Usage
pfilter(mn, un, bn, da, pn, bc, perCount=NULL, pnthresh = NULL, perc = NULL,
pthresh = NULL,logical.return=FALSE)
Arguments
mn
matrix of methylated signal intensities, each column representing a sample
(default method), or an object for which a method is available e.g
MethyLumiSet or RGChannelSetExtended. N.B. Bead count filtering will
not work unless data read in as an RGGhannelSetExtended rather than an
RGChannelSet.
un
matrix of unmethylated signal intensities, each column representing a sample
(default method) or NULL when mn is a MethyLumiSet or RGChannelSetExtended
object
bn
matrix of precalculated betas, each column representing a sample, or NULL when
mn is a MethyLumiSet or RGChannelSetExtended object
da
annotation data frame, such as x@featureData@data #methylumi package, or
NULL when mn is a MethyLumiSet or RGChannelSetExtended object pn
matrix of detection p-values, each column representing a sample, a
MethyLumiSet or RGChannelSetExtended object
bc
matrix of arbitrary values, each column representing a sample and eeach row
representing a probe, in which "NA" represents beadcount
perCount
remove sites having this percentage of samples with a beadcount
pnthresh
cutoff for detection p-value, default set to 0.05
perc
remove samples having this percentage of sites with a detection p-value
greater than pnthresh, default set to 1
pthresh
remove sites having this percentage of samples with a detection p-value
greater than pnthresh, default set to 1
logical.return
If it is TRUE, FALSE or TRUE is returned to indicate success