An expectation and maximization algorithm for multivariate genome-wide association studies (EMmvGWAS).

Genome-wide association studies (GWAS) commonly focus on one quantitative trait at a time, even when multiple traits are collected. However, joint analysis of multiple traits can increase the power to detect genetic associations by leveraging trait correlations. Multivariate GWAS is particularly important for identifying pleiotropic effects and uncovering shared genetic architecture underlying complex traits. Despite its great potential, multivariate GWAS methods face substantial computational challenges due to the high dimensionality of polygenic covariance structures and the cost of scanning genome-wide markers. We present EMmvGWAS, an efficient computational framework implemented in R, which dramatically reduces computational time for multivariate GWAS involving a moderate number of traits. The algorithm estimates the genetic and environmental covariance matrices from a pure polygenic model using an Expectation-Maximization algorithm. To improve computational efficiency during genome-wide scanning, we use a semi-exact method that fixes the estimated covariance matrices and treats their ratio, defined as the genetic covariance matrix multiplied by the inverse of the environmental covariance matrix, as a known constant across all markers. This approach enables closed-form solutions for marker effects and residual covariance matrix at each locus, dramatically reducing the computational time without compromising statistical power. We demonstrate the scalability and performance of our method through both simulation studies and real dataset analyses from rice, mice and human populations. The method is implemented in R and is designed to support multivariate GWAS involving a moderate number of traits, while also accommodating univariate analyses as a special case. The R package is available at https://github.com/Jason-Teng/EMmvGWAS.