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Plate efficiency was calculated using control cells and the following formula: PE = (number of colonies formed/number of cells seeded).
PCR efficiency was calculated using the following equation: Efficiency % = (10^ -1/ Slope -1)*100% Amplification factor waSlope -1ated using the following equation: Amplification factor=10^(-1/Slope).
Efficiency was calculated using a constant return to scale with an input-oriented Charnes-Cooper-Rhodes (CCR) formulation method.
Cutoff diameter at the 50% collection efficiency was calculated using both linear and non-linear regression techniques.
Individual band intensity was quantified using ImageLab and the HDR efficiency was calculated using the following equation: (b + c) / (a + b + c) × 100 (a = uncleaved PCR amplicon, b and c = the cleavage products).
The efficiency was calculated using Rct and corrosion current density (Icorr) process and found that 3 and 5% inhibitor exhibit around 89 and 96%, respectively after 1 h of exposure in SCP + 3.5 wt% NaCl solution.
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Device isolation efficiency is calculated using the Yeh's matrix formalism for anisotropic multilayers.
The output power and energy conversion efficiency are calculated using engineering power factor (PF eng and figure of merit (ZT eng.
In this method, the detection efficiency is calculated using a physical and statistical model of the photon distribution emitted by the source.
The corrosion rate and inhibition efficiency were calculated using the formulae (1) and (2).
The results of the drug loading and encapsulation efficiency were calculated using Eqs. 2 and 3, respectively.
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