gr.end | R Documentation |
GRanges
Alternative to GenomicRanges::flank
that will provide end positions *within* intervals
Shortcut for gr.end
gr1 <- GRanges(1, IRanges(10,20), strand="+") gr1
Shortcut for gr.end
gr1 <- GRanges(1, IRanges(10,20), strand="+") gr1
Shortcut for gr.end
gr1 <- GRanges(1, IRanges(10,20), strand="+") gr1
Shortcut for gr.end
gr1 <- GRanges(1, IRanges(10,20), strand="+") gr1
gr.end(x, width = 1, force = FALSE, ignore.strand = TRUE, clip = TRUE)
x %)% ...
x %))% ...
x %(% ...
x %((% ...
x |
|
width |
integer Specify subranges of greater width including the start of the range. (default = 1) |
force |
boolean Allows returned |
ignore.strand |
boolean If set to |
clip |
boolean Trims returned |
y |
num bases to get from left side of interval |
GRanges object of width = width
ranges representing end of each genomic range in the input.
GRanges
right sides of input intervals
GRanges
3' sides of input intervals
GRanges
left sides of input intervals
GRanges
5' sides of input intervals
Marcin Imielinski
Marcin Imielinski
Marcin Imielinski
Marcin Imielinski
Marcin Imielinski
gr.end(example_dnase, width=200, clip=TRUE)
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