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Panel 1: Population attributable fraction P A F = p (R R − 1 ) p (R R − 1 ) + 1 RR = relative risk; p = prevalence of exposure The available disease burden estimates have been developed with variations of the above method, or different approaches supported by differing levels of evidence.
Improved fixation method or different localization to avoid accidental sensor removal.
To rank indicators with respect to their importance and enhance the transparency of the quality of care assessment, several approaches can be applied such as a survey, a Delphi method or different variants of conjoint analyses.
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Indeed, several other constraints, e.g. costs of edge deployment and maintenance, capacities, weights (see Materials and Methods), or different routing strategies should be taken into account for more precise and system specific analysis.
These conflicting results might be due to different analysis methods or different gene sequence selection.
They often suffer, however, from poor quality, be it due to different sampling methods or different taxonomic resolution.
Although we assume that most laboratories used immunohistochemistry assays and consistent cutoff points, it is possible that some laboratories used different methods or different cutoff points.
Therefore, either more powerful methods or different approaches will be needed to address the task of assigning sequences to species or taxa.
If we the data sources lead in different directions, then we attempt to understand why, for instance, by examining for modifying variables, different sampling methods or different study quality.
The incongruence between molecular trees obtained with different methods or different data sets is also frequently encountered [ 23, 24] Studies on several other systems reveal similar uncertainty as we observed in our analysis [ 25, 26].
The contrast between case-fatality and severity found in this analysis and that observed in previous studies in South Africa might be the result of different methods or different study periods.
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