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Newly designed assays must always be validated using methods that can discriminate between individual alleles.
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Furthermore, identified interactors of proteins should always be validated using different methods and/or different constructs of the protein.
The accuracy of protein recognition depends on the specificity of the primary antibody that should be validated using parallel methods.
Furthermore, it is expected that more biomarkers of mycotoxin exposure will be validated using these methods by means of a dose response relationship.
Promising candidates can then be validated using a method with higher accuracy and proven reliability, such as ELISA.
The present improved method may be validated using the conventional Hertz Sneddon method, which is widely reported in the literature.
Moreover, the composite pressure vessel design will be validated using the finite element method.
This corresponds to a study where the questionnaire has already been validated using classical methods (face validity, reliability, structure validity...), but not using an IRT model.
The predictive ability and robustness of the proposed model was validated using various methods, including cross-validation and y-randomization experiments.
Pharmacophore models were validated using various methods and utilized in database searching to identify potential hits.
Selected PrPC interactors were validated using independent methods.
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CEO of Professional Science Editing for Scientists @ prosciediting.com