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The results of the paired-samples t-test with the t-value of 1.55 and the p-value of.132 > .05 show that there was no significant difference between the friend and non-friend corrections (Table 5).
To validate this quantification method, we reconstructed the well-known fluorescence emission spectrum of GFP and the bioluminescence spectrum of Aeq by means of the above four channel measurements and corrections (Table 1).
Results were consistent between models after multiple testing corrections (Table 1).
First, we tested hypothesis-driven within-group effects only when higher order interactions were significant (using Greenhouse-Geisser corrections; Table S1).
The age-adjusted incidence of endometrial cancer in 1999 was 146/10, but 188 per million after applying uteri-at-risk corrections (Table 1).
None of the G-statistics compared between males and females were significantly different from each other after multiple testing corrections (Table 4).
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Using both kinds of correction (Table 3) resulted in inversions showing higher corrected values relative to the DNA sequence characters in seven out of eight comparisons.
KEGG enrichment analysis results showed that 30 genes were significantly enriched in the complement and coagulation cascade pathway (ID: bta04610, P = 6.95 × 10−12) after Bonferroni correction (Table S4, Figure S4).
In particular, the specificity (80.8%) remained constant regardless of MTV correction (Table 3).
However, this effect was no longer significant when applying a multiple comparison correction (Table 3).
Seven haplotypes remained significant after Bonferroni correction (Table 4).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com