| norm_TSS {benchdamic} | R Documentation |
Calculate the raw library sizes from a phyloseq object. If used to divide counts, known as Total Sum Scaling normalization (TSS).
norm_TSS(object, method = "TSS", verbose = TRUE)
object |
phyloseq object containing the counts to be normalized. |
method |
normalization method to be used. |
verbose |
an optional logical value. If |
A new column containing the TSS scaling factors is added to the
phyloseq sample_data slot.
setNormalizations and runNormalizations
to fastly set and run normalizations.
set.seed(1)
# Create a very simple phyloseq object
counts <- matrix(rnbinom(n = 60, size = 3, prob = 0.5), nrow = 10, ncol = 6)
metadata <- data.frame("Sample" = c("S1", "S2", "S3", "S4", "S5", "S6"),
"group" = as.factor(c("A", "A", "A", "B", "B", "B")))
ps <- phyloseq::phyloseq(phyloseq::otu_table(counts, taxa_are_rows = TRUE),
phyloseq::sample_data(metadata))
# Calculate the scaling factors
ps_NF <- norm_TSS(object = ps)
# The phyloseq object now contains the scaling factors:
scaleFacts <- phyloseq::sample_data(ps_NF)[, "NF.TSS"]
head(scaleFacts)
# VERY IMPORTANT: to convert scaling factors to normalization factors
# multiply them by the library sizes and renormalize.
normFacts = scaleFacts * phyloseq::sample_sums(ps_stool_16S)
# Renormalize: multiply to 1
normFacts = normFacts/exp(colMeans(log(normFacts)))