A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways.
other · Level V
Where this comes from
- Record sourced from PubMed, PMID 26140448.
- Also identified by DOI 10.1016/j.ajhg.2015.05.015 and PMC identifier 4572492.
- Licence recorded as CC BY-NC-ND.
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Abstract
Gene-based, pathway, and other multivariate association methods are motivated by the possibility of GxG and GxE interactions; however, accounting for such interactions is limited by the challenges associated with adequate modeling information. Here we propose an easy-to-implement joint location-scale (JLS) association testing framework for single-variant and multivariate analysis that accounts for interactions without explicitly modeling them. We apply the JLS method to a gene-set analysis of cystic fibrosis (CF) lung disease, which is influenced by multiple environmental and genetic factors. We identify and replicate an association between the constituents of the apical plasma membrane and CF lung disease (p = 0.0099 and p = 0.0180, respectively) and highlight a role for the SLC9A3-SLC9A3R1/2-EZR complex in contributing to CF lung disease. Many association studies could benefit from re-analysis with the JLS method that leverages complex genetic architecture for SNP, gene, and pathway identification. Analytical verification, simulation, and additional proof-of-principle applications support our approach.
Medical subject headings
- Cell Membrane
- Cystic Fibrosis
- Diabetes Complications
- Genetic Association Studies
- Multiprotein Complexes
- Polymorphism, Single Nucleotide