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EEG power and isolated effective coherence of delta (1 3.5 Hz), theta (4 7.5 Hz), alpha (8 12.5 Hz), and beta (13 30 Hz) bands were calculated in the frontal, central, temporal, parietal, and occipital regions.
Simple "reference bands" were calculated in the volunteer group assuming normal distribution for visual comparison [ 31].
Intensity values of the PCR product bands were calculated in comparison with a regression line, with the correlation coefficient ≥ 0.99, generated from measurements of at least four Marker M5 bands of different concentration values.
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To determine the fold-change in the expressions of BIM and p21 proteins in the individual samples, the intensities of the bands were calculated using Quantity One, version 4.7 software in GS 800 calibrated Densitometer (Bio Rad, Gurgaon, Haryana, India) followed with normalization with the respective ß-actin expression.
Signal intensities from target protein bands were calculated relative to GAPDH signal intensities in liver homogenates.
Molecular sizes of the RNA bands were calculated based on the migration distances of the ladder bands in each individual gel.
Corresponding 90% confidence bands were calculated.
The deformation-induced shift in transmission spectrum valleys for different bands is calculated, and the changes in the width of these reflectance peaks are also obtained.
Band structures for other models were calculated in the same fashion.
The electron density of states (DOS) was determined for these two surfaces and the d-band center and fractional filling were calculated in different situations.
Transient amplitude, rise time and pulse duration were measured in the time domain to obtain the associated empirical distributions; the power spectrum and the frequency content were calculated in the bands of interest; finally a time frequency representation has been used to observe the evolution of the power spectrum over time and determine the location of the main contributions.
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CEO of Professional Science Editing for Scientists @ prosciediting.com