URL: https://github.com/im3sanger/dndscv
Proper Citation: dndSCV (RRID:SCR_017093)
Description: Software R package as suite of dN/dS methods 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 genome level. Used to detect cancer driver genes on datasets.
Resource Type: software resource, software application, data analysis software, data processing software
Keywords: dN/dS, method, quantify, selection, cancer, somatic, evolution, missense, nonsense, essential, splice, mutation, gene, genome, dataset
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