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**Providers (n = 45) completed both the hip and knee instruments and the distributions here combine their responses.
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In other words, the distribution here is critical.
As for the summed scores, the distribution here was left-skewed.
The choice of the variational family is restricted only by the tractability of computing expectations with respect to the variational distributions; here, we choose parametric distributions that are conjugate to the distributions in the likelihood function.
The fusion of distributions here is proposed as an alternative to the pixel-level fusion of the SI frames.
Thus, instead of the ancestor distribution, here we study the distribution of the common ancestors of the population (the last common ancestor and its ancestors).
The first important point to note here is that these observations emerged only with an increased sampling of eukaryotic molecular diversity, implying that the distributions reported here are likely to change further as taxon sampling becomes even more comprehensive.
The distributions analysed here consisted of vectors of variables, of which some entries had a large mass at zero and others had a large mass away from zero.
In those cases where one genome contains more than one ortholog encoding the same reaction, I calculated pairwise distances for each of these orthologs separately, and include these distances in the distributions reported here.
However, the overall similarity of the distributions found here to those found by Schwanhausser et al. (2013) indicates that our data are sufficient as a guide for our mass-action model (below).
We would like to emphasize that the γ distribution here refers to raw mutation rate rather than γ distribution of ω itself.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com