Rahaf M. Ahmad, Noura AlDhaheri, Mohd Saberi Mohamad, Bassam R. Ali
Breast cancer (BC) remains one of the most prevalent and lethal malignancies worldwide, with its onset shaped by complex interactions between germline predispositions, environmental exposures, and accumulated somatic mutations. Accurate prediction of variant pathogenicity is essential for identifying high-risk individuals, guiding early detection, and tailoring treatment strategies. However, existing computational tools often lack disease-specific training and fail to generalize across diverse variant datasets. To address this gap, we systematically benchmarked the predictive utility of four distinct variant datasets using three Automated Machine Learning (AutoML) frameworks-TPOT, H2O AutoML, and MLJAR. Our goal was to evaluate how dataset composition influences classification performance and to identify the optimal dataset for BC-specific pathogenicity prediction. Among the datasets evaluated, Dataset-2-curated from both cancer-specific and non-cancer databases, consistently yielded the highest predictive performance across all frameworks. H2O AutoML achieved a peak accuracy of 99.99 %, while TPOT and MLJAR also exhibited robust generalization on this dataset. Feature importance analyses revealed strong convergence across frameworks, highlighting conservation scores and pathogenicity metrics as dominant predictors. Interpretability techniques including SHAP, permutation importance, and LIME further validated the biological relevance and transparency of the models. This study presents a scalable, interpretable AutoML benchmarking framework tailored to the clinical prioritization of BC variants. By demonstrating the superiority of cancer-specific, disease-relevant datasets, our findings underscore the critical importance of thoughtful dataset design in machine learning pipelines for genomic medicine. Beyond BC, this framework is readily transferable to other genetic disorders, providing a foundational tool for precision diagnostics and the advancement of personalized oncology. © 2025 The Authors
Department of Genetics and Genomics, College of Medicine and Health Sciences, United Arab Emirates University, United Arab Emirates; Centre for Advanced Analytics, CoE for Artificial Intelligence, Faculty of Engineering & Technology, Multimedia University, Melaka, 75450, Malaysia; Department of Biosystems Engineering, Faculty of Agricultural Technology, Universitas Brawijaya, East Java, Malang, Indonesia; Institute For Data Innovation and Artificial Intelligence, Cranbourne East, Victoria, 3977, Australia
