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Participants were asked to use the same values for parameters such as fiber volume fraction, injection pressure and fluid viscosity to minimize sources of scatter.
The parameter setups of the DM, MDI, and NMF methods use the same values as the best performing systems in the experiments of our previous studies [17, 18].
However, since these rates using oxalic acid are smaller by a factor of 10, it is chosen here to use the same values for all different saline conditions.
In the analysis, we use the same values used in [30] for the number of rail nodes in a station N ST, and R/T which are taken as 16 and 3/8, respectively.
In Figure 11b, the incorrect value is (bar {n}=200), way in excess of the actual value of n=60 but in agreement with the simulations of Figure 9 which use the same values of n,m, and k. Figure 11 The change in (bar {n}) per iteration vs. (bar {n}) for different values of ({h}, left (c(bar {n})=left (1+frac {h}{sqrt {bar {n}}}right)right)).
For infection in the light, we use the same values of parameters Vr, Kmr, tr and ε, and found that λ = 1,027,800 (dNTP h−1 cell−1) gave a reasonable description of phage genome replication (Fig. 3).
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The accuracy results change gradually with the value of, and this allows us to use the same value for all regions and still outperform other approaches.
We use the same value of k = 1.5 used by Wu et al. for consistency.
For convenience in the derivation, we use the same value of the threshold for recall, θ, for both screening tests.
For the whole range of the parameter, we can use the same value for the random variation, and a difference of more than 0.2 is beyond the random variation.
Further, while R0 has to be redetermined for each bond type separately, it should be possible to use the same value of b for all bond types at a given pressure.
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