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This framework emphasizes the importance of evaluating multiple alternative models when evaluating the validity of the model.
Multiple realizations and multiple alternative models can be constructed to quantitatively examine the probability of specific parameters of interest such as pore volume and connectivity.
The concept of evaluating multiple alternative models to determine ecological response form is over a century old and is ever more relevant as modern computing power allows ever more complicated models to be routinely used but often without a reasonable model verification process, particularly in fields where the ecological conceptual model is still developing.
The paper focuses on the question of whether a threshold model is appropriate, and demonstrates the importance of evaluating multiple alternative models in the detection of ecological thresholds, and illustrates how choosing an inappropriate model can lead to erroneous conclusion regarding the existence of thresholds.
Although PSR-induced histone modification is a plausabile hypothesis that remains to be proven, there are multiple alternative models that could explain PSR's mode of action.
The evidence gathered so far should not be considered satisfactory as it leads to multiple alternative models of how dysbindin may act in the cell.
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Due to serious concerns about the validity of model structures and kinetics, many studies include the parallel development and analysis of multiple alternative model structures [ 1– 3].
Our preferred model specification, however, was conservative; multiple alternative modeling specifications tested in sensitivity analyses produced considerably narrower 95% confidence intervals for all analyses.
Following this procedure, potential ORFs that spanned high-scoring matches to the splice site model were represented by multiple alternative gene models.
For the combined or branched component of a cause-effect (CE) model, multiple alternative modules have been proposed.
One other possible improvement is to incorporate MHC flexibility by sampling peptide-contacting MHC residue rotamer conformations or utilizing multiple alternative rigid models of the binding cleft in the docking procedure.
More suggestions(15)
multiple other models
multiple alternative developments
multiple alternative pathways
multiple alternative transcripts
multiple alternative outcomes
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multiple alternative futures
multiple alternative workflows
multiple alternative methods
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multiple alternative theories
multiple alternative performances
multiple alternative runs
multiple alternative modules
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