BREAD: Baseline-Referenced Explanations for Anomaly Diagnosis

Unsupervised anomaly detection scores each point of an unlabelled, contaminated sample in a single pass, and increasingly must also explain why a point is flagged. Yet the dominant detectors give a score with no account of which features drive it, and explanations are bolted on post-hoc with SHAP or LIME, which re-query the detector thousands of times per point and only approximate it. We introduce WAND, an unsupervised tabular anomaly detector that is explainable by design. WAND organises its computation around directions on the unit sphere, scoring each point by how far its projection escapes a sub-Gaussian extreme-value baseline. The originality of our approach is that the witness directions that flag a point, being vectors in feature space, are its explanation, a per-feature attribution obtained at no cost over scoring and, since the score is differentiable, recoverable by gradients. Scoring is linear in the sample size, and a probe-efficiency bound guarantees every anomaly a witness, hence an explanation. Across 47 ADBench datasets WAND attains the best mean Friedman rank at ROC-AUC parity with 16 unsupervised baselines, so the gain is interpretability at no accuracy cost; its native explanations are more accurate and faithful than post-hoc SHAP/LIME and ECOD at a fraction of the query cost. WAND is thus a practical, interpretable solution for explainable anomaly detection.

This paper considers a practical few-shot anomaly detection (FSAD) setting, termed discriminative FSAD, where a limited number of both normal and anomalous examples are available as references during inference. Existing FSAD methods rely on normal-only references through normality matching, ignoring the discriminative clues in anomalous references, while directly fitting both references can overfit to the seen anomalies. We introduce IDEAL, an intrinsic deviation learning framework that leverages both reference types to learn intrinsic deviation patterns characterizing generalizable abnormality as deviations from normality. IDEAL decomposes the learning process into two novel components: 1) a Normal Variation Eraser to suppress nuisance normal variations that may lead to noisy deviations from normality, thereby highlighting anomaly-relevant deviation representations; 2) an Intrinsic Deviation Encoder to decompose these denoised deviation representations into intrinsic deviation vectors capturing the most discriminative orthogonal deviation directions. At inference, IDEAL scores query-to-normal deviations preserved after projection onto the learned intrinsic deviation vectors, enabling generalization for both seen and unseen anomalies. Extensive experiments on eight real-world datasets show that IDEAL generalizes effectively to unseen anomalies and consistently outperforms existing state-of-the-art FSAD methods. Code and data will be available at \href{https://github.com/mala-lab/IDEAL}{https://github.com/mala-lab/IDEAL}.

Anomaly detection in physiological sensor data from Wireless Body Area Networks (WBANs) can be caused by sensor faults, network disruptions, or missing data, leading to false alarms. Hence, it demands both high predictive accuracy and clinically interpretable explanations. Existing approaches rely either on black-box models that achieve strong performance but offer no transparency, or on post-prediction explanation methods such as SHAP and LIME. In this paper, we propose the Distilled Explanation Model (DEM), a three-stage glass-box framework that distills the non-linear knowledge of a gradient boosting expert into an interpretable decision tree operating on residuals relative to a linear baseline, so that the explanation is not an approximation but the prediction itself. DEM introduces a novel distillation fidelity metric that quantifies how faithfully the explanation tree captures the expert model's non-linear contribution, providing a principled measure of explanation trustworthiness absent from prior interpretable models. Evaluated across four physiological datasets, including MIMIC-IV, WESAD, eICU, and an in-house SmartNet WBAN corpus, DEM achieves an AUC of 0.9964 on clinical contextual anomaly detection and 0.9047 on wearable stress detection while producing human-readable if-then rules at a controllable depth. Inference requires 0.17ms per 1000 samples, rendering DEM 1235x faster than SHAP-based post-hoc explanation and suitable for real-time physiological monitoring. Ablation studies confirm that the XGBoost distillation step provides measurable gains over naive residual fitting, and depth-sensitivity analysis demonstrates an explicit, user-controlled accuracy-interpretability trade-off unique to DEM among existing intrinsically interpretable models.