Rare Variant Sharing (RVS) implements tests of association and linkage between rare genetic variant genotypes and a dichotomous phenotype, e.g. a disease status, in family samples. The tests are based on probabilities of rare variant sharing by relatives under the null hypothesis of absence of linkage and association between the rare variants and the phenotype and apply to single variants or multiple variants in a region (e.g. gene-based test).
RVS is a bioconductor R package and so the release version can be installed as follows:
The most up-to-date version of RVS can be installed directly from Github:
Follow the vignette here
If you encounter a bug in the package, or have any questions about RVS, please open an issue at https://github.com/sherman5/RVS/issues
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