NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3979062 Query DataSets for GSM3979062
Status Public on Jul 27, 2019
Title PFC-COC3-RNAseq
Sample type SRA
 
Source name Cocaine-treated
Organism Rattus norvegicus
Characteristics tissue: PFC
strain: Sprague-Dawley
Sex: male
Extracted molecule total RNA
Extraction protocol Total RNA was harvested using Trizol reagent. KAPA Stranded RNA-Seq Library Prep Kit was used with 1 ug of total RNA for the construction of sequencing libraries.
ATAC-seq: Nuclei from flash frozen PFC tissue were extracted and 100,000 nuclei were tagmented. DNA were prepared using Nextera library prep kit.
RNA and DNA libraries were prepared for sequencing using standard Illumina protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description Cocaine-treated
PFC_FPKM.xls
sample name in processed data file:
Coc_3
Data processing Reads were aligned using the BWA algorithm (mem mode; default settings). Duplicate reads were removed, and only reads mapping as matched pairs and being uniquely mapped (mapping quality >= 1) were used for further analysis. The 42 base pair (bp) length of the reads were used for peak-calling and the generic term “interval” was used to describe genomic regions with local enrichments in tag numbers. Intervals were defined by the chromosome number, and a start and end coordinate.
Peaks were identified using the MACS 2.1.0 algorithm at a cutoff p-value of 1e-7 and with the –nomodel option. Peaks that were on the ENCODE blacklist of known false ChIP-Seq peaks were removed.
HISAT2 was used to map filtered sequenced reads to the reference rat genome, HTSeq was used to analyze gene expression levels (in union mode)
DESeq was used for differential gene expression analysis
rMATS (replicate multivariate analysis of transcript splicing) was used for detection of differential alternative splicing (AS)
Genome_build: RN6(Nacc-RNAseq and ATACseq), RN5(PFC-RNAseq)
Supplementary_files_format_and_content: xlsx files including FPKM value for each sample
 
Submission date Jul 26, 2019
Last update date Jul 27, 2019
Contact name Philippe Melas
Organization name Columbia University
Lab Kandel's lab
Street address 1051 Riverside Drive
City New York
ZIP/Postal code 10032
Country USA
 
Platform ID GPL14844
Series (1)
GSE134935 Cannabinoid exposure in rat adolescence reprograms the initial behavioral, molecular, and epigenetic response to cocaine
Relations
BioSample SAMN12370772
SRA SRX6597837

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