View source: R/somenone_variantconsensus.R
rdata_gr_list | R Documentation |
run function to make list of GRanges per caller
rdata_gr_list(in_vec, germline_id, callers, out_ext, raw_vcf_pattern)
in_vec |
vector of VCFs to parse |
germline_id |
ID for germline_id sample |
callers |
the variant callers for which VCFs are present in dir |
out_ext |
the extension after caller in filename of VCF |
raw_vcf_pattern |
pattern to match raw unannotated, unfiltered VCFs unfiltered |
none, creates an RData object
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