Sentence examples for decay was calculated from inspiring English sources

The theoretical current decay was calculated as a weighted algebraic summation of the deactivation kinetics of hERG1a and hERG1b homomeric channels.

The LD decay was calculated as previously described [ 71].

LD decay was calculated using the method described by Remington et al. [ 40] in which a non-linear least squares estimate of r per base pair is estimated.

At a scan rate of 100 mV/s, the slope of the decay was calculated to be 1.43 × 10 –2 a.u./s, whilst the slower scan rate (10 mV/s) induced a lower value of 1.01 × 10 –2 a.u./s, with consistently higher absorbance values in parallel over the same time scale.

Zero-order rate coefficients of greigite decay were calculated by linear regression of the time-dependent data from the maximum value to the point where the constant final value was reached (Table 3).

MRI PDFF and T2* decay were calculated in the same ROI.

Rates of NO decay were calculated for each protein by determining the time taken for peak NO concentrations to decay by 0.5 μM and were expressed per μM heme, determined spectrally by the peak in the Soret region at 410 nm.

The decay rate was calculated as follows: fruit decay rate = (the decayed count of fruits × 100/the total count of fruits) [ 3].

The mean decay parameter (slope) in a biexponential fit model of correlation decay curve was calculated and plotted for each sample (matched HMD and LMD samples, indicated on the x-axis).

The "decay" data set was analyzed in R. The slope of the decay curves was calculated using the following equation: where Y is the natural logarithm of the expression level and X is the time of incubation with actinomycin D in hours.

The LD decay rate was calculated as the chromosomal distance where the correlation coefficient (r 2 ) between SNP pairs dropped to half its maximum estimated value.