fillGenome | R Documentation |
finds all ranges not present in the input segments, e.g. non-coding regions in a list of coding regions
fillGenome(seg, chrS, indexed = TRUE, expand = TRUE)
seg |
input segments with indexed coordinates (see
|
chrS |
a chromosome index, indicating at wich positions chromosomes start; this is required for handling chromosome ends and forward and reverse strand values |
indexed |
boolean value indicating whether the coordinates
in argument |
expand |
if |
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