Description Usage Arguments Details Author(s) References See Also Examples
This function plots X, Y and pseudoautosomal SNPs on BAF/LRR plots.
1 2 3 |
scan.ids |
A vector containing the sample indices of the plots. |
intenData |
|
main |
A character vector containing the titles to be used for
each plot. If |
plotY |
If |
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 |
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.
Caitlin McHugh
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.
pseudoautosomal
,
IntensityData
, GenotypeData
,
BAFfromGenotypes
1 2 3 4 5 6 7 8 9 | 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)
|
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