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The potential of the TASTE method towards entirely novel 3D profile variants is high and will direct towards new applications where those varieties are needed.
The application of CAD and CAM to the manufacture of helicoidal surfaces as threads and their mated elements, together with their generating tools, is especially important in individual manufacture where the number of variants is high, and consequently the variety of tools required is high as well.
In this case, the relative intensity is low whereas the number of gene variants is high (Figure 1B).
The more VSG variants that are present at a time, the less chance each variant subpopulation has of reaching the threshold to induce an antibody response, meaning that, when the number of variants is high, overall population numbers are predicted to be controlled by differentiation.
When the LD between the two causal variants is high (r 2 >0.8), there is almost no difference in the results of the SNP-based meta-analyses of all three populations at higher Type I errors as compared with the power observed in our earlier simulations with only one causal variant.
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The rate of accumulation of telomeric variants is higher in the proximal region than in the distal region [25], suggesting that the proximal region has rarely been reconstructed by telomerase on an evolutionary time scale.
The frequency of potentially pathological variants is higher in our SS subset than in the Exome Variant Server healthy controls (Peto's OR = 208.3, 95% CI = 1.5 29137.8).
Test whether the proportion of cases carrying two or more variants is higher than would be expected under independence and HWE.
Such a model is consistent with the hypothesis that a large number of variants increase the rate at which key mutational events occur, and the increased relative risk conferred by at least some variants is higher at younger ages.
Since the specific fluorescence generated from GFP-tagged Cx43 and mutant variants was high, this prevented the use a dye which fluoresces with the same emission as GFP.
Although the precision of imbalance detection using partial genotypes and common variants was high across datasets, the number of imbalances detected varied greatly (minimum = 0, maximum = 291, median 19).
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