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Both tests used the same CDC-produced antigen, the microsomal fraction of adult S. mansoni fluke, which has both a sensitivity and specificity for S. mansoni of 99%.
All tests used the same molecule with the same parameters: a fatty acid amide hydrolase molecule that, once ported to the cubic grid, consisted of 29880 charges on 297 × 297 × 297 grid points.
Virulence comparison and pathogenicity screening tests used the same methodology except that in the former tests G. sturtianum seedlings were inoculated when 4 weeks old with a conidial suspension (1.0 ± 0.2 × 10 conidia/mL) from which hyphae had been removed by straining through tissue.
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These consistencies have been perceptually confirmed by naturalness evaluation tests using the same two-phrase samples with different F0 heights.
The hardware and software architectures of ADCWAN are described in detail and some ADC tests using the same test setup are presented.
The AAA and modified AAA tests use the same movement assessment criteria, with the exception of the chin-up and total AAA score.
To evaluate the resolution of each dataset and our joint source inversion analysis, we conducted checkerboard resolution tests using the same previously determined parameters.
It should however be noted that the likelihood of statistical errors vastly increases when doing multiple tests using the same dataset.
When a dose group effect was found to be significant, pairwise tests using the same model were used to further investigate specific comparisons.
Our initial observation of increased infection causing higher dauer formation involved RNAi tests using the same bacterial strain (HT115) for control and sample.
The PCR-RLB was added to these tests, using the same criteria as for culture.
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