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Series GSE111120 Query DataSets for GSE111120
Status Public on Dec 11, 2019
Title Deep transcriptomic analysis of human vascular cells identifies novel risk genes for common vascular diseases
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Several genome-wide association studies have to date been carried out to identify genetic risk loci associated with vascular diseases. Many of the established common variants likely perturb the expression of disease-relevant genes within the vascular tissue itself. To identify such genes on a genome-wide level, we analyzed the transcriptome of human coronary artery smooth muscle and endothelial cells for Allele-Specific Expression (ASE).
 
Overall design observation of mRNA expression in 2 different cell types from paired donor samples
 
Contributor(s) Brown CD, Quertermous T, Rader DJ
Citation(s) 31917787
Submission date Feb 26, 2018
Last update date Feb 10, 2020
Contact name Sylvia T Nurnberg
E-mail(s) sylvian@upenn.edu
Organization name University of Pennsylvania
Department Medicine
Lab Rader
Street address 3400 Civic Center Blvd
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (38)
GSM3022370 Donor1.SMC
GSM3022371 Donor2.SMC
GSM3022372 Donor3.SMC
Relations
BioProject PRJNA435966
SRA SRP133483

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE111120_083016_DESeq2_paired_hg19_ALL.csv.gz 2.0 Mb (ftp)(http) CSV
GSE111120_RAW.tar 156.0 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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