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However, these validation experiments are cumbersome, and, as a result, there are only a few validated miRNA targets.
These validation tests demonstrate the precise estimation of shield thickness.
These validation parameters were the mean of the ten repeats of each model.
We do not show these validation results due to space constraints.
Sections 7 and 8 will demonstrate that these validation results are more than satisfactory.
Overall, these validation experiments further suggest that mRNA-Seq can provide strong evidence of transcript expression.
However, we could not find any published equilibrium sampling methods able to fulfil these validation requirements.
On the basis of these validation analyses, FK was modeled into four hierarchical levels.
Only patients with data satisfying these validation criteria were included in the analysis.
These validation parameters demonstrate that electrochemical CUPRAC methods are comparable with the classical spectrophotometric method.
Relevant impact of temporal reporting accuracy was found for these validation datasets.
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