| Literature DB >> 29300829 |
Jhih-Rong Lin1, Daniel Jaroslawicz1, Ying Cai1, Quanwei Zhang1, Zhen Wang1, Zhengdong D Zhang1.
Abstract
Summary: Although the genome-wide association study (GWAS) is a powerful method to identify disease-associated variants, it does not directly address the biological mechanisms underlying such genetic association signals. Here, we present PGA, a Perl- and Java-based program for post-GWAS analysis that predicts likely disease genes given a list of GWAS-reported variants. Designed with a command line interface, PGA incorporates genomic and eQTL data in identifying disease gene candidates and uses gene network and ontology data to score them based upon the strength of their relationship to the disease in question. Availability and implementation: http://zdzlab.einstein.yu.edu/1/pga.html. Contact: zhengdong.zhang@einstein.yu.edu. Supplementary information: Supplementary data are available at Bioinformatics online.Entities:
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Year: 2018 PMID: 29300829 PMCID: PMC5946835 DOI: 10.1093/bioinformatics/btx845
Source DB: PubMed Journal: Bioinformatics ISSN: 1367-4803 Impact factor: 6.937