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dc.contributor.advisorBruce Tidor.en_US
dc.contributor.authorHagen, David Roberten_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Biological Engineering.en_US
dc.date.accessioned2014-09-19T21:42:36Z
dc.date.available2014-09-19T21:42:36Z
dc.date.copyright2014en_US
dc.date.issued2014en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/90148
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Department of Biological Engineering, 2014.en_US
dc.descriptionCataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 157-169).en_US
dc.description.abstractA major effort of systems biology is the building of accurate and detailed models of biological systems. Because biological models are large, complex, and highly nonlinear, building accurate models requires large quantities of data and algorithms appropriate to translate this data into a model of the underlying system. This thesis describes the development and application of several algorithms for simulation, quantification of uncertainty, and optimal experimental design for reducing uncertainty. We applied a previously described algorithm for choosing optimal experiments for reducing parameter uncertainty as estimated by the Fisher information matrix. We found, using a computational scenario where the true parameters were unknown, that the parameters of the model could be recovered from noisy data in a small number of experiments if the experiments were chosen well. We developed a method for quickly and accurately approximating the probability distribution over a set of topologies given a particular data set. The method was based on a linearization applied at the maximum a posteriori parameters. This method was found to be about as fast as existing heuristics but much closer to the true probability distribution as computed by an expensive Monte Carlo routine. We developed a method for optimal experimental design to reduce topology uncertainty based on the linear method for topology probability. This method was a Monte Carlo method that used the linear method to quickly evaluate the topology uncertainty that would result from possible data sets of each candidate experiment. We applied the method to a model of ErbB signaling. Finally, we developed a method for reducing the size of models defined as rule-based models. Unlike existing methods, this method handles compartments of models and allows for cycles between monomers. The methods developed here generally improve the detail at which models can be built, as well as quantify how well they have been built and suggest experiments to build them even better.en_US
dc.description.statementofresponsibilityby David Robert Hagen.en_US
dc.format.extent169 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectBiological Engineering.en_US
dc.titleParameter and topology uncertainty for optimal experimental designen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.identifier.oclc890197490en_US


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