View source: R/somenone_variantconsensus.R
master_intersect_snv_grlist | R Documentation |
Find intersect from list of SNV GRanges
master_intersect_snv_grlist(gr_list, ps_vec, dp_vec, tag, which_genome)
gr_list |
list of named GRanges objects |
ps_vec |
mcols columns to keep p(er) s(ample; appended with list element's name) |
dp_vec |
mcols columns to d(edu)p(licate); appended as-is if all same; if varaitions, usual 'dot number' formatting applies) |
tag |
to apply to output file (master) |
which_genome |
hg19 or hg38 |
list of GRanges object of shared intersecting, and all mutations with ps_vec, dp_vec columns, and original rownames (should be unique therefore)
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