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Consequently, we derived a normalization factor by normalizing each disease interaction ratio to the one in the VisANT database (Table S5).
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Relative stoichiometries were calculated by normalizing each protein by iBAQ value against the bait protein (CSA).
By normalizing each row of this matrix, we obtain a transition matrix U = (u ij) m× m, where, representing the probability that a random walker moves from the i-th disease to the j-th disease.
By normalizing each row of this matrix, we obtain a transition matrix R = (r ij) m × n, where, representing the probability that a random walker jumps from the i-th disease to the j-th gene.
Relative percent viability was determined by normalizing each condition to DMSO treatment only.
The analysis was conducted by normalizing each protein band to its respective loading control.
Fold-change in expression was calculated by ΔΔCt normalized to GAPDH for each sample and normalizing each of the cell lines to the cell line SKBR3.
The action potential wave is retrieved by normalizing the time-series in each pixel in the co-moving frame.
Relative gene expression was determined by normalizing the gene expression of each target gene to GAPDH.
The relative densities for each protein were determined by normalizing with that of β-actin.
Enrichment of 5-hmC gains at each element was then calculated by normalizing for element length.
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