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Data background correction was done within GenomeStudio (Illumina), and then exported to the lumi R package.
For each plate, background correction was performed with blank control wells containing no compounds.
Bias Correction and Background Correction was checked for protein quantification and normalization.
Background correction was done using the normexp method by Ritchie et al.62.62
No background correction was performed.
Background correction was done for autofluorescence.
A robust Edwards background correction was applied.
No background correction was performed before normalization.
Background correction was achieved by subtracting the changes in absorbance obtained with BSA.
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Background-correction was conducted according to the recommended methods for each platform.
The background correction was set to: offset = 50.
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