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We have trained both methods on the FRGCv2 database and evaluated them using high-resolution images.
Figure 6 gives the error on quantification with both methods, on the whole image and different bags.
To study the effect of both methods on the duration of overhead conductors, comparative fretting fatigue tests with real conductor/clamp contacts were carried out.
We first tested both methods on the positive subset of the training set (Table 6).
The convergence of both methods on the same biochemical pathways underlines the complementarity of both techniques and exemplifies the power of this combined approach.
Similar results are obtained when comparing both methods on the D. melanogaster genome.
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We tested the performance of both methods on different subsets of the GSIs.
No external EHG model is currently available to compare both methods on signals with characteristics close to the real ones.
The purity of the cells was almost identical with both methods based on the analysis of the combined expression of Gr-1 and CD11b on the isolated cells (Fig. 2A and table 2).
It should be kept in mind that for a single measurement the statistical error of both methods depends on the size of the particles and can be in the range of a few nanometer.
The efficiency of both methods depends on the accuracy of the genome sequence for selection of target sites and recombination events.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.
Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com