While the search for associations between genetic markers and complex traits has discovered tens of thousands of trait-related genetic variants, the vast majority of these only explain a tiny fraction of observed phenotypic variation. One possible strategy to detect stronger associations is to aggregate the effects of several genetic markers and to test entire genes, pathways or (sub)networks of genes for association to a phenotype. The latter, network-based genome-wide association studies, in particular suffers from a huge search space and an inherent multiple testing problem. As a consequence, current approaches are either based on greedy feature selection, thereby risking that they miss relevant associations, and/or neglect doing a multiple testing correction, which can lead to an abundance of false positive findings. To address the shortcomings of current approaches of network-based genome-wide association studies, we propose <tt>networkGWAS</tt>, a computationally efficient and statistically sound approach to gene-based genome-wide association studies based on mixed models and neighborhood aggregation. It allows for population structure correction and for well-calibrated p-values, which we obtain through a block permutation scheme. <tt>networkGWAS</tt> successfully detects known or plausible associations on simulated rare variants from H. sapiens data as well as semi-simulated and real data with common variants from A. thaliana and enables the systematic combination of gene-based genome-wide association studies with biological network information.
EigenGWAS: finding loci under selection through genome-wide association studies of eigenvectors in structured populations