,0.96472,0.03479,0.03377,0.7234,0.73113,0.45541,0.46895,74,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49349,SRR7891995,SRX4729603,SRS3812040,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample2 Lane1,10.I2 epi gfp 2 Lane1,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample2 Lane1|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample2 Lane1,10.I2 epi gfp 2 Lane1,10.I2 epi gfp 2 Lane1,mH2A2 75% epiboly GFP sample2 Lane1,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,10.I2-epi-gfp-2-Lane1-R1.fastq 10.I2-epi-gfp-2-Lane1-R2.fastq,fastq fastq,283096715.0,1877442.0,10.I2 epi gfp 2 Lane1 R2.fastq,0:75.48 1:75.31,A:71033881;C:69720110;G:70846628;T:71338427;N:157669,75,75,,,71033881,69720110,70846628,71338427,157669,SRX4729603,SRS3812040,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.9661,0.96876,0.05255,0.05163,0.75532,0.75824,0.48277,0.48181,75,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49355,SRR7892001,SRX4729597,SRS3812034,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo sample2 Lane1,5.I1 ep wy 2 Lane1,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo sample2 Lane1|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo sample2 Lane1,5.I1 ep wy 2 Lane1,5.I1 ep wy 2 Lane1,mH2A1 75% epiboly whole embryo sample2 Lane1,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,5.I1-ep-wy-2-Lane1-R1.fastq 5.I1-ep-wy-2-Lane1-R2.fastq,fastq fastq,348574840.0,2310385.0,5.I1 ep wy 2 Lane1 R2.fastq,0:75.51 1:75.36,A:87586701;C:85471128;G:86825811;T:88495175;N:196025,75,75,,,87586701,85471128,86825811,88495175,196025,SRX4729597,SRS3812034,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96823,0.97031,0.05454,0.05391,0.74888,0.75128,0.4766,0.47474,76,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49356,SRR7892002,SRX4729596,SRS3812033,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo sample2 Lane2,5.I1 ep wy 2 Lane2,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo sample2 Lane2|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo sample2 Lane2,5.I1 ep wy 2 Lane2,5.I1 ep wy 2 Lane2,mH2A1 75% epiboly whole embryo sample2 Lane2,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,5.I1-ep-wy-2-Lane2-R1.fastq 5.I1-ep-wy-2-Lane2-R2.fastq,fastq fastq,340915369.0,2259615.0,5.I1 ep wy 2 Lane2 R2.fastq,0:75.52 1:75.36,A:85706953;C:83634858;G:84896890;T:86487487;N:189181,75,75,,,85706953,83634858,84896890,86487487,189181,SRX4729596,SRS3812033,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96775,0.96955,0.05347,0.05233,0.74809,0.75233,0.47816,0.47993,76,75,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49359,SRR7892005,SRX4729593,SRS3812030,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo sample2 Lane3,5.I1 ep wy 2 Lane3,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo sample2 Lane3|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo sample2 Lane3,5.I1 ep wy 2 Lane3,5.I1 ep wy 2 Lane3,mH2A1 75% epiboly whole embryo sample2 Lane3,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,5.I1-ep-wy-2-Lane3-R1.fastq 5.I1-ep-wy-2-Lane3-R2.fastq,fastq fastq,352736044.0,2337910.0,5.I1 ep wy 2 Lane3 R1.fastq,0:75.52 1:75.36,A:88637067;C:86501628;G:87864984;T:89524754;N:207611,75,75,,,88637067,86501628,87864984,89524754,207611,SRX4729593,SRS3812030,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96809,0.97112,0.05336,0.0528,0.74718,0.75079,0.47718,0.47679,75,35,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49360,SRR7892006,SRX4729592,SRS3812029,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo sample2 Lane4,5.I1 ep wy 2 Lane4,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo sample2 Lane4|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo sample2 Lane4,5.I1 ep wy 2 Lane4,5.I1 ep wy 2 Lane4,mH2A1 75% epiboly whole embryo sample2 Lane4,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,5.I1-ep-wy-2-Lane4-R1.fastq 5.I1-ep-wy-2-Lane4-R2.fastq,fastq fastq,341106146.0,2260869.0,5.I1 ep wy 2 Lane4 R2.fastq,0:75.51 1:75.36,A:85837100;C:83646068;G:84779770;T:86645340;N:197868,75,75,,,85837100,83646068,84779770,86645340,197868,SRX4729592,SRS3812029,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96757,0.97029,0.05363,0.05278,0.74848,0.75136,0.47365,0.47505,76,35,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49362,SRR7892008,SRX4729590,SRS3812027,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample2 Lane4,10.I2 epi gfp 2 Lane4,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample2 Lane4|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample2 Lane4,10.I2 epi gfp 2 Lane4,10.I2 epi gfp 2 Lane4,mH2A2 75% epiboly GFP sample2 Lane4,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,10.I2-epi-gfp-2-Lane4-R1.fastq 10.I2-epi-gfp-2-Lane4-R2.fastq,fastq fastq,275588852.0,1827633.0,10.I2 epi gfp 2 Lane4 R1.fastq,0:75.47 1:75.32,A:69217962;C:67868461;G:68900002;T:69448617;N:153810,75,75,,,69217962,67868461,68900002,69448617,153810,SRX4729590,SRS3812027,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96617,0.96905,0.05181,0.05089,0.75444,0.75724,0.48295,0.48648,75,35,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49368,SRR7892014,SRX4729584,SRS3812021,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample1 Lane1,9.I2 epi gfp 1 Lane1,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample1 Lane1|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample1 Lane1,9.I2 epi gfp 1 Lane1,9.I2 epi gfp 1 Lane1,mH2A2 75% epiboly GFP sample1 Lane1,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,9.I2-epi-gfp-1-Lane1-R1.fastq 9.I2-epi-gfp-1-Lane1-R2.fastq,fastq fastq,496992545.0,3293963.0,9.I2 epi gfp 1 Lane1 R2.fastq,0:75.50 1:75.38,A:128042542;C:118343159;G:122636262;T:127690969;N:279613,75,75,,,128042542,118343159,122636262,127690969,279613,SRX4729584,SRS3812021,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96413,0.96584,0.06548,0.06473,0.76185,0.76445,0.50648,0.48968,76,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49369,SRR7892015,SRX4729583,SRS3812020,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample2 Lane2,10.I2 epi gfp 2 Lane2,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample2 Lane2|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample2 Lane2,10.I2 epi gfp 2 Lane2,10.I2 epi gfp 2 Lane2,mH2A2 75% epiboly GFP sample2 Lane2,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,10.I2-epi-gfp-2-Lane2-R1.fastq 10.I2-epi-gfp-2-Lane2-R2.fastq,fastq fastq,274447059.0,1820114.0,10.I2 epi gfp 2 Lane2 R1.fastq,0:75.47 1:75.31,A:68897661;C:67603576;G:68690482;T:69098427;N:156913,75,75,,,68897661,67603576,68690482,69098427,156913,SRX4729583,SRS3812020,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96618,0.96899,0.05169,0.05083,0.75329,0.75562,0.48252,0.48334,76,75,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49370,SRR7892016,SRX4729582,SRS3812019,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample1 Lane2,9.I2 epi gfp 1 Lane2,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample1 Lane2|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample1 Lane2,9.I2 epi gfp 1 Lane2,9.I2 epi gfp 1 Lane2,mH2A2 75% epiboly GFP sample1 Lane2,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,9.I2-epi-gfp-1-Lane2-R1.fastq 9.I2-epi-gfp-1-Lane2-R2.fastq,fastq fastq,487522081.0,3231144.0,9.I2 epi gfp 1 Lane2 R1.fastq,0:75.51 1:75.38,A:125725899;C:116093393;G:120228604;T:125197332;N:276853,75,75,,,125725899,116093393,120228604,125197332,276853,SRX4729582,SRS3812019,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96515,0.96702,0.06617,0.06504,0.76228,0.76487,0.50462,0.50964,76,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49379,SRR7892025,SRX4729573,SRS3812010,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A2 75% epiboly GFP sample2 Lane3,10.I2 epi gfp 2 Lane3,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo without xxx|genotype:TgmH2A2:GFP mH2A2.|samples information:mH2A2 75% epiboly GFP sample2 Lane3|BioSampleModel:Model organism or animal,,,,,,,,,mH2A2 75% epiboly GFP sample1 Lane3,10.I2 epi gfp 2 Lane3,10.I2 epi gfp 2 Lane3,mH2A2 75% epiboly GFP sample2 Lane3,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,10.I2-epi-gfp-2-Lane3-R1.fastq 10.I2-epi-gfp-2-Lane3-R2.fastq,fastq fastq,283548008.0,1880401.0,10.I2 epi gfp 2 Lane3 R2.fastq,0:75.47 1:75.32,A:71164597;C:69817830;G:70971963;T:71419845;N:173773,75,75,,,71164597,69817830,70971963,71419845,173773,SRX4729573,SRS3812010,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96659,0.96842,0.05301,0.05119,0.75574,0.75765,0.48105,0.48291,75,35,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49385,SRR7892031,SRX4729567,SRS3812005,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane4,6.I1 ep woy 2 Lane4,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo whitout yolk|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo without xxx sample2 Lane4|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane4,6.I1 ep woy 2 Lane4,6.I1 ep woy 2 Lane4,mH2A1 75% epiboly whole embryo without xxx sample2 Lane4,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,6.I1-ep-woy-2-Lane4-R1.fastq 6.I1-ep-woy-2-Lane4-R2.fastq,fastq fastq,399315530.0,2646139.0,6.I1 ep woy 2 Lane4 R2.fastq,0:75.53 1:75.38,A:101597801;C:96127596;G:100204030;T:101154602;N:231501,75,75,,,101597801,96127596,100204030,101154602,231501,SRX4729567,SRS3812005,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96719,0.96886,0.06314,0.06238,0.76094,0.76546,0.47959,0.47867,75,35,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49386,SRR7892032,SRX4729566,SRS3812054,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane3,6.I1 ep woy 2 Lane3,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo whitout yolk|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo without xxx sample2 Lane3|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane3,6.I1 ep woy 2 Lane3,6.I1 ep woy 2 Lane3,mH2A1 75% epiboly whole embryo without xxx sample2 Lane3,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,6.I1-ep-woy-2-Lane3-R2.fastq 6.I1-ep-woy-2-Lane3-R1.fastq,fastq fastq,413007665.0,2736835.0,6.I1 ep woy 2 Lane3 R1.fastq,0:75.53 1:75.38,A:104836023;C:99402397;G:104036766;T:104479363;N:253116,75,75,,,104836023,99402397,104036766,104479363,253116,SRX4729566,SRS3812054,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96709,0.96695,0.06398,0.06227,0.764,0.76832,0.47279,0.48091,76,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49387,SRR7892033,SRX4729565,SRS3812002,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane2,6.I1 ep woy 2 Lane2,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo whitout yolk|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo without xxx sample2 Lane2|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane2,6.I1 ep woy 2 Lane2,6.I1 ep woy 2 Lane2,mH2A1 75% epiboly whole embryo without xxx sample2 Lane2,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,6.I1-ep-woy-2-Lane2-R1.fastq 6.I1-ep-woy-2-Lane2-R2.fastq,fastq fastq,400065434.0,2651135.0,6.I1 ep woy 2 Lane2 R1.fastq,0:75.53 1:75.38,A:101671787;C:96307451;G:100694248;T:101171404;N:220544,75,75,,,101671787,96307451,100694248,101171404,220544,SRX4729565,SRS3812002,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96698,0.96785,0.06431,0.0634,0.76357,0.76816,0.47461,0.47488,73,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures 49388,SRR7892034,SRX4729564,SRS3812003,SRP162371,PRJNA492713,Zebrafish macroH2A variants analysis reveals distinct embryo localization and function RNASeq Information,PRJNA492713,Other,Most mouse and cell based studies have shown that macroH2A histone variants predominantly associate with heterochromatin and have been associated with gene repression and with an important function in cell differentiation and inhibiting acquisition of pluripotency of pluripotency. However fewer studies have analysed the role of macroH2A during early embryo development. In the project transgenic zebrafish lines were developed expressing macroH2A isoforms mH2A1 and mH2A2 fusion proteins GFP under endogenous identified promoters to study their function during embryogenesis.,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane1,6.I1 ep woy 2 Lane1,,strain:TAB.L ABxTL|dev stage:75% epiboly|sex:pooled male and female|tissue:whole embryo whitout yolk|genotype:Tg mH2A1:GFP mH2A1|samples information:mH2A1 75% epiboly whole embryo without xxx sample2 Lane1|BioSampleModel:Model organism or animal,,,,,,,,,mH2A1 75% epiboly whole embryo without xxx sample2 Lane1,6.I1 ep woy 2 Lane1,6.I1 ep woy 2 Lane1,mH2A1 75% epiboly whole embryo without xxx sample2 Lane1,,,RNA-Seq,TRANSCRIPTOMIC,PolyA,PAIRED,ILLUMINA,NextSeq 500,,SRP162371,,,6.I1-ep-woy-2-Lane1-R1.fastq 6.I1-ep-woy-2-Lane1-R2.fastq,fastq fastq,409551882.0,2714002.0,6.I1 ep woy 2 Lane1 R1.fastq,0:75.53 1:75.38,A:103918289;C:98573178;G:103190444;T:103638452;N:231519,75,75,,,103918289,98573178,103190444,103638452,231519,SRX4729564,SRS3812003,SRA782245,University of Nebraska Lincoln|Electrical and Computer Engineering,University of Nebraska Lincoln,2,0.96801,0.96789,0.06315,0.06224,0.76025,0.76451,0.47347,0.47998,76,76,B,B,biological fallback assumption,illumina,nextseq,unknown,poly_a,unknown,bulk,unknown,unknown,,United States,2019-10-21,Gastrula,Embryo,Whole Organism,All anatomical structures