Parameter Estimation and Model Selection in Computational Biology

被引:230
作者
Lillacci, Gabriele [1 ]
Khammash, Mustafa [1 ]
机构
[1] Univ Calif Santa Barbara, Ctr Control Dynam Syst & Computat, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会;
关键词
STATE-SPACE MODELS; BIOCHEMICAL PATHWAYS; MONTE-CARLO; OPTIMIZATION; ALGORITHMS; NETWORK;
D O I
10.1371/journal.pcbi.1000696
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A central challenge in computational modeling of biological systems is the determination of the model parameters. Typically, only a fraction of the parameters (such as kinetic rate constants) are experimentally measured, while the rest are often fitted. The fitting process is usually based on experimental time course measurements of observables, which are used to assign parameter values that minimize some measure of the error between these measurements and the corresponding model prediction. The measurements, which can come from immunoblotting assays, fluorescent markers, etc., tend to be very noisy and taken at a limited number of time points. In this work we present a new approach to the problem of parameter selection of biological models. We show how one can use a dynamic recursive estimator, known as extended Kalman filter, to arrive at estimates of the model parameters. The proposed method follows. First, we use a variation of the Kalman filter that is particularly well suited to biological applications to obtain a first guess for the unknown parameters. Secondly, we employ an a posteriori identifiability test to check the reliability of the estimates. Finally, we solve an optimization problem to refine the first guess in case it should not be accurate enough. The final estimates are guaranteed to be statistically consistent with the measurements. Furthermore, we show how the same tools can be used to discriminate among alternate models of the same biological process. We demonstrate these ideas by applying our methods to two examples, namely a model of the heat shock response in E. coli, and a model of a synthetic gene regulation system. The methods presented are quite general and may be applied to a wide class of biological systems where noisy measurements are used for parameter estimation or model selection.
引用
收藏
页数:17
相关论文
共 39 条
[1]  
[Anonymous], 1982, Practical Optimization
[2]  
[Anonymous], 2000, PRACTICAL METHODS OP
[3]  
[Anonymous], 2005, Dover Books on Engineering
[4]  
[Anonymous], Probability, Random Variables and Stochastic Processes
[5]   Parameter estimation and determinability analysis applied to Drosophila gap gene circuits [J].
Ashyraliyev, Maksat ;
Jaeger, Johannes ;
Blom, Joke G. .
BMC SYSTEMS BIOLOGY, 2008, 2
[6]   An ensemble method for identifying regulatory circuits with special reference to the qa gene cluster of Neurospora crassa [J].
Battogtokh, D ;
Asch, DK ;
Case, ME ;
Arnold, J ;
Schüttler, HB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (26) :16904-16909
[7]   Model selection and mixed-effects modeling of HIV infection dynamics [J].
Bortz, D. M. ;
Nelson, P. W. .
BULLETIN OF MATHEMATICAL BIOLOGY, 2006, 68 (08) :2005-2025
[8]  
Brooks SP, 1998, J ROY STAT SOC D-STA, V47, P69, DOI 10.1111/1467-9884.00117
[9]   Statistical mechanical approaches to models with many poorly known parameters [J].
Brown, KS ;
Sethna, JP .
PHYSICAL REVIEW E, 2003, 68 (02) :9
[10]  
Bullinger E, 1997, IEEE DECIS CONTR P, P4348, DOI 10.1109/CDC.1997.649541