To control the stability of the variance, the variance calculation was tested for 2, 3, 5, 7, and 10 samples per group.
5 The accuracy of the calculation was tested by simulation of traction force recovery, which demonstrates the validity of our traction force computation method.
Finally, when a modified ML calculation was tested by using variable weightings for each genomic locus, there was improved performance of ML with an AUC of 0.97, compared with the current method of ML calculation that had an AUC of 0.95.
The inhibitory activities of 15 top-ranking compounds from the docking calculations were tested on a recombinant methyltransferase with the RNA substrate 7MeGpppAC5.
Approximations included in the calculations were tested; for example, calculations were repeated with a much larger QM region for CM, showing a change in barrier of only 0.7 kcal/mol.
Different spectral processing calculations were tested: a combination of either multiplicative scatter correction or standard normal variate, and first or second order Savitzky Golay algorithm with a three or five-point window was used depending on the model (Table 2).
Different spectral processing calculations were tested on both sub-sets in Matlab; first derivative with a window width of 5, with either multiplicative scatter correction or standard normal variate.
These calculations were tested using simulation of selection of dogs born in 2005 (n = 2489, 756 males, 1733 females).
The calculations were tested for validity using simulation studies.
The sample size calculations were tested using simulation, to check that they provided the desired power and α, or the desired confidence interval width.
