Quantifies how partition stability, minority class recovery, and topological interpretability trade off across K-means, SOMs, consensus K-means, and four modern baselines on 10,095 TCGA cancer RNA samples (13,634 genes, 19 cancer types). At matched prototype budgets, K-means outperforms SOMs on both stability and minority recovery, while SOMs uniquely provide 2D topological visualization. No single method optimizes all three properties.
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