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Stochastic modelling in biological systemsLuo, Yang January 2012 (has links)
No description available.
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Multiscale Monte Carlo methods to cope with separation of scales in stochastic simulation of biological networksSamant, Asawari. January 2007 (has links)
Thesis (M.Ch.E.)--University of Delaware, 2007. / Principal faculty advisors: Dionisios G. Vlachos and Babatunde Ogunnaike, Dept. of Chemical Engineering. Includes bibliographical references.
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Processing sequences of chromatophore images with application to a signal transduction pathway modeling /Orhanovic, Iva. January 2004 (has links)
Thesis (Ph. D.)--Oregon State University, 2005. / Printout. Includes bibliographical references (leaves 100-102). Also available on the World Wide Web.
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Growing brains in silico : integrating biochemistry, genetics and neural activity in neurodevelopmental simulations /Storjohann, Rasmus. January 1900 (has links)
Thesis (M.Sc. (Computing Sc.)) - Simon Fraser University, 2004. / Theses (School of Computing Science) / Simon Fraser University. Also available on the World Wide Web.
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Dynamic flux estimation a novel framework for metabolic pathway analysis /Goel, Gautam. January 2009 (has links)
Thesis (Ph.D)--Biomedical Engineering, Georgia Institute of Technology, 2010. / Committee Chair: Voit, Eberhard O.; Committee Member: Butera, Robert; Committee Member: Chen, Rachel; Committee Member: Kemp, Melissa; Committee Member: Neves, Ana Rute. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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New analytical tools for systems biologyTang, Xiaoting, January 2006 (has links) (PDF)
Thesis (Ph. D.)--Washington State University, December 2006. / Includes bibliographical references.
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Measuring system dynamics mRNA, protein and metabolite profiling /Lu, Peng, Marcotte, Edward Michael, January 2005 (has links) (PDF)
Thesis (Ph. D.)--University of Texas at Austin, 2005. / Supervisor: Edward M. Marcotte. Vita. Includes bibliographical references.
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Modelling techniques for biological systemsBilling, Alison Emslie January 1987 (has links)
The objective of this investigation has been to develop and evaluate techniques which are appropriate to the modelling and simulation of biological reaction system behaviour. The model used as the basis for analysis of modelling and simulation techniques is a reduced version of the biological model proposed by the IAWPRC Task Group for mathematical modell ing in wastewater treatment design. This limited model has the advantage of being easily manageable in terms of analysis and presentation of the simulation techniQues whilst at the same time incorporating a range of features encountered with biological growth applications in general. Because a model may incorporate a number of different components and large number of biological conversion processes, a convenient method of presentation was found to be a matrix format. The matrix representation ensures clarity as to what compounds, processes and react ion terms are to be incorporated and allows easy comparison of different models. In addition, it facilitates transforming the model into a computer program. Simulation of the system response first involves specifying the reactor configuration and flow patterns. With this information fixed, mass balances for each compound in each reactor can be completed. These mass balances constitute a set of simultaneous non-linear differential and algebraic eQuations which, when solved, characterise the system behaviour.
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Constraints on Patterns of Abundance and Aggregation in Biological SystemsLocey, Kenneth J. 01 December 2013 (has links)
Understanding the mechanisms that structure biological systems is a primary goal of biology. My research shows that the biological structure is constrained in important ways by general variables such as the number of base pairs in a genome and the number of individuals and species in a community. I used a combination of macroecology, bioinformatics, statistics, mathematics, and advanced computing to pursue my research and published several peer-reviewed scientific manuscripts and open-source software as a result.I was funded through a combination of fellowships and scholarships awarded by the Utah State University School of Graduate Studies, College of Science, and Department of Biology, as well as teaching assistantships awarded through the Department of Biology at Utah State University, and research assistantships funded through a CAREER grant from the U.S. National Science Foundation (DEB-0953694) awarded to my advisor, Dr. Ethan White. With the help of my advisor, I also obtained a computing grant from Amazon Web Services in the amount of $7,500. Altogether, funding for my research and education totaled approximately $123,500.
Using over 9000 communities of plants, animals, fungi, and microorganisms, I demonstrated that the forms of empirical species abundance distributions (SADs) are constrained by total abundance and species richness. Using over 300 microbial genomes, I demonstrate that nucleotide aggregation is constrained by genome length and differs between regions of coding and noncoding DNA. General state variables of genomes and ecological communities (i.e. genome length, total abundance and species richness) constrain simple structural properties of each system.
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Applications of mathematical models to resolving questions in animal behavior, ecology and epidemiology /Fefferman, Nina H. January 1900 (has links)
Thesis (Ph.D.)--Tufts University, 2005. / Adviser: J. Michael Reed. Submitted to the Dept. of Biology. Includes bibliographical references (leaves 126-135). Access restricted to members of the Tufts University community. Also available via the World Wide Web;
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