Description Usage Arguments Value
View source: R/GenerateDPinput_strelka_vcf.R
Converts snv counts from vcf into input format for DPClust
1 2 3 4 5 6 7 8 9 10 11 | GenerateDPinput_strelka_vcf(
tumourplatekey,
normalplatekey,
gender,
vcffilepath,
rhoandpsifilepath,
subcloneshg38filepath,
output_loci_file,
output_file,
output_DPinput_file
)
|
Loci |
of SNP positions used in CNV call Allele frequencies of same SNP positions File containing purity and ploidy of tumour sample Subclones file from Battenberg containing copy number segments across genome Sex of patient |
A file containing all snv loci, their mutation copy number status, and their CCF (cancer cell fraction)
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