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Both strains were compared to the C. elegans reference genome (release 195).
In this regard, a similar response has been found when both strains were compared in batch cultures using gluconate as carbon source; the production of mcl-PHA was 10-fold higher for KT2440 relative to KT2442 [ 34].
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To further study inhibition of the strains by these compounds, ethanol production of both strains was compared in the presence of 13 inhibitory compounds (Table 2) and in the absence of any inhibitors.
The predicted env protein from both FIV Ple strains were compared to other published FIV strains with respect to inferred structural elements, with particular focus on regions known to be important for receptor binding.
Evidence for this was inferred by the marked absence of correlation when results obtained by pp-NT for both HPAI H5 strains were compared to those obtained by HI assay.
The translated CDS sets from both HUS- and HUS+ strains were compared by localized BlastP analyses and the proteins were annotated on the basis of orthologous proteins identified by comparison against the NCBI non-redundant protein database (Additional file 2: Table S2).
Geometric mean titer (GMT) ratios against the three influenza antigen strains were compared for both routes.
Deletion strains were compared to their respective control strain, which expression was set to 1 for each time point.
Enzyme activities were determined by spectrophotometric measurements based on optical densities, and the two strains were compared using the Mann-Whitney U-test.
The measured strains were compared with the standard Nakajima tests containing sharp local necks.
The recombinant yeast strains were compared for their ability to perform fermentation on soluble starch.
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