Projects per year
Abstract / Description of output
Bio-PEPA is a process algebra for modelling biological systems. An important aspect of Bio-PEPA is the ability it provides to discretise concentrations resulting in a smaller, more manageable state space. The discretisation is based on a step size which determines the size of each discrete level and also the maximum number of levels. This paper considers the relationship between two discretisations of the same Bio-PEPA model that differ only in the step size and hence the maximum number of levels, by using the idea of equivalence from concurrency and process algebra. We present a novel behavioural semantic equivalence, compression bisimulation, that equates two discretisations of the same model and we show that this equivalence is a congruence with respect to the synchronisation operator.
Original language | English |
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Title of host publication | Computational Methods in Systems Biology |
Subtitle of host publication | 7th International Conference, CMSB 2009, Bologna, Italy, August 31-September 1, 2009. Proceedings |
Editors | Pierpaolo Degano, Roberto Gorriero |
Publisher | Springer |
Pages | 189-204 |
Number of pages | 16 |
ISBN (Print) | 978-3-642-03844-0 |
DOIs | |
Publication status | Published - 2009 |
Publication series
Name | Lecture Notes in Computer Science |
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Publisher | Springer Berlin / Heidelberg |
Volume | 5688 |
ISSN (Print) | 0302-9743 |
ISSN (Electronic) | 1611-3349 |
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Dive into the research topics of 'Equivalence and discretisation in Bio-PEPA'. Together they form a unique fingerprint.Projects
- 4 Finished
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SIGNAL: SIGNAL -Stochastic process algebra for biochemical signaling pathway analysis
1/09/07 → 31/01/11
Project: Research
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SynthSys; formerly CSBE: Centre for Systems Biology at Edinburgh
Millar, A., Beggs, J., Ghazal, P., Goryanin, I., Hillston, J., Plotkin, G., Tollervey, D., Walton, A. & Robertson, K.
8/01/07 → 31/12/12
Project: Research
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