dumpCounts.Broad | R Documentation |
Dump allele counts stored in the sample columns of the VCF file. Output will go into a file supplied as tumour_outfile and optionally normal_outfile. It will be a fully formatted allele counts file as returned by alleleCounter.
dumpCounts.Broad(
vcf_infile,
tumour_outfile,
normal_outfile = NA,
refence_genome = "hg19",
samplename = NA
)
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 |
sd11
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