A quantitative framework For large-scale model estimation and discrimination In systems biology

Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2013.

Bibliographic Details
Main Author: Eydgahi, Hoda
Other Authors: Peter K. Sorger and John N. Tsitsiklis.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2013
Subjects:
Online Access:http://hdl.handle.net/1721.1/82347
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author Eydgahi, Hoda
author2 Peter K. Sorger and John N. Tsitsiklis.
author_facet Peter K. Sorger and John N. Tsitsiklis.
Eydgahi, Hoda
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description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2013.
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spelling mit-1721.1/823472019-04-10T10:33:04Z A quantitative framework For large-scale model estimation and discrimination In systems biology Eydgahi, Hoda Peter K. Sorger and John N. Tsitsiklis. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science. Electrical Engineering and Computer Science. Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2013. Cataloged from PDF version of thesis. Includes bibliographical references (p. 103-111). Using models to simulate and analyze biological networks requires principled approaches to parameter estimation and model discrimination. We use Bayesian and Monte Carlo methods to recover the full probability distributions of free parameters (initial protein concentrations and rate constants) for mass action models of receptor-mediated cell death. The width of the individual parameter distributions is largely determined by non-identifiability but co-variation among parameters, even those that are poorly determined, encodes essential information. Knowledge of joint parameter distributions makes it possible to compute the uncertainty of model-based predictions whereas ignoring it (e.g. by treating parameters as a simple list of values and variances) yields nonsensical predictions. Computing the Bayes factor from joint distributions yields the odds ratio (~20-fold) for competing "direct" and "indirect" apoptosis models having different numbers of parameters. The methods presented in this thesis were then extended to make predictions in eight apoptosis mini-models. Despite topological uncertainty, the simulated predictions can be used to drive experimental design. Our results illustrate how Bayesian approaches to model calibration and discrimination combined with single-cell data represent a generally useful and rigorous approach to discriminating between competing hypotheses in the face of parametric and topological uncertainty. by Hoda Eydgahi. Ph.D. 2013-11-18T19:11:48Z 2013-11-18T19:11:48Z 2013 2013 Thesis http://hdl.handle.net/1721.1/82347 861703201 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 111 p. application/pdf Massachusetts Institute of Technology
spellingShingle Electrical Engineering and Computer Science.
Eydgahi, Hoda
A quantitative framework For large-scale model estimation and discrimination In systems biology
title A quantitative framework For large-scale model estimation and discrimination In systems biology
title_full A quantitative framework For large-scale model estimation and discrimination In systems biology
title_fullStr A quantitative framework For large-scale model estimation and discrimination In systems biology
title_full_unstemmed A quantitative framework For large-scale model estimation and discrimination In systems biology
title_short A quantitative framework For large-scale model estimation and discrimination In systems biology
title_sort quantitative framework for large scale model estimation and discrimination in systems biology
topic Electrical Engineering and Computer Science.
url http://hdl.handle.net/1721.1/82347
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