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SGA-DT: An adaptive fusion framework for missing data imputation and interpretable healthcare classification

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  • Monalisa Jena
  • Satchidananda Dehuri
  • Sung-Bae Cho

Abstract

Despite advances in machine learning and medical data processing, handling missing values remains a critical and complex challenge in healthcare analytics. Missing data, especially in non-class attributes can severely compromise model accuracy, clinical reliability, and interpretability. In sensitive domains such as healthcare, improper imputation may lead to biased outcomes or delayed interventions. To address this challenge, we propose SGA-DT, an adaptive and interpretable learning framework that combines the best features of genetically optimized support vector regression (SVR) with a decision tree (DT) classifier for robust healthcare prediction. The framework adaptively selects an imputation strategy based on the level of missingness. It uses standard SVR for low, iterative SVR for moderate, and k-Nearest Neighbor (KNN) followed by SVR refinement for high missingness. Genetic algorithm (GA) is used to select the best SVR kernel and tune its hyperparameters, enhancing imputation accuracy across different data patterns. The complete dataset is then classified using DT, providing both robustness and transparency in prediction. The SGA-DT framework is evaluated on three healthcare datasets, Breast Cancer, Mammographic, and Hepatitis, along with other real-world and synthetic datasets. For interpretability analysis, decision trees are generated under varying missingness levels to support clinical transparency. Comparative results show that SGA-DT consistently outperforms multiple integrated frameworks across accuracy, precision, recall, and F-measure, demonstrating its robustness, interpretability, and generalizability in healthcare prediction tasks.

Suggested Citation

  • Monalisa Jena & Satchidananda Dehuri & Sung-Bae Cho, 2026. "SGA-DT: An adaptive fusion framework for missing data imputation and interpretable healthcare classification," PLOS ONE, Public Library of Science, vol. 21(3), pages 1-31, March.
  • Handle: RePEc:plo:pone00:0343619
    DOI: 10.1371/journal.pone.0343619
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