run_metadata
23 rows where devstage_curation = "Gastrula" and experiment.library_selection = "PolyA"
This data as json, CSV (advanced)
| Link | 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 | 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 | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>152</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC><READ_SPEC><READ_INDEX>1</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Reverse</READ_TYPE><BASE_COORD>77</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 |
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CREATE TABLE run_metadata("run.accession" VARCHAR, "experiment.accession" VARCHAR, "sample.accession" VARCHAR, "study.accession" VARCHAR, bioproject VARCHAR, "study.title" VARCHAR, "study.alias" VARCHAR, "study.type" VARCHAR, "study.abstract" VARCHAR, "study.attributes" VARCHAR, "study.PMIDs" VARCHAR, "sample.description" VARCHAR, "sample.title" VARCHAR, "sample.alias" VARCHAR, "sample.centername" VARCHAR, "sample.attributes" VARCHAR, "GEOsample.title" VARCHAR, "GEOsample.dataprocessing" VARCHAR, "GEOsample.source" VARCHAR, "GEOsample.treatmentprotocol" VARCHAR, "GEOsample.extractprotocol" VARCHAR, "GEOsample.growthprotocol" VARCHAR, "GEOsample.characteristics" VARCHAR, "GEOsample.accession" VARCHAR, "experiment.title" VARCHAR, "experiment.alias" VARCHAR, "experiment.library_name" VARCHAR, "experiment.design_description" VARCHAR, "experiment.library_construction_protocol" VARCHAR, "experiment.attributes" VARCHAR, "experiment.library_strategy" VARCHAR, "experiment.library_source" VARCHAR, "experiment.library_selection" VARCHAR, "experiment.library_layout" VARCHAR, "experiment.platform" VARCHAR, "experiment.instrument_model" VARCHAR, "experiment.spot_descriptor" VARCHAR, "experiment.study_ref" VARCHAR, "run.title" VARCHAR, "run.attributes" VARCHAR, "run.filename" VARCHAR, "run.semantic_name" VARCHAR, "run.total_bases" DOUBLE, "run.total_spots" DOUBLE, "run.alias" VARCHAR, "run.read_lengths" VARCHAR, "run.base_counts" VARCHAR, "run.r1_length" BIGINT, "run.r2_length" BIGINT, "run.r3_length" BIGINT, "run.r4_length" BIGINT, "run.Acount" BIGINT, "run.Ccount" BIGINT, "run.Gcount" BIGINT, "run.Tcount" BIGINT, "run.Ncount" BIGINT, "run.experiment" VARCHAR, "run.pool_member" VARCHAR, "submission.accession" VARCHAR, "submission.srasource" VARCHAR, "submission.bioprojectsource" VARCHAR, "seqdetective.n_mates" BIGINT, "seqdetective.mapping_rate.mate1" DOUBLE, "seqdetective.mapping_rate.mate2" DOUBLE, "seqdetective.nofeature_rate.mate1" DOUBLE, "seqdetective.nofeature_rate.mate2" DOUBLE, "seqdetective.sparsity.mate1" DOUBLE, "seqdetective.sparsity.mate2" DOUBLE, "seqdetective.pos_strand_rate.mate1" DOUBLE, "seqdetective.pos_strand_rate.mate2" DOUBLE, "seqdetective.readlen.mate1" BIGINT, "seqdetective.readlen.mate2" BIGINT, "seqdetective.judgement.mate1" VARCHAR, "seqdetective.judgement.mate2" VARCHAR, "seqdetective.judgement.reason" VARCHAR, platform_family VARCHAR, instrument_generation VARCHAR, read_bias VARCHAR, selection_class VARCHAR, prep_kit VARCHAR, sc_or_bulk VARCHAR, tech_class VARCHAR, technology VARCHAR, tech_variant VARCHAR, "submission.bioprojectsource.country" VARCHAR, earliest_date DATE, devstage_curation VARCHAR, devstage_curation_coarse VARCHAR, tissue_curation VARCHAR, tissue_curation_coarse VARCHAR);;
CREATE INDEX idx_run_bioproject ON run_metadata(bioproject);;
CREATE INDEX idx_run_run_accession ON run_metadata("run.accession");;