A suite for analysis of rare genomic variants in whole genome
sequencing data
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Documentation for package ‘RareVariantVis’ version 2.34.0
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 |