dumpCounts.ICGCconsensusSNV: Dump allele counts from vcf - ICGC pancancer consensus SNV...

View source: R/allelecount.R

dumpCounts.ICGCconsensusSNVR Documentation

Dump allele counts from vcf - ICGC pancancer consensus SNV pipeline

Description

Dump allele counts stored in the info column of the VCF file. Output will go into a file supplied as tumour_outfile. It will be a fully formatted allele counts file as returned by alleleCounter. There are no counts for the matched normal.

Usage

dumpCounts.ICGCconsensusSNV(
  vcf_infile,
  tumour_outfile,
  normal_outfile = NA,
  refence_genome = "hg19",
  samplename = NA
)

Arguments

vcf_infile

The vcf file to read in

tumour_outfile

File to save the tumour counts to

normal_outfile

Optional parameter specifying where the normal output should go

refence_genome

Optional parameter specifying the reference genome build used

samplename

Optional parameter specifying the samplename to be used for matching the right column in the VCF

Author(s)

sd11


Wedge-lab/dpclust3p documentation built on June 14, 2025, 4:24 p.m.