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Bruce Tidor. King, Bracken Matheny Massachusetts Institute of Technology. Dept. of Biological Engineering. Massachusetts Institute of Technology. Department of Biological Engineering 2011-02-23T14:19:40Z 2011-02-23T14:19:40Z 2010 2010 http://hdl.handle.net/1721.1/61143 698095409 Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biological Engineering, 2010. Cataloged from PDF version of thesis. Includes bibliographical references (p. 115-123). The identification and quantification of high-dimensional relationships is a major challenge in the analysis of both biological and chemical systems. To address this challenge, a variety of experimental and computational tools have been developed to generate multivariate samples from these systems. Information theory provides a general framework for the analysis of such data, but for many applications, the large sample sizes needed to reliably compute high-dimensional information theoretic statistics are not available. In this thesis we develop, validate, and apply a novel framework for approximating high-dimensional information theoretic statistics using associated terms of arbitrarily low order. For a variety of synthetic, biological, and chemical systems, we find that these low-order approximations provide good estimates of higher-order multivariate relationships, while dramatically reducing the number of samples needed to reach convergence. We apply the framework to the analysis of multiple biological systems, including a phospho-proteomic data set in which we identify a subset of phospho-peptides that is maximally informative of cellular response (migration and proliferation) across multiple conditions (varying EGF or heregulin stimulation, and HER2 expression). This subset is shown to produce statistical models with superior performance to those built with subsets of similar size. We also employ the framework to extract configurational entropies from molecular dynamics simulations of a series of small molecules, demonstrating improved convergence relative to existing methods. As these disparate applications highlight, our framework enables the use of general information theoretic phrasings even in systems where data quantities preclude direct estimation of the high-order statistics. Furthermore, because the framework provides a hierarchy of approximations of increasing order, as data collection and analysis techniques improve, the method extends to generate more accurate results, while maintaining the same underlying theory. by Bracken Matheny King. Ph.D. 123 p. eng Massachusetts Institute of Technology MIT 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. http://dspace.mit.edu/handle/1721.1/7582 Biological Engineering. Analysis of biological and chemical systems using information theoretic approximations Thesis application/pdf Publication unknown unknown <Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="869edd10-edd4-402b-b928-47ecf29b1d2a"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Analysis of biological and chemical systems using information theoretic approximations</Title> <PublishedIn> <Publication> </Publication> </PublishedIn> <PublicationDate>2010</PublicationDate> <Authors> <Author> <DisplayName>King, Bracken Matheny</DisplayName> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Massachusetts Institute of Technology</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>http://dspace.mit.edu/handle/1721.1/7582</License> <Keyword>Biological Engineering.</Keyword> <Abstract>The identification and quantification of high-dimensional relationships is a major challenge in the analysis of both biological and chemical systems. To address this challenge, a variety of experimental and computational tools have been developed to generate multivariate samples from these systems. Information theory provides a general framework for the analysis of such data, but for many applications, the large sample sizes needed to reliably compute high-dimensional information theoretic statistics are not available. In this thesis we develop, validate, and apply a novel framework for approximating high-dimensional information theoretic statistics using associated terms of arbitrarily low order. For a variety of synthetic, biological, and chemical systems, we find that these low-order approximations provide good estimates of higher-order multivariate relationships, while dramatically reducing the number of samples needed to reach convergence. We apply the framework to the analysis of multiple biological systems, including a phospho-proteomic data set in which we identify a subset of phospho-peptides that is maximally informative of cellular response (migration and proliferation) across multiple conditions (varying EGF or heregulin stimulation, and HER2 expression). This subset is shown to produce statistical models with superior performance to those built with subsets of similar size. We also employ the framework to extract configurational entropies from molecular dynamics simulations of a series of small molecules, demonstrating improved convergence relative to existing methods. As these disparate applications highlight, our framework enables the use of general information theoretic phrasings even in systems where data quantities preclude direct estimation of the high-order statistics. Furthermore, because the framework provides a hierarchy of approximations of increasing order, as data collection and analysis techniques improve, the method extends to generate more accurate results, while maintaining the same underlying theory.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication>