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Unlike previous methods, we thus achieve discrete global conservation in terms of interface interactions and a consistently sharp interface representation.
For all of these methods, we thus can obtain 33 × 11 sequences of PTT data (denoted as T for each sequence as before) and 33 × 11 sequences of BP data (also denoted as P for each sequence as before).
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For each instance of each sampling method, we thus build the resulting surrogate aggregated contact network and rank nodes according to each centrality measure.
Beyond the development of a new hybrid method, we thus conclude that birth-rate fluctuations are central to a quantitatively accurate description of invasive phenomena such as tumour growth.
It was not possible to recover a particular region inside the env gene using this method, and we thus used a PERL assembly script to fill this region using overlapping reads.
Using this method, we could thus probe immobilised Protein A ligand directly on agarose beads using ATR-FTIR spectroscopy for the first time.
Then, for all methods, we ranked these genes, thus obtaining ranking lists of genes.
Thus, in Methods, we derive again the main results of MCA without relying on such an assumption.
Thus, the methods we used are inappropriate in some respects but we attempted to put some boundaries on the forces applied in femoral impaction grafting to reduce the risk of fracture.
We will insert the network graph that will be used in Dijkstra's method it will use the reduced graph from SGR the method we used before thus reducing the size of the graph and will help in giving a better upgrade in performance wise in Dijkstra's method.
We thus kept method (iii) as a representative for alignment-free methods.
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