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After exclusions, the full sample provided 4,448,612 annual observations.
*Median ages (ranges) of study participants were as follows: 1 blood sample provided: 25 y (18 41 y); 2 blood samples provided, 29 y (16 67 y); p = 0.005.
Incidence, sensitivity, specificity, positive predictive value and F-measure were calculated from each sample providing 10 000 measures from which to calculate the 95% CIs.
Genetic screening of these samples provided 233 authenticated tiger samples, which we attempted to amplify at 10 highly polymorphic microsatellite loci.
Together, the GROG and Sentinelles samples provided 838 laboratory-confirmed pandemic A(H1N1) influenza cases ≥6 month-old that were described for pandemic vaccination and age, and were included in the analysis of pandemic vaccines.
The 4 sets of samples provided 3 sets of paired sera.
Additionally, thin sections made from selected plug samples provide 2D information with a much higher detail than the μCT data.
Therefore, our approach allowed us to detect the pre-leukemic clone in all samples providing 1 3 positive cells were present in the analyzed sample.
All the 18 cases came from different households, and all provided at least one sputum sample; 14 provided 2 sputum samples and 13 provided three sputum samples.
Our estimation sample thus provided 10,608 usable choice responses from 442 respondents.
Our sample size provided 99.9% statistical power to detect differences between drugs regarding clinical response and mortality.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com