View source: R/normalize_loess.R
normalize_loess | R Documentation |
Perform Loess normalization
normalize_loess(omicsData, method = "fast", span = 0.4)
omicsData |
an object of the class 'pepData', 'proData', 'metabData',
'lipidData', or 'nmrData', created by |
method |
character string specifying which variant of the cyclic loess method to use. Options are "fast" (default), "affy", or "pairs" |
span |
span of loess smoothing window, between 0 and 1. |
A wrapper for the normalizeCyclicLoess function from the limma package.
The normalized data is returned in an object of the appropriate S3 class (e.g. pepData), on the same scale as omicsData (e.g. if omicsData contains log2 transformed data, the normalization will be performed on the non-log2 scale and then re-scaled after normalization to be returned on the log2 scale).
Bolstad, B. M., Irizarry R. A., Astrand, M., and Speed, T. P. (2003). A comparison of normalization methods for high density oligonucleotide array data based on bias and variance. Bioinformatics 19, 185-193.
Ballman, KV Grill, DE, Oberg, AL and Therneau, TM (2004). Faster cyclic loess: normalizing RNA arrays via linear models. Bioinformatics 20, 2778-2786.
normalizeCyclicLoess
in the limma
package
library(pmartRdata)
mypep <- edata_transform(pep_object, "log2")
result <- normalize_loess(mypep)
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