Description Usage Arguments Methods Accessors Fields Class-Based Methods Author(s) See Also Examples
A Snapshot
-class to visualize genomic data from
BAM files with zoom and pan functionality.
1 |
files |
A character() or |
range |
A |
... |
Additional, optional, arguments to be passed to the
Snapshot
|
signature(x = "Snapshot")
: Zoom (in or out) the
current plot.
signature(x = "Snapshot")
: Pan (right or left)
the current plot.
signature(x = "Snapshot")
: Toggle the current
functions which imported records are to be immediately
evaluated. Note that the active range will be changed to the
current active window.
signature(x = "Snapshot")
: Toggle the panning
effects.
signature(x = "Snapshot")
: Toggle the zooming
effects.
signature(object = "Snapshot")
: Display a
Snapshot
object.
signature(x = "Snapshot")
: Get the files
field (object of class BamFileList
) of a Snapshot
object.
signature(x = "Snapshot")
: Get the
functions
field (object of SnapshotFunctionList
) of a
Snapshot
object.
signature(x = "Snapshot")
: Get the view
field (object of SpTrellis
) of a Snapshot
object.
signature(x = "Snapshot")
: Get the
.range
field (object of GRanges
) of a Snapshot
object.
signature(x = "Snapshot")
: Get the
trellis
object, a field of the SpTrellis
object.
.debug
:Object of class function
to display
messages while in debug mode
.auto_display
:Object of class logical
to
automatically display the coverage plot.
.range
:Object of class GRanges
indicating
which ranges of records to be imported from BAM fields.
.zin
:Object of class logical
indicating
whether the current zooming effect is zoom in.
.pright
:Object of class logical
indicating
whether the current panning effect is right.
.data
:Object of class data.frame
containing
coverage a position is represented for each strand and BAM file.
.data_dirty
:Object of class logical
indicating whether to re-evaluate the imported records.
.initial_functions
:Object of class
SnapshotFunctionList
available by the Snapshot
object.
.current_function
:Object of class character
of the function the imported recorded are currently evaluated and
visualized.
annTrack
:Default to NULL
if not intended to
visualize the annotation track. If default visualization
function(s) is intended to be used to plot the annotation,
annTrack
has to be a GRanges
instance.
functions
:Object of class
SnapshotFunctionList
of customized functions to evaluate
and visualize the imported records.
files
:Object of class BamFileList
to be imported.
view
:Object of class SpTrellis
that is
essentially a reference class wrapper of Trellis
objects.
display()
:Display the current Snapshot
object.
pan()
:Pan (right or left) the current plot.
zoom()
:Zoom (in or out) the current plot.
toggle(zoom, pan, currentFunction)
:Toggle zooming, panning effects or the currentFuction in which the imported records are to be evaluated and visualized.
Martin Morgan and Chao-Jen Wong cwon2@fhcrc.org
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 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 | ## example 1: Importing specific ranges of records
file <- system.file("extdata", "SRR002051.chrI-V.bam",
package="yeastNagalakshmi")
which <- GRanges("chrI", IRanges(1, 2e5))
s <- Snapshot(file, range=which)
## methods
zoom(s) # zoom in
## zoom in to a specific region
zoom(s, range=GRanges("chrI", IRanges(7e4, 7e4+8000)))
pan(s) # pan right
togglez(s) # change effect of zooming
zoom(s) # zoom out
togglep(s) # change effect of panning
pan(s)
## accessors
functions(s)
vrange(s)
show(s)
ignore.strand(s)
view(s) ## extract the spTrellis object
getTrellis(s) ## extract the trellis object
## example 2: ignore strand
s <- Snapshot(file, range=which, ignore.strand=TRUE)
##
## example 3: visualizing annotation track
##
library(GenomicFeatures)
getAnnGR <- function(txdb, which) {
ex <- exonsBy(txdb, by="gene")
seqlevels(ex, pruning.mode="coarse") <- seqlevels(which)
r <- range(ex)
gr <- unlist(r)
values(gr)[["gene_id"]] <- rep.int(names(r), times=lengths(r))
gr
}
txdbFile <- system.file("extdata", "sacCer2_sgdGene.sqlite",
package="yeastNagalakshmi")
# txdb <- makeTxDbFromUCSC(genome="sacCer2", tablename="sgdGene")
txdb <- loadDb(txdbFile)
which <- GRanges("chrI", IRanges(1, 2e5))
gr <- getAnnGR(txdb, which)
## note that the first column of the elementMetadata annotates of the
## range of the elements.
gr
s <- Snapshot(file, range=which, annTrack=gr)
annTrack(s)
## zoom in to an interesting region
zoom(s, range=GRanges("chrI", IRanges(7e4, 7e4+8000)))
togglez(s) ## zoom out
zoom(s)
pan(s)
## example 4, 5, 6: multiple BAM files with 'multicoarse_covarage'
## and 'multifine_coverage' view.
## Resolution does not automatically switch for views of multiple
## files. It is important to note if width(which) < 10,000, use
## multifine_coverage. Otherwise use multicoarse_coverage
file <- system.file("extdata", "SRR002051.chrI-V.bam",
package="yeastNagalakshmi")
which <- GRanges("chrI", IRanges(1, 2e5))
s <- Snapshot(c(file, file), range=which,
currentFunction="multicoarse_coverage")
## grouping files and view by 'multicoarse_coverage'
bfiles <- BamFileList(c(a=file, b=file))
values(bfiles) <- DataFrame(sampleGroup=factor(c("normal", "tumor")))
values(bfiles)
s <- Snapshot(bfiles, range=which,
currentFunction="multicoarse_coverage", fac="sampleGroup")
## grouping files and view by 'multifine_coverage'
which <- GRanges("chrI", IRanges(7e4, 7e4+8000))
s <- Snapshot(bfiles, range=which,
currentFunction="multifine_coverage", fac="sampleGroup")
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