MARV: a tool for genome-wide multi-phenotype analysis of rare variants.
Marika A KaakinenReedik MägiKrista FischerJani HeikkinenMarjo-Riitta JärvelinAndrew P MorrisInga ProkopenkoPublished in: BMC bioinformatics (2017)
MARV is a computationally efficient, flexible and user-friendly software tool allowing rapid identification of rare variant effects on multiple phenotypes, thus paving the way for novel discoveries and insights into biology of complex traits.