zhuangyh/easyVAF
Somatic sequence variants are associated with a cancer diagnosis, prognostic stratification, and treatment response. Variant allele frequency (VAF) is the percentage of sequence reads with a specific DNA variant over the read depth at that locus. VAFs on targeted loci under different (experimental) conditions are often compared. We present our R package ‘ esayVAF’ for parametric and non-parametric comparison of VAFs among multiple treatment groups.
RGPL-3.0