Description findOverlaps methods Accessors See Also Examples
Methods for GRanges objects
findOverlaps(query, subject, ...):
Find the feature indices in subject that overlap the
genomic intervals in query, where query is a
GRanges object and subject is a gSet-derived object.
Additional arguments to the findOverlaps method in the
package IRanges can be passed through the ...
operator.
object is an instance of the GRanges class.
coverage2(object):
For the GRanges and GRangesList objects returned by
the hidden Markov model implemented in the "VanillaICE" package
and the segmentation algorithm in the "MinimumDistance" package,
the intervals are annotated by the number of probes (markers) for
SNPs and nonpolymorphic regions. coverage2 and
numberProbes are convenient accessors for these
annotations.
genomeBuild(object):
Accessor for the UCSC genome build.
numberProbes(object):
Integer vector indicating the number of probes (markers) for each
range in object. Equivalent to coverage2.
state(object):
Accessor for the elementMetadata column 'state', when
applicable. State is used to contain the index of the inferred
copy number state for various hmm methods defined in the
VanillaICE.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 | library(IRanges)
library(GenomicRanges)
gr1 <- GRanges(seqnames = "chr2", ranges = IRanges(3, 6),
state=3L, numberProbes=100L)
## convenience functions
state(gr1)
numberProbes(gr1)
gr2 <- GRanges(seqnames = c("chr1", "chr1"),
ranges = IRanges(c(7,13), width = 3),
state=c(2L, 2L), numberProbes=c(200L, 250L))
gr3 <- GRanges(seqnames = c("chr1", "chr2"),
ranges = IRanges(c(1, 4), c(3, 9)),
state=c(1L, 4L), numberProbes=c(300L, 350L))
## Ranges organized by sample
grl <- GRangesList("sample1" = gr1, "sample2" = gr2, "sample3" = gr3)
sampleNames(grl) ## same as names(grl)
numberProbes(grl)
chromosome(grl)
state(grl)
gr <- stack(grl)
sampleNames(gr)
chromosome(gr)
state(gr)
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