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Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits
To date, most genetic analyses of phenotypes have focused on analyzing single traits or analyzing each phenotype independently. However, joint epistasis analysis of multiple complementary traits will increase statistical power and improve our understanding of the complicated genetic structure of the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841563/ https://www.ncbi.nlm.nih.gov/pubmed/27104857 http://dx.doi.org/10.1371/journal.pgen.1005965 |
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author | Zhang, Futao Xie, Dan Liang, Meimei Xiong, Momiao |
author_facet | Zhang, Futao Xie, Dan Liang, Meimei Xiong, Momiao |
author_sort | Zhang, Futao |
collection | PubMed |
description | To date, most genetic analyses of phenotypes have focused on analyzing single traits or analyzing each phenotype independently. However, joint epistasis analysis of multiple complementary traits will increase statistical power and improve our understanding of the complicated genetic structure of the complex diseases. Despite their importance in uncovering the genetic structure of complex traits, the statistical methods for identifying epistasis in multiple phenotypes remains fundamentally unexplored. To fill this gap, we formulate a test for interaction between two genes in multiple quantitative trait analysis as a multiple functional regression (MFRG) in which the genotype functions (genetic variant profiles) are defined as a function of the genomic position of the genetic variants. We use large-scale simulations to calculate Type I error rates for testing interaction between two genes with multiple phenotypes and to compare the power with multivariate pairwise interaction analysis and single trait interaction analysis by a single variate functional regression model. To further evaluate performance, the MFRG for epistasis analysis is applied to five phenotypes of exome sequence data from the NHLBI’s Exome Sequencing Project (ESP) to detect pleiotropic epistasis. A total of 267 pairs of genes that formed a genetic interaction network showed significant evidence of epistasis influencing five traits. The results demonstrate that the joint interaction analysis of multiple phenotypes has a much higher power to detect interaction than the interaction analysis of a single trait and may open a new direction to fully uncovering the genetic structure of multiple phenotypes. |
format | Online Article Text |
id | pubmed-4841563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48415632016-04-29 Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits Zhang, Futao Xie, Dan Liang, Meimei Xiong, Momiao PLoS Genet Research Article To date, most genetic analyses of phenotypes have focused on analyzing single traits or analyzing each phenotype independently. However, joint epistasis analysis of multiple complementary traits will increase statistical power and improve our understanding of the complicated genetic structure of the complex diseases. Despite their importance in uncovering the genetic structure of complex traits, the statistical methods for identifying epistasis in multiple phenotypes remains fundamentally unexplored. To fill this gap, we formulate a test for interaction between two genes in multiple quantitative trait analysis as a multiple functional regression (MFRG) in which the genotype functions (genetic variant profiles) are defined as a function of the genomic position of the genetic variants. We use large-scale simulations to calculate Type I error rates for testing interaction between two genes with multiple phenotypes and to compare the power with multivariate pairwise interaction analysis and single trait interaction analysis by a single variate functional regression model. To further evaluate performance, the MFRG for epistasis analysis is applied to five phenotypes of exome sequence data from the NHLBI’s Exome Sequencing Project (ESP) to detect pleiotropic epistasis. A total of 267 pairs of genes that formed a genetic interaction network showed significant evidence of epistasis influencing five traits. The results demonstrate that the joint interaction analysis of multiple phenotypes has a much higher power to detect interaction than the interaction analysis of a single trait and may open a new direction to fully uncovering the genetic structure of multiple phenotypes. Public Library of Science 2016-04-22 /pmc/articles/PMC4841563/ /pubmed/27104857 http://dx.doi.org/10.1371/journal.pgen.1005965 Text en © 2016 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zhang, Futao Xie, Dan Liang, Meimei Xiong, Momiao Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits |
title | Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits |
title_full | Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits |
title_fullStr | Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits |
title_full_unstemmed | Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits |
title_short | Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits |
title_sort | functional regression models for epistasis analysis of multiple quantitative traits |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841563/ https://www.ncbi.nlm.nih.gov/pubmed/27104857 http://dx.doi.org/10.1371/journal.pgen.1005965 |
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