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Optimized cancer gene selection using armadillo optimization algorithm and support vector machine.

Abrar Yaqoob1, Mushtaq Ahmad Mir2, Mohd Asif Shah3

  • 1Department of Mathematics, VIT Bhopal University located at Kothrikalan, Sehore, Bhopal 466114, India.

Cancer Treatment and Research Communications
|October 31, 2025
PubMed
Summary
This summary is machine-generated.

A novel hybrid approach, AOA-SVM, efficiently selects key genes for accurate cancer classification. This method achieves high precision and computational efficiency, aiding in precision medicine and cancer diagnostics.

Keywords:
AlgorithmsGene expression profilingMachine learningMicroarray analysisNeoplasmsSupport vector machine

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • High-dimensional cancer datasets pose challenges for classification due to irrelevant or redundant features.
  • Effective feature selection is critical to enhance accuracy and reduce computational load in cancer data analysis.

Purpose of the Study:

  • To develop and evaluate a hybrid AOA-SVM method for efficient and accurate feature selection in cancer datasets.
  • To identify minimal, biologically relevant gene markers for improved cancer diagnostics.

Main Methods:

  • A hybrid AOA-SVM method was proposed, combining AOA's optimization and diversity maintenance with SVM classification.
  • Gene selection involved local optimization within subgroups and a shuffling phase to identify informative gene subsets.
  • The method was validated on leukaemia, ovarian, and CNS cancer datasets.

Main Results:

  • The AOA-SVM method achieved high accuracy across all tested cancer datasets.
  • For the ovarian dataset, 99.12% accuracy and 98.83% AUC-ROC were obtained with 15 genes.
  • Perfect classification (100% accuracy) was achieved for leukaemia (34 genes) and CNS (43 genes) datasets.

Conclusions:

  • The AOA-SVM hybrid is a highly accurate and computationally efficient tool for cancer diagnostics.
  • It demonstrates potential for precision medicine by identifying minimal gene markers.
  • The method effectively distinguishes between cancerous and healthy tissues using selected gene subsets.