Description Usage Arguments Value
This function computes the proportion of an input genomic interval (eg: an intron or an exon) that is contained in a read.
NB: it takes into account possible gaps and splicing in read alignments.
1 | computeRegionOverlap(align.gr, intron.gr)
|
align.gr |
A |
intron.gr |
A |
The fraction of intron.gr
contained in the sequence align.gr
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