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The applicability of the new LightCycler assays for routine molecular testing was evaluated by testing 96 clinical samples.
To assess the effect of this antigenic divergence between field isolates and the official vaccine strain, serologic testing was evaluated by means of HI assays.
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Factors associated with MVCT participation, risk selection among MVCT clients, and barriers to HIV testing, were evaluated by comparing characteristics of clients presenting for HIV testing and randomly selected community respondents who did not present for testing.
Reactions during the application period and after patch testing were evaluated by a dermatologist-allergologist at 24, 48, and 72 hours after patching.
The reproducibility of the cobas KRAS test was evaluated by comparing the results from testing the evaluable FFPET tumour panel at the two independent clinical laboratory sites.
The stability test was evaluated by injecting the same sample solution at 0, 2, 4, 8, 12 and 24 h after preparation.
Repeatability within-test was evaluated in a mixed model with pig as a random effect, and agreement between days, handlers and tests was evaluated by partial correlations after controlling for replicate, pen and day effects.
Agreement between the tests was evaluated by kappa statistics.
Significance of the neutrality test was evaluated by simulations implemented in BOTTLENECK [71] performed under the two-phase mutation model (TPM) with one-step mutations occurring at a frequency of 95% of the total.
The performance of the test was evaluated by Christian Medical College (CMC), Vellore in 2002 [ 17].
Significance of the homozygosity test was evaluated by simulations implemented in BOTTLENECK.
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