A set of functions which use Ensembl and Bioconductor genome objects to map between given protein sequences to corresponding coding DNA sequences, extract single-amino acid variants (SNVs) and corresponding nucleotide substitutions. Map mutational signatures for all possible substitutions.
Package details |
|
---|---|
Maintainer | Joseph Ng <joseph.chifung.ng@gmail.com> |
License | GPL-3 + file LICENSE |
Version | 0.2.0 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.