A Systematic Evaluation of Imbalance Handling Methods in Biomedical Binary Classification

arXiv cs.LG Papers

Summary

This paper systematically evaluates five imbalance handling methods (RUS, ROS, SMOTE, re-weighting, direct F1 optimization) on three biomedical datasets (tabular, text, image) using models of varying complexity. Results show that benefits depend on model complexity and data modality, with ROS, re-weighting, and direct F1 optimization being effective for complex models on unstructured data.

arXiv:2605.14147v1 Announce Type: new Abstract: Objective: The primary goal of this study was to systematically examine the impact of commonly used imbalance handling methods (IHMs) on predictive performance in biomedical binary classification, considering the interplay between model complexity and diverse data modalities. Material and Methods: We evaluated five representative IHMs: random undersampling (RUS), random oversampling (ROS), SMOTE, re-weighting (RW), and direct F1-score optimization (DMO), against a raw training (RAW) baseline. The evaluation encompassed three public biomedical datasets: MIMIC-III (tabular), ADE-Corpus-V2 (text), and MURA (image), spanning three common biomedical data modalities. To assess varying model complexity, we employed a range of architectures, from classical logistic regression and random forest to deep neural networks, including multilayer perceptron (MLP), BiLSTM, BERT, DenseNet, and DINOv2. Results: For simpler models such as logistic regression on tabular data, IHMs yielded no significant advantage over the RAW baseline, aligning with prior findings. However, clear benefits were observed for more complex models and unstructured data: (a) ROS and RW consistently enhanced the performance of powerful models; (b) direct F1-score optimization demonstrated utility primarily for unstructured text and image data; and (c) RUS and SMOTE consistently degraded performance and are therefore not recommended. Conclusion: The effectiveness of IHMs depends on both model complexity and data modality. Performance gains are most pronounced when leveraging appropriate IHMs, such as ROS, RW, and DMO, on high-complexity models.
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# A Systematic Evaluation of Imbalance Handling Methods in Biomedical Binary Classification
Source: [https://arxiv.org/abs/2605.14147](https://arxiv.org/abs/2605.14147)
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> Abstract:Objective: The primary goal of this study was to systematically examine the impact of commonly used imbalance handling methods \(IHMs\) on predictive performance in biomedical binary classification, considering the interplay between model complexity and diverse data modalities\. Material and Methods: We evaluated five representative IHMs: random undersampling \(RUS\), random oversampling \(ROS\), SMOTE, re\-weighting \(RW\), and direct F1\-score optimization \(DMO\), against a raw training \(RAW\) baseline\. The evaluation encompassed three public biomedical datasets: MIMIC\-III \(tabular\), ADE\-Corpus\-V2 \(text\), and MURA \(image\), spanning three common biomedical data modalities\. To assess varying model complexity, we employed a range of architectures, from classical logistic regression and random forest to deep neural networks, including multilayer perceptron \(MLP\), BiLSTM, BERT, DenseNet, and DINOv2\. Results: For simpler models such as logistic regression on tabular data, IHMs yielded no significant advantage over the RAW baseline, aligning with prior findings\. However, clear benefits were observed for more complex models and unstructured data: \(a\) ROS and RW consistently enhanced the performance of powerful models; \(b\) direct F1\-score optimization demonstrated utility primarily for unstructured text and image data; and \(c\) RUS and SMOTE consistently degraded performance and are therefore not recommended\. Conclusion: The effectiveness of IHMs depends on both model complexity and data modality\. Performance gains are most pronounced when leveraging appropriate IHMs, such as ROS, RW, and DMO, on high\-complexity models\.

## Submission history

From: Jiandong Chen \[[view email](https://arxiv.org/show-email/77194b39/2605.14147)\] **\[v1\]**Wed, 13 May 2026 21:57:38 UTC \(948 KB\)

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