run_metadata: 60453
This data as json
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 60453 | SRR12283716 | SRX8787095 | SRS7055742 | SRP273008 | PRJNA647599 | Transcriptome of nkx2.2a+ olig2+ dbx1b+ cells from 14hpf zebrafish embryo | GSE154885 | Transcriptome Analysis | cDNA extracted from FACS sorted GFP positive cells taken from trunk region of 14hpf zebrafish embryo with transgenic reporter TgBACnkx2.2a:memGFP TgBAColig2:GFP or TgBACdbx1b:GFP Overall design: transcriptome of nkx2.2a+ olig2+ dbx1b+ cells from 14hpf zebrafish embryo | pubmed:33004519 | TgBAColig2:GFP positive cells 2 | GSM4681844 | tissue:FACS sorted olig2 + neural progenitors|age:14hpf|genotype:WT | TgBAColig2:GFP positive cells 2 | Sequenced reads were filtered by fastqc 0.11.3 then mapped to GRCz10 whole genome using bowtie 1.1.1 with parameters q n 2 l 28 e 1000 I 0 X 1000 k 1 m 200 Reads Per Kilobase of exon per Megabase of library size RPKM were calculated. Genome build: GRCz10 Supplementary files format and content: tab delimited text files include gene names gene length mapped count unmapped count Supplementary files format and content: excel spreadsheet with gene names and transcript count in each sample | FACS sorted olig2 + neural progenitors | 14hpf zebrafish embryos were dissected to remove the brain and tail region. The trunk region is dissociated by mechanical pipetting in FACSMax solution. The dissociated cells are resuspended in PBS FACS sorted for GFP positive cells. The sorted cells are spun down and the pellet was flash frozen in Trizol for RNA extraction. RNA libraries were prepared for sequencing using standard Illumina protocols | age:14hpf|genotype:WT | GSM4681844 | GSM4681844: TgBAColig2:GFP positive cells 2; Danio rerio; RNA Seq | GSM4681844 | 1 | 14hpf zebrafish embryos were dissected to remove the brain and tail region. The trunk region is dissociated by mechanical pipetting in FACSMax solution. The dissociated cells are resuspended in PBS FACS sorted for GFP positive cells. The sorted cells are spun down and the pellet was flash frozen in Trizol for RNA extraction. RNA libraries were prepared for sequencing using standard Illumina protocols | GEO Accession:GSM4681844 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP273008 | LIB018768_TRA00046535_S12_L002_R1.fastq LIB018768_TRA00046535_S12_L002_R2.fastq | fastq fastq | 1883562500.0 | 18835625.0 | GSM4681844 r1 | 0:50 1:50 | A:538880974;C:389273777;G:399233943;T:555933855;N:239951 | 50 | 50 | 538880974 | 389273777 | 399233943 | 555933855 | 239951 | SRX8787095 | SRS7055742 | SRA1102160 | GEO | Sean Megason, Systems Biology, Harvard Medical School | 2 | 0.83434 | 0.81762 | 0.28607 | 0.27612 | 0.77804 | 0.78137 | 0.67234 | 0.67724 | 50 | 50 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | random_priming | unknown | bulk | unknown | unknown | United States | 2020-07-22 | Segmentation | Embryo | Multi-tissue | Multi-system |