View source: R/somenone_variantconsensus.R
variant_consensus | R Documentation |
Primary function to call others and produce plots, table
variant_consensus( germline_id, vep_vcf_pattern, raw_vcf_pattern = "raw.vcf", tag = "somatic_n_of_1", which_genome, included_order = NULL, name_callers = NULL, impacts = NULL )
germline_id |
ID for germline_id sample |
vep_vcf_pattern |
pattern to match VEP annotated VCFs |
raw_vcf_pattern |
pattern to match raw unannotated, unfiltered VCFs unfiltered |
tag |
is a string to tag output files |
which_genome |
hg19 or hg38 |
included_order |
oredering of samples for plotting |
name_callers |
named variant callers to use primary to random selection |
vector of single-letter HGVS protein IDs
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