Comparison of Gene Regulatory Networks via Steady-State Trajectories

被引:6
|
作者
Brun, Marcel [1 ]
Kim, Seungchan [1 ,2 ]
Choi, Woonjung [3 ]
Dougherty, Edward R. [1 ,4 ,5 ]
机构
[1] Translat Genom Res Inst, Computat Biol Div, Phoenix, AZ 85004 USA
[2] Arizona State Univ, Ira A Fulton Sch Engn, Sch Comp & Informat, Tempe, AZ 85287 USA
[3] Arizona State Univ, Coll Liberal Arts & Sci, Dept Math & Stat, Tempe, AZ 85287 USA
[4] Texas A&M Univ, Dept Elect & Comp Engn, College Stn, TX 77843 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Canc Genom Lab, Houston, TX 77030 USA
基金
美国国家科学基金会;
关键词
D O I
10.1155/2007/82702
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The modeling of genetic regulatory networks is becoming increasingly widespread in the study of biological systems. In the abstract, one would prefer quantitatively comprehensive models, such as a differential-equation model, to coarse models; however, in practice, detailed models require more accurate measurements for inference and more computational power to analyze than coarse-scale models. It is crucial to address the issue ofmodel complexity in the framework of a basic scientific paradigm: the model should be of minimal complexity to provide the necessary predictive power. Addressing this issue requires a metric by which to compare networks. This paper proposes the use of a classical measure of difference between amplitude distributions for periodic signals to compare two networks according to the differences of their trajectories in the steady state. The metric is applicable to networks with both continuous and discrete values for both time and state, and it possesses the critical property that it allows the comparison of networks of different natures. We demonstrate application of the metric by comparing a continuous-valued reference network against simplified versions obtained via quantization. Copyright (C) 2007 Marcel Brun et al.
引用
收藏
页数:11
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