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As a comparison, between two trials of the quadratic method each trial was obtained by averaging over 10 EM runs the Pearson correlation was 0.98.
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Each animal received between seven and twelve trials of both food combinations in each of the three time intervals (mean = 9.52, SD = 1.30).
High correlation was shown between the two trials of static standing [ICC 1,1) = 0.92].
There was a 1-h interval between the two trials of the test, trial 1 took place at 2, 4, or 6 h after the first treatment on different testing days.
Participants received feedback about a high average group contribution level (between 16 and 18 MUs) in two trials of each block, and in the rest the feedback was medium (between 7 and 12 MUs).
Another difference between the two trials is, of course, the new set of jurors.
The effect of each blood specimen γ was expected to be different between the two trials. of which, εijk1 and εijk2 were within-individual errors of the first and the second trial respectively.
However, differences in methodology for Ki67 immunohistochemistry and scoring between the two trials precluded combination of Ki67 response data.
There was significant heterogeneity (P<0.00001) between the two trials comparing length of hospitalisation, which could have been due to differences in fluoroquinolone treatment durations (3 days v 7 days).
As we discussed previously [ 5], this analysis demonstrates a surprising degree of statistical heterogeneity, which remains despite minimal methodologic differences between the two trials and further minimization of clinical heterogeneity by selecting a more uniform subgroup of patients with severe sepsis and a high risk for death.
A major difference between these two trials is the proportion of evaluable tumor samples that were p16 positive.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com