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Multiple Quantitative Trait Analysis Using Bayesian Networks
Author(s) -
Marco Scutari,
Phil Howell,
David J. Balding,
Ian Mackay
Publication year - 2014
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.114.165704
Subject(s) - biology , trait , pleiotropy , quantitative trait locus , bayesian probability , genetic association , population , inference , linear model , genetics , quantitative genetics , genome wide association study , computational biology , evolutionary biology , statistics , phenotype , computer science , genetic variation , single nucleotide polymorphism , artificial intelligence , genotype , mathematics , gene , demography , sociology , programming language
Models for genome-wide prediction and association studies usually target a single phenotypic trait. However, in animal and plant genetics it is common to record information on multiple phenotypes for each individual that will be genotyped. Modeling traits individually disregards the fact that they are most likely associated due to pleiotropy and shared biological basis, thus providing only a partial, confounded view of genetic effects and phenotypic interactions. In this article we use data from a Multiparent Advanced Generation Inter-Cross (MAGIC) winter wheat population to explore Bayesian networks as a convenient and interpretable framework for the simultaneous modeling of multiple quantitative traits. We show that they are equivalent to multivariate genetic best linear unbiased prediction (GBLUP) and that they are competitive with single-trait elastic net and single-trait GBLUP in predictive performance. Finally, we discuss their relationship with other additive-effects models and their advantages in inference and interpretation. MAGIC populations provide an ideal setting for this kind of investigation because the very low population structure and large sample size result in predictive models with good power and limited confounding due to relatedness.

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