| Literature DB >> 31777110 |
Yi Yang1, Saonli Basu1, Lin Zhang1.
Abstract
While genome-wide association studies (GWASs) have been widely used to uncover associations between diseases and genetic variants, standard SNP-level GWASs often lack the power to identify SNPs that individually have a moderate effect size but jointly contribute to the disease. To overcome this problem, pathway-based GWASs methods have been developed as an alternative strategy that complements SNP-level approaches. We propose a Bayesian method that uses the generalized fused hierarchical structured variable selection prior to identify pathways associated with the disease using SNP-level summary statistics. Our prior has the flexibility to take in pathway structural information so that it can model the gene-level correlation based on prior biological knowledge, an important feature that makes it appealing compared to existing pathway-based methods. Using simulations, we show that our method outperforms competing methods in various scenarios, particularly when we have pathway structural information that involves complex gene-gene interactions. We apply our method to the Wellcome Trust Case Control Consortium Crohn's disease GWAS data, demonstrating its practical application to real data.Entities:
Keywords: generalized fused lasso; group lasso; hierarchical variable selection; pathway-based GWAS; summary statistics
Mesh:
Year: 2019 PMID: 31777110 PMCID: PMC7690328 DOI: 10.1002/sim.8442
Source DB: PubMed Journal: Stat Med ISSN: 0277-6715 Impact factor: 2.497