| gr.end | R Documentation |
GRangesAlternative 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
gr.end(example_dnase, width=200, clip=TRUE)
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