
Genetic association studies have yielded a wealth of biological discoveries. However, these studies have mostly analyzed one trait and one SNP at a time, thus failing to capture the underlying complexity of the data sets. Joint genotype-phenotype analyses of complex, high-dimensional data sets represent an important way to move beyond simple genome-wide association studies (GWAS) with great potential. The move to high-dimensional phenotypes will raise many new statistical problems. Here we address the central issue of missing phenotypes in studies with any level of relatedness between samples. We propose a multiple-phenotype mixed model and use a computationally efficient variational Bayesian algorithm to fit the model. On a variety of simulated and real data sets from a range of organisms and trait types, we show that our method outperforms existing state-of-the-art methods from the statistics and machine learning literature and can boost signals of association.
Blood Platelets, Male, Models, Genetic, T-Lymphocytes, Bayes Theorem, Polymorphism, Single Nucleotide, Article, Rats, Phenotype, Animals, Outbred Strains, Animals, Humans, Female, Chickens, Algorithms, Triticum, Genome-Wide Association Study
Blood Platelets, Male, Models, Genetic, T-Lymphocytes, Bayes Theorem, Polymorphism, Single Nucleotide, Article, Rats, Phenotype, Animals, Outbred Strains, Animals, Humans, Female, Chickens, Algorithms, Triticum, Genome-Wide Association Study
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