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Reverse Engineering Biological Networks: Opportunities and Challenges in Computational Methods for Pathway Inference Volume 1115 published November 2007
Ann. N.Y. Acad. Sci. 1115: 212–220 (2007). doi: 10.1196/annals.1407.007
Copyright © 2007 by the New York Academy of Sciences
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Articles by MAIWALD, T.
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Articles by MAIWALD, T.
Articles by TIMMER, J.

Part VI. Reverse Engineering of Parameters in Quantitative Models

Dynamic Pathway Modeling

Feasibility Analysis and Optimal Experimental Design

THOMAS MAIWALDa, CLEMENS KREUTZa, ANDREA C. PFEIFERb, SEBASTIAN BOHLb, URSULA KLINGMÜLLERb AND JENS TIMMERa

a Freiburg Center for Data Analysis and Modeling, Freiburg University, 79104 Freiburg, Germany b German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany

Key Words: systems biology • mathematical modeling • experimental design • null hypothesis • multi-experiment fitting

Address for correspondence: Thomas Maiwald, Freiburg Center for Data Analysis and Modeling, Freiburg University, Eckerstrasse 1, 79104 Freiburg, Germany. Voice: +49-761-1528-703; fax: +49-761-203-5967.  maiwald{at}fdm.uni-freiburg.de

A major challenge in systems biology is to evaluate the feasibility of a biological research project prior to its realization. Since experiments are animals-, cost- and time-consuming, approaches allowing researchers to discriminate alternative hypotheses with a minimal set of experiments are highly desirable. Given a null hypothesis and alternative model, as well as laboratory constraints like observable players, sample size, noise level, and stimulation options, we suggest a method to obtain a list of required experiments in order to significantly reject the null hypothesis model M0 if a specified alternative model MA is realized. For this purpose, we estimate the power to detect a violation of M0 by means of Monte Carlo simulations. Iteratively, the power is maximized over all feasible stimulations of the system using multi-experiment fitting, leading to an optimal combination of experimental settings to discriminate the null hypothesis and alternative model. We prove the importance of simultaneous modeling of combined experiments with quantitative, highly sampled in vivo measurements from the Jak/STAT5 signaling pathway in fibroblasts, stimulated with erythropoietin (Epo). Afterwards we apply the presented iterative experimental design approach to the Jak/STAT3 pathway of primary hepatocytes stimulated with IL-6. Our approach offers the possibility of deciding which scientific questions can be answered based on existing laboratory constraints. To be able to concentrate on feasible questions on account of inexpensive computational simulations yields not only enormous cost and time saving, but also helps to specify realizable, systematic research projects in advance.




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G. STOLOVITZKY, D. MONROE, and A. CALIFANO
Dialogue on Reverse-Engineering Assessment and Methods: The DREAM of High-Throughput Pathway Inference
Ann. N.Y. Acad. Sci., December 1, 2007; 1115(1): 1 - 22.
[Abstract] [Full Text] [PDF]



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