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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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 |
work_keys_str_mv |
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