Structure identification for gene regulatory networks via linearization and robust state estimation

被引:11
作者
Xiong, Jie [1 ]
Zhou, Tong [1 ,2 ]
机构
[1] Tsinghua Univ, Dept Automat, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Tsinghua Natl Lab Informat Sci & Technol TNList, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Causal relationships; Extended Kalman filter; Gene regulatory networks; Robust state estimator; Modelling error; EXTENDED KALMAN FILTER; EXPRESSION PROFILES; LINEAR-SYSTEMS; TIME-SERIES; MODELS; INFERENCE;
D O I
10.1016/j.automatica.2014.08.003
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Inferring causal relationships among cellular components is one of the fundamental problems in understanding biological behaviours. The well known extended Kalman filter (EKF) has been proved to be a useful tool in simultaneously estimating both structure and actual gene expression levels of a gene regulatory network (GRN). First-order approximations, however, unavoidably result in modelling errors, but the EKF based method does not take either unmodelled dynamics or parametric uncertainties into account, which makes its estimation performances not very satisfactory. To overcome these problems, a sensitivity penalization based robust state estimator is adopted in this paper for revealing the structure of a GRN. Based on the specific structure of the estimation problem, it has been proved that under some weak conditions, both the EKF based method and the method suggested in this paper provide a consistent estimate, but the suggested method has a faster convergence speed. Compared with both the EKF and the unscented Kalman filter (UKF) based methods, simulation results and real data based estimations consistently show that both convergence speed and parametric estimation accuracy can be appreciably improved. These lead to significant reductions in both false positive errors and false negative errors, and may imply helpfulness of the suggested method in better understanding the structure and dynamics of actual GRNs. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2765 / 2776
页数:12
相关论文
共 37 条
[1]  
Akutsu T, 1999, Pac Symp Biocomput, P17
[2]  
[Anonymous], 1985, COMPUTER SCI APPL MA
[3]  
[Anonymous], 1999, SYSTEM IDENTIFICATIO
[4]   A tutorial on particle filters for online nonlinear/non-Gaussian Bayesian tracking [J].
Arulampalam, MS ;
Maskell, S ;
Gordon, N ;
Clapp, T .
IEEE TRANSACTIONS ON SIGNAL PROCESSING, 2002, 50 (02) :174-188
[5]   Inference of gene regulatory networks and compound mode of action from time course gene expression profiles [J].
Bansal, M ;
Della Gatta, G ;
di Bernardo, D .
BIOINFORMATICS, 2006, 22 (07) :815-822
[6]  
Butte A J, 2000, Pac Symp Biocomput, P418
[7]   Modeling and simulation of genetic regulatory systems: A literature review [J].
De Jong, H .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2002, 9 (01) :67-103
[8]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[9]   Large-scale mapping and validation of Escherichia coli transcriptional regulation from a compendium of expression profiles [J].
Faith, Jeremiah J. ;
Hayete, Boris ;
Thaden, Joshua T. ;
Mogno, Ilaria ;
Wierzbowski, Jamey ;
Cottarel, Guillaume ;
Kasif, Simon ;
Collins, James J. ;
Gardner, Timothy S. .
PLOS BIOLOGY, 2007, 5 (01) :54-66
[10]   Using Bayesian networks to analyze expression data [J].
Friedman, N ;
Linial, M ;
Nachman, I ;
Pe'er, D .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2000, 7 (3-4) :601-620