4,680 research outputs found
Time-delayed models of gene regulatory networks
We discuss different mathematical models of gene regulatory networks as relevant to the onset and development of cancer. After discussion of alternativemodelling approaches, we use a paradigmatic two-gene network to focus on the role played by time delays in the dynamics of gene regulatory networks. We contrast the dynamics of the reduced model arising in the limit of fast mRNA dynamics with that of the full model. The review concludes with the discussion of some open problems
Therapeutic target discovery using Boolean network attractors: improvements of kali
In a previous article, an algorithm for identifying therapeutic targets in
Boolean networks modeling pathological mechanisms was introduced. In the
present article, the improvements made on this algorithm, named kali, are
described. These improvements are i) the possibility to work on asynchronous
Boolean networks, ii) a finer assessment of therapeutic targets and iii) the
possibility to use multivalued logic. kali assumes that the attractors of a
dynamical system, such as a Boolean network, are associated with the phenotypes
of the modeled biological system. Given a logic-based model of pathological
mechanisms, kali searches for therapeutic targets able to reduce the
reachability of the attractors associated with pathological phenotypes, thus
reducing their likeliness. kali is illustrated on an example network and used
on a biological case study. The case study is a published logic-based model of
bladder tumorigenesis from which kali returns consistent results. However, like
any computational tool, kali can predict but can not replace human expertise:
it is a supporting tool for coping with the complexity of biological systems in
the field of drug discovery
A survey of models for inference of gene regulatory networks
In this article, I present the biological backgrounds of microarray, ChIP-chip and ChIPSeq technologies and the application of computational methods in reverse engineering of gene regulatory networks (GRNs). The most commonly used GRNs models based on Boolean networks, Bayesian networks, relevance networks, differential and difference equations are described. A novel model for integration of prior biological knowledge in the GRNs inference is presented, too. The advantages and disadvantages of the described models are compared. The GRNs validation criteria are depicted. Current trends and further directions for GRNs inference using prior knowledge are given at the end of the paper
A survey of models for inference of gene regulatory networks
In this article, I present the biological backgrounds of microarray, ChIP-chip and ChIPSeq technologies and the application of computational methods in reverse engineering of gene regulatory networks (GRNs). The most commonly used GRNs models based on Boolean networks, Bayesian networks, relevance networks, differential and difference equations are described. A novel model for integration of prior biological knowledge in the GRNs inference is presented, too. The advantages and disadvantages of the described models are compared. The GRNs validation criteria are depicted. Current trends and further directions for GRNs inference using prior knowledge are given at the end of the paper
Hybrid-Controlled Neurofuzzy Networks Analysis Resulting in Genetic Regulatory Networks Reconstruction
Reverse engineering of gene regulatory networks (GRNs) is the process of estimating genetic interactions of a cellular system from gene expression data. In this paper, we propose a novel hybrid systematic algorithm based on neurofuzzy network for reconstructing GRNs from observational gene expression data when only a medium-small number of measurements are available. The approach uses fuzzy logic to transform gene expression values into qualitative descriptors that can be evaluated by using a set of defined rules. The algorithm uses neurofuzzy network to model genes effects on other genes followed by four stages of decision making to extract gene interactions. One of the main features of the proposed algorithm is that an optimal number of fuzzy rules can be easily and rapidly extracted without overparameterizing. Data analysis and simulation are conducted on microarray expression profiles of S. cerevisiae cell cycle and demonstrate that the proposed algorithm not only selects the patterns of the time series gene expression data accurately, but also provides models with better reconstruction accuracy when compared with four published algorithms: DBNs, VBEM, time delay ARACNE, and PF subjected to LASSO. The accuracy of the proposed approach is evaluated in terms of recall and F-score for the network reconstruction task
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