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Patterns were normalized using the molecular weight marker (PFGE Lambda Marker, Fermentas, Germany).
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Patterns were normalized using a molecular weight marker (Lambda Ladder PFGE Marker, New England Biolabs, USA) [ 3, 9].
The data were normalized using the default normalization method.
Expressed data were normalized using the Median normalization.
Expression levels were normalized using the quantile normalization method [ 44].
Data were normalized using the Controls Normalization method (Illumina, San Diego, CA).
The background-corrected data were normalized using the Gene Expression Pattern Analysis Suite v3.1 (GEPAS, http://www.gepas.org) and the global loess method [ 69].
The values were normalized using the LOWESS algorithm.
Extracts were normalized using the BCA assay (Novagen).
Database and expression levels were normalized using the GCRMA algorithm.
Signal intensities were normalized using the global Lowess regression algorithm.
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