Title of article :
Biological phenomena are often modeled by differential equations, where states of a model system are described by continuous real values. When we consider concentrations of molecules as dynamical variables for a set of biochemical reactions, we implicitly
Author/Authors :
Mariam Kiran، نويسنده , , Simon Coakley، نويسنده , , Neil Walkinshaw، نويسنده , , Phil McMinn، نويسنده , , Mike Holcombe، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Abstract :
Simulation software is often a fundamental component in systems biology projects and provides a key aspect of the integration of experimental and analytical techniques in the search for greater understanding and prediction of biology at the systems level. It is important that the modelling and analysis software is reliable and that techniques exist for automating the analysis of the vast amounts of data which such simulation environments generate. A rigorous approach to the development of complex modelling software is needed. Such a framework is presented here together with techniques for the automated analysis of such models and a process for the automatic discovery of biological phenomena from large simulation data sets. Illustrations are taken from a major systems biology research project involving the in vitro investigation, modelling and simulation of epithelial tissue.
Keywords :
Validation and testing , X-machines , Parallel computation , Agent-based modelling , simulation
Journal title :
BioSystems
Journal title :
BioSystems