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There are three components that are central to estimating this accumulation of costs: 1) defining the prevalent cohort and its heterogeneity, 2) the diabetes incidence model, and 3) the lifetime simulation model for diabetes progression.
We consider two approaches to estimating this threshold, accounting for the correlation within the genome: one based on a permutation scheme, and the other using linear algebra to estimate an effective number of tests directly from genotype data [ Patterson et al., 2006].
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Third, since this law required an inaccessible state, a Kalman estimator has been introduced to estimate this state.
The Kaplan-Meier estimator is often used to estimate this probability.
The current estimation methods based on statistical theory could not be used to estimate this kind of small samples.
To estimate this vector, we provide two methods: a "difference of models" estimator and a "multiple-impute matched pairs" estimator.
Is there a rule of thumb to estimate this?
It is not possible to estimate this great waste of talent, of potential.
We have to estimate this DC value.
The greedy algorithm is used to estimate this.
We suggest using sampling to estimate this proportion.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com