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In our variant, we have a third hierarchical level, two categories of link costs, and the number of concentrators is unknown.
Beginning the analysis with the tf variant, we have observed that for smaller codebooks, the term 'l' (log-weighted term frequency) behaves better.
For both, Dissociation and Convey variant, we have selected the time range such that each concentration can reach steady state.
The variant we have called Ty101 is related to Ty1' (89% identity).
In addition, for each variant, we have information about the number of reads supporting it.
With the des-Cys Pfu pol variant, we have introduced pairs of Cys residues at different locations.
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Since only the C-terminal amino acids are different for each variant we had limited options for antibody selection.
The study included one variant we had previously classified as pathogenic by multifactorial likelihood analysis (G1738R) and three variants that remained unclassified after multifactorial analysis (R1699Q, A1708V, and A1708E) [ 3- 5].
To confirm de novo sequence variants, we have undertaken clinical and genetic screening of affected offspring and their parents.
By applying the approach on the composition of a set of formalized architectural patterns, including their variants, we have shown that composed patterns have become traceable and reconstructable.
While evolving a lipase in vitro from mesophilic Bacillus subtilis to generate thermostable variants, we have designed protocols that combine stringent three-tier testing, sequencing and stability assessments on the protein at the end of each generation.
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CEO of Professional Science Editing for Scientists @ prosciediting.com