varianceStabilizingTransformation
(VST)
that provides much faster estimation of the dispersion trend used to determine
the formula for the VST. The speed-up is accomplished by
subsetting to a smaller number of genes in order to estimate this dispersion trend.
The subset of genes is chosen deterministically, to span the range
of genes' mean normalized count.
This wrapper for the VST is not blind to the experimental design:
the sample covariate information is used to estimate the global trend
of genes' dispersion values over the genes' mean normalized count.
It can be made strictly blind to experimental design by first
assigning a design
of ~1
before running this function,
or by avoiding subsetting and using varianceStabilizingTransformation
.
vst(object, blind = TRUE, nsub = 1000, fitType = "parametric")
varianceStabilizingTransformation
)estimateDispersions
(options described there)
dds <- makeExampleDESeqDataSet(n=20000, m=20)
vsd <- vst(dds)
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