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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
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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).
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Overall design |
observation of mRNA expression in 2 different cell types from paired donor samples
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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
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Organization name |
University of Pennsylvania
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Department |
Medicine
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Lab |
Rader
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Street address |
3400 Civic Center Blvd
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City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19104 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (38)
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Relations |
BioProject |
PRJNA435966 |
SRA |
SRP133483 |