| overlapsToCoverage {ORFik} | R Documentation |
Get overlaps and convert to coverage list
overlapsToCoverage(gr, reads, keep.names = TRUE, type = "any")
gr |
a |
reads |
a GAlignment or GRanges object of RiboSeq, RnaSeq etc |
keep.names |
logical (T), keep names or not. |
type |
a string (any), argument for countOverlaps. |
a Rle, one list per group with # of hits per position.
Other ExtendGenomicRanges: asTX,
coveragePerTiling,
pmapFromTranscriptF,
reduceKeepAttr, tile1,
txSeqsFromFa, windowPerGroup
ORF <- GRanges(seqnames = "1",
ranges = IRanges(start = c(1, 10, 20),
end = c(5, 15, 25)),
strand = "+")
names(ORF) <- "tx1"
reads <- GRanges("1", IRanges(25, 25), "+")
overlapsToCoverage(ORF, reads)