Leveraging prior information to detect causal variants via multi-variant regression.

PLoS Comput Biol

Center for Human Genome Variation, Duke University School of Medicine, Durham, North Carolina, United States of America.

Published: January 2014

Although many methods are available to test sequence variants for association with complex diseases and traits, methods that specifically seek to identify causal variants are less developed. Here we develop and evaluate a Bayesian hierarchical regression method that incorporates prior information on the likelihood of variant causality through weighting of variant effects. By simulation studies using both simulated and real sequence variants, we compared a standard single variant test for analyzing variant-disease association with the proposed method using different weighting schemes. We found that by leveraging linkage disequilibrium of variants with known GWAS signals and sequence conservation (phastCons), the proposed method provides a powerful approach for detecting causal variants while controlling false positives.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675126PMC
http://dx.doi.org/10.1371/journal.pcbi.1003093DOI Listing

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