run_metadata: 52233
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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| 52233 | SRR9022957 | SRX5800871 | SRS4730903 | SRP195753 | PRJNA541476 | Transcriptomic profiling of zebrafish livers with nAtf6 overexpression at collected at 78 hpf and 120 hpf | GSE130800 | Transcriptome Analysis | Activting transcription factor 6 Atf6 is one of three main mediators of the Unfolded Protein Response and it gets cleaved cleaved in the Golgi and its N terminal consisting of the bZip domain translocates into the nucleus to generate a transcriptional response nAtf6. This study carries out RNAseq on an established transgenic overexpression of nAtf6 in zebrafish hepatocytes tgfabp10:nAtf6 cherry; cmlc2:GFP C allele. Samples were collected at 78 hpf and 120 hpf to detect gene expression changes at early and late time points post nAtf6 is overexpressed. Overall design: We used two transgenic lines: Tgfabp10a: CAAX EGFP to use as a marker of the liver for dissction and tgfabp10:nAtf6 cherry; cmlc2:GFP C allele to overexpress nAtf6 specifically in hepatocytes.This experiment was conducted by natural spawnings between tg:fabp10:nAtf6 cherry; cmlc2:GFP C and tgfabp10a:CAAX EGFP . Using GFP to guide microdissscion of 20 25 livers at 78 hpf and 120 hpf . Total RNA isolated using TRIZOL and treated by DNAse I. Libraries were prepared using RiboZero for 120 hpf samples or polyA selection for 78 hpf samples. Samples from 2 clutches collected at 78 hpf and 3 clutches at 120 hpf. Samples were sequenced on NextSeq550 Illumina | parent bioproject:PRJNA541472 | sibslivr1: 5 dpf Livers non transgenic siblings 1 | GSM3754093 | source name:liver/pooled|tissue:pooled liver|genotype/variation:WT | sibslivr1: 5 dpf Livers non transgenic siblings 1 | Illumina Casava1.8 software used for basecalling. The raw reads were quality assessed using FastQC v0.11.5. The raw reads were then quality trimmed using Trimmomatic trimmomatic adapter.fa:2:30:10 TRAILING:3 LEADING:3 SLIDINGWINDOW:4:15 MINLEN:36 Alignments of trimmed reads were performed using tophat2 v2.1.0 with the parameters “–no novel junctions” and “–G” Accepted bam files were used for counting gene read numbers with HTSeq a 10 s no Test of differential expression of each transposonis was implemented by DESeq2 in Bioconductor Genome build: GRCz10 Supplementary files format and content: .txt Reads count of genes | liver/pooled | Tgfabp10:nAtf6 cherry; cmlc2:GFPC+/ were outcrossed to WT TAB 14 and the embryos were sorted and segregated basing on the expression of Cmlc2:GFP. The three different clutches of embryos were collected and dissected over three different days. The embryos were collected inbetween 10 11 AM. The Liver dissection was also performed on the 5dpf larvae before noon. 25 livers from 5dpf embryos were pooled per sample Transgenic and WT siblings in two different tubes and RNA extracted with Trizol as per manufacturer's instructions.The RNA was later treated with DNAse to remove any DNA. They RNA concentration was taken on the Q bit and then analysed on the Bioanalyser for the integrety and quality of RNA. The RIN score for the samples was above 8.5 RNA seq libraries were prepared according to Illumina TruSeq RNA sample preparation version 2 protocol with Ribo Zero Gold Catalog #: RS 122 2501 | tissue:pooled liver|genotype/variation:WT | GSM3754093 | GSM3754093: sibslivr1: 5 dpf Livers non transgenic siblings 1; Danio rerio; RNA Seq | GSM3754093 | 1 | Tgfabp10:nAtf6 cherry; cmlc2:GFPC+/ were outcrossed to WT TAB 14 and the embryos were sorted and segregated basing on the expression of Cmlc2:GFP. The three different clutches of embryos were collected and dissected over three different days. The embryos were collected inbetween 10 11 AM. The Liver dissection was also performed on the 5dpf larvae before noon. 25 livers from 5dpf embryos were pooled per sample Transgenic and WT siblings in two different tubes and RNA extracted with Trizol as per manufacturer's instructions.The RNA was later treated with DNAse to remove any DNA. They RNA concentration was taken on the Q bit and then analysed on the Bioanalyser for the integrety and quality of RNA. The RIN score for the samples was above 8.5 RNA seq libraries were prepared according to Illumina TruSeq RNA sample preparation version 2 protocol with Ribo Zero Gold Catalog #: RS 122 2501 | GEO Accession:GSM3754093 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP195753 | Sample_sibslivr1_read1.fastq.gz Sample_sibslivr1_read2.fastq.gz | fastq fastq | 6725147216.0 | 33292808.0 | GSM3754093 r1 | 0:101 1:101 | A:1807945249;C:1550856849;G:1534573991;T:1826050327;N:5720800 | 101 | 101 | 1807945249 | 1550856849 | 1534573991 | 1826050327 | 5720800 | SRX5800871 | SRS4730903 | SRA883585 | GEO | Biology, New York University Abu Dhabi | 2 | 0.90678 | 0.9037 | 0.2571 | 0.25652 | 0.76278 | 0.76577 | 0.58002 | 0.58511 | 101 | 101 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | poly_a | ribozero | bulk | unknown | unknown | United Arab Emirates | 2019-05-07 | Larval | Larval | Liver | Liver and Biliary System |