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Based on the proposed method, we identify eight potential greenway networks, each highlighting different sets of priorities.
In the second method, we identify one photon candidate in the EMC and one which has converted into an e +e − pair due to interaction with detector material, and we measure absolute product branching fractions.
Using our method we identify HIV-1 broadly neutralizing antibodies (bNAbs) from an HIV-1 slow progressor and high-affinity neutralizing antibodies against Ebola virus glycoprotein and influenza hemagglutinin.
Using this method, we identify a novel mutant resistant to Al. Physiological analysis reveals that decreased Al binding capacity to the cell wall is responsible for the increased resistance of ral1 mutant to Al. RAL1 gene is mapped on the long arm of chromosome 6, and cloning of the gene is currently undertaken.
Using this method, we identify known disease cell-type associations andisease cell-typeassociationsurther study.
Then, using a tree-based jack-knife method, we identify clownfish species likely stemming from hybridisation events.
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Applying our screening method, we identified 51 lncRNAs that can positively or negatively regulate human cancer cell growth.
With this method, we identified five CRPs, which summarized the activity of all recorded single units (Fig. 3).
By using a hierarchical clustering method, we identified 4 groups of co-expressed lncRNAs and mRNAs, termed 'modules'modules
Using a nonparametric kernel smoothing method we identified the most sensitive items of the SPIN.
With this method, we identified two clinically relevant subtypes of GBM: the 'Classical-like subtype' (CL) characterised by EGFR-positive, p53-negative and PDGFRA-negative staining and the 'Proneural-like subtype' (PNL) characterised by p53- and/or PDGFRA-positive staining.
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CEO of Professional Science Editing for Scientists @ prosciediting.com