Evidence map›Paper›PMID 34252959›Full record

ArticleBioinformatics (Oxford, England)2021

A novel constrained genetic algorithm-based Boolean network inference method from steady-state gene expression data.

Hung-Cuong Trinh, Yung-Keun Kwon

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Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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11citing papers in PubMed
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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
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  3. Automated model refinement using perturbation-observation pairs.NPJ systems biology and applications · 2025
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  6. Review
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5 · Who and what money

Authors and funding

2 authors.

Hung-Cuong TrinhFaculty of Information Technology, Ton Duc Thang University, Ho Chi Minh 758307, Vietnam.
Yung-Keun KwonDepartment of IT Convergence, University of Ulsan, Ulsan 680-749, Korea.

Funding

2021 Research Fund of University of Ulsan
6 · The paper itself

Abstract

motivationIt is a challenging problem in systems biology to infer both the network structure and dynamics of a gene regulatory network from steady-state gene expression data. Some methods based on Boolean or differential equation models have been proposed but they were not efficient in inference of large-scale networks. Therefore, it is necessary to develop a method to infer the network structure and dynamics accurately on large-scale networks using steady-state expression.

resultsIn this study, we propose a novel constrained genetic algorithm-based Boolean network inference (CGA-BNI) method where a Boolean canalyzing update rule scheme was employed to capture coarse-grained dynamics. Given steady-state gene expression data as an input, CGA-BNI identifies a set of path consistency-based constraints by comparing the gene expression level between the wild-type and the mutant experiments. It then searches Boolean networks which satisfy the constraints and induce attractors most similar to steady-state expressions. We devised a heuristic mutation operation for faster convergence and implemented a parallel evaluation routine for execution time reduction. Through extensive simulations on the artificial and the real gene expression datasets, CGA-BNI showed better performance than four other existing methods in terms of both structural and dynamics prediction accuracies. Taken together, CGA-BNI is a promising tool to predict both the structure and the dynamics of a gene regulatory network when a highest accuracy is needed at the cost of sacrificing the execution time. AVAILABILITY AND IMPLEMENTATION: Source code and data are freely available at https://github.com/csclab/CGA-BNI. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsGene Regulatory NetworksGene ExpressionModels, GeneticSoftwareSystems Biology

Identifiers

PMID34252959
PMCPMC8275338

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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.