Part V: New approaches complexity management and matrix methods: A Universal Complexity Criterion for Model Selection in Dynamic Models of Cooperative Work Based on the DSM

2013 ◽  
pp. 97-105 ◽  
Author(s):  
Christopher M. Schlick ◽  
Sebastian Schneider ◽  
Sönke Duckwitz
2010 ◽  
Vol 175 (6) ◽  
pp. 762-764 ◽  
Author(s):  
Benjamin D. Dalziel ◽  
Juan M. Morales ◽  
John M. Fryxell

Biostatistics ◽  
2018 ◽  
Vol 21 (3) ◽  
pp. 400-416 ◽  
Author(s):  
Theresa Stocks ◽  
Tom Britton ◽  
Michael Höhle

Summary Despite the wide application of dynamic models in infectious disease epidemiology, the particular modeling of variability in the different model components is often subjective rather than the result of a thorough model selection process. This is in part because inference for a stochastic transmission model can be difficult since the likelihood is often intractable due to partial observability. In this work, we address the question of adequate inclusion of variability by demonstrating a systematic approach for model selection and parameter inference for dynamic epidemic models. For this, we perform inference for six partially observed Markov process models, which assume the same underlying transmission dynamics, but differ with respect to the amount of variability they allow for. The inference framework for the stochastic transmission models is provided by iterated filtering methods, which are readily implemented in the R package pomp by King and others (2016, Statistical inference for partially observed Markov processes via the R package pomp. Journal of Statistical Software69, 1–43). We illustrate our approach on German rotavirus surveillance data from 2001 to 2008, discuss practical difficulties of the methods used and calculate a model based estimate for the basic reproduction number $R_0$ using these data.


2010 ◽  
Vol 13 (2) ◽  
pp. 177-204 ◽  
Author(s):  
Hwan-sik Choi ◽  
Nicholas M. Kiefer

2020 ◽  
Vol 17 (168) ◽  
pp. 20200204
Author(s):  
Fredrik Ohlsson ◽  
Johannes Borgqvist ◽  
Marija Cvijovic

Understanding the complex interactions of biochemical processes underlying human disease represents the holy grail of systems biology. When processes are modelled in ordinary differential equation (ODE) fashion, the most common tool for their analysis is linear stability analysis where the long-term behaviour of the model is determined by linearizing the system around its steady states. However, this asymptotic behaviour is often insufficient for completely determining the structure of the underlying system. A complementary technique for analysing a system of ODEs is to consider the set of symmetries of its solutions. Symmetries provide a powerful concept for the development of mechanistic models by describing structures corresponding to the underlying dynamics of biological systems. To demonstrate their capability, we consider symmetries of the nonlinear Hill model describing enzymatic reaction kinetics and derive a class of symmetry transformations for each order of the model. We consider a minimal example consisting of the application of symmetry-based methods to a model selection problem, where we are able to demonstrate superior performance compared to ordinary residual-based model selection. Moreover, we demonstrate that symmetries reveal the intrinsic properties of a system of interest based on a single time series. Finally, we show and propose that symmetry-based methodology should be considered as the first step in a systematic model building and in the case when multiple time series are available it should complement the commonly used statistical methodologies.


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