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A Bayesian hierarchical variable selection prior for pathway-based GWAS using summary statistics.
Yang, Yi; Basu, Saonli; Zhang, Lin.
Afiliação
  • Yang Y; Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
  • Basu S; Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
  • Zhang L; Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
Stat Med ; 39(6): 724-739, 2020 03 15.
Article em En | MEDLINE | ID: mdl-31777110
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Stat Med Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Stat Med Ano de publicação: 2020 Tipo de documento: Article