R: Plot copy number and physical position for a set of genomic...
xyplot
R Documentation
Plot copy number and physical position for a set of genomic intervals.
Description
Plot copy number and physical position given by a
CNSet object for a set of genomic intervals stored in a
RangedDataCVN object.
Usage
xyplot2(x, data, range, frame=50e3L, ...)
Arguments
x
A formula. Currently, the formula must be one of cn~x,
cn ~ x | id or cn ~ x | range when data is a
CNSet. If data is a BeadStudioSet, the formula
has the form lrr ~ x| range or baf ~ x | range.
data
A CNSet, BeadStudioSet, or SnpSet object.
...
A RangedDataCNV object must be passed by the name
'range'. Arguments for xyplot are passed to
xyplot2. Additional arguments are passed to xypanel and panel.xyplot.
range
A RangedDataCNV object.
frame
The genomic distance (basepairs) to the left and right of the start and stop
coordinates in the range object.
Details
These functions plot copy number estimates versus physical
position. The function is particularly useful for multi-panel displays
in which the copy number estimates for a single range of a
GRanges object appears in one panel. The size of the
multi-panel display depends on the number of ranges (rows) in the
GRanges object.
Value
An object of class trellis.
Author(s)
R. Scharpf
See Also
xyplot, xypanel
To modify the plot appearance from the default, additional arguments
can be passed to panel.xyplot, lpoints, and
lrect.
Examples
## simulated data
library(oligoClasses)
library(IRanges)
library(VanillaICE)
data(oligoSetExample, package="oligoClasses")
## The oligoSnpSet class will likely be deprecated and made defunct
## in a future release. Instead, we favor
## RangedSummarizedExperiment-derived classes defined in VanillaICE
oligoSet <- oligoSet[chromosome(oligoSet) == 1, ]
grl <- hmm(oligoSet, p.hom=0, TAUP=1e10, is.log=FALSE)
g <- grl[[1]]
## To visualize each range in it's own panel surrounded by a
## frame of 2,000,000 bases:
## (here the frames are overlapping, but the method could be
## applied more generally to a collection of ranges from
## different chromsomes and samples)
xyplot2(cn~x | range, data=oligoSet,
range=g,
frame=2e6, panel=xypanel,
cex=2,
pch=".",
col.het="salmon",
fill.het="salmon",
col.hom="royalblue",
fill.hom="royalblue",
state.cex=0.5,
border="orange", scales=list(x="free"),
par.strip.text=list(cex=0.5),
xlab="Mb", ylab=expression(log[2]("copy number")))
Results
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
Copyright (C) 2016 The R Foundation for Statistical Computing
Platform: x86_64-pc-linux-gnu (64-bit)
R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.
R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.
Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.
> library(SNPchip)
Welcome to SNPchip version 2.18.0
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/SNPchip/xyplot.Rd_%03d_medium.png", width=480, height=480)
> ### Name: xyplot
> ### Title: Plot copy number and physical position for a set of genomic
> ### intervals.
> ### Aliases: xyplot2 xyplot2,formula,gSet-method
> ### xyplot2,formula,SnpSet-method
> ### Keywords: dplot methods
>
> ### ** Examples
>
> ## simulated data
> library(oligoClasses)
Welcome to oligoClasses version 1.34.0
> library(IRanges)
Loading required package: BiocGenerics
Loading required package: parallel
Attaching package: 'BiocGenerics'
The following objects are masked from 'package:parallel':
clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
clusterExport, clusterMap, parApply, parCapply, parLapply,
parLapplyLB, parRapply, parSapply, parSapplyLB
The following objects are masked from 'package:stats':
IQR, mad, xtabs
The following objects are masked from 'package:base':
Filter, Find, Map, Position, Reduce, anyDuplicated, append,
as.data.frame, cbind, colnames, do.call, duplicated, eval, evalq,
get, grep, grepl, intersect, is.unsorted, lapply, lengths, mapply,
match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, rank,
rbind, rownames, sapply, setdiff, sort, table, tapply, union,
unique, unsplit
Loading required package: S4Vectors
Loading required package: stats4
Attaching package: 'S4Vectors'
The following objects are masked from 'package:base':
colMeans, colSums, expand.grid, rowMeans, rowSums
> library(VanillaICE)
Loading required package: GenomicRanges
Loading required package: GenomeInfoDb
Loading required package: SummarizedExperiment
Loading required package: Biobase
Welcome to Bioconductor
Vignettes contain introductory material; view with
'browseVignettes()'. To cite Bioconductor, see
'citation("Biobase")', and for packages 'citation("pkgname")'.
Welcome to VanillaICE version 1.34.0
> data(oligoSetExample, package="oligoClasses")
> ## The oligoSnpSet class will likely be deprecated and made defunct
> ## in a future release. Instead, we favor
> ## RangedSummarizedExperiment-derived classes defined in VanillaICE
> oligoSet <- oligoSet[chromosome(oligoSet) == 1, ]
> grl <- hmm(oligoSet, p.hom=0, TAUP=1e10, is.log=FALSE)
Warning message:
executing %dopar% sequentially: no parallel backend registered
> g <- grl[[1]]
>
> ## To visualize each range in it's own panel surrounded by a
> ## frame of 2,000,000 bases:
> ## (here the frames are overlapping, but the method could be
> ## applied more generally to a collection of ranges from
> ## different chromsomes and samples)
> xyplot2(cn~x | range, data=oligoSet,
+ range=g,
+ frame=2e6, panel=xypanel,
+ cex=2,
+ pch=".",
+ col.het="salmon",
+ fill.het="salmon",
+ col.hom="royalblue",
+ fill.hom="royalblue",
+ state.cex=0.5,
+ border="orange", scales=list(x="free"),
+ par.strip.text=list(cex=0.5),
+ xlab="Mb", ylab=expression(log[2]("copy number")))
>
>
>
>
>
> dev.off()
null device
1
>