MARV: a tool for genome-wide multi-phenotype analysis of rare variants. (2017)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s12859-017-1530-2
PubMed Identifier: 28209135
Publication URI: http://europepmc.org/abstract/MED/28209135
Type: Journal Article/Review
Volume: 18
Parent Publication: BMC bioinformatics
Issue: 1
ISSN: 1471-2105