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The data was normalized using RMA normalization.
The data was normalized using quantile normalization as described in [ 22].
The data was normalized using the software's LOWESS and linear normalization methods.
The data was normalized using the ubiquitin gene (OsUG) as an endogenous control and analyzed to calculate relative expression values using 2−ΔΔCt method (Livak and Schmittgen 2001).
The data was normalized using the print tip loess method as described in the methods section.
The data was normalized using Affymetrix ExACT software to sketch normalize exon array data.
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The data were normalized using quantile normalization (BOLSTAD http://www.ncbi.nlm.nih.gov/pubmed/12538238).nih.gov/pubmed/12538238
Once the background is corrected using DFCM, the data are normalized using quantile normalization and summarized with median polish.
The data were normalized using quantile normalization, and expression measures were produced by fitting the RMA robust linear model.
The data were normalized using TMM normalization, implemented through the edgeR package in R (Robinson and Oshlack 2010).
The data were normalized using the default normalization method.
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