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Article

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

BMC bioinformatics - 16 Feb 2017

Kaakinen Marika, Mägi Reedik, Fischer Krista, Heikkinen Jani, Järvelin Marjo-Riitta, Morris Andrew P, Prokopenko Inga

Abstract excerpt

BACKGROUND: Genome-wide association studies have enabled identification of thousands of loci for hundreds of traits. Yet, for most human traits a substantial part of the estimated heritability is unexplained. This and recent advances in technology to produce high-dimensional data cost-effectively have led to method development beyond standard common variant analysis, including single-phenotype rare variant and...

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PMID: 28209135
DOI: 10.1186/s12859-017-1530-2
PMCID: PMC5311849

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