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The RMS deviation is given by (Kim and Kim 2004) {text{RMS}} = sqrt {frac{1}{N}sumlimits_{i = 1}^{N} {frac{{left( {C_{text{exp,i}} - C_{text{pred,i}} } right)^{2} }}{{C_{text{exp,i}}^{ 2} }}} }, (15 where C exp,i and C pred,i are 2-CP concentrations of experiment and model prediction, respectively, and N is the number of data points.
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The colloid breakthrough concentrations of Experiments A (Stage 1), B (Stages 1 2), and C (Stages 1 4) are shown in Figure 1.
aPercentage of the total variance for each source of variation for supernatant ethanol concentration of experiment 1 (S. bicolor bmr near-isogenic lines) and experiment 2 (15 S. bicolor ssp. accessions) 3 days after inoculation with Clostridium phytofermentans.
Algal concentrations were deliberately chosen to differ from concentrations of previous experiment so as to be able to observe the effect of these algal concentrations as well.
Shown are mean values of 4-TTri concentrations of duplicate experiments.
Shown are mean values of benzotriazole concentrations of duplicate experiments with error bars indicating standard deviations (n = 2).
Shown are mean values of 5-TTri concentrations of duplicate experiments with error bars indicating standard deviations (n = 2).
The stated concentrations of described experiments are those in the mixing chamber, unless shown otherwise.
Furthermore, Fig. 8 (right side) displays the PPP concentrations of the lab experiment in comparision to the field work.
The working solution was diluted to the required concentration of the experiments.
In addition, ethanol was also used as a carrier by a few studies, in concentrations of 0.001% for experiments with larvae [40,41] or 0.435% for experiments with zebrafish adults [42].
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