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Differentiation between all the species tested was achieved by combined analysis of the rDNA fragments produced by primer pairs FR1 + NS1 and FR1+FF390.
In all validations prior to its application on test situations, the algorithm was successively modified until the hypothesised outcome of the effect of the particular property being tested was achieved.
The highest agreement among all weighting schemes tested was achieved when the clinical chemistry data was given all of the weight.
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The pilot testing was achieved in January 2013.
The anti-bacterial test was achieved for the treated substrates.
The multi-axial testing was achieved by internally pressurizing and uniaxially loading hollow cylinders.
A statistically significant discriminative accuracy of 86% (p = 0.002) after a permutation test was achieved.
In situ accelerated lightfastness testing was achieved with a Newport-Oriel style microfadeometer previously described by Whitmore et al. [6].
If statistical significance at the 0.05 level using Kruskal Wallis test was achieved, Bonferroni correction was used for post hoc comparison of pairs of groups (P < 0.0125).
Lastly, freezing/thawing cycles test was achieved via storing each prepared formula at −21 °C and +25 °C for two days at each temperature.
The worst performance in cavitation erosion tests was achieved by the WC 12%Co coating, which showed the highest mass loss throughout the test.
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