R/mutationalpatterns.R
sig_count_snv.Rd
Counts SNV Contexts.
sig_count_snv(vcf_gr, ref_genome)
GRanges containing all mutation types from a single sample.
The BSGenome reference genome to use.
A list with two elements:
snv_counts: matrix containing the number of SNVs per COSMIC context per gr.
gr_snv: GRanges object containing the SNVs.