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For all electrophysiological measures presented here, outliers were removed based on the 2 SD rule.
The limited nature of the single-item self-reported measures presented here restrict our inferences.
Finally, the scoring measures presented here can be used generally to evaluate and compare results of simulated genome assemblies.
While our findings are supported by previous randomized research in other settings, the trends in outcome measures presented here may have alternative explanations.
It can be noted, however, that it may be possible to apply the sequence sensitive measures presented here to these previous analyses.
The Five Cause Taxonomy and the strategy for defining appropriate measures presented here address gaps that have limited significant reductions in TDE and patient harm.
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The Q′ R measure presented here allows the estimation of the proportion of interactions established between different modules in a network.
All volume measures are presented here in this corrected form.
The optimum number of clusters, provided by at least two of these measures, was presented here.
The measured spectra presented here were normalized by sample transmission at B=0 and then divided by the rate of reference signals (signal without sample) at nonzero and zero magnetic fields.
Some of the measured parameters presented here are used today as is in biology, such as cell dry mass and surface area.
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