A vector containing the sample indices of the plots.
intenData
IntensityData object, must contain
'BAlleleFreq' and 'LogRRatio'
main
A character vector containing the titles to be used for
each plot. If NULL then the title will be the sample number and
the chromosome.
plotY
If plotY is TRUE, the Y chromosome will be
plotted in addition to X.
hg.build
Human genome bulid number
snp.exclude
An integer vector giving the IDs of SNPs to exclude
from the plot.
cex
cex value for points on the plots
...
Other parameters to be passed directly to plot.
Details
The pseudoautosomal regions are highlighted on the plots
(PAR1 and PAR2 in gray, XTR in yellow),
and the X, Y, and XY SNPs are plotted in different colors. The base
positions for these regions depend on genome build (hg.build).
Currently hg18 and hg19 are supported.
By default the output is a 2-panel plot with LRR and BAF for the X
chromosome. if plotY is TRUE, the output is a 4-panel
plot with the Y chromosome plotted as well.
Author(s)
Caitlin McHugh
References
Ross, Mark. T. et al. (2005), The DNA sequence of the human X chromosome.
Nature, 434: 325-337. doi:10.1038/nature03440
Mumm, S., Molini, B., Terrell, J., Srivastava, A., and Schlessinger, D.
(1997), Evolutionary features of the 4-Mb Xq21.3 XY homology region revealed
by a map at 60-kb resolution. Genome Res. 7: 307-314.
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
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> library(GWASTools)
Loading required package: Biobase
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
Welcome to Bioconductor
Vignettes contain introductory material; view with
'browseVignettes()'. To cite Bioconductor, see
'citation("Biobase")', and for packages 'citation("pkgname")'.
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/GWASTools/pseudoautoIntensityPlot.Rd_%03d_medium.png", width=480, height=480)
> ### Name: pseudoautoIntensityPlot
> ### Title: Plot B Allele Frequency and Log R Ratio for the X and Y
> ### chromosomes, overlaying XY SNPs
> ### Aliases: pseudoautoIntensityPlot
> ### Keywords: hplot
>
> ### ** Examples
>
> library(GWASdata)
> data(illuminaScanADF)
> blfile <- system.file("extdata", "illumina_bl.gds", package="GWASdata")
> blgds <- GdsIntensityReader(blfile)
> intenData <- IntensityData(blgds, scanAnnot=illuminaScanADF)
>
> scanID <- getScanID(illuminaScanADF, index=1)
> pseudoautoIntensityPlot(intenData=intenData, scan.ids=scanID)
> close(intenData)
>
>
>
>
>
> dev.off()
null device
1
>