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Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants
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 “FiniM...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326304/ https://www.ncbi.nlm.nih.gov/pubmed/37348543 http://dx.doi.org/10.1093/bioinformatics/btad396 |
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author | Karhunen, Ville Launonen, Ilkka Järvelin, Marjo-Riitta Sebert, Sylvain Sillanpää, Mikko J |
author_facet | Karhunen, Ville Launonen, Ilkka Järvelin, Marjo-Riitta Sebert, Sylvain Sillanpää, Mikko J |
author_sort | Karhunen, Ville |
collection | PubMed |
description | 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/. |
format | Online Article Text |
id | pubmed-10326304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103263042023-07-08 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 Bioinformatics Original Paper 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/. Oxford University Press 2023-06-22 /pmc/articles/PMC10326304/ /pubmed/37348543 http://dx.doi.org/10.1093/bioinformatics/btad396 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/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. |
spellingShingle | Original Paper Karhunen, Ville Launonen, Ilkka Järvelin, Marjo-Riitta Sebert, Sylvain Sillanpää, Mikko J Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants |
title | Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants |
title_full | Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants |
title_fullStr | Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants |
title_full_unstemmed | Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants |
title_short | Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants |
title_sort | genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326304/ https://www.ncbi.nlm.nih.gov/pubmed/37348543 http://dx.doi.org/10.1093/bioinformatics/btad396 |
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