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When we consider different absence rates for team workers and non-team workers, the coefficients do not change much, which suggests our main analyses are robust.
Findings are comparable across different levels of correlation (R = 0.50, 0.74, 0.84 and 0.94), therefore the meta-analysis (and subsequent meta-regression analyses) are robust to the imputed R = 0.84 (full details of sensitivity analyses are presented in Additional file 1: Table S8 and S9).
PARM has certain advantages: (a) it can be used for many systems, regardless of whether the 3D structure of the receptor is known; (b) PARM models were demonstrated to be highly statistically reliable; and (c) PARM analyses are robust and reproducible.
However, biologically meaningful patterns occur between hosts and parasites despite this dilemma [33], [41], and nestedness analyses are robust to variation in sampling effort [42].
Yet, given the fact that FUSION data are a minor part of the meta-analysis and that effect estimates of Danish and DIAGRAM+ data are virtually similar (OR 1.060 and 1.065, respectively) we argue that the current analyses are robust.
Our analyses are robust despite the potential for uneven sampling of amino acid transporters across lineages.
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All fetal growth analyses were robust to further adjustment for maternal socioeconomic status and smoking during pregnancy.
The analyses were robust to plausible changes in all variables.
The trial design, including randomisation, blinded outcome ascertainment, and the adjusted analyses, was robust.
Results of survival analyses were robust to linkage step or certainty of a correct link.
Results of permutation tests demonstrated that our analyses were robust and not obtained by chance.
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