Usage
dmrPlot(dmr, which.table=1:length(dmr$tabs), which.plot=1:30, legend.size=1, all.lines=TRUE, all.points=FALSE, colors.l, colors.p, outpath=".", cpg.islands, Genome, plotG=FALSE, dat=NULL, buffer=NULL, plot.p=TRUE)
Arguments
dmr
a list object as returned by dmrFinder.
which.table
a vector of indices identifying which tables in the dmr list to plot regions from.
which.plot
a vector of indices identifying which regions (rows) from each table to plot.
legend.size
cex argument for the legend (factor by which to magnify/shrink the legend).
all.lines
if TRUE, plot the smooth lines for all groups. If FALSE, only for the 2 groups being compared.
all.points
if TRUE, plot the points for all groups. If FALSE, only for the 2 groups being compared.
colors.l
a vector of line colors, one color for each group whose line is to be plotted (in alphabetical order).
colors.p
a vector of point colors, one color for each group whose points are to be plotted (in alphabetical order).
outpath
where to save the output pdf file.
cpg.islands
a table with columns "chr","start", and "end" for CpG islands to plot in the second panel.
Genome
the BSgenome object for the organism based upon which your array was designed.
plotG
if TRUE, a third panel of each DMR plot will show the difference between the median green channel value (after subtracting probe medians and correcting for gc content) between the 2 groups. If true, dat must be provided.
dat
if plotG=TRUE, this must be provided. It is the TilingFeatureSet object used when estimating the matrix of percent methylation estimates used in dmrFinder when it produced dmr.
buffer
Number of base pairs to plot on either side of each DMR candidate.
plot.p
set to FALSE if you want to plot the methlation values (the "l" output from dmrFinder) instead of the percentage methylation values (the "p" output). If dmrFinder was run on l instead of p, plot.p=FALSE necessarily.