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Genome-Wide Gene-Based Multi-Trait Analysis
Genome-wide association studies focusing on a single phenotype have been broadly conducted to identify genetic variants associated with a complex disease. The commonly applied single variant analysis is limited by failing to consider the complex interactions between variants, which motivated the dev...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248273/ https://www.ncbi.nlm.nih.gov/pubmed/32508874 http://dx.doi.org/10.3389/fgene.2020.00437 |
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author | Deng, Yamin He, Tao Fang, Ruiling Li, Shaoyu Cao, Hongyan Cui, Yuehua |
author_facet | Deng, Yamin He, Tao Fang, Ruiling Li, Shaoyu Cao, Hongyan Cui, Yuehua |
author_sort | Deng, Yamin |
collection | PubMed |
description | Genome-wide association studies focusing on a single phenotype have been broadly conducted to identify genetic variants associated with a complex disease. The commonly applied single variant analysis is limited by failing to consider the complex interactions between variants, which motivated the development of association analyses focusing on genes or gene sets. Moreover, when multiple correlated phenotypes are available, methods based on a multi-trait analysis can improve the association power. However, most currently available multi-trait analyses are single variant-based analyses; thus have limited power when disease variants function as a group in a gene or a gene set. In this work, we propose a genome-wide gene-based multi-trait analysis method by considering genes as testing units. For a given phenotype, we adopt a rapid and powerful kernel-based testing method which can evaluate the joint effect of multiple variants within a gene. The joint effect, either linear or nonlinear, is captured through kernel functions. Given a series of candidate kernel functions, we propose an omnibus test strategy to integrate the test results based on different candidate kernels. A p-value combination method is then applied to integrate dependent p-values to assess the association between a gene and multiple correlated phenotypes. Simulation studies show a reasonable type I error control and an excellent power of the proposed method compared to its counterparts. We further show the utility of the method by applying it to two data sets: the Human Liver Cohort and the Alzheimer Disease Neuroimaging Initiative data set, and novel genes are identified. Our method has broad applications in other fields in which the interest is to evaluate the joint effect (linear or nonlinear) of a set of variants. |
format | Online Article Text |
id | pubmed-7248273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72482732020-06-05 Genome-Wide Gene-Based Multi-Trait Analysis Deng, Yamin He, Tao Fang, Ruiling Li, Shaoyu Cao, Hongyan Cui, Yuehua Front Genet Genetics Genome-wide association studies focusing on a single phenotype have been broadly conducted to identify genetic variants associated with a complex disease. The commonly applied single variant analysis is limited by failing to consider the complex interactions between variants, which motivated the development of association analyses focusing on genes or gene sets. Moreover, when multiple correlated phenotypes are available, methods based on a multi-trait analysis can improve the association power. However, most currently available multi-trait analyses are single variant-based analyses; thus have limited power when disease variants function as a group in a gene or a gene set. In this work, we propose a genome-wide gene-based multi-trait analysis method by considering genes as testing units. For a given phenotype, we adopt a rapid and powerful kernel-based testing method which can evaluate the joint effect of multiple variants within a gene. The joint effect, either linear or nonlinear, is captured through kernel functions. Given a series of candidate kernel functions, we propose an omnibus test strategy to integrate the test results based on different candidate kernels. A p-value combination method is then applied to integrate dependent p-values to assess the association between a gene and multiple correlated phenotypes. Simulation studies show a reasonable type I error control and an excellent power of the proposed method compared to its counterparts. We further show the utility of the method by applying it to two data sets: the Human Liver Cohort and the Alzheimer Disease Neuroimaging Initiative data set, and novel genes are identified. Our method has broad applications in other fields in which the interest is to evaluate the joint effect (linear or nonlinear) of a set of variants. Frontiers Media S.A. 2020-05-19 /pmc/articles/PMC7248273/ /pubmed/32508874 http://dx.doi.org/10.3389/fgene.2020.00437 Text en Copyright © 2020 Deng, He, Fang, Li, Cao and Cui. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Deng, Yamin He, Tao Fang, Ruiling Li, Shaoyu Cao, Hongyan Cui, Yuehua Genome-Wide Gene-Based Multi-Trait Analysis |
title | Genome-Wide Gene-Based Multi-Trait Analysis |
title_full | Genome-Wide Gene-Based Multi-Trait Analysis |
title_fullStr | Genome-Wide Gene-Based Multi-Trait Analysis |
title_full_unstemmed | Genome-Wide Gene-Based Multi-Trait Analysis |
title_short | Genome-Wide Gene-Based Multi-Trait Analysis |
title_sort | genome-wide gene-based multi-trait analysis |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248273/ https://www.ncbi.nlm.nih.gov/pubmed/32508874 http://dx.doi.org/10.3389/fgene.2020.00437 |
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