This package provides an association test that is capable of dealing with very rare and even private variants. This is accomplished by a kernel-based approach that takes the positions of the variants into account. The test can be used for pre-processed matrix data, but also directly for variant data stored in VCF files. Association testing can be performed whole-genome, whole-exome, or restricted to pre-defined regions of interest. The test is complemented by tools for analyzing and visualizing the results.
|Bioconductor views||Annotation DataImport Genetics Sequencing VariantAnnotation WholeGenome|
|Maintainer||Ulrich Bodenhofer <[email protected]>|
|License||GPL (>= 2)|
|Package repository||View on GitHub|
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