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Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics

Many complex diseases, such as psychiatric and behavioral disorders, are commonly characterized through various measurements that reflect physical, behavioral and psychological aspects of diseases. While it remains a great challenge to find a unified measurement to characterize a disease, the availa...

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Autores principales: Li, Ming, Wei, Changshuai, Wen, Yalu, Wang, Tong, Lu, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320542/
https://www.ncbi.nlm.nih.gov/pubmed/28479869
http://dx.doi.org/10.2174/1389202917666160513100946
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author Li, Ming
Wei, Changshuai
Wen, Yalu
Wang, Tong
Lu, Qing
author_facet Li, Ming
Wei, Changshuai
Wen, Yalu
Wang, Tong
Lu, Qing
author_sort Li, Ming
collection PubMed
description Many complex diseases, such as psychiatric and behavioral disorders, are commonly characterized through various measurements that reflect physical, behavioral and psychological aspects of diseases. While it remains a great challenge to find a unified measurement to characterize a disease, the available multiple phenotypes can be analyzed jointly in the genetic association study. Simultaneously testing these phenotypes has many advantages, including considering different aspects of the disease in the analysis, and utilizing correlated phenotypes to improve the power of detecting disease-associated variants. Furthermore, complex diseases are likely caused by the interplay of multiple genetic variants through complicated mechanisms. Considering gene-gene interactions in the joint association analysis of complex diseases could further increase our ability to discover genetic variants involving complex disease pathways. In this article, we propose a stepwise U-test for joint association analysis of multiple loci and multiple phenotypes. Through simulations, we demonstrated that testing multiple phenotypes simultaneously could attain higher power than testing one single phenotype at a time, especially when there are shared genes contributing to multiple phenotypes. We also illustrated the proposed method with an application to Nicotine Dependence (ND), using datasets from the Study of Addition, Genetics and Environment (SAGE). The joint analysis of three ND phenotypes identified two SNPs, rs10508649 and rs2491397, and reached a nominal P-value of 3.79e-13. The association was further replicated in two independent datasets with P-values of 2.37e-05 and 7.46e-05.
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spelling pubmed-53205422017-05-05 Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics Li, Ming Wei, Changshuai Wen, Yalu Wang, Tong Lu, Qing Curr Genomics Article Many complex diseases, such as psychiatric and behavioral disorders, are commonly characterized through various measurements that reflect physical, behavioral and psychological aspects of diseases. While it remains a great challenge to find a unified measurement to characterize a disease, the available multiple phenotypes can be analyzed jointly in the genetic association study. Simultaneously testing these phenotypes has many advantages, including considering different aspects of the disease in the analysis, and utilizing correlated phenotypes to improve the power of detecting disease-associated variants. Furthermore, complex diseases are likely caused by the interplay of multiple genetic variants through complicated mechanisms. Considering gene-gene interactions in the joint association analysis of complex diseases could further increase our ability to discover genetic variants involving complex disease pathways. In this article, we propose a stepwise U-test for joint association analysis of multiple loci and multiple phenotypes. Through simulations, we demonstrated that testing multiple phenotypes simultaneously could attain higher power than testing one single phenotype at a time, especially when there are shared genes contributing to multiple phenotypes. We also illustrated the proposed method with an application to Nicotine Dependence (ND), using datasets from the Study of Addition, Genetics and Environment (SAGE). The joint analysis of three ND phenotypes identified two SNPs, rs10508649 and rs2491397, and reached a nominal P-value of 3.79e-13. The association was further replicated in two independent datasets with P-values of 2.37e-05 and 7.46e-05. Bentham Science Publishers 2016-10 2016-10 /pmc/articles/PMC5320542/ /pubmed/28479869 http://dx.doi.org/10.2174/1389202917666160513100946 Text en © 2016 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Li, Ming
Wei, Changshuai
Wen, Yalu
Wang, Tong
Lu, Qing
Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics
title Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics
title_full Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics
title_fullStr Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics
title_full_unstemmed Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics
title_short Detecting Gene-Gene Interactions Associated with Multiple Complex Traits with U-Statistics
title_sort detecting gene-gene interactions associated with multiple complex traits with u-statistics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320542/
https://www.ncbi.nlm.nih.gov/pubmed/28479869
http://dx.doi.org/10.2174/1389202917666160513100946
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