run_metadata: 39947
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 |
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| 39947 | SRR2541817 | SRX1297639 | SRS1095797 | SRP064360 | PRJNA297460 | Female Reproductive Impacts of Dietary Methylmercury in Yellow Perch Perca flavescens and Zebrafish Danio rerio | GSE73615 | Transcriptome Analysis | This study sought to evaluate the effects of dietary MeHg exposure on adult female yellow perch Perca flavescens and zebrafish Danio rerio reproduction by relating controlled exposures with subsequent reproductive effects. Yellow perch were used in the study for their socioeconomic and ecological importance within the Great Lakes basin and the use of zebrafish allowed for a detailed analysis of the molecular effects of MeHg. MeHg exposures at environmentally relevant levels were done in zebrafish for a full life cycle mimicking a realistic exposure scenario and in adult yellow perch for twenty weeks capturing early seasonal ovarian development. In zebrafish several genes involved in reproductive processes were shown to be dysregulated by RNA seq and QPCR but no significant phenotypic or physiological changes were observed with ovarian staging fecundity or embryo mortality. Yellow perch did not appear to be affected by MeHg either at a molecular level as assessed by QPCR of eight genes in the pituitary liver and ovary tissue or a physiological level as seen with ovarian somatic index circulating estradiol and ovarian staging. Lack of impact in yellow perch limits the usefulness of zebrafish as a model and suggests that the reproductive sensitivity to environmentally relevant levels of MeHg differs between yellow perch and zebrafish. Overall design: 12 samples of total RNA isolated from adult zebrafish ovaries were analyzed. Each exposure group 1 3 and 10 ppm MeHg had three replicates as did the vehicle control. Each sample was comprised of pooled total RNA of up to 6 individual fish. | pubmed:29272799 | zfish 0ppm R3 | GSM1899548 | source name:ovary|tissue:ovary|strain:EK|mehg exposure:0 ppm | zfish 0ppm R3 | Basecalling was performed using CASAVA 1.8.2. Adapters and low quality bases were removed from the initial 2x101bp Illumina TruSeq reads and trimmed using Cutadapt The cleaned reads for each sample were independently aligned to the reference zebrafish genome Zv9 UCSC using TopHat The alignment output from TopHat was converted into a transcriptome using Cufflinks v. 2.2.1 and alignment data was confirmed using RNAseQC against the Zv9 reference transcriptome of zebrafish Sample specific transcriptomes were assembled using Cufflinks with the Zv9 transcriptome as a reference to correct fragment biases by better identifying the start/end point of each exon Transcriptomes from each sample were merged into an ovary specific transcriptome using Cuffmerge Differential expression was conducted with Cuffdiff using pooled dispersion geometric normalization and the merged ovary transcriptome. Genome build: UCSC Zv9 Supplementary files format and content: Cuffdiff outputs FPKM files which show expression values. Included in ovary.zip | ovary | Ovaries were flash frozen in RNA later and placed on dry ice immediately post dissection until proper storage at 80C. | High quality total RNA was extracted from the ovary using Direct zol* RNA MiniPrep kit Zymo Research. Total RNA for each sample was comprised of pooled RNA from up to six individual fish in order to reduce biological variance. Each library was generated using a paired end approach following the Illumina “TruSeq RNA Sample Preparation Guide” and the Illumina TruSeq RNA Sample Preparation Kit Illumina Inc. San Diego CA USA. Samples were run with 12 samples per lane with 100 base pair paired end reads. | Adult EK female zebrafish were exposed to MeHg 0 1 3 or 10 ppm with ethanol as the vehicle for an entire life cycle starting with maternal exposure. Fish were exposed until euthanized. | tissue:ovary|strain:EK|mehg exposure:0 ppm | GSM1899548 | GSM1899548: zfish 0ppm R3; Danio rerio; RNA Seq | GSM1899548 | 1 | High quality total RNA was extracted from the ovary using Direct zol* RNA MiniPrep kit Zymo Research. Total RNA for each sample was comprised of pooled RNA from up to six individual fish in order to reduce biological variance. Each library was generated using a paired end approach following the Illumina “TruSeq RNA Sample Preparation Guide” and the Illumina TruSeq RNA Sample Preparation Kit Illumina Inc. San Diego CA USA. Samples were run with 12 samples per lane with 100 base pair paired end reads. | GEO Accession:GSM1899548 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | SRP064360 | run448.R3-control_GGCTAC_L003_R1.fastq.gz run448.R3-control_GGCTAC_L003_R2.fastq.gz | fastq fastq | 1772836840.0 | 8776420.0 | GSM1899548 r1 | 0:101 1:101 | A:479859924;C:405519938;G:400658916;T:482250457;N:4547605 | 101 | 101 | 479859924 | 405519938 | 400658916 | 482250457 | 4547605 | SRX1297639 | SRS1095797 | SRA302185 | GEO | School of Freshwater Sciences, University of Wisconsin-Milwaukee | 2 | 0.91754 | 0.91556 | 0.02431 | 0.02395 | 0.74998 | 0.75012 | 0.45157 | 0.45334 | 101 | 101 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | trueseq | bulk | unknown | unknown | United States | 2015-09-30 | Adult | Adult | Gonad | Reproductive System |