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Materials and methods A positive gram stain was defined as the visualization of bacterial cells or "many neutrophils" (> 5 per high-power field) in the smear.
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Using this method, a positive fold change would represent up-regulation of the sample gene compared to the calibrator; whereas a negative fold change would represent down-regulation of the sample gene compared to the calibrator.
Using this method, a positive clone was identified and sequenced.
Using this method, a positive difference corresponded to a functional decline.
An additional 36 patients (56% increase, 100 patients in total), who were not recognized as pneumococcal CAP patients using the conventional methods, had a positive result in any of the three alternative methods.
However, we argue that this relationship must still be discussed because both methods showed a positive association even though the relationship in the PQL2 method was not statistically significant.
The SEPs were listed positively in the supplemental table only when both methods returned a positive signal peptide prediction.
The two methods showed a positive and highly significant correlation.
The simulations showed that for camera polygons that were smaller than approximately one home range density estimates for all methods had a positive bias.
These methods have a positive impact on protein function prediction.
All analysis methods show a positive correlation between local symmetry and human eye fixations.
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