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To directly illustrate the performance of these methods, we utilize the tool of Dolan and Moré [58] to analyze their efficiency.
Within both of these methods, we utilize either the scaled BFBt, or an identity matrix scaled by the local cell viscosity (LV) to define a preconditioner for the Schur complement.
Therefore no matter what methods we utilize, duplicated genes in Group I seem much younger than those in Groups II and III.
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Methods: We utilized a sampled National Health Insurance claims database containing one million beneficiaries.
Among these object modeling methods, we utilized the tetrahedrons to generate the deformable objects which can express its strain effectively, but it requires a lot of calculations.
Methods: We utilized a co-twin design to assess how twin pairs discordant for chronic fatigue and CFS cope with stress.
The methods we utilized can be separated into two broad categories: analyses that attempt to discern differences across the experimental procedures (ST vs. ST + HS), and analyses that attempt to define mechanistic drivers within ST or ST + HS.
In this report, we describe in detail the methods we utilized to study chromatin assembly, both in vitro and in vivo.
Methods: We utilized an in vitro model in which human lung epithelial BEAS-2B cells were transformed through long-term exposure to arsenic.
To exemplify these methods we utilized data from a nested case control study examining repeated measures of urinary phthalate metabolites during pregnancy in association with preterm birth.
To determine how accurately our method detects low-frequency variants in a viral population, and to demonstrate how it compares with currently available methods, we utilized published data generated by Wilm et al.
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CEO of Professional Science Editing for Scientists @ prosciediting.com