Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.

Extensive genetic studies have identified a large number of causal genetic variations in many human phenotypes; however, these could not completely explain heritability in complex diseases. Some researchers have proposed that the "missing heritability" may be attributable to gene-gene and...

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Main Authors: Chin Lin, Chi-Ming Chu, John Lin, Hsin-Yi Yang, Sui-Lung Su
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4414456?pdf=render
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spelling doaj-3e95835145434a84b7a876fe1f1227d92020-11-25T00:40:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01104e012496710.1371/journal.pone.0124967Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.Chin LinChi-Ming ChuJohn LinHsin-Yi YangSui-Lung SuExtensive genetic studies have identified a large number of causal genetic variations in many human phenotypes; however, these could not completely explain heritability in complex diseases. Some researchers have proposed that the "missing heritability" may be attributable to gene-gene and gene-environment interactions. Because there are billions of potential interaction combinations, the statistical power of a single study is often ineffective in detecting these interactions. Meta-analysis is a common method of increasing detection power; however, accessing individual data could be difficult. This study presents a simple method that employs aggregated summary values from a "case" group to detect these specific interactions that based on rare disease and independence assumptions. However, these assumptions, particularly the rare disease assumption, may be violated in real situations; therefore, this study further investigated the robustness of our proposed method when it violates the assumptions. In conclusion, we observed that the rare disease assumption is relatively nonessential, whereas the independence assumption is an essential component. Because single nucleotide polymorphisms (SNPs) are often unrelated to environmental factors and SNPs on other chromosomes, researchers should use this method to investigate gene-gene and gene-environment interactions when they are unable to obtain detailed individual patient data.http://europepmc.org/articles/PMC4414456?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Chin Lin
Chi-Ming Chu
John Lin
Hsin-Yi Yang
Sui-Lung Su
spellingShingle Chin Lin
Chi-Ming Chu
John Lin
Hsin-Yi Yang
Sui-Lung Su
Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.
PLoS ONE
author_facet Chin Lin
Chi-Ming Chu
John Lin
Hsin-Yi Yang
Sui-Lung Su
author_sort Chin Lin
title Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.
title_short Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.
title_full Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.
title_fullStr Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.
title_full_unstemmed Gene-gene and gene-environment interactions in meta-analysis of genetic association studies.
title_sort gene-gene and gene-environment interactions in meta-analysis of genetic association studies.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Extensive genetic studies have identified a large number of causal genetic variations in many human phenotypes; however, these could not completely explain heritability in complex diseases. Some researchers have proposed that the "missing heritability" may be attributable to gene-gene and gene-environment interactions. Because there are billions of potential interaction combinations, the statistical power of a single study is often ineffective in detecting these interactions. Meta-analysis is a common method of increasing detection power; however, accessing individual data could be difficult. This study presents a simple method that employs aggregated summary values from a "case" group to detect these specific interactions that based on rare disease and independence assumptions. However, these assumptions, particularly the rare disease assumption, may be violated in real situations; therefore, this study further investigated the robustness of our proposed method when it violates the assumptions. In conclusion, we observed that the rare disease assumption is relatively nonessential, whereas the independence assumption is an essential component. Because single nucleotide polymorphisms (SNPs) are often unrelated to environmental factors and SNPs on other chromosomes, researchers should use this method to investigate gene-gene and gene-environment interactions when they are unable to obtain detailed individual patient data.
url http://europepmc.org/articles/PMC4414456?pdf=render
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