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The data was normalized using RMA normalization.
Data was normalized by Lowess normalization [ 49].
Data was normalized by quantile normalization.
Data was normalized by loessM normalization [ 55, 56].
The data was normalized by variance stabilization normalization [ 68].
The OCR and ECAR data was normalized using protein concentration that was assayed with Pierce BSA kit (Thermofisher).
The data was normalized to the control group.
Moreover, the data was normalized with logarithmic transformation.
Data was normalized against ACTB.
Gene expression data was normalized by GAPDH.
Intensity data was normalized using the Beadstudio cubic spline algorithm.
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