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Sample GSM2536620 Query DataSets for GSM2536620
Status Public on Dec 17, 2018
Title 5456_NAcc_pos (RNA-Seq)
Sample type SRA
 
Source name NeuN positive nuclei sorted from nucleus accumbens (NAcc)
Organism Homo sapiens
Characteristics cell type: NeuN pos
tissue: nucleus accumbens (NAcc)
individual id: 5456
Treatment protocol RNA was extracted from neuronal and non-neuronal nuclei isolated from nucleus accumbens or prefrontal cortex (BA9) tissues (for samples with "_pos" or "_neg" at end of sample ID) and sorted via FACS based on NeuN staining as in Montano et al. 2013.
Extracted molecule total RNA
Extraction protocol RNA was extracted using the Qiagen RNeasy Mini kit (cat#: 74104 )
SMARTer Stranded Total RNA-Seq Kit – Pico Input Mammalian
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 4000
 
Data processing We trimmed the first 3 bp of read1, which were derived from template switching oligos and not the cDNA of interest, using seqtk (https://github.com/lh3/seqtk; v1.2-r94) with the following parameters: seqtk trimfq -b 3 ${READ1}. We then quasi-mapped these trimmed reads to a FASTA file of protein-coding and lncRNA genes from GENCODE v19 (http://www.gencodegenes.org/releases/19.html) and performed transcript-level quantification using Salmon (v0.7.2).
We used tximport (v1.2.0) to compute normalized gene-level counts from the transcript-level abundance estimates (scaling these using the average transcript length over samples and the library size). Only autosomal genes with at least 1 cpm in at least 4 libraries (the size of the smallest group of samples) were retained for downstream analysis.
Genome_build: hg19/GRCh37
Supplementary_files_format_and_content: Matrix of gene-level read counts for each gene from all samples.
 
Submission date Mar 14, 2017
Last update date May 15, 2019
Contact name Andrew P. Feinberg
Organization name Johns Hopkins University School of Medicine
Street address 855 N. Wolfe St
City Baltimore
State/province MD
ZIP/Postal code 21205
Country USA
 
Platform ID GPL20301
Series (2)
GSE96613 Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability [RNA-Seq]
GSE96615 Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability
Relations
BioSample SAMN06603216
SRA SRX2640560

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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