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Several data sets corresponding to production-scale runs with a load from 120 to 485 L have been compared with simulations.
Several data sets contained information on annotated but not translated pseudogenes.
Several data sets were built in order to calculate the MI for sequence-agonist, sequence-antagonists, sequence-Gi, sequence-Gs and sequence-Gq correlations.
Several data sets from the United States and Canada are used in this paper.
Several data sets from the Saskatchewan health administrative databases were used for our analysis.
Several data sets were constructed by varying how the positive and negative alignments were generated.
Several data sets show that these probabilities are indeed closer, but the differences remain very large [ 21, 31].
The algorithm has been tested in several data sets.
The method is tested for several data sets including synthetic as well as real-world data.
To evaluate its validity, the model was applied to several data sets from column experiments.
We use several data sets to demonstrate the feasibility of this TVQ approach.
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