Evidence map›Paper›PMID 21545720›Full record

ArticleBMC systems biology2011

Inference of gene regulatory networks from time series by Tsallis entropy.

Fabrício Martins Lopes, Evaldo A de Oliveira, Roberto M Cesar

Abstract read
In one paragraph

Article in BMC systems biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Stable Gene Regulatory Network Modeling From Steady-State Data.Bioengineering (Basel, Switzerland) · 2016
    Article
  5. Article
  6. Article
  7. Learning delayed influences of biological systems.Frontiers in bioengineering and biotechnology · 2014
    Article
  8. Article
  9. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Fabrício Martins LopesFederal University of Technology - Paraná, Brazil. fabricio@utfpr.edu.br
Evaldo A de Oliveira
Roberto M Cesar

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe inference of gene regulatory networks (GRNs) from large-scale expression profiles is one of the most challenging problems of Systems Biology nowadays. Many techniques and models have been proposed for this task. However, it is not generally possible to recover the original topology with great accuracy, mainly due to the short time series data in face of the high complexity of the networks and the intrinsic noise of the expression measurements. In order to improve the accuracy of GRNs inference methods based on entropy (mutual information), a new criterion function is here proposed.

resultsIn this paper we introduce the use of generalized entropy proposed by Tsallis, for the inference of GRNs from time series expression profiles. The inference process is based on a feature selection approach and the conditional entropy is applied as criterion function. In order to assess the proposed methodology, the algorithm is applied to recover the network topology from temporal expressions generated by an artificial gene network (AGN) model as well as from the DREAM challenge. The adopted AGN is based on theoretical models of complex networks and its gene transference function is obtained from random drawing on the set of possible Boolean functions, thus creating its dynamics. On the other hand, DREAM time series data presents variation of network size and its topologies are based on real networks. The dynamics are generated by continuous differential equations with noise and perturbation. By adopting both data sources, it is possible to estimate the average quality of the inference with respect to different network topologies, transfer functions and network sizes.

conclusionsA remarkable improvement of accuracy was observed in the experimental results by reducing the number of false connections in the inferred topology by the non-Shannon entropy. The obtained best free parameter of the Tsallis entropy was on average in the range 2.5 ≤ q ≤ 3.5 (hence, subextensive entropy), which opens new perspectives for GRNs inference methods based on information theory and for investigation of the nonextensivity of such networks. The inference algorithm and criterion function proposed here were implemented and included in the DimReduction software, which is freely available at http://sourceforge.net/projects/dimreduction and http://code.google.com/p/dimreduction/.

Indexed as

EntropyGene Regulatory NetworksComputational BiologyModels, GeneticTime Factors

Identifiers

PMID21545720
PMCPMC3117729

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.