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The question to address are the following: (i) What would happen if some of the trials were detected with large synchronization errors?
The main effect of group was not significant (F = 0.9, p = 0.36 1 That is, regardless of side or group, targets in congruent trials were detected faster than targets in incongruent trials.
These trials were detected as they happened, discarded, and rerun within the same block.
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Significant statistical heterogeneity among trials was detected.
No significant statistical heterogeneity among trials was detected.
No heterogeneity across trials was detected by the χ2 test, and the P value was 0.537 (I2 = 0.0%; Figure 4).
Of note, 68% of the cancers in the screening arm in the Swedish trial were detected through screening, compared with 74% in our study, and adjuvant therapy was not given, 20 whereas it was in the Canadian National Breast Screening Study. 1 Tumours in the control group of the Swedish Two-County study were on average 2.8 cm, larger than in our study.
However, no significant time effect for evapotranspiration rate (ET) in growth chamber trial was detected.
No association between breed and likelihood of responding to a diet trial was detected in this sample.
In NHL trials, ADAs were detected in patients and neutralizing antibody assays were not yet available.
Four Y-coordinates from trial one were detected as outliers as they were not plotted on, or close to, the 45° line.
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CEO of Professional Science Editing for Scientists @ prosciediting.com