PT  - JOURNAL ARTICLE
AU  - Francesco Paolo Casale
AU  - Danilo Horta
AU  - Barbara Rakitsch
AU  - Oliver Stegle
TI  - Joint genetic analysis using variant sets reveals polygenic gene-context interactions
AID  - 10.1101/097477
DP  - 2016 Jan 01
TA  - bioRxiv
PG  - 097477
4099  - http://biorxiv.org/content/early/2016/12/31/097477.short
4100  - http://biorxiv.org/content/early/2016/12/31/097477.full
AB  - Joint genetic models for multiple traits have helped to enhance association analyses. Most existing multi-trait models have been designed to increase power for detecting associations, whereas the analysis of interactions has received considerably less attention. Here, we propose iSet, a method based on linear mixed models to test for interactions between sets of variants and environmental states or other contexts. Our model generalizes previous interaction tests and in particular provides a test for local differences in the genetic architecture between contexts. We first use simulations to validate iSet before applying the model to the analysis of genotype-environment interactions in an eQTL study. Our model retrieves a larger number of interactions than alternative methods and reveals that up to 20% of cases show context-specific configurations of causal variants. Finally, we apply iSet to test for sub-group specific genetic effects in human lipid levels in a large human cohort, where we identify a gene-sex interaction for C-reactive protein that is missed by alternative methods.Author summary Genetic effects on phenotypes can depend on external contexts, including environment. Statistical tests for identifying such interactions are important to understand how individual genetic variants may act in different contexts. Interaction effects can either be studied using measurements of a given phenotype in different contexts, under the same genetic backgrounds, or by stratifying a population into subgroups. Here, we derive a method based on linear mixed models that can be applied to both of these designs. iSet enables testing for interactions between context and sets of variants, and accounts for polygenic effects. We validate our model using simulations, before applying it to the genetic analysis of gene expression studies and genome-wide association studies of human blood lipid levels. We find that modeling interactions with variant sets offers increased power, thereby uncovering interactions that cannot be detected by alternative methods.