scholarly journals Identifying regulational alterations in gene regulatory networks by state space representation of vector autoregressive models and variational annealing

BMC Genomics ◽  
2012 ◽  
Vol 13 (Suppl 1) ◽  
pp. S6 ◽  
Author(s):  
Kaname Kojima ◽  
Seiya Imoto ◽  
Rui Yamaguchi ◽  
André Fujita ◽  
Mai Yamauchi ◽  
...  
2008 ◽  
Vol 06 (05) ◽  
pp. 961-979 ◽  
Author(s):  
ANDRÉ FUJITA ◽  
JOÃO RICARDO SATO ◽  
HUMBERTO MIGUEL GARAY-MALPARTIDA ◽  
MARI CLEIDE SOGAYAR ◽  
CARLOS EDUARDO FERREIRA ◽  
...  

In cells, molecular networks such as gene regulatory networks are the basis of biological complexity. Therefore, gene regulatory networks have become the core of research in systems biology. Understanding the processes underlying the several extracellular regulators, signal transduction, protein–protein interactions, and differential gene expression processes requires detailed molecular description of the protein and gene networks involved. To understand better these complex molecular networks and to infer new regulatory associations, we propose a statistical method based on vector autoregressive models and Granger causality to estimate nonlinear gene regulatory networks from time series microarray data. Most of the models available in the literature assume linearity in the inference of gene connections; moreover, these models do not infer directionality in these connections. Thus, a priori biological knowledge is required. However, in pathological cases, no a priori biological information is available. To overcome these problems, we present the nonlinear vector autoregressive (NVAR) model. We have applied the NVAR model to estimate nonlinear gene regulatory networks based entirely on gene expression profiles obtained from DNA microarray experiments. We show the results obtained by NVAR through several simulations and by the construction of three actual gene regulatory networks (p53, NF-κB, and c-Myc) for HeLa cells.


2011 ◽  
Vol 5 (Suppl 3) ◽  
pp. S3 ◽  
Author(s):  
Xi Wu ◽  
Peng Li ◽  
Nan Wang ◽  
Ping Gong ◽  
Edward J Perkins ◽  
...  

2016 ◽  
Vol 13 (120) ◽  
pp. 20160179 ◽  
Author(s):  
S. E. Ahnert ◽  
T. M. A. Fink

Network motifs have been studied extensively over the past decade, and certain motifs, such as the feed-forward loop, play an important role in regulatory networks. Recent studies have used Boolean network motifs to explore the link between form and function in gene regulatory networks and have found that the structure of a motif does not strongly determine its function, if this is defined in terms of the gene expression patterns the motif can produce. Here, we offer a different, higher-level definition of the ‘function’ of a motif, in terms of two fundamental properties of its dynamical state space as a Boolean network. One is the basin entropy, which is a complexity measure of the dynamics of Boolean networks. The other is the diversity of cyclic attractor lengths that a given motif can produce. Using these two measures, we examine all 104 topologically distinct three-node motifs and show that the structural properties of a motif, such as the presence of feedback loops and feed-forward loops, predict fundamental characteristics of its dynamical state space, which in turn determine aspects of its functional versatility. We also show that these higher-level properties have a direct bearing on real regulatory networks, as both basin entropy and cycle length diversity show a close correspondence with the prevalence, in neural and genetic regulatory networks, of the 13 connected motifs without self-interactions that have been studied extensively in the literature.


2013 ◽  
Vol 2013 ◽  
pp. 1-12 ◽  
Author(s):  
Amina Noor ◽  
Erchin Serpedin ◽  
Mohamed Nounou ◽  
Hazem Nounou ◽  
Nady Mohamed ◽  
...  

The large influx of data from high-throughput genomic and proteomic technologies has encouraged the researchers to seek approaches for understanding the structure of gene regulatory networks and proteomic networks. This work reviews some of the most important statistical methods used for modeling of gene regulatory networks (GRNs) and protein-protein interaction (PPI) networks. The paper focuses on the recent advances in the statistical graphical modeling techniques, state-space representation models, and information theoretic methods that were proposed for inferring the topology of GRNs. It appears that the problem of inferring the structure of PPI networks is quite different from that of GRNs. Clustering and probabilistic graphical modeling techniques are of prime importance in the statistical inference of PPI networks, and some of the recent approaches using these techniques are also reviewed in this paper. Performance evaluation criteria for the approaches used for modeling GRNs and PPI networks are also discussed.


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