View source: R/BSmooth.fstat.R
smoothSds | R Documentation |
Smooth the standard deviations using a thresholded running mean based on smoothed whole-genome bisulfite sequencing data.
smoothSds(BSseqStat, k = 101, qSd = 0.75, mc.cores = 1, maxGap = 10^8,
verbose = TRUE)
BSseqStat |
An object of class |
k |
A positive scalar, see details. |
qSd |
A scalar between 0 and 1, see details. |
mc.cores |
The number of cores used. Note that setting
|
maxGap |
A scalar greater than 0, see details. |
verbose |
Should the function be verbose? |
The standard deviation estimates are smoothed using a running mean with a
width of k
and thresholded using qSd
which sets the minimum
standard deviation to be the qSd
-quantile.
An object of class BSseqStat. More speciically, the input
BSseqStat object with the computed statistics added to the
stats
slot (accessible with getStats
).
Kasper Daniel Hansen khansen@jhsph.edu
BSmooth.fstat
for the function to create the appropriate
BSseqStat
input object.
BSseqStat
also describes the return class. This
function is likely to be followed by the use of computeStat
.
if(require(bsseqData)) {
# library(limma) required for makeContrasts()
library(limma)
data(keepLoci.ex)
data(BS.cancer.ex.fit)
BS.cancer.ex.fit <- updateObject(BS.cancer.ex.fit)
## Remember to subset the BSseq object, see vignette for explanation
## TODO: Kind of a forced example
design <- model.matrix(~0 + BS.cancer.ex.fit$Type)
colnames(design) <- gsub("BS\\.cancer\\.ex\\.fit\\$Type", "",
colnames(design))
contrasts <- makeContrasts(
cancer_vs_normal = cancer - normal,
levels = design
)
BS.stat <- BSmooth.fstat(BS.cancer.ex.fit[keepLoci.ex,],
design,
contrasts)
BS.stat <- smoothSds(BS.stat)
## Comparing the raw standard deviations to the smoothed standard
## deviations
summary(getStats(BS.stat, what = "rawSds"))
summary(getStats(BS.stat, what = "smoothSds"))
}
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