NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4131024 Query DataSets for GSM4131024
Status Public on Oct 20, 2020
Title cattle_muscle_3
Sample type SRA
 
Source name high IMF
Organism Bos taurus
Characteristics intramuscular fat: high IMF
tissue: muscle
Treatment protocol Animals were weaned at three months of age, castrated at six months of age, started to fatten at 18 months of age, and slaughtered at 30 months of age.
Growth protocol Three Xinyang buffalo and three Nanyang cattle were raised in the breeding farm of Xinyang Buffalo (Guangshan, Henan province, P.R. China) and the breeding center of Nanyang cattle (Nanyang, Henan province, P.R. China), respectively, with equivalent forage and feeding management conditions.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using TRIzol reagent (Invitrogen, USA). The quality and concentration of total RNA were determined by the NanoDrop 2,000 (Nanodrop, Wilmington, DE) and 1% agarose gel.
Approximately 2 μg total RNA per sample was used for library construction according to protocol of the TruSeq® RNA LT Sample Prep Kit v2 (Illumina, USA).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 3000
 
Data processing Low-quality reads and those containing adapters were removed to obtain clean reads using Trim Galore. High-quality data were used for the subsequent analysis. Each read was aligned to the reference genome using STAR. Mapped reads were assembled using Cufflinks v2.2.1. These assemblies were merged to the reference gene model annotation by Cuffmerge.
For mRNAs and lncRNAs, fragments per kilobase of transcript per million mapped reads (FPKM) was used as index to calculate the expression level of each transcript in every library using Cuffdiff program.
For circRNA prediction, the CIRCexplorer2 was employed to identify the back-spliced junction of circRNAs. To calculate the expression levels of circRNAs, back-spliced reads per million mapped reads (BSRP) was used.
Genome_build: UMD3.1
Supplementary_files_format_and_content: (1) Tab-delimited text files include FPKM values (mRNAs and lncRNAs) or BSRP values (circRNAs) for each sample. (2) The .fa files include sequences of lncRNAs and circRNAs predicted in this study.
 
Submission date Oct 18, 2019
Last update date Oct 20, 2020
Contact name Huang JiePing
E-mail(s) [email protected]
Organization name Guangxi University
Street address Xixiangtang District
City Nanning
ZIP/Postal code 530000
Country China
 
Platform ID GPL21659
Series (1)
GSE139102 Comparative transcriptome analysis in adipose and muscle between Chinese buffalo and cattle.
Relations
BioSample SAMN13059396
SRA SRX7023484

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap