View source: R/preprocessing.R
maf2loci | R Documentation |
Function that dumps the loci of snvs from a series of vcf files into a single loci file
maf2loci(maf_file, outfile, dummy_alt_allele = NA, dummy_ref_allele = NA)
outfile |
Where to store the output |
dummy_alt_allele |
The alt allele to store, supply when you want to override what is in the VCF (Default: NA) |
dummy_ref_allele |
The reference allele to store, supply when you want to override what is in the VCF (Default: NA) |
vcf_files |
A vector of vcf files to be considered |
fai_file |
Reference genome index |
ign_file |
A file with chromosomes to be excluded from consideration |
sd11
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