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ERX2187518: Illumina HiSeq 2000 sequencing; An RNASeq normal tissue atlas for mouse and rat
1 ILLUMINA (Illumina HiSeq 2000) run: 25.1M spots, 1.3G bases, 783.8Mb downloads

Design: An RNASeq normal tissue atlas for mouse and rat
Submitted by: Boehringer Ingelheim Pharma GmbH & Co. KG Target Discovery Research (Boehringer Ingelheim Pharma GmbH & Co. KG Target )
Study: An RNASeq normal tissue atlas for mouse and rat
show Abstracthide Abstract
The function of a gene is closely connected to its expression specificity across tissues and cell types. RNA-Seq is a powerful quantitative tool to explore genome wide expression. The aim of the present study is to provide a comprehensive RNA-Seq dataset across the same 13 tissues for mouse and rat, two of the most relevant species for biomedical research. The dataset provides the transcriptome across tissues from three male C57BL6 mice and three male Han Wistar rats. We also describe our bioinformatics pipeline to process and technically validate the data. Principal component analysis shows that tissue samples from both species cluster similarly. By comparative genomics we show that many genes with high sequence identity with respect to their human orthologues have also a highly correlated tissue distribution profile and are in agreement with manually curated literature data for human. These results make us confident that the present study provides a unique resource for comparative genomics and will facilitate the analysis of tissue specificity and cross-species conservation in higher organisms.
Sample: Sample 75
SAMEA104310481 • ERS1935459 • All experiments • All runs
Library:
Name: Sample 75_s
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: SINGLE
Construction protocol: Male Wistar Han rats (Crl:WI(Han)) and male BL/6J mice (C57BL/6J) were obtained from Charles River Laboratories (Germany). Experimental protocols concerning the use of laboratory animals were reviewed by a German Federal Ethics Committee and approved by German governmental authorities. Animals were housed in groups of three on a 12-h light/dark cycle and fed ad libitum a standard pelleted rodent diet (Diet No. 3438, Provimi Kliba Switzerland) with free access to water. Rats with a body weight of 160-180 g and rats and mice at the age of 7-8 weeks were used for tissue sampling. Retrobulbar blood samples were collected in the morning at 9 a.m. under isofluran anesthesia immediately prior to dissection. Animals (n = 3 for each species) were sacrificed thereafter by intraperitoneal injection of pentobarbital (rats) or cervical dislocation (mice) and tissues (esophagus, stomach, duodenum, jejunum, ileum, colon, pancreas, liver, thymus, kidney, heart, brain, quadriceps muscle) were harvested and transferred immediately to RNA Later at 4 degrees celsius. Total RNAs were individually extracted using the Ambion Magmax™-96 total RNA isolation kit (Life Sciences) according to the manufacturer’s instructions. Briefly, 5 mg of tissue was placed in the lysis solution and homogenized in Qiagen Tissuelyzer™ for a period of 30 sec. Nucleic acids were captured onto magnetic beads, washed and treated with DNase. Total RNA was then eluted in 50 μl elution buffer. RNA quality and concentration was measured using an RNA Pico chip on an Agilent Bioanalyzer. The Sequencing library preparation has been done using 200 ng of total RNA input with the TrueSeq RNA Sample Prep Kit v2-Set B (RS-122-2002, Illumina Inc, San Diego, CA) producing a 275bp fragment including adapters in average size. In the final step before sequencing, eight individual libraries were normalized and pooled together using the adapter indices supplied by the manufacturer.
Experiment attributes:
Experimental Factor: organism: Rattus norvegicus
Experimental Factor: organism part: heart
Runs: 1 run, 25.1M spots, 1.3G bases, 783.8Mb
Run# of Spots# of BasesSizePublished
ERR213066625,058,5661.3G783.8Mb2017-09-24

ID:
4516967

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