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The cut-off for this categorized variable was set at the 75th percentile of MMP-11 in the total group.
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For this study we categorized this CNV as non-pathogenic, although further study is required to determine whether this CNV is translated and pathogenic through a dominant-negative effect.
Therefore, we utilized this latter definition for this analysis and categorized patients as a 20%-responder or 20%-nonresponder based on whether their mean of all T25FW assessments during double-blind visits improved by 20% or more from the mean of the pre-randomization visits baseline.
Self-reported medications for each of the above chronic conditions were queried, and for this analysis were categorized as "None", "One", "Two", or "Three or more".
In conclusion, based on the above evaluations of these five aspects of p-oncomirs and p-mirsupps, we conclude that the p-oncomirs and the p-mirsupps used for this analysis were categorized correctly.
For this purpose we categorized PaO2/FIO2 ratios.
The validation studies included for this analysis are categorized into internal and external.
For this study, we categorized exposure groups using mean individual air benzene measurements obtained during the 3 months preceding phlebotomy.
The main analytical variables for this study were categorized based on WHO, UNICEF, and the Government of Bangladesh treatment guidelines.
We constructed two cumulative lifetime cyanazine exposure metrics for this analysis, each categorized into terthiles, based on the tertile levels among all cancer cases.
For this study, we categorized severity of CI into 4 groups: No/Mild (0, 1); Moderate (2, 3); Severe (4, 5); Very Severe (6).
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