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Specifically, we based our simulations on the quantitative trait model corresponding to recursion (14).
We based our simulations on the approach described by Mandl et al[ 18].
For time-to-event outcomes, we based our simulations on the PBC trial.
For binary outcomes, we based our simulations on the Acute Upper Gastrointestinal Bleeding (AUGIB) audit dataset.
We based our simulations on realistic scenarios inspired by our case study.
We based our simulations on this real pedigree and assumed that the genotyped animals were those in the pedigree.
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We base our simulations of vaccines on our previously described model for the natural history and epidemiology of P. falciparum malaria [12].
Henceforth, we base our simulation on Jones matrix analysis, incorporating the extended Jones matrix calculus which takes into account off axis light propagation in birefringent multi-layered structures.
We base our simulation environment on the random way-point algorithm implemented in the network simulation (ns) tool.
To account for the uncertainty surrounding the relationship between mortality and heath, we base our simulation study on all three hypotheses.
We base our simulation approach on a mathematical model describing human CML as a competition phenomenon between normal and malignant cells.
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