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| 21 November 2009 | |
Dr Laurence Loewe
Research InterestsMy research centres on computer models that integrate biological knowledge. Such models regularly struggle with the complexity of intracellular biochemical reaction networks. To facilitate the analysis of more complex models, I work with Prof. Jane Hillston on extending the applicability of the Bio-PEPA process algebra. A process algebra is a compositional, formal system description technique that is supported by formal reasoning and model manipulation methods. The formality means that a software tool can apply these methods automatically in order to help with the analysis of a model. Bio-PEPA has recently been developed in order to model intracellular biochemical reaction networks. I am currently working on the following applied and methodological projects together with other researchers in CSBE in the groups of Prof. A. Millar, Prof. P. Ghazal and Prof. I. Goryanin:
Having quality modelling tools that are applicable to a wide range of systems biology problems is important. For example, such tools can facilitate analyses of robustness that are based on a mechanistic understanding in corresponding models. Robustness is a pervasive feature of biological systems that needs to be understood for many other questions, including effective drug design. I also have some interest in how systems biology might interact with evolutionary genetics. Selected SoftwareSBGNtext2BioPEPA: From SBGN to quantitative analysis in Bio-PEPA SBGNtext2BioPEPA is a tool that automatically translates from a textual representation of SBGN Process Diagrams to the process algebra Bio-PEPA to facilitate quantitative analysis. While the ready-to-download code is tailored towards generating Bio-PEPA code, the underlying principles are general and can help translate to other quantitative analysis formalisms too. This work has also led to a possible textual representation of SBGN Process Diagrams that is formally defined by a BNF grammar. For more details, see the dedicated SBGNtext2BioPEPA site. Selected PublicationsLoewe L., Moodie S., Hillston J. 2009. Quantifying the implicit process flow abstraction in SBGN-PD diagrams with Bio-PEPA. Submitted to the Proceedings of the "2nd International Workshop on Computational Models for Cell Processes" (CompMod 2009). Preliminary PDF Loewe L., Moodie S., Hillston J. 2009. Technical Report: Defining a textual representation for SBGN Process Diagrams and translating it to Bio-PEPA for quantitative analysis of the MAPK signal transduction cascade. Technical Report EDI-INF-RR-1334, School for Informatics, University of Edinburgh. PDF Duguid A, Gilmore S, Guerriero ML, Hillston J & Loewe L (2009) “Design and development of software tools for Bio-PEPA”, Proceedings of the 2009 Winter Simulation Conference (WSC’09), eds.: Rossetti RMD, Hill RR, Johansson B, Dunkin A & Ingalls RG. Austin, Texas, to appear in December. PDF Loewe, L. 2009. A framework for evolutionary systems biology. BMC Systems Biology 3:27. Abstract; PDF Loewe, L., and J. Hillston. 2008. Meeting report: Computational models in systems biology. Genome Biol 9:328. PDF Loewe, L. 2008. Designing a Front-End for Bio-PEPA in S. Gilmore, ed. Proceedings of the 7th Workshop on Process Algebra and Stochastically Timed Activities, 30-31 July 2008, Edinburgh, UK. PDF Loewe, L., and J. Hillston. 2008. The distribution of mutational effects on fitness in a simple circadian clock. pp. 156-175 in: M. Heiner, and A. M. Uhrmacher, eds. Computational Methods in Systems Biology CMSB-08. Springer, Rostock, Germany. Lecture Notes in Bioinformatics 5307:156-175. PDF | |
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