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Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants.
Karhunen, Ville; Launonen, Ilkka; Järvelin, Marjo-Riitta; Sebert, Sylvain; Sillanpää, Mikko J.
Afiliação
  • Karhunen V; Research Unit of Mathematical Sciences, University of Oulu, Oulu, P.O.Box 8000, FI-90014, Finland.
  • Launonen I; Research Unit of Population Health, University of Oulu, Oulu, Finland.
  • Järvelin MR; Research Unit of Mathematical Sciences, University of Oulu, Oulu, P.O.Box 8000, FI-90014, Finland.
  • Sebert S; Research Unit of Population Health, University of Oulu, Oulu, Finland.
  • Sillanpää MJ; Department of Epidemiology and Biostatistics, Imperial College London, London, United Kingdom.
Bioinformatics ; 39(7)2023 07 01.
Article em En | MEDLINE | ID: mdl-37348543
ABSTRACT
MOTIVATION Genome-wide association studies (GWAS) have been successful in identifying genomic loci associated with complex traits. Genetic fine-mapping aims to detect independent causal variants from the GWAS-identified loci, adjusting for linkage disequilibrium patterns.

RESULTS:

We present "FiniMOM" (fine-mapping using a product inverse-moment prior), a novel Bayesian fine-mapping method for summarized genetic associations. For causal effects, the method uses a nonlocal inverse-moment prior, which is a natural prior distribution to model non-null effects in finite samples. A beta-binomial prior is set for the number of causal variants, with a parameterization that can be used to control for potential misspecifications in the linkage disequilibrium reference. The results of simulations studies aimed to mimic a typical GWAS on circulating protein levels show improved credible set coverage and power of the proposed method over current state-of-the-art fine-mapping method SuSiE, especially in the case of multiple causal variants within a locus. AVAILABILITY AND IMPLEMENTATION https//vkarhune.github.io/finimom/.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genômica / Estudo de Associação Genômica Ampla Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genômica / Estudo de Associação Genômica Ampla Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article