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


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Documentation for package ‘RareVariantVis’ version 2.22.0

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