Abstract:The Platonic Representation Hypothesis claims that recent foundation models are converging to a shared representation space as a function of their downstream task performance, irrespective of the objectives and data modalities used to train these models. Representational similarity is generally measured for individual datasets and is not necessarily consistent across datasets. Thus, one may wonder whether this convergence of model representations is confounded by the datasets commonly used in machine learning. Here, we propose a systematic way to measure how representational similarity between models varies with the set of stimuli used to construct the representations. We find that the objective function is the most crucial factor in determining the consistency of representational similarities across datasets. Specifically, self-supervised vision models learn representations whose relative pairwise similarities generalize better from one dataset to another compared to those of image classification or image-text models. Moreover, the correspondence between representational similarities and the models' task behavior is dataset-dependent, being most strongly pronounced for single-domain datasets. Our work provides a framework for systematically measuring similarities of model representations across datasets and linking those similarities to differences in task behavior.
Abstract:Multiple instance learning (MIL) is an effective and widely used approach for weakly supervised machine learning. In histopathology, MIL models have achieved remarkable success in tasks like tumor detection, biomarker prediction, and outcome prognostication. However, MIL explanation methods are still lagging behind, as they are limited to small bag sizes or disregard instance interactions. We revisit MIL through the lens of explainable AI (XAI) and introduce xMIL, a refined framework with more general assumptions. We demonstrate how to obtain improved MIL explanations using layer-wise relevance propagation (LRP) and conduct extensive evaluation experiments on three toy settings and four real-world histopathology datasets. Our approach consistently outperforms previous explanation attempts with particularly improved faithfulness scores on challenging biomarker prediction tasks. Finally, we showcase how xMIL explanations enable pathologists to extract insights from MIL models, representing a significant advance for knowledge discovery and model debugging in digital histopathology.