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Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model
Predicting organismal phenotypes from genotype data is important for preventive and personalized medicine as well as plant and animal breeding. Although genome-wide association studies (GWAS) for complex traits have discovered a large number of trait- and disease-associated variants, phenotype predi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815501/ https://www.ncbi.nlm.nih.gov/pubmed/25873147 http://dx.doi.org/10.1038/hdy.2015.9 |
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author | Jiang, J Zhang, Q Ma, L Li, J Wang, Z Liu, J-F |
author_facet | Jiang, J Zhang, Q Ma, L Li, J Wang, Z Liu, J-F |
author_sort | Jiang, J |
collection | PubMed |
description | Predicting organismal phenotypes from genotype data is important for preventive and personalized medicine as well as plant and animal breeding. Although genome-wide association studies (GWAS) for complex traits have discovered a large number of trait- and disease-associated variants, phenotype prediction based on associated variants is usually in low accuracy even for a high-heritability trait because these variants can typically account for a limited fraction of total genetic variance. In comparison with GWAS, the whole-genome prediction (WGP) methods can increase prediction accuracy by making use of a huge number of variants simultaneously. Among various statistical methods for WGP, multiple-trait model and antedependence model show their respective advantages. To take advantage of both strategies within a unified framework, we proposed a novel multivariate antedependence-based method for joint prediction of multiple quantitative traits using a Bayesian algorithm via modeling a linear relationship of effect vector between each pair of adjacent markers. Through both simulation and real-data analyses, our studies demonstrated that the proposed antedependence-based multiple-trait WGP method is more accurate and robust than corresponding traditional counterparts (Bayes A and multi-trait Bayes A) under various scenarios. Our method can be readily extended to deal with missing phenotypes and resequence data with rare variants, offering a feasible way to jointly predict phenotypes for multiple complex traits in human genetic epidemiology as well as plant and livestock breeding. |
format | Online Article Text |
id | pubmed-4815501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48155012016-07-15 Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model Jiang, J Zhang, Q Ma, L Li, J Wang, Z Liu, J-F Heredity (Edinb) Original Article Predicting organismal phenotypes from genotype data is important for preventive and personalized medicine as well as plant and animal breeding. Although genome-wide association studies (GWAS) for complex traits have discovered a large number of trait- and disease-associated variants, phenotype prediction based on associated variants is usually in low accuracy even for a high-heritability trait because these variants can typically account for a limited fraction of total genetic variance. In comparison with GWAS, the whole-genome prediction (WGP) methods can increase prediction accuracy by making use of a huge number of variants simultaneously. Among various statistical methods for WGP, multiple-trait model and antedependence model show their respective advantages. To take advantage of both strategies within a unified framework, we proposed a novel multivariate antedependence-based method for joint prediction of multiple quantitative traits using a Bayesian algorithm via modeling a linear relationship of effect vector between each pair of adjacent markers. Through both simulation and real-data analyses, our studies demonstrated that the proposed antedependence-based multiple-trait WGP method is more accurate and robust than corresponding traditional counterparts (Bayes A and multi-trait Bayes A) under various scenarios. Our method can be readily extended to deal with missing phenotypes and resequence data with rare variants, offering a feasible way to jointly predict phenotypes for multiple complex traits in human genetic epidemiology as well as plant and livestock breeding. Nature Publishing Group 2015-07 2015-04-15 /pmc/articles/PMC4815501/ /pubmed/25873147 http://dx.doi.org/10.1038/hdy.2015.9 Text en Copyright © 2015 The Genetics Society http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Original Article Jiang, J Zhang, Q Ma, L Li, J Wang, Z Liu, J-F Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model |
title | Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model |
title_full | Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model |
title_fullStr | Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model |
title_full_unstemmed | Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model |
title_short | Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model |
title_sort | joint prediction of multiple quantitative traits using a bayesian multivariate antedependence model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815501/ https://www.ncbi.nlm.nih.gov/pubmed/25873147 http://dx.doi.org/10.1038/hdy.2015.9 |
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