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Samples with VL ≥1000 copies/mL were selected for HIV drug resistance testing by using an in-house PCR.
We have attempted to reduce the potential problems associated with multiple testing by using an a priori approach for choosing the pollutant metric, pollutant lag structure, and modeling approach; however, we have conducted numerous statistical tests.
These patients were given treatment for a dengue-like illness, and blood samples were obtained for complete blood counts and serologic testing by using an ELISA specific for IgG and IgM against DENV.
We performed susceptibility testing by using an agar proportion method on enriched Middlebrook 7H10 medium (BBL Microbiology Systems, Cockeysville, MD, USA) at the following concentrations: rifampicin 1 μg/mL, isoniazid 0.2 μg/mL, streptomycin 2 μg/mL and 10 μg/mL, and ethambutol 5 μg/mL.
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The image quality requirement was determined through empirical testing by using a videotaped National Institutes of Health Stroke Scale examination.
We accounted for multiple testing by using a significance level of p<0.01 and adjusted for follow-up time.
P-values were adjusted for multiple testing by using a Holm correction [ 44].
The results were corrected for multiple testing by using a Bonferroni correction.
The RIVM performed drug susceptibility testing by using a modified agar dilution method (5 ).
Histopathologic testing of the skin biopsy specimen showed a leukoclastic vasculitis, and immunohistochemical testing by using a rabbit polyclonal antibody directed against SFG rickettsiae showed positive result.
The activity of CLEAs was tested by using an appropriate aliquot of CLEAs that guaranteed a linear response.
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CEO of Professional Science Editing for Scientists @ prosciediting.com