View source: R/somenone_facets.R
facets_jointsegs_parse_to_gr | R Documentation |
Parse jointsegs into GRanges object
facets_jointsegs_parse_to_gr( jointseg, sampleID, which_genome, anno = NULL, cgc_gr = NULL, bsgenome = NULL, work_dir )
jointseg |
filename (output from Facets) with columns: "seg", "num.mark", "nhet", "cnlr.median", "mafR", "segclust", "cnlr.median.clust", "mafR.clust", "cf.em", "tcn.em", "lcn.em" |
sampleID |
the sample identifier, taken as the string before first dot in jointseg |
which_genome |
the genome assembly used, "hg19" or "hg38" |
anno |
annotation strategy, "ENS" or "CGC" |
cgc_gr |
GRanges object of cancer gene census from COSMIC |
bsgenome |
which version of bsgenome to use |
work_dir |
character path of where files should be found, written (default: ./) |
a GRanges object with annotated jointsegs from input
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