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An information-gain approach to detecting three-way epistatic interactions in genetic association studies
BACKGROUND: Epistasis has been historically used to describe the phenomenon that the effect of a given gene on a phenotype can be dependent on one or more other genes, and is an essential element for understanding the association between genetic and phenotypic variations. Quantifying epistasis of or...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721169/ https://www.ncbi.nlm.nih.gov/pubmed/23396514 http://dx.doi.org/10.1136/amiajnl-2012-001525 |
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author | Hu, Ting Chen, Yuanzhu Kiralis, Jeff W Collins, Ryan L Wejse, Christian Sirugo, Giorgio Williams, Scott M Moore, Jason H |
author_facet | Hu, Ting Chen, Yuanzhu Kiralis, Jeff W Collins, Ryan L Wejse, Christian Sirugo, Giorgio Williams, Scott M Moore, Jason H |
author_sort | Hu, Ting |
collection | PubMed |
description | BACKGROUND: Epistasis has been historically used to describe the phenomenon that the effect of a given gene on a phenotype can be dependent on one or more other genes, and is an essential element for understanding the association between genetic and phenotypic variations. Quantifying epistasis of orders higher than two is very challenging due to both the computational complexity of enumerating all possible combinations in genome-wide data and the lack of efficient and effective methodologies. OBJECTIVES: In this study, we propose a fast, non-parametric, and model-free measure for three-way epistasis. METHODS: Such a measure is based on information gain, and is able to separate all lower order effects from pure three-way epistasis. RESULTS: Our method was verified on synthetic data and applied to real data from a candidate-gene study of tuberculosis in a West African population. In the tuberculosis data, we found a statistically significant pure three-way epistatic interaction effect that was stronger than any lower-order associations. CONCLUSION: Our study provides a methodological basis for detecting and characterizing high-order gene-gene interactions in genetic association studies. |
format | Online Article Text |
id | pubmed-3721169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37211692013-12-11 An information-gain approach to detecting three-way epistatic interactions in genetic association studies Hu, Ting Chen, Yuanzhu Kiralis, Jeff W Collins, Ryan L Wejse, Christian Sirugo, Giorgio Williams, Scott M Moore, Jason H J Am Med Inform Assoc Focus on Translational Bioinformatics BACKGROUND: Epistasis has been historically used to describe the phenomenon that the effect of a given gene on a phenotype can be dependent on one or more other genes, and is an essential element for understanding the association between genetic and phenotypic variations. Quantifying epistasis of orders higher than two is very challenging due to both the computational complexity of enumerating all possible combinations in genome-wide data and the lack of efficient and effective methodologies. OBJECTIVES: In this study, we propose a fast, non-parametric, and model-free measure for three-way epistasis. METHODS: Such a measure is based on information gain, and is able to separate all lower order effects from pure three-way epistasis. RESULTS: Our method was verified on synthetic data and applied to real data from a candidate-gene study of tuberculosis in a West African population. In the tuberculosis data, we found a statistically significant pure three-way epistatic interaction effect that was stronger than any lower-order associations. CONCLUSION: Our study provides a methodological basis for detecting and characterizing high-order gene-gene interactions in genetic association studies. BMJ Publishing Group 2013-07 2013-02-08 /pmc/articles/PMC3721169/ /pubmed/23396514 http://dx.doi.org/10.1136/amiajnl-2012-001525 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Focus on Translational Bioinformatics Hu, Ting Chen, Yuanzhu Kiralis, Jeff W Collins, Ryan L Wejse, Christian Sirugo, Giorgio Williams, Scott M Moore, Jason H An information-gain approach to detecting three-way epistatic interactions in genetic association studies |
title | An information-gain approach to detecting three-way epistatic interactions in genetic association studies |
title_full | An information-gain approach to detecting three-way epistatic interactions in genetic association studies |
title_fullStr | An information-gain approach to detecting three-way epistatic interactions in genetic association studies |
title_full_unstemmed | An information-gain approach to detecting three-way epistatic interactions in genetic association studies |
title_short | An information-gain approach to detecting three-way epistatic interactions in genetic association studies |
title_sort | information-gain approach to detecting three-way epistatic interactions in genetic association studies |
topic | Focus on Translational Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721169/ https://www.ncbi.nlm.nih.gov/pubmed/23396514 http://dx.doi.org/10.1136/amiajnl-2012-001525 |
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