RVPedigree
RVPedigree is an R package that enables genome-wide analysis of the association between a quantitative trait and autosomal region-based genetic variation, with the ability to accurately test for rare variant association with non-normally distributed traits and adjust for related individuals. It includes the calculation of kinship matrices, triaging for efficient use of computationally-intensive calculations, and a parallelization option for genome-wide analysis.
Topic
Genotype and phenotype;Genetic variation;Transcription factors and regulatory sites
Detail
Operation: Quantification;Gene expression QTL analysis;Genotyping
Software interface: Library
Language: R
License: GNU General Public License v3
Cost: Free
Version name: 0.0.3
Credit: The Canadian Institutes of Health Research, the Fonds de la Recherche en Santé au Québec.
Input: -
Output: -
Contact: Oualkacha Karim oualkacha.karim@uqam.ca
Collection: -
Maturity: Emerging
Publications
- Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits.
- Oualkacha K, et al. Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits. Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits. 2016; 45:402-7. doi: 10.1093/ije/dyw047
- https://doi.org/10.1093/ije/dyw047
- PMID: 27085080
- PMC: PMC5841637
Download and documentation
Source: https://github.com/GreenwoodLab/RVPedigree/releases/tag/v0.0.3
Documentation: https://github.com/GreenwoodLab/RVPedigree/blob/master/vignettes/vignette.Rnw
Home page: https://github.com/GreenwoodLab/RVPedigree
Links: https://github.com/GreenwoodLab/RVPedigree/tree/master/man
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