run_metadata: 8100
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8100 | ERR2402424 | ERX2443278 | ERS2295352 | ERP107516 | PRJEB25583 | The transcriptome of Gfi1aa and/or Gfi1b depleted primitive red blood cells in zebrafish embryos | ena-STUDY-DPSQ-14-03-2018-19:09:10:340-151 | Other | The zebrafish gene trap line qmc551 carries a gene trap transposon in intron 1 of the gene gfi1aa which a encodes a transcriptional repressor. The presence of the transposon interferes with the transcription of the gfi1aa gene during haematopoiesis. Despite the lack of Gfi1aa expression primitive red blood cell development appears to be normal due to functional redundancy with a second gene called gfi1b. Loss of Gfi1aa and Gfi1b protein expression in embryos that are homozygous for qmc551 and injected with gfi1b morpholinos leads to maturation defects in primitive red blood cells. Here we performed an RNA sequencing experiment to study the early programming of Gfi1aa and/or Gfi1b depleted primitive red blood cells. For this purpose we made use of the gene trap's gfp reporter gene expression in the primitive red blood cells to isolate these cells by fluorescence activated cell sorting from either qmc551 heterozygous or homozygous 20 hpf embryos that were or were not injected with the gfi1b morpholinos at the one cell stage. Batches of 200 embryos were dissociated in a Liberase Blendzyme solution. GFP positive primitive red blood cells were isolated by fluorescence activated cell sorting. 3 samples of between 1700 and 4000 cells were collected per batch. Total RNA was isolated from the cells of each of the 4 x 3 samples Het1 3 HetMO1 3 Hom1 3 and HomMO1 3 and used to generate full length cDNA of polyadenylated transcripts. Following cDNA amplification and library preparation paired end 75 bp reads were generated on the Illumina NextSeq500 sequencing platform. | ENA FIRST PUBLIC:2018 10 12|ENA LAST UPDATE:2018 03 14 | Het MO rep1 | Gfi1aa and/or Gfi1b depleted primitive red blood cells in zebrafish embryos | SAMEA104693969 | DPSQ | ENA FIRST PUBLIC:2018 10 12T17:03:15Z|ENA LAST UPDATE:2018 03 14T19:09:14Z|External Id:SAMEA104693969|INSDC center name:DPSQ|INSDC first public:2018 10 12T17:03:15Z|INSDC last update:2018 03 14T19:09:14Z|INSDC status:public|Submitter Id:CM4|common name:zebrafish|sample name:CM4|scientific name:Danio rerio | NextSeq 500 paired end sequencing | ena EXPERIMENT DPSQ 14 03 2018 19:09:09:420 4 | unspecified | 1 | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | NextSeq 500 | ERP107516 | NextSeq 500 paired end sequencing | ENA FIRST PUBLIC:2018 10 12|ENA LAST UPDATE:2018 11 16 | CM4.trimmed.read_1.fastq.gz CM4.trimmed.read_2.fastq.gz | fastq fastq | 5803404091.0 | 41335851.0 | ena RUN DPSQ 14 03 2018 19:09:09:420 4 | 0:70.72 1:69.67 | A:1590577583;C:1305683925;G:1331895549;T:1575219146;N:27888 | 70 | 69 | 1590577583 | 1305683925 | 1331895549 | 1575219146 | 27888 | ERX2443278 | ERS2295352 | ERA1246315 | European Nucleotide Archive | Deep Seq department, Centre for Genetics and Genomics, The University of Nottingham, United Kingdom | 2 | 0.9216 | 0.91971 | 0.05719 | 0.05738 | 0.77333 | 0.77761 | 0.47789 | 0.47244 | 76 | 74 | B | B | biological fallback assumption | illumina | nextseq | full_length | poly_a | unknown | bulk | unknown | unknown | United Kingdom | 2018-03-14 | Undetermined | Embryo | Blood | Hematopoietic System |