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Hence, it must be corrected against bias coming from multiple hypothesis testing to determine statistical significance.
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Peak areas were calculated in El Maven (https://elucidatainc.github.io/ElMaven/) and stable isotopic measurements were corrected against the naturally occurring isotopes for each metabolite measured.
The hypocretin contents were corrected against protein concentrations.
Urinary amino acid concentrations were corrected against creatinine values.
The assay results were corrected against β-gal activity assayed using Promega β-gal reporter kit.
For each replicate, the radioactivity of the samples was corrected against a blank which corresponded to the pre-fixed sediment cores submitted to the protocol described above.
Signal intensities were corrected against the membrane background.
Absorbance levels from drug treated cells and untreated controls were corrected against medium only blank controls.
Gene expression was corrected against GAPDH and GUS mRNA level in each sample.
Ag levels were corrected against cellular total protein and presented as ng TFPI/mg total protein.
Results were corrected against cellular total protein measured in the cell lysate.
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