Evidence map›Paper›PMID 39090538›Full record

ArticleBMC bioinformatics2024

Ant colony optimization for the identification of dysregulated gene subnetworks from expression data.

Eileen Marie Hanna, Ghadi El Hasbani, Danielle Azar

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Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Eileen Marie HannaDepartment of Computer Science and Mathematics, Lebanese American University, Byblos, Lebanon. eileenmarie.hanna@lau.edu.lb.
Ghadi El HasbaniDepartment of Computer Science and Mathematics, Lebanese American University, Byblos, Lebanon.
Danielle AzarDepartment of Computer Science and Mathematics, Lebanese American University, Byblos, Lebanon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-throughput experimental technologies can provide deeper insights into pathway perturbations in biomedical studies. Accordingly, their usage is central to the identification of molecular targets and the subsequent development of suitable treatments for various diseases. Classical interpretations of generated data, such as differential gene expression and pathway analyses, disregard interconnections between studied genes when looking for gene-disease associations. Given that these interconnections are central to cellular processes, there has been a recent interest in incorporating them in such studies. The latter allows the detection of gene modules that underlie complex phenotypes in gene interaction networks. Existing methods either impose radius-based restrictions or freely grow modules at the expense of a statistical bias towards large modules. We propose a heuristic method, inspired by Ant Colony Optimization, to apply gene-level scoring and module identification with distance-based search constraints and penalties, rather than radius-based constraints.

resultsWe test and compare our results to other approaches using three datasets of different neurodegenerative diseases, namely Alzheimer's, Parkinson's, and Huntington's, over three independent experiments. We report the outcomes of enrichment analyses and concordance of gene-level scores for each disease. Results indicate that the proposed approach generally shows superior stability in comparison to existing methods. It produces stable and meaningful enrichment results in all three datasets which have different case to control proportions and sample sizes.

conclusionThe presented network-based gene expression analysis approach successfully identifies dysregulated gene modules associated with a certain disease. Using a heuristic based on Ant Colony Optimization, we perform a distance-based search with no radius constraints. Experimental results support the effectiveness and stability of our method in prioritizing modules of high relevance. Our tool is publicly available at github.com/GhadiElHasbani/ACOxGS.git.

Indexed as

Gene Regulatory NetworksAlgorithmsAnimalsAntsComputational BiologyDatabases, GeneticGene Expression ProfilingHumansNeurodegenerative DiseasesAnt Colony OptimizationEnrichment analysisGene expressionGene interaction network

Identifiers

PMID39090538
PMCPMC11295523

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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.