| Literature DB >> 32719112 |
Gaspard Kerner1,2, Matthieu Bouaziz1,2, Aurélie Cobat1,2, Benedetta Bigio1,2,3, Andrew T Timberlake4,5,6,7, Jacinta Bustamante1,2,3,8, Richard P Lifton4,5,9,10, Jean-Laurent Casanova11,2,3,5,12, Laurent Abel11,2,3.
Abstract
Whole-exome sequencing (WES) has facilitated the discovery of genetic lesions underlying monogenic disorders. Incomplete penetrance and variable expressivity suggest a contribution of additional genetic lesions to clinical manifestations and outcome. Some monogenic disorders may therefore actually be digenic. However, only a few digenic disorders have been reported, all discovered by candidate gene approaches applied to at least one locus. We propose here a two-locus genome-wide test for detecting digenic inheritance in WES data. This approach uses the gene as the unit of analysis and tests all pairs of genes to detect pairwise gene × gene interactions underlying disease. It is a case-only method, which has several advantages over classic case-control tests, in particular by avoiding recruitment of controls. Our simulation studies based on real WES data identified two major sources of type I error inflation in this case-only test: linkage disequilibrium and population stratification. Both were corrected by specific procedures. Moreover, our case-only approach is more powerful than the corresponding case-control test for detecting digenic interactions in various population stratification scenarios. Finally, we confirmed the potential of our unbiased, genome-wide approach by successfully identifying a previously reported digenic lesion in patients with craniosynostosis. Our case-only test is a powerful and timely tool for detecting digenic inheritance in WES data from patients.Entities:
Keywords: case-only; craniosynostosis; digenic inheritance; genome-wide; next-generation sequencing
Mesh:
Year: 2020 PMID: 32719112 PMCID: PMC7430978 DOI: 10.1073/pnas.1920650117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205