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In order to address this possibility a comparison of expression data from somatic embryos, callus and leaf was conducted.
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Vicario et al. (2007) previously proposed this possibility in a comparison of codon usage in the genomes of 12 Drosophila species.
Among others, one can cite the automatic tuning of regularization coefficients, the selection of the most important input variables, the derivation of an uncertainty interval on the model output and the possibility to perform a comparison of different models and, therefore, select the optimal model.
We discuss the possibilities below based on a comparison of the amino acid sequences of amoebal p22 phox and other p22 phox orthologs.
This possibility is also supported by a comparison of EC10 values for superfemale induction in M. cornuarietis via water (13.9 ng/L, this study) and in P. antipodarum via sediments (0.22 μg/kg, Duft et al. 2003).
A more detailed assessment of this possibility will require further analysis, including a comparison of the transcriptome of islets from βLKBKO and wild-type islets.
To normalize for this possibility, the comparison of normal and abnormal cells adhered to a strict side-by-side analysis of cultures, which had been generated and maintained under identical conditions.
This offers a possibility for the comparison of thresholds for biomarkers of exposure versus biomarkers of effect.
Farther, let us analyze the possibility of comparison of the last two summands at the right part of Equation 8 with the basic potential summand ( {displaystyle {sum}_{n=1}^{N_a}}Qleft left|mathbf{r}-{mathbf{R}}_N_a}}Qleft left|mathbf{r}-{mathbf{R}n 4).
The methods used in these studies differ from the present one, which limit the possibility for comparison of the results.
There is also the possibility for comparison of the results with other forms of quantitative objective assessments for at least a subset of the data.
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