inter-range-methods {GenomicRanges} | R Documentation |
This man page documents inter range transformations of a GenomicRanges object (i.e. of an object that belongs to the GenomicRanges class or one of its subclasses, this includes for example GRanges objects), or a GRangesList object.
See ?`intra-range-methods`
and
?`inter-range-methods`
in the IRanges
package for a quick introduction to intra range and inter
range transformations.
See ?`intra-range-methods`
for
intra range transformations of a GenomicRanges object or
GRangesList object.
## S4 method for signature 'GenomicRanges' range(x, ..., with.revmap=FALSE, ignore.strand=FALSE, na.rm=FALSE) ## S4 method for signature 'GRangesList' range(x, ..., with.revmap=FALSE, ignore.strand=FALSE, na.rm=FALSE) ## S4 method for signature 'GenomicRangesList' range(x, ..., with.revmap=FALSE, ignore.strand=FALSE, na.rm=FALSE) ## S4 method for signature 'GenomicRanges' reduce(x, drop.empty.ranges=FALSE, min.gapwidth=1L, with.revmap=FALSE, with.inframe.attrib=FALSE, ignore.strand=FALSE) ## S4 method for signature 'GRangesList' reduce(x, drop.empty.ranges=FALSE, min.gapwidth=1L, with.revmap=FALSE, with.inframe.attrib=FALSE, ignore.strand=FALSE) ## S4 method for signature 'GenomicRangesList' reduce(x, drop.empty.ranges=FALSE, min.gapwidth=1L, with.inframe.attrib=FALSE, ignore.strand=FALSE) ## S4 method for signature 'GenomicRanges' gaps(x, start=1L, end=seqlengths(x)) ## S4 method for signature 'GenomicRanges' disjoin(x, with.revmap=FALSE, ignore.strand=FALSE) ## S4 method for signature 'GRangesList' disjoin(x, with.revmap=FALSE, ignore.strand=FALSE) ## S4 method for signature 'GenomicRangesList' disjoin(x, with.revmap=FALSE, ignore.strand=FALSE) ## S4 method for signature 'GenomicRanges' isDisjoint(x, ignore.strand=FALSE) ## S4 method for signature 'GRangesList' isDisjoint(x, ignore.strand=FALSE) ## S4 method for signature 'GenomicRangesList' isDisjoint(x, ignore.strand=FALSE) ## S4 method for signature 'GenomicRanges' disjointBins(x, ignore.strand=FALSE)
x |
A GenomicRanges or GenomicRangesList object. |
drop.empty.ranges, min.gapwidth, with.revmap, with.inframe.attrib, start, end |
See |
ignore.strand |
|
... |
For |
na.rm |
Ignored. |
range
returns an object of the same type as x
containing range bounds for each distinct (seqname, strand) pairing.
The names (names(x)
) and the metadata columns in x
are
dropped.
reduce
returns an object of the same type as x
containing reduced ranges for each distinct (seqname, strand) pairing.
The names (names(x)
) and the metadata columns in x
are
dropped.
See ?reduce
for more information about range
reduction and for a description of the optional arguments.
gaps
returns an object of the same type as x
containing complemented ranges for each distinct (seqname, strand) pairing.
The names (names(x)
) and the columns in x
are dropped.
For the start and end arguments of this gaps method, it is expected that
the user will supply a named integer vector (where the names correspond to
the appropriate seqlevels). See ?gaps
for more
information about range complements and for a description of the optional
arguments.
disjoin
returns an object of the same type as x
containing disjoint ranges for each distinct (seqname, strand) pairing.
The names (names(x)
) and the metadata columns in x
are
dropped. If with.revmap=TRUE
, a metadata column that maps the
ouput ranges to the input ranges is added to the returned object.
See ?disjoin
for more information.
isDisjoint
returns a logical value indicating whether the ranges
in x
are disjoint (i.e. non-overlapping).
disjointBins
returns bin indexes for the ranges in x
, such
that ranges in the same bin do not overlap. If ignore.strand=FALSE
,
the two features cannot overlap if they are on different strands.
When they are supported on GRangesList object x
, the above inter
range transformations will apply the transformation to each of the list
elements in x
and return a list-like object parallel to
x
(i.e. with 1 list element per list element in x
).
If x
has names on it, they're propagated to the returned object.
H. Pagès and P. Aboyoun
The GenomicRanges and GRanges classes.
The Ranges class in the IRanges package.
The inter-range-methods man page in the IRanges package.
GenomicRanges-comparison for comparing and ordering genomic ranges.
endoapply
in the S4Vectors package.
gr <- GRanges( seqnames=Rle(paste("chr", c(1, 2, 1, 3), sep=""), c(1, 3, 2, 4)), ranges=IRanges(1:10, width=10:1, names=letters[1:10]), strand=Rle(strand(c("-", "+", "*", "+", "-")), c(1, 2, 2, 3, 2)), score=1:10, GC=seq(1, 0, length=10) ) gr gr1 <- GRanges(seqnames="chr2", ranges=IRanges(3, 6), strand="+", score=5L, GC=0.45) gr2 <- GRanges(seqnames="chr1", ranges=IRanges(c(10, 7, 19), width=5), strand=c("+", "-", "+"), score=3:5, GC=c(0.3, 0.5, 0.66)) gr3 <- GRanges(seqnames=c("chr1", "chr2"), ranges=IRanges(c(1, 4), c(3, 9)), strand=c("-", "-"), score=c(6L, 2L), GC=c(0.4, 0.1)) grl <- GRangesList(gr1=gr1, gr2=gr2, gr3=gr3) grl ## --------------------------------------------------------------------- ## range() ## --------------------------------------------------------------------- ## On a GRanges object: range(gr) range(gr, with.revmap=TRUE) ## On a GRangesList object: range(grl) range(grl, ignore.strand=TRUE) range(grl, with.revmap=TRUE, ignore.strand=TRUE) # --------------------------------------------------------------------- ## reduce() ## --------------------------------------------------------------------- reduce(gr) gr2 <- reduce(gr, with.revmap=TRUE) revmap <- mcols(gr2)$revmap # an IntegerList ## Use the mapping from reduced to original ranges to group the original ## ranges by reduced range: relist(gr[unlist(revmap)], revmap) ## Or use it to split the DataFrame of original metadata columns by ## reduced range: relist(mcols(gr)[unlist(revmap), ], revmap) # a SplitDataFrameList ## [For advanced users] Use this reverse mapping to compare the reduced ## ranges with the ranges they originate from: expanded_gr2 <- rep(gr2, elementNROWS(revmap)) reordered_gr <- gr[unlist(revmap)] codes <- pcompare(expanded_gr2, reordered_gr) ## All the codes should translate to "d", "e", "g", or "h" (the 4 letters ## indicating that the range on the left contains the range on the right): alphacodes <- rangeComparisonCodeToLetter(pcompare(expanded_gr2, reordered_gr)) stopifnot(all(alphacodes %in% c("d", "e", "g", "h"))) ## On a big GRanges object with a lot of seqlevels: mcols(gr) <- NULL biggr <- c(gr, GRanges("chr1", IRanges(c(4, 1), c(5, 2)), strand="+")) seqlevels(biggr) <- paste0("chr", 1:2000) biggr <- rep(biggr, 25000) set.seed(33) seqnames(biggr) <- sample(factor(seqlevels(biggr), levels=seqlevels(biggr)), length(biggr), replace=TRUE) biggr2 <- reduce(biggr, with.revmap=TRUE) revmap <- mcols(biggr2)$revmap expanded_biggr2 <- rep(biggr2, elementNROWS(revmap)) reordered_biggr <- biggr[unlist(revmap)] codes <- pcompare(expanded_biggr2, reordered_biggr) alphacodes <- rangeComparisonCodeToLetter(pcompare(expanded_biggr2, reordered_biggr)) stopifnot(all(alphacodes %in% c("d", "e", "g", "h"))) table(alphacodes) ## On a GRangesList object: reduce(grl) # Doesn't really reduce anything but note the reordering # of the inner elements in the 2nd and 3rd list elements: # the ranges are reordered by sequence name first (which # should appear in the same order as in 'seqlevels(grl)'), # and then by strand. reduce(grl, ignore.strand=TRUE) # 2nd list element got reduced ## --------------------------------------------------------------------- ## gaps() ## --------------------------------------------------------------------- gaps(gr, start=1, end=10) ## --------------------------------------------------------------------- ## disjoin(), isDisjoint(), disjointBins() ## --------------------------------------------------------------------- disjoin(gr) disjoin(gr, with.revmap=TRUE) disjoin(gr, with.revmap=TRUE, ignore.strand=TRUE) isDisjoint(gr) stopifnot(isDisjoint(disjoin(gr))) disjointBins(gr) stopifnot(all(sapply(split(gr, disjointBins(gr)), isDisjoint))) ## On a GRangesList object: disjoin(grl) # doesn't really disjoin anything but note the reordering disjoin(grl, with.revmap=TRUE)