Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions

Genome-wide association studies (GWASs) have identified thousands of single nucleotide polymorphisms (SNPs) robustly associated with hundreds of complex human diseases including cancers. However, the large number of G WAS-identified genetic loci only explains a small proportion of the disease herita...

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Published in:Cancer Informatics
Main Authors: Yaping Wang, Donghui Li, Peng Wei
Format: Article
Language:English
Published: SAGE Publishing 2015-01-01
Online Access:https://doi.org/10.4137/CIN.S17305
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author Yaping Wang
Donghui Li
Peng Wei
author_facet Yaping Wang
Donghui Li
Peng Wei
author_sort Yaping Wang
collection DOAJ
container_title Cancer Informatics
description Genome-wide association studies (GWASs) have identified thousands of single nucleotide polymorphisms (SNPs) robustly associated with hundreds of complex human diseases including cancers. However, the large number of G WAS-identified genetic loci only explains a small proportion of the disease heritability. This “missing heritability” problem has been partly attributed to the yet-to-be-identified gene-gene (G × G) and gene-environment (G × E) interactions. In spite of the important roles of G × G and G × E interactions in understanding disease mechanisms and filling in the missing heritability, straightforward GWAS scanning for such interactions has very limited statistical power, leading to few successes. Here we propose a two-step statistical approach to test G × G/G × E interactions: the first step is to perform principal component analysis (PCA) on the multiple SNPs within a gene region, and the second step is to perform Tukey's one degree-of-freedom (1-df) test on the leading PCs. We derive a score test that is computationally fast and numerically stable for the proposed Tukey's 1-df interaction test. Using extensive simulations we show that the proposed approach, which combines the two parsimonious models, namely, the PCA and Tukey's 1-df form of interaction, outperforms other state-of-the-art methods. We also demonstrate the utility and efficiency gains of the proposed method with applications to testing G × G interactions for Crohn's disease using the Wellcome Trust Case Control Consortium (WTCCC) GWAS data and testing G × E interaction using data from a case-control study of pancreatic cancer.
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spelling doaj-art-3eea6a1e328a4b09ae8a67adb2c6d5982025-08-19T22:06:49ZengSAGE PublishingCancer Informatics1176-93512015-01-0114s210.4137/CIN.S17305Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment InteractionsYaping Wang0Donghui Li1Peng Wei2Department of Biostatistics, School of Public Health, University of Texas Health Science Center, University of Texas Health Science Center, Houston, TX, USA.Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, University of Texas Health Science Center, Houston, TX, USA.Human Genetics Center, School of Public Health, University of Texas Health Science Center, Houston, TX, USA.Genome-wide association studies (GWASs) have identified thousands of single nucleotide polymorphisms (SNPs) robustly associated with hundreds of complex human diseases including cancers. However, the large number of G WAS-identified genetic loci only explains a small proportion of the disease heritability. This “missing heritability” problem has been partly attributed to the yet-to-be-identified gene-gene (G × G) and gene-environment (G × E) interactions. In spite of the important roles of G × G and G × E interactions in understanding disease mechanisms and filling in the missing heritability, straightforward GWAS scanning for such interactions has very limited statistical power, leading to few successes. Here we propose a two-step statistical approach to test G × G/G × E interactions: the first step is to perform principal component analysis (PCA) on the multiple SNPs within a gene region, and the second step is to perform Tukey's one degree-of-freedom (1-df) test on the leading PCs. We derive a score test that is computationally fast and numerically stable for the proposed Tukey's 1-df interaction test. Using extensive simulations we show that the proposed approach, which combines the two parsimonious models, namely, the PCA and Tukey's 1-df form of interaction, outperforms other state-of-the-art methods. We also demonstrate the utility and efficiency gains of the proposed method with applications to testing G × G interactions for Crohn's disease using the Wellcome Trust Case Control Consortium (WTCCC) GWAS data and testing G × E interaction using data from a case-control study of pancreatic cancer.https://doi.org/10.4137/CIN.S17305
spellingShingle Yaping Wang
Donghui Li
Peng Wei
Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions
title Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions
title_full Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions
title_fullStr Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions
title_full_unstemmed Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions
title_short Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions
title_sort powerful tukey s one degree of freedom test for detecting gene gene and gene environment interactions
url https://doi.org/10.4137/CIN.S17305
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