Description Usage Arguments Value See Also Examples
Finds a common genome for a series of BigWig-files, either using only levels present in all files (intersect) or in any file (union).
1 | bwCommonGenome(plusStrand, minusStrand, method = "intersect")
|
plusStrand |
BigWigFileList: BigWig files with plus-strand CTSS data. |
minusStrand |
BigWigFileList: BigWig files with minus-strand CTSS data. |
method |
character: Either 'intersect' or 'union'. |
Sorted Seqinfo-object.
Other BigWig functions:
bwGenomeCompatibility()
,
bwValid()
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 | if (.Platform$OS.type != "windows") {
# Use the BigWig-files included with the package:
data('exampleDesign')
bw_plus <- system.file('extdata', exampleDesign$BigWigPlus,
package = 'CAGEfightR')
bw_minus <- system.file('extdata', exampleDesign$BigWigMinus,
package = 'CAGEfightR')
# Create two named BigWigFileList-objects:
bw_plus <- BigWigFileList(bw_plus)
bw_minus <- BigWigFileList(bw_minus)
names(bw_plus) <- exampleDesign$Name
names(bw_minus) <- exampleDesign$Name
# Find the smallest common genome (intersect) across the BigWigList-objects:
bwCommonGenome(plusStrand=bw_plus, minusStrand=bw_minus, method='intersect')
# Find the most inclusive genome (union) across the BigWigList-objects:
bwCommonGenome(plusStrand=bw_plus, minusStrand=bw_minus, method='union')
}
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