Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits

Int J Epidemiol. 2016 Apr;45(2):402-7. doi: 10.1093/ije/dyw047. Epub 2016 Apr 16.

Abstract

Motivation: RVPedigree (Rare Variant association tests in Pedigrees) implements a suite of programs facilitating genome-wide analysis of association between a quantitative trait and autosomal region-based genetic variation. The main features here are the ability to appropriately test for association of rare variants with non-normally distributed quantitative traits, and also to appropriately adjust for related individuals, either from families or from population structure and cryptic relatedness.

Implementation: RVPedigree is available as an R package.

General features: The package includes calculation of kinship matrices, various options for coping with non-normality, three different ways of estimating statistical significance incorporating triaging to enable efficient use of the most computationally-intensive calculations, and a parallelization option for genome-wide analysis.

Availability: The software is available from the Comprehensive R Archive Network [CRAN.R-project.org] under the name 'RVPedigree' and at [https://github.com/GreenwoodLab]. It has been published under General Public License (GPL) version 3 or newer.

Keywords: kernel tests; kinship; kurtosis; mixed models; pedigrees; region-based tests.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Family
  • Genetic Variation*
  • Genome-Wide Association Study
  • Humans
  • Pedigree*
  • Quantitative Trait Loci
  • Software*

Grants and funding