4.5 Article

Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model

Journal

HEREDITY
Volume 115, Issue 1, Pages 29-36

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/hdy.2015.9

Keywords

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Funding

  1. National High Technology Research and Development Program of China (863 Program) [2013AA102503, 2011AA100302]
  2. National Natural Science Foundations of China [31272419]
  3. New-Century Training Program Foundation for the Talents by the State Education Commission of China [NETC-10-0783]
  4. Program for Changjiang Scholar and Innovation Research Team in University [IRT1191]

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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.

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