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Two types of sectional model, a twin-deck bluff model (model A) and a partially streamlined box girder model (model B) are tested with two extreme cases of relative amplitude.
The first model (model A) is based on the existence of two types of sites on the modified substrate: active (normal) and completely deactivated, whereas the second model (model B) also considers infected sites, ie, partially active sites.
The simplest null model (Model A) is that based on the amino acid propensity this assumes that repeats occur randomly [18], [28].
Recently, using a molecular dynamics approach, we built a model (Model A) for the complex formed between residues 29 138 of Ets-1 and ERK2, which reveals how the SAM domain may bind ERK2 [13].
The initial model (model A) controlled for age only.
The first model (model A) examined the contribution of a/oligomenorrhoea.
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Output results of age modeling (Model A) using OxCal.
In each of the two groups, we selected a pair of female models (model A and model B) so that there were four models in total.
All freely estimated longitudinal models (models A) had a good fit.
We conducted LRT for each branch using the branch-site models, model A null and model A [24].
In the branch-site models, model A identified 14 sites under positive selection.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com