RVPedigree
RVPedigree tests associations between rare genetic variants and non-normally distributed quantitative traits while accounting for relatedness.
Key Features:
- Rare Variant Association with Relatedness Adjustment: Performs association testing for rare variants using kinship matrices to correct for family structure, population structure, and cryptic relatedness.
- Non-Normal Trait Handling and Significance Estimation: Supports analysis of non-normally distributed quantitative traits and provides multiple statistical significance estimation methods with triaging strategies and parallel computation for genome-wide studies.
Scientific Applications:
- Family-Based Rare Variant Analysis: Identifies genetic contributions of rare variants to complex traits in pedigree and population-based studies.
Methodology:
RVPedigree integrates kinship matrix calculation with statistical models robust to non-normal trait distributions, applying optimized significance testing and parallelization for large-scale rare variant association analyses.
Topics
Details
- License:
- GPL-3.0
- Tool Type:
- library
- Programming Languages:
- R
- Added:
- 5/27/2018
- Last Updated:
- 12/10/2018
Operations
Publications
Oualkacha K, Lakhal-Chaieb L, Greenwood CM. Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits. International Journal of Epidemiology. 2016;45(2):402-407. doi:10.1093/ije/dyw047. PMID:27085080. PMCID:PMC5841637.