normalizeNbpseq | R Documentation |
This function is a wrapper over DESeq normalization. It accepts a matrix of gene counts (e.g. produced by importing an externally generated table of counts to the main metaseqr2 pipeline).
normalizeNbpseq(geneCounts, sampleList,
normArgs = NULL, libsizeList = NULL,
output = c("matrix", "native"))
geneCounts |
a table where each row represents a gene and each column a sample. Each cell contains the read counts for each gene and sample. Such a table can be produced outside metaseqr2 and is imported during the basic metaseqr2 workflow. |
sampleList |
the list containing condition names and the samples under each condition. |
normArgs |
a list of NBPSeq normalization
parameters. See the result of
|
libsizeList |
an optional named list where names
represent samples (MUST be the same as the samples in
|
output |
the class of the output object. It can be
|
A matrix with normalized counts or a list with the normalized counts and other NBPSeq specific parameters.
Panagiotis Moulos
dataMatrix <- metaseqR2:::exampleCountData(2000)
sampleList <- list(A=c("A1","A2"),B=c("B1","B2","B3"))
diagplotBoxplot(dataMatrix,sampleList)
normDataMatrix <- normalizeNbpseq(dataMatrix,sampleList)
diagplotBoxplot(normDataMatrix,sampleList)
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