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SRX843456: GSM1585504: tbi2 (RRBS); Rattus norvegicus; Bisulfite-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 29.8M spots, 3G bases, 2.6Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: DNA methylation profile for male SD rats with and without traumatic brain injury (TBI) by RRBS
show Abstracthide Abstract
To investigate the effects of TBI on affecting the DNA methylation in the hippocampus of male SD rats by sequencing the methylome (RRBS). Overall design: Male Sprague–Dawley (SD) rats weighing between 200 and 240 g were housed in cages and maintained in environmentally-controlled rooms (22–24C) with a 12-h light/dark cycle. After acclimatization for 1 week on standard rat chow, the rats were subjected to TBI by fluid percussion injury (FPI) or sham surgery. At 1 week post-surgery the rats were tested for learning abilities, and then were sacrificed by decapitation. The fresh tissues including the hippocampus were dissected out, flash frozen, and stored at -70°C for later transcriptome and DNA methylome sequencing experiments. All experiments were performed in accordance with the United States National Institutes of Health Guide for the Care and Use of Laboratory Animals and were approved by the University of California at Los Angeles Chancellor’s Animal Research Committee.
Sample: tbi2 (RRBS)
SAMN03284610 • SRS819611 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: Reduced Representation
Layout: SINGLE
Construction protocol: Geome DNA was extracted with Qiagen AllPrep DNA/RNA Mini Kit. Quantity and quality of DNA were checked using Nanodrop (Thermo Fisher Scientific, MA, USA), Qubit RNA assay (Life Technologies, NY, USA) and gel electrophoresis Reduced representation bisulfite sequencing (RRBS) libraries were constructed as described previously with some modifications (Chen, P.Y. et al. Physiol Genomics 45, 565-576). Briefly, about 1,000 ng genomic DNA was digested with the MspI enzyme. Digested DNA was then purified, end-repaired, and adenylated, followed by ligation to Illumina TruSeq barcode adapters (Illumina Inc, CA, USA). Fragments of 150-300 bp in size were selected, bisulfite-treated, and sequenced using an Illumina Hiseq 2500 System (Illumina Inc, CA, USA).
Experiment attributes:
GEO Accession: GSM1585504
Links:
External link:
Runs: 1 run, 29.8M spots, 3G bases, 2.6Gb
Run# of Spots# of BasesSizePublished
SRR175937829,838,3403G2.6Gb2017-03-09

ID:
1193287

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