Description: Package that takes Battenberg copy number output and somatic point mutations and transforms the allele frequencies into an estimate of fraction of cells (CCF). It can also perform mutation to mutation and mutation to SNP phasing and contains a number of other convenience functions.
Package details |
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Author | Stefan Dentro |
Maintainer | Stefan Dentro <sd11@sanger.ac.uk> |
License | GPL-3 |
Version | 1.0.8 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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