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For instance, by determining the sample size for statistical tests in advance, the type-II-risk is guaranteed to be taken into account and, foremost, only relevant effects are likely to become significant.
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The optimum experimental design for systems following the first-order Arrhenius model under linearly increasing temperature profiles was studied by determining the sampling conditions that lead to a minimum confidence region of the model parameters.
Reconstruction was calibrated by determining the APT sample geometric parameters, such as tip radius and shank angle.
Motif-X also computes a fold increase of the kinase motif in the sample by determining the total number of motifs found in the entire rat database.
The relative quantification (ΔΔCq) was performed by determining the difference between ΔCq sample and ΔCq calibrator.
The degradation was followed by determining the residual mass of the samples at the predetermined times.
Power was calculated by determining the predicted proportion of samples with counts greater than noncompliance threshold values (eqs 1a− 1a−.
Mass spectrometry is used to determine the composition of a sample by determining the mass and charge of its component parts.
The reporter luciferase activity was normalized for each sample by determining the firefly: Renillaluciferase activity ratios.
The band gap energy (eV) was calculated for the calcined samples by determining the relation between hν and (αhν) [2] [Additional file 1: Figure S1].
The methylmercury exposure was measured by determining the inorganic mercury in hair samples.
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