URL: https://github.com/im3sanger/dndscv
Proper Citation: dNdScv (RRID:SCR_023123)
Description: Software R package is group of maximum likelihood dN/dS methods designed to quantify selection in cancer and somatic evolution. Contains functions to quantify dN/dS ratios for missense, nonsense and essential splice mutations, at level of individual genes, groups of genes or at whole-exome level.Used to detect cancer driver genes on datasets ranging from few samples to thousands of samples, in whole-exome/genome or targeted sequencing studies.
Synonyms: dN/dScv
Resource Type: data processing software, data analysis software, software application, software resource
Keywords: quantify dN/dS ratios, missense, nonsense, essential splice mutations, detect cancer driver genes on datasets, whole-exome/genome, targeted sequencing studies,
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