Cellwise Robust Twoblock Dimension Reduction

TL;DR

CRTB is a novel robust dimension reduction method that effectively handles scattered cellwise outliers in multivariate data, maintaining interpretability and high fidelity in outlier detection.

Contribution

It introduces the first cellwise robust two-block dimension reduction technique with efficient algorithms and demonstrates superior performance over existing methods.

Findings

Resists contamination in over 50% of rows.

Recovers cellwise outlier patterns with high fidelity.

Produces interpretable results in practical examples.

Abstract

Cellwise Robust Twoblock (CRTB) is introduced, the first cellwise robust method for simultaneous dimension reduction of multivariate predictor and response blocks, in both a dense and a sparse variable-selecting variant. Classical robust methods protect against casewise outliers by downweighting or removing entire observations, a strategy that becomes inefficient -- and eventually breaks down -- when contamination is scattered across individual cells rather than concentrated in whole rows. CRTB combines a column-wise pre-filter for cellwise outlier detection with model-based imputation of flagged cells inside an iteratively reweighted M-estimation loop, retaining the clean cells of partially contaminated rows instead of discarding the observation. An efficient algorithm is provided that uses the classical twoblock SVD as a warm start and converges in a handful of IRLS iterations at a moderate computational cost. The method resists settings where more than $50\%$ of rows contain contaminated cells while retaining comparable efficiency on clean data. A simulation study confirms these properties and shows that CRTB additionally recovers the underlying cellwise outlier pattern with high fidelity and, in the sparse setting, the correct set of informative variables. Two compelling examples illustrate CRTB's practical utility. In each of these, CRTB is shown to be conducive to results that are highly interpretable in the respective domains in the presence of cellwise outliers. As a by-product, the corresponding cells are identified with high fidelity.