Calculates the Variant Allele Fraction for variants sites in VCF and/or BED file This script performs comparative analysis of variant sites in multiple tumour/normal samples in an individual. Also facilitates the merging of varinats sites across the samples in a sample group defined by set of related samples in an individual and provides unbiased pileup[MNV] and exonerate[Indel] output for each variant site.
- Download current installer version from git repository
- ./setup.sh <INSTALL_PATH>