run_metadata: 38302
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 38302 | SRR1695730 | SRX798420 | SRS781712 | SRP050879 | PRJNA269540 | zebrafish transciptsome sequencing | PRJNA269540 | Other | we aimed to calculate the expression level of some special genes | Testis from Danio rerio | testis of zebrafish | strain:AB|dev stage:adult|sex:male|tissue:testis|biomaterial provider:zebrafish facilities of the Institute of Hydrobiology Chinese Academy of Sciences|BioSampleModel:Model organism or animal | RNA seq of zebrafish testis | testis of zebrafish | Zebrafish facilities of the Institute of Hydrobiology Chinese Academy of Sciences | Wild type zebrafish from an AB background were maintained in the zebrafish facilities of the Institute of Hydrobiology Chinese Academy of Sciences. Testis of adult is collected for RNA extraction. Total RNA extraction was performed with TRIZOL reagents from Takara following the manufacturer’s instructions. Total RNA contents were measured using the NanoDrop 2000. Then 5 μg total RNA was used for mRNA isolation with oligo dT magnetic beads and fragmented into small pieces in fragmentation buffer at 70°C for 4 min before cDNA synthesis. First strand cDNA was synthesized from the cleaved RNA using SuperScript II reverse transcriptase and random hexamer primers followed by second strand cDNA synthesis using DNA polymerase I and RNaseH. post purification with a QIAquick PCR Purification Kit Qiagen Dusseldorf Germany the double stranded cDNA was treated to repair ends by T4 DNA polymerase Klenow enzyme and T4 polynucleotide kinase NEB. This was followed by addition of a single A base using Klenow exo polymerase and ligation with an adapter using DNA ligase NEB. post ligation the DNA was purified using a QIAquick PCR Purification Kit. PCR amplification with 10 to 12 cycles was performed with primers complementary to the adapter sequences to enrich the samples for the desired fragments. post purification using a QIAquick PCR Purification Kit the product was dissolved in 30 µL of Qiagen EB buffer. These DNA fragments represented the designated mRNA library. The cDNA library was quantified with Qubit Invitrogen and a cluster of the DNA fragment was amplified using bridge PCR on the surface of a flow cell chip. Multiplexed libraries were sequenced for 101bp at both ends using an Illumina HiSeqTM 2000 platform. | RNA-Seq | TRANSCRIPTOMIC | RANDOM | PAIRED | ILLUMINA | Illumina HiSeq 2000 | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>202</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>102</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP050879 | Zebrafish_256-T14-VI_good_1.fq.gz Zebrafish_256-T14-VI_good_2.fq.gz | fastq fastq | 5252571430.0 | 26005174.0 | testis of zebrafish | 0:100.99 1:100.99 | A:1353125230;C:1273042497;G:1273793183;T:1350916239;N:1694281 | 100 | 100 | 1353125230 | 1273042497 | 1273793183 | 1350916239 | 1694281 | SRX798420 | SRS781712 | SRA210676 | CAS|systematic evolution | Institute of Hydrobiology, Chinese Academy of sciences | 2 | 0.93036 | 0.93332 | 0.09196 | 0.09372 | 0.64559 | 0.64806 | 0.48865 | 0.48746 | 101 | 101 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | random_priming | unknown | bulk | unknown | unknown | China | 2015-09-23 | Adult | Adult | Gonad | Reproductive System |