Nothing
if(dev.cur() <= 1) get(getOption("device"))()
opar <-
par(ask = interactive() &&
(.Device %in% c("X11", "GTK", "windows","quartz"))
)
#datadir <- system.file("examples", package = "DNAcopy")
#Read in two example by Snijders et al.
data(coriell)
#Combine into one CNA object to prepare for analysis on Chromosomes 1-23
CNA.object <- CNA(cbind(coriell$Coriell.05296,coriell$Coriell.13330),
coriell$Chromosome,coriell$Position,
data.type="logratio",sampleid=c("c05296","c13330"))
#We generally recommend smoothing single point outliers before analysis
#Make sure to check that the smoothing is proper
smoothed.CNA.object <- smooth.CNA(CNA.object)
#Segmentation at default parameters
segment.smoothed.CNA.object <- segment(smoothed.CNA.object, verbose=1)
#Plot whole studies
plot(segment.smoothed.CNA.object, plot.type="w")
#Plot each study by chromosome
plot(segment.smoothed.CNA.object, plot.type="s")
#Plot each chromosome across studies (6 per page)
plot(segment.smoothed.CNA.object, plot.type="c", cbys.layout=c(2,1), cbys.nchrom=6)
#Plot by plateaus
plot(segment.smoothed.CNA.object, plot.type="p")
#Segment again but making sure that splits correspond are 3SDs separated
segment.smoothed.CNA.object <- segment(smoothed.CNA.object, undo.splits="sdundo", verbose=1)
#All the non-obvious splits have been removed
plot(segment.smoothed.CNA.object,plot.type="s")
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