Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants
Karhunen, Ville; Launonen, lkka; Järvelin, Marjo-Riitta; Sebert, Sylvain; Sillanpää, Mikko J. (2023-06-22)
Ville Karhunen, Ilkka Launonen, Marjo-Riitta Järvelin, Sylvain Sebert, Mikko J Sillanpää, Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants, Bioinformatics, Volume 39, Issue 7, July 2023, btad396, https://doi.org/10.1093/bioinformatics/btad396
© The Author(s) 2023. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
https://creativecommons.org/licenses/by/4.0/
https://urn.fi/URN:NBN:fi-fe20230908121884
Tiivistelmä
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.
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