GRanges-class {GenomicRanges} | R Documentation |
The GRanges class is a container for the genomic locations and their associated annotations.
GRanges is a vector of genomic locations and associated annotations. Each element in the vector is comprised of a sequence name, an interval, a strand, and optional metadata columns (e.g. score, GC content, etc.). This information is stored in four components:
seqnames
a 'factor' Rle object containing the sequence names.
ranges
an IRanges object containing the ranges.
strand
mcols
a DataFrame object
containing the metadata columns. Columns cannot be named
"seqnames"
, "ranges"
, "strand"
,
"seqlevels"
, "seqlengths"
, "isCircular"
,
"start"
, "end"
, "width"
, or "element"
.
seqinfo
a Seqinfo object containing information about the set of genomic sequences present in the GRanges object.
GRanges(seqnames = Rle(), ranges = IRanges(),
strand = Rle("*", length(seqnames)),
...,
seqlengths = NULL, seqinfo = NULL)
:
Creates a GRanges object.
seqnames
Rle object, character vector, or factor containing the sequence names.
ranges
IRanges object containing the ranges.
strand
Rle object, character vector, or factor containing the strand information.
...
Optional metadata columns.
These columns cannot be named
"start"
, "end"
, "width"
, or
"element"
. A named integer vector "seqlength"
can be used instead of seqinfo
.
seqlengths
an integer vector named with the
sequence names and containing the lengths (or NA) for each
level(seqnames)
.
seqinfo
a Seqinfo object containing allowed
sequence names and lengths (or NA) for each
level(seqnames)
.
In the code snippets below, x
is a GRanges object.
as(from, "GRanges")
: Creates a GRanges object from a
RangedData, RangesList, RleList or RleViewsList object.
Coercing a data.frame or DataFrame into a GRanges object is also
supported. See makeGRangesFromDataFrame
for the details.
as(from, "RangedData")
:
Creates a RangedData object from a GRanges
object. The strand
and metadata columns become columns
in the result. The seqlengths(from)
, isCircular(from)
,
and genome(from)
vectors are stored in the metadata columns
of ranges(rd)
.
as(from, "RangesList")
:
Creates a RangesList object from a GRanges
object. The strand
and metadata columns become inner
metadata columns (i.e. metadata columns on the ranges).
The seqlengths(from)
, isCircular(from)
, and
genome(from)
vectors become the metadata columns.
as.data.frame(x, row.names = NULL, optional = FALSE, ...)
:
Creates a data.frame with columns seqnames
(factor),
start
(integer), end
(integer), width
(integer),
strand
(factor), as well as the additional metadata columns
stored in mcols(x)
. Pass an explicit
stringsAsFactors=TRUE/FALSE
argument via ...
to
override the default conversions for the metadata columns in
mcols(x)
.
In the following code snippets, x
is a GRanges object.
length(x)
:
Get the number of elements.
seqnames(x)
, seqnames(x) <- value
:
Get or set the sequence names.
value
can be an Rle object, a character vector,
or a factor.
ranges(x)
, ranges(x) <- value
:
Get or set the ranges. value
can be a Ranges object.
names(x)
, names(x) <- value
:
Get or set the names of the elements.
strand(x)
, strand(x) <- value
:
Get or set the strand. value
can be an Rle object, character
vector, or factor.
mcols(x, use.names=FALSE)
, mcols(x) <- value
:
Get or set the metadata columns.
If use.names=TRUE
and the metadata columns are not NULL
,
then the names of x
are propagated as the row names of the
returned DataFrame object.
When setting the metadata columns, the supplied value must be NULL
or a data.frame-like object (i.e. DataTable or data.frame)
object holding element-wise metadata.
elementMetadata(x)
, elementMetadata(x) <- value
,
values(x)
, values(x) <- value
:
Alternatives to mcols
functions. Their use is discouraged.
seqinfo(x)
, seqinfo(x) <- value
:
Get or set the information about the underlying sequences.
value
must be a Seqinfo object.
seqlevels(x)
, seqlevels(x, force=FALSE) <- value
:
Get or set the sequence levels.
seqlevels(x)
is equivalent to seqlevels(seqinfo(x))
or to levels(seqnames(x))
, those 2 expressions being
guaranteed to return identical character vectors on a GRanges object.
value
must be a character vector with no NAs.
See ?seqlevels
for more information.
seqlengths(x)
, seqlengths(x) <- value
:
Get or set the sequence lengths.
seqlengths(x)
is equivalent to seqlengths(seqinfo(x))
.
value
can be a named non-negative integer or numeric vector
eventually with NAs.
isCircular(x)
, isCircular(x) <- value
:
Get or set the circularity flags.
isCircular(x)
is equivalent to isCircular(seqinfo(x))
.
value
must be a named logical vector eventually with NAs.
genome(x)
, genome(x) <- value
:
Get or set the genome identifier or assembly name for each sequence.
genome(x)
is equivalent to genome(seqinfo(x))
.
value
must be a named character vector eventually with NAs.
seqlevelsStyle(x)
, seqlevelsStyle(x) <- value
:
Get or set the seqname style for x
.
See the seqlevelsStyle generic getter and setter
in the GenomeInfoDb package for more information.
score(x), score(x) <- value
: Get or set the “score”
column from the element metadata.
In the following code snippets, x
is a GRanges object.
start(x)
, start(x) <- value
:
Get or set start(ranges(x))
.
end(x)
, end(x) <- value
:
Get or set end(ranges(x))
.
width(x)
, width(x) <- value
:
Get or set width(ranges(x))
.
In the code snippets below, x
is a GRanges object.
append(x, values, after = length(x))
:
Inserts the values
into x
at the position given by
after
, where x
and values
are of the same
class.
c(x, ...)
:
Combines x
and the GRanges objects in ...
together.
Any object in ...
must belong to the same class as x
,
or to one of its subclasses, or must be NULL
.
The result is an object of the same class as x
.
c(x, ..., ignore.mcols=FALSE)
If the GRanges
objects have metadata columns (represented as one
DataFrame per object), each such DataFrame must have the
same columns in order to combine successfully. In order to circumvent
this restraint, you can pass in an ignore.mcols=TRUE
argument
which will combine all the objects into one and drop all of their
metadata columns.
split(x, f, drop=FALSE)
:
Splits x
according to f
to create a
GRangesList object.
If f
is a list-like object then drop
is ignored
and f
is treated as if it was
rep(seq_len(length(f)), sapply(f, length))
,
so the returned object has the same shape as f
(it also
receives the names of f
).
Otherwise, if f
is not a list-like object, empty list
elements are removed from the returned object if drop
is
TRUE
.
tile(x, n, width)
: Splits x
into a
GRangesList
, each element of which corresponds to a tile,
or partition, of x
. Specify the tile geometry with either
n
or width
(not both). Passing n
creates
n
tiles of approximately equal width, truncated by sequence
end, while passing width
tiles the region with ranges of
the given width, again truncated by sequence end.
In the code snippets below, x
is a GRanges object.
x[i, j]
, x[i, j] <- value
:
Get or set elements i
with optional metadata columns
mcols(x)[,j]
, where i
can be missing; an NA-free
logical, numeric, or character vector; or a 'logical' Rle object.
x[i,j] <- value
:
Replaces elements i
and optional metadata columns j
with value
.
head(x, n = 6L)
:
If n
is non-negative, returns the first n elements of the
GRanges object.
If n
is negative, returns all but the last abs(n)
elements
of the GRanges object.
rep(x, times, length.out, each)
:
Repeats the values in x
through one of the following conventions:
times
Vector giving the number of times to repeat each
element if of length length(x)
, or to repeat the whole vector
if of length 1.
length.out
Non-negative integer. The desired length of the output vector.
each
Non-negative integer. Each element of x
is
repeated each
times.
subset(x, subset)
:
Returns a new object of the same class as x
made of the subset
using logical vector subset
, where missing values are taken as
FALSE
.
tail(x, n = 6L)
:
If n
is non-negative, returns the last n elements of the
GRanges object.
If n
is negative, returns all but the first abs(n)
elements
of the GRanges object.
window(x, start = NA, end = NA, width = NA, frequency = NULL, delta = NULL, ...)
:
Extracts the subsequence window from the GRanges object using:
start
, end
, width
The start, end, or width of the window. Two of the three are required.
frequency
, delta
Optional arguments that specify the sampling frequency and increment within the window.
In general, this is more efficient than using "["
operator.
window(x, start = NA, end = NA, width = NA, keepLength = TRUE) <- value
:
Replaces the subsequence window specified on the left (i.e. the subsequence
in x
specified by start
, end
and width
)
by value
.
value
must either be of class class(x)
, belong to a subclass
of class(x)
, be coercible to class(x)
, or be NULL
.
If keepLength
is TRUE
, the elements of value
are
repeated to create a GRanges object with the same number of elements
as the width of the subsequence window it is replacing.
If keepLength
is FALSE
, this replacement method can modify
the length of x
, depending on how the length of the left
subsequence window compares to the length of value
.
x$name
, x$name <- value
:
Shortcuts for mcols(x)$name
and mcols(x)$name <- value
,
respectively. Provided as a convenience, for GRanges objects *only*,
and as the result of strong popular demand.
Note that those methods are not consistent with the other $
and $<-
methods in the IRanges/GenomicRanges infrastructure,
and might confuse some users by making them believe that a GRanges
object can be manipulated as a data.frame-like object.
Therefore we recommend using them only interactively, and we discourage
their use in scripts or packages. For the latter, use
mcols(x)$name
and mcols(x)$name <- value
, instead
of x$name
and x$name <- value
, respectively.
show(x)
:
By default the show
method displays 5 head and 5 tail
elements. This can be changed by setting the global options
showHeadLines
and showTailLines
. If the object
length is less than (or equal to) the sum of these 2 options
plus 1, then the full object is displayed.
Note that these options also affect the display of
GAlignments and
GAlignmentPairs objects (defined in
the GenomicAlignments package), as well as other objects
defined in the IRanges and Biostrings packages (e.g.
IRanges and DNAStringSet objects).
P. Aboyoun and H. Pages
makeGRangesFromDataFrame
,
GRangesList-class,
seqinfo
,
Vector-class,
Ranges-class,
Rle-class,
DataFrame-class,
intra-range-methods,
inter-range-methods,
setops-methods,
findOverlaps-methods,
nearest-methods,
coverage-methods
seqinfo <- Seqinfo(paste0("chr", 1:3), c(1000, 2000, 1500), NA, "mock1") gr <- GRanges(seqnames = Rle(c("chr1", "chr2", "chr1", "chr3"), c(1, 3, 2, 4)), ranges = IRanges( 1:10, width = 10:1, names = head(letters,10)), strand = Rle( strand(c("-", "+", "*", "+", "-")), c(1, 2, 2, 3, 2)), score = 1:10, GC = seq(1, 0, length=10), seqinfo=seqinfo) gr ## Summarizing elements table(seqnames(gr)) sum(width(gr)) summary(mcols(gr)[,"score"]) ## Renaming the underlying sequences seqlevels(gr) seqlevels(gr) <- sub("chr", "Chrom", seqlevels(gr)) gr seqlevels(gr) <- sub("Chrom", "chr", seqlevels(gr)) # revert ## Combining objects gr2 <- GRanges(seqnames=Rle(c('chr1', 'chr2', 'chr3'), c(3, 3, 4)), IRanges(1:10, width=5), strand='-', score=101:110, GC = runif(10), seqinfo=seqinfo) gr3 <- GRanges(seqnames=Rle(c('chr1', 'chr2', 'chr3'), c(3, 4, 3)), IRanges(101:110, width=10), strand='-', score=21:30, seqinfo=seqinfo) some.gr <- c(gr, gr2) ## all.gr <- c(gr, gr2, gr3) ## (This would fail) all.gr <- c(gr, gr2, gr3, ignore.mcols=TRUE) ## The number of lines displayed in the 'show' method ## are controlled with two global options. longGR <- c(gr[,"score"], gr2[,"score"], gr3) longGR options("showHeadLines"=7) options("showTailLines"=2) longGR ## Revert to default values options("showHeadLines"=NULL) options("showTailLines"=NULL)