MEGA-V: detection of variant gene sets in patient cohorts.
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- Record sourced from PubMed, PMID 28003259.
- Also identified by DOI 10.1093/bioinformatics/btw809 and PMC identifier 5408849.
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Abstract
: Detecting significant associations between genetic variants and disease may prove particularly challenging when the variants are rare in the population and/or act together with other variants to cause the disease. We have developed a statistical framework named Mutation Enrichment Gene set Analysis of Variants (MEGA-V) that specifically detects the enrichments of genetic alterations within a process in a cohort of interest. By focusing on the mutations of several genes contributing to the same function rather than on those affecting a single gene, MEGA-V increases the power to detect statistically significant associations. MEGA-V is available at https://github.com/ciccalab/MEGA. francesca.ciccarelli@kcl.ac.uk. Supplementary data are available at Bioinformatics online.
Medical subject headings
- Mutation
- Software