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A two-stage testing strategy for detecting genes×environment interactions in association studies

Identifying gene×environment (G×E) interactions, especially when rare variants are included in genome-wide association studies, is a major challenge in statistical genetics. However, the detection of G×E interactions is very important for understanding the etiology of complex diseases. Although curr...

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Detalles Bibliográficos
Autores principales: Zhou, Jiabin, Li, Shitao, Zhou, Ying, Sheng, Xiaona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496220/
https://www.ncbi.nlm.nih.gov/pubmed/34568910
http://dx.doi.org/10.1093/g3journal/jkab220
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author Zhou, Jiabin
Li, Shitao
Zhou, Ying
Sheng, Xiaona
author_facet Zhou, Jiabin
Li, Shitao
Zhou, Ying
Sheng, Xiaona
author_sort Zhou, Jiabin
collection PubMed
description Identifying gene×environment (G×E) interactions, especially when rare variants are included in genome-wide association studies, is a major challenge in statistical genetics. However, the detection of G×E interactions is very important for understanding the etiology of complex diseases. Although currently some statistical methods have been developed to detect the interactions between genes and environment, the detection of the interactions for the case of rare variants is still limited. Therefore, it is particularly important to develop a new method to detect the interactions between genes and environment for rare variants. In this study, we extend an existing method of adaptive combination of P-values (ADA) and design a novel strategy (called iSADA) for testing the effects of G×E interactions for rare variants. We propose a new two-stage test to detect the interactions between genes and environment in a certain region of a chromosome or even for the whole genome. First, the score statistic is used to test the associations between trait value and the interaction terms of genes and environment and obtain the original P-values. Then, based on the idea of the ADA method, we further construct a full test statistic via the P-values of the preliminary tests in the first stage, so that we can comprehensively test the interactions between genes and environment in the considered genome region. Simulation studies are conducted to compare our proposed method with other existing methods. The results show that the iSADA has higher power than other methods in each case. A GAW17 data set is also applied to illustrate the applicability of the new method.
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spelling pubmed-84962202021-10-07 A two-stage testing strategy for detecting genes×environment interactions in association studies Zhou, Jiabin Li, Shitao Zhou, Ying Sheng, Xiaona G3 (Bethesda) Investigation Identifying gene×environment (G×E) interactions, especially when rare variants are included in genome-wide association studies, is a major challenge in statistical genetics. However, the detection of G×E interactions is very important for understanding the etiology of complex diseases. Although currently some statistical methods have been developed to detect the interactions between genes and environment, the detection of the interactions for the case of rare variants is still limited. Therefore, it is particularly important to develop a new method to detect the interactions between genes and environment for rare variants. In this study, we extend an existing method of adaptive combination of P-values (ADA) and design a novel strategy (called iSADA) for testing the effects of G×E interactions for rare variants. We propose a new two-stage test to detect the interactions between genes and environment in a certain region of a chromosome or even for the whole genome. First, the score statistic is used to test the associations between trait value and the interaction terms of genes and environment and obtain the original P-values. Then, based on the idea of the ADA method, we further construct a full test statistic via the P-values of the preliminary tests in the first stage, so that we can comprehensively test the interactions between genes and environment in the considered genome region. Simulation studies are conducted to compare our proposed method with other existing methods. The results show that the iSADA has higher power than other methods in each case. A GAW17 data set is also applied to illustrate the applicability of the new method. Oxford University Press 2021-07-01 /pmc/articles/PMC8496220/ /pubmed/34568910 http://dx.doi.org/10.1093/g3journal/jkab220 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Investigation
Zhou, Jiabin
Li, Shitao
Zhou, Ying
Sheng, Xiaona
A two-stage testing strategy for detecting genes×environment interactions in association studies
title A two-stage testing strategy for detecting genes×environment interactions in association studies
title_full A two-stage testing strategy for detecting genes×environment interactions in association studies
title_fullStr A two-stage testing strategy for detecting genes×environment interactions in association studies
title_full_unstemmed A two-stage testing strategy for detecting genes×environment interactions in association studies
title_short A two-stage testing strategy for detecting genes×environment interactions in association studies
title_sort two-stage testing strategy for detecting genes×environment interactions in association studies
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496220/
https://www.ncbi.nlm.nih.gov/pubmed/34568910
http://dx.doi.org/10.1093/g3journal/jkab220
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