Genomics Inform.  2022 Mar;20(1):e8. 10.5808/gi.21080.

Bayesian mixed models for longitudinal genetic data: theory, concepts, and simulation studies

Affiliations
  • 1Department of Statistics and Actuarial Science, Soongsil University, Seoul 06978, Korea
  • 2Program in Genetic Epidemiology and Statistical Genetics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA

Abstract

Despite the success of recent genome-wide association studies (GWAS) investigating longitudinal traits, a large fraction of overall heritability remains unexplained. This suggests that some of the missing heritability may be accounted for by gene-gene and gene-time/environment interactions. In this paper, we develop a Bayesian variable selection method for longitudinal genetic data based on mixed models. The method jointly models the main effects and interactions of all candidate genetic variants and non-genetic factors and has higher statistical power than previous approaches. To account for the within-subject dependence structure, we propose a grid-based approach that models only one fixed-dimensional covariance matrix, which is thus applicable to data where subjects have different numbers of time points. We provide the theoretical basis of our Bayesian method and then illustrate its performance using data from the 1000 Genome Project with various simulation settings. Several simulation studies show that our multivariate method increases the statistical power compared to the corresponding univariate method and can detect gene-time/environment interactions well. We further evaluate our method with different numbers of individuals, variants, and causal variants, as well as different trait-heritability, and conclude that our method performs reasonably well with various simulation settings.

Keyword

Bayesian mixed model; gene-time interaction; grid-based model; longitudinal data
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