Extrapolated cross-validation for randomized ensembles
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Ensemble methods such as bagging and random forests are ubiquitous in fields ranging from finance to genomics. However, the question of the efficient tuning of ensemble parameters has received relatively little attention. In this paper, we propose a cross-validation method, ECV (Extrapolated Cross-Validation), for tuning the ensemble and subsample sizes of randomized ensembles. Our method builds on two main ingredients: two initial estimators for small ensemble sizes using out-of-bag errors and a novel risk extrapolation technique leveraging the structure of the prediction risk decomposition. By establishing uniform consistency over ensemble and subsample sizes, we show that ECV yields δ-optimal (with respect to the oracle-tuned risk) ensembles for squared prediction risk. Our theory accommodates general ensemble predictors, requires mild moment assumptions, and allows for high-dimensional regimes where the feature dimension grows with the sample size. As an illustrative example, we employ ECV to predict surface protein abundances from gene expressions in single-cell multiomics using random forests. Compared to sample-split cross-validation and K-fold cross-validation, ECV achieves higher accuracy avoiding sample splitting. Meanwhile, its computational cost is considerably lower owing to the use of the risk extrapolation technique. Further numerical results demonstrate the finite-sample accuracy of ECV for several common ensemble predictors.
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