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MARV: a tool for genome-wide multi-phenotype analysis of rare variants.

Marika A KaakinenReedik MägiKrista FischerJani HeikkinenMarjo-Riitta JärvelinAndrew P MorrisInga Prokopenko
Published 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.
Keyphrases
  • genome wide
  • copy number
  • dna methylation
  • loop mediated isothermal amplification