Cargando…

Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies

Epistasis, commonly defined as the interaction between genetic loci, is known to play an important role in the phenotypic variation of complex traits. As a result, many statistical methods have been developed to identify genetic variants that are involved in epistasis, and nearly all of these approa...

Descripción completa

Detalles Bibliográficos
Autores principales: Stamp, Julian, DenAdel, Alan, Weinreich, Daniel, Crawford, Lorin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484060/
https://www.ncbi.nlm.nih.gov/pubmed/37243672
http://dx.doi.org/10.1093/g3journal/jkad118
_version_ 1785102520432984064
author Stamp, Julian
DenAdel, Alan
Weinreich, Daniel
Crawford, Lorin
author_facet Stamp, Julian
DenAdel, Alan
Weinreich, Daniel
Crawford, Lorin
author_sort Stamp, Julian
collection PubMed
description Epistasis, commonly defined as the interaction between genetic loci, is known to play an important role in the phenotypic variation of complex traits. As a result, many statistical methods have been developed to identify genetic variants that are involved in epistasis, and nearly all of these approaches carry out this task by focusing on analyzing one trait at a time. Previous studies have shown that jointly modeling multiple phenotypes can often dramatically increase statistical power for association mapping. In this study, we present the “multivariate MArginal ePIstasis Test” (mvMAPIT)—a multioutcome generalization of a recently proposed epistatic detection method which seeks to detect marginal epistasis or the combined pairwise interaction effects between a given variant and all other variants. By searching for marginal epistatic effects, one can identify genetic variants that are involved in epistasis without the need to identify the exact partners with which the variants interact—thus, potentially alleviating much of the statistical and computational burden associated with conventional explicit search-based methods. Our proposed mvMAPIT builds upon this strategy by taking advantage of correlation structure between traits to improve the identification of variants involved in epistasis. We formulate mvMAPIT as a multivariate linear mixed model and develop a multitrait variance component estimation algorithm for efficient parameter inference and P-value computation. Together with reasonable model approximations, our proposed approach is scalable to moderately sized genome-wide association studies. With simulations, we illustrate the benefits of mvMAPIT over univariate (or single-trait) epistatic mapping strategies. We also apply mvMAPIT framework to protein sequence data from two broadly neutralizing anti-influenza antibodies and approximately 2,000 heterogeneous stock of mice from the Wellcome Trust Centre for Human Genetics. The mvMAPIT R package can be downloaded at https://github.com/lcrawlab/mvMAPIT.
format Online
Article
Text
id pubmed-10484060
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-104840602023-09-08 Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies Stamp, Julian DenAdel, Alan Weinreich, Daniel Crawford, Lorin G3 (Bethesda) Investigation Epistasis, commonly defined as the interaction between genetic loci, is known to play an important role in the phenotypic variation of complex traits. As a result, many statistical methods have been developed to identify genetic variants that are involved in epistasis, and nearly all of these approaches carry out this task by focusing on analyzing one trait at a time. Previous studies have shown that jointly modeling multiple phenotypes can often dramatically increase statistical power for association mapping. In this study, we present the “multivariate MArginal ePIstasis Test” (mvMAPIT)—a multioutcome generalization of a recently proposed epistatic detection method which seeks to detect marginal epistasis or the combined pairwise interaction effects between a given variant and all other variants. By searching for marginal epistatic effects, one can identify genetic variants that are involved in epistasis without the need to identify the exact partners with which the variants interact—thus, potentially alleviating much of the statistical and computational burden associated with conventional explicit search-based methods. Our proposed mvMAPIT builds upon this strategy by taking advantage of correlation structure between traits to improve the identification of variants involved in epistasis. We formulate mvMAPIT as a multivariate linear mixed model and develop a multitrait variance component estimation algorithm for efficient parameter inference and P-value computation. Together with reasonable model approximations, our proposed approach is scalable to moderately sized genome-wide association studies. With simulations, we illustrate the benefits of mvMAPIT over univariate (or single-trait) epistatic mapping strategies. We also apply mvMAPIT framework to protein sequence data from two broadly neutralizing anti-influenza antibodies and approximately 2,000 heterogeneous stock of mice from the Wellcome Trust Centre for Human Genetics. The mvMAPIT R package can be downloaded at https://github.com/lcrawlab/mvMAPIT. Oxford University Press 2023-05-27 /pmc/articles/PMC10484060/ /pubmed/37243672 http://dx.doi.org/10.1093/g3journal/jkad118 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of The Genetics Society of America. 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 Investigation
Stamp, Julian
DenAdel, Alan
Weinreich, Daniel
Crawford, Lorin
Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies
title Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies
title_full Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies
title_fullStr Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies
title_full_unstemmed Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies
title_short Leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies
title_sort leveraging the genetic correlation between traits improves the detection of epistasis in genome-wide association studies
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484060/
https://www.ncbi.nlm.nih.gov/pubmed/37243672
http://dx.doi.org/10.1093/g3journal/jkad118
work_keys_str_mv AT stampjulian leveragingthegeneticcorrelationbetweentraitsimprovesthedetectionofepistasisingenomewideassociationstudies
AT denadelalan leveragingthegeneticcorrelationbetweentraitsimprovesthedetectionofepistasisingenomewideassociationstudies
AT weinreichdaniel leveragingthegeneticcorrelationbetweentraitsimprovesthedetectionofepistasisingenomewideassociationstudies
AT crawfordlorin leveragingthegeneticcorrelationbetweentraitsimprovesthedetectionofepistasisingenomewideassociationstudies