Computation of Steady-State Probability Distributions in Stochastic Models of Cellular Networks
Author(s) -
Mark A. Hallen,
Bochong Li,
Yu Tanouchi,
Cheemeng Tan,
Mike West,
Lingchong You
Publication year - 2011
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1002209
Subject(s) - noise (video) , computer science , computation , convolution (computer science) , gene regulatory network , biological system , stochastic process , steady state (chemistry) , master equation , systems biology , network analysis , stochastic modelling , key (lock) , statistical physics , algorithm , mathematics , bioinformatics , artificial intelligence , physics , biology , chemistry , statistics , biochemistry , gene expression , computer security , quantum mechanics , artificial neural network , image (mathematics) , quantum , gene
Cellular processes are “noisy”. In each cell, concentrations of molecules are subject to random fluctuations due to the small numbers of these molecules and to environmental perturbations. While noise varies with time, it is often measured at steady state, for example by flow cytometry. When interrogating aspects of a cellular network by such steady-state measurements of network components, a key need is to develop efficient methods to simulate and compute these distributions. We describe innovations in stochastic modeling coupled with approaches to this computational challenge: first, an approach to modeling intrinsic noise via solution of the chemical master equation, and second, a convolution technique to account for contributions of extrinsic noise. We show how these techniques can be combined in a streamlined procedure for evaluation of different sources of variability in a biochemical network. Evaluation and illustrations are given in analysis of two well-characterized synthetic gene circuits, as well as a signaling network underlying the mammalian cell cycle entry.
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