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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