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ERX4030522: Illumina HiSeq 2500 paired end sequencing; RNA-seq of tissue panel samples from zebrafish (Danio rerio), medaka (Oryzias latipes), and rainbow trout (Oncorhynchus mykiss)
1 ILLUMINA (Illumina HiSeq 2500) run: 20.4M spots, 5.1G bases, 2.2Gb downloads

Design: RNA-seq of tissue panel samples from zebrafish (Danio rerio), medaka (Oryzias latipes), and rainbow trout (Oncorhynchus mykiss)
Submitted by: CIGENE, Faculty of Biosciences, The Norwegian University of Life Sciences (CIGENE, Faculty of Biosciences, The Norwegian Univ)
Study: RNA-seq of tissue panel samples from zebrafish (Danio rerio), medaka (Oryzias latipes), and rainbow trout (Oncorhynchus mykiss)
show Abstracthide Abstract
The aim of this sequencing experiment was to make available tissue expression panels for selected fish species for comparative expression studies between the species. Tissue samples were collected for zebrafish (Danio rerio), medaka (Oryzias latipes), and rainbow trout (Oncorhynchus mykiss). Tissue types included liver, skin, muscle, heart, gut, gill, eye, brain for all three species, with additionally pyloric caeca, kidney, head kidney, and spleen for rainbow trout. Only liver samples were taken in replicate of four or three for rainbow trout. All fish were raised under standard rearing conditions for the species. Total RNA was extracted from the tissue samples and paired-end sequencing of sample libraries was completed on an Illumina HiSeq 2500 with 125-bp reads. Processed count tables per species as raw counts, FPKM, or TPM, were generated from read alignment to the Ensembl genomes of the respective species using STAR and gene level counting using RSEM and Ensembl gene annotation.
Sample: RT_HK_1
SAMEA6786280 • ERS4513960 • All experiments • All runs
Library:
Name: RT_HK_1_p
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: Oligo-dT
Layout: PAIRED
Construction protocol: Tissue samples of multiple types were collected from adult individuals of zebrafish, medaka, and rainbow trout. Liver tissue samples were taken in replicates of four, or three in the case of rainbow trout. All fish were raised in fresh water under standard rearing conditions in aquaculture facilities (rainbow trout: Aquagen broodstock, tanks at NIVA solbergstranda), or animal laboratory facilities (zebrafish, medaka: VetBio, adamstuen). Total RNA was extracted from the tissue samples using the RNeasy Plus Universal Kit (QIAGEN). Quality was determined on a 2100 Bioanalyzer using the RNA 6000 Nano Kit (Agilent). Concentration was determined using a Nanodrop 8000 spectrophotometer (Thermo Scientific). cDNA libraries were prepared using the TruSeq Stranded mRNA HT Sample Prep Kit (Illumina). Library mean length was determined by running on a 2100 Bioanalyzer using the DNA 1000 Kit (Agilent) and library concentration was determined with the Qbit BR Kit (Thermo Scientific).
Experiment attributes:
Experimental Factor: organism part: head kidney
Experimental Factor: organism: Oncorhynchus mykiss
Runs: 1 run, 20.4M spots, 5.1G bases, 2.2Gb
Run# of Spots# of BasesSizePublished
ERR402920620,383,5625.1G2.2Gb2020-05-01

ID:
10711259

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