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The AE for –500 nm looks different in Figures 5(c) and 5 d) because of the aforementioned scaling.
Note that while the signal and background noise ratios are different in Figures 5(a) and 5(b), the geometrical appearance of the signal as compared to the interfering random signal has not been changed.
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It would also be nice to discuss possible differences in Z+ PCs across modules - because they look different in Figure 1 figure supplement 3E, yet there is no direct comparison.
The enhancement results in Figure 8c,d by SDRCLCE and PNAE, respectively, have almost the same visual effects, but the situations are different in Figure 9.
The original regions in (A) and (B) are the same as that in Figure 1A, B. The binarization results of the two regions are the same, but different in Figure 1. Figure 3 Two different regions.
7) Figure 3A: why does the sFlt-1 IHC look so completely different in Figure 3A compared to Figure 1C?
For changing the value of β1, we get different results in Figures 7 and 8.
The color coding of the different populations in Figures 3B and 3C matches the colors in Figure 3D.
The release kinetics of CrmA from different microspheres was quite different, depicted in Figure 2.
We then used a qualitative approach to see whether the main MTBC lineages inferred by MLSA (indicated in different colours in Figure 2 and Figure 3A) were reproduced across the different genotyping datasets.
Note that the scale of the velocity vectors is different in each figure.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com