A single specimen from each norovirus-positive outbreak was selected for characterisation (except for the similarity criteria experiments described below).
Based on this criterion experiment design of H∞-type is derived.
A total of 37,403 SNPs met these criteria in Experiment 1 and were subsequently used for validation within Experiment 1. Across Experiment 1 and 2, 18,695 SNP markers were in common after SNP preprocessing.
The inclusion of these studies was based on three criteria: (i) experiments involving commercial broiler lines; (ii) experiments reporting at least two of these variables: average daily feed intake (ADFI), average daily gain (ADG) or FCR; (iii) experiments detailing ingredients lists and basic nutritional characteristics of experimental diets.
We use two main and popular external evaluation metrics including cluster purity and F-measure criteria for experiments.
The benefits of these new waveforms for the foreseen 5G use cases are clearly highlighted on representative criteria and experiments.
High and equal peeling effect in convex and concave areas, and low peel losses, were the criteria of experiments.
The zebrafish embryos were staged by hours post fertilization (hpf) at 28.5°C and also by morphological criteria for experiments [81].
Based on these criteria, we experimented with a few potential scores in the training sample taking into account both relative risk estimates and the net reclassification improvement by the score, and proceeded with the best ones to the validation sample.
When we compared the number of trials necessary to reach criterion in Experiment 1 (when all numerical and non-numerical cues were available) and Experiment 2 (where only numerical cues were available), we found no difference between experiments (trials in Experiment 1: 25.2±11.7; trials in Experiment 2: 29.14±9.7; F(1,33) = 1.064, p = 0.170; power = 0.170).
Following stringent selection criteria, these experiments revealed 156 genes (165 probe sets) to be two-fold or higher differentially expressed (Fig. 4A, Table S1), with 134 genes (142 probe sets) up-regulated upon proliferation, and 22 genes (23 probe sets) associated with quiescence/slow proliferation.
