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Using evolutionary and biostatistics methodologies, we evaluated deaths and births of protein families and domains, and duplications and deletions of protein family and domain members within the target species.
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Following the same methodology, we evaluated the ruffling activity of the binary input gates.
Due to the known limitations of non-quantitative methodology, we evaluated biomarkers frequently reported to be hypermethylated in HNSCC with three quantitative methodologies, in order to identify meaningful correlations with patient outcome.
Using the direct measurement methodology, we evaluate the T-SIMn framework by collecting traces using an iPhone, which is representative of a wide variety of one antenna devices.
Using two distinct methodologies, we next evaluated whether BM macrophages had a defect in neutrophil clearance in vivo (4), (45).
Pretreatment parameters were optimized using a response surface methodology and we evaluated the efficiency of pretreatment through the biomass to ethanol ratio (BTER).
Through a single replacement scan library using the SPOT methodology we have evaluated both the contribution of sequence positioning and amino acid singularity towards the peptide biological and physicochemical properties.
Using this methodology, we first evaluated how polarization of a fluorescently labelled peptide encompassing the dimerization motif was affected by titration of TRPM6- 1730 end) (which lacks the dimerization motif).
With the fixed p e value, obtained via the methodology described above, we evaluated the FER performance via simulations, where Link 1 and Link 2 were assumed to suffer from statistically independent block Rayleigh fading.
Using the HLA-predictive methodology described above, we evaluated testing accuracies given various flanking-region sizes following Li et al.'s [ 13].
Since these predictions were generated using different methodologies, we were interested in evaluating the level of agreement among them, as well as between each one of them and the NCBI Refseq database.
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