|
Status |
Public on Oct 31, 2014 |
Title |
F2 ind29 |
Sample type |
SRA |
|
|
Source name |
Liver
|
Organism |
Rattus norvegicus |
Characteristics |
Sex: Male tissue: liver genotype/variation: F2
|
Growth protocol |
The rats were bred and maintained in an approved animal facility in microisolator caging on a 12-hour light-dark cycle.
|
Extracted molecule |
polyA RNA |
Extraction protocol |
Total RNA was isolated from liver tissue using standard TRIzol methods (Chomczynski and Sacchi 1987). RNA quality was determined via a BioAnalyzer 2100 (Agilent Technologies, Santa Clara, CA, USA), using an RIN threshold of 7. RNA-Seq libraries were prepared with TruSeq RNA Sample Preparation Kits v2 (Illumina, San Diego, CA) according to manufacturer’s instructions.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Tophat (version 1.4.1) were used to map RNA-Seq reads to rat Ensembl transcripts first allowing up to 1 mismatch and the reads that were not fully mapped to the transcriptome will then be mapped to rat rn4 Ensembl genome allowing up to 2 mismatch. Only the uniquely mapped read pairs were subjected to downstream analyses. FPKMs (fragments per kb of exon per million sequence reads) were calculated using Cufflinks (version 2.0.0). Genome_build: rn4 Supplementary_files_format_and_content: Supplemental excel file includes the FPKM values of all samples.
|
|
|
Submission date |
Aug 20, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Jinkai Wang |
Organization name |
University of California, Los Angeles
|
Street address |
650 Charles E. Young Drive South, CHS 33-228
|
City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90095-7278 |
Country |
USA |
|
|
Platform ID |
GPL14844 |
Series (1) |
GSE50027 |
Systems biology with high-throughput sequencing revealed genetic mechanisms underlying the Metabolic Syndrome in the Lyon Hypertensive Rat |
|
Relations |
BioSample |
SAMN02319496 |
SRA |
SRX337425 |