# A suite for analysis of rare genomic variants in whole genome sequencing data

## Documentation for package ‘RareVariantVis’ version 2.38.0

- DESCRIPTION file.
- User guides, package vignettes and other documentation.

## Help Pages

callHomozygous | Call homozygous regions from sequencing data
chromosomeVis | Visualization of all genomic variants on the chromosome
getCrisprGuides | Retrieve CRISPR/Cas9 guides.
movingAverage | Computation of moving average
multipleVis | Interactive visualization of rare variants on the chromosome, applicable for multiple files
rareVariantVis | Interactive visualization of rare variants on the chromosome