Prototypical-part methods, e.g., ProtoPNet, enhance interpretability in image recognition by linking predictions to training prototypes, thereby offering intuitive insights into their decision-making. Existing methods, which rely on a point-based learning of prototypes, typically face two critical issues: 1) the learned prototypes have limited representation power and are not suitable to detect Out-of-Distribution (OoD) inputs, reducing their decision trustworthiness; and 2) the necessary projection of the learned prototypes back into the space of training images causes a drastic degradation in the predictive performance. Furthermore, current prototype learning adopts an aggressive approach that considers only the most active object parts during training, while overlooking sub-salient object regions which still hold crucial classification information. In this paper, we present a new generative paradigm to learn prototype distributions, termed as Mixture of Gaussian-distributed Prototypes (MGProto). The distribution of prototypes from MGProto enables both interpretable image classification and trustworthy recognition of OoD inputs. The optimisation of MGProto naturally projects the learned prototype distributions back into the training image space, thereby addressing the performance degradation caused by prototype projection. Additionally, we develop a novel and effective prototype mining strategy that considers not only the most active but also sub-salient object parts. To promote model compactness, we further propose to prune MGProto by removing prototypes with low importance priors. Experiments on CUB-200-2011, Stanford Cars, Stanford Dogs, and Oxford-IIIT Pets datasets show that MGProto achieves state-of-the-art image recognition and OoD detection performances, while providing encouraging interpretability results.

Constructing effective representation of lesions is essential for disease classification and localization in medical image analysis. Prototype-based models address this by leveraging visual prototypes to capture representative lesion patterns, yet effectively handling the complexity of diverse lesion characteristics remains a critical challenge, as they typically rely on single-level, fixed-size prototypes and suffer from prototype redundancy. In this paper, we present HierProtoPNet, a new prototype-based framework designed to handle the complexity of lesions in medical images. HierProtoPNet leverages hierarchical visual prototypes across different semantic feature granularities to effectively capture diverse lesion patterns. To prevent redundancy and increase utility of the prototypes, we devise a novel prototype mining paradigm to progressively discover semantically distinct prototypes, offering multi-level complementary analysis of lesions. Also, we introduce a dynamic knowledge distillation strategy that allows transferring essential classification information across hierarchical levels, thereby improving generalisation performance. Comprehensive experiments show that HierProtoPNet achieves state-of-the-art classification performances in three benchmarks: binary breast cancer screening, multi-class retinal disease diagnosis, and multi-label chest X-ray classification. Quantitative assessments also illustrate HierProtoPNet's significant advantages in weakly-supervised disease localisation and segmentation.

Recent advances in prototypical learning have shown remarkable potential to provide useful decision interpretations associating activation maps and predictions with class-specific training prototypes. Such prototypical learning has been well-studied for various single-label diseases, but for quite relevant and more challenging multi-label diagnosis, where multiple diseases are often concurrent within an image, existing prototypical learning models struggle to obtain meaningful activation maps and effective class prototypes due to the entanglement of the multiple diseases. In this paper, we present a novel Cross- and Intra-image Prototypical Learning (CIPL) framework, for accurate multi-label disease diagnosis and interpretation from medical images. CIPL takes advantage of common cross-image semantics to disentangle the multiple diseases when learning the prototypes, allowing a comprehensive understanding of complicated pathological lesions. Furthermore, we propose a new two-level alignment-based regularisation strategy that effectively leverages consistent intra-image information to enhance interpretation robustness and predictive performance. Extensive experiments show that our CIPL attains the state-of-the-art (SOTA) classification accuracy in two public multi-label benchmarks of disease diagnosis: thoracic radiography and fundus images. Quantitative interpretability results show that CIPL also has superiority in weakly-supervised thoracic disease localisation over other leading saliency- and prototype-based explanation methods.

Audio-visual segmentation (AVS) is a challenging task that involves accurately segmenting sounding objects based on audio-visual cues. The effectiveness of audio-visual learning critically depends on achieving accurate cross-modal alignment between sound and visual objects. Successful audio-visual learning requires two essential components: 1) a challenging dataset with high-quality pixel-level multiclass annotated images associated with audio files, and 2) a model that can establish strong links between audio information and its corresponding visual object. However, these requirements are only partially addressed by current methods, with training sets containing biased audio-visual data, and models that generalise poorly beyond this biased training set. In this work, we propose a new cost-effective strategy to build challenging and relatively unbiased high-quality audio-visual segmentation benchmarks. We also propose a new informative sample mining method for audio-visual supervised contrastive learning to leverage discriminative contrastive samples to enforce cross-modal understanding. We show empirical results that demonstrate the effectiveness of our benchmark. Furthermore, experiments conducted on existing AVS datasets and on our new benchmark show that our method achieves state-of-the-art (SOTA) segmentation accuracy11This work was supported by Australian Research Council through grant FT190100525.

The deployment of automated deep-learning classifiers in clinical practice has the potential to streamline the diagnosis process and improve the diagnosis accuracy, but the acceptance of those classifiers relies on both their accuracy and interpretability. In general, accurate deep-learning classifiers provide little model interpretability, while interpretable models do not have competitive classification accuracy. In this paper, we introduce a new deep-learning diagnosis framework, called InterNRL, that is designed to be highly accurate and interpretable. InterNRL consists of a student-teacher framework, where the student model is an interpretable prototype-based classifier (ProtoPNet) and the teacher is an accurate global image classifier (GlobalNet). The two classifiers are mutually optimised with a novel reciprocal learning paradigm in which the student ProtoPNet learns from optimal pseudo labels produced by the teacher GlobalNet, while GlobalNet learns from ProtoPNet's classification performance and pseudo labels. This reciprocal learning paradigm enables InterNRL to be flexibly optimised under both fully- and semi-supervised learning scenarios, reaching state-of-the-art classification performance in both scenarios for the tasks of breast cancer and retinal disease diagnosis. Moreover, relying on weakly-labelled training images, InterNRL also achieves superior breast cancer localisation and brain tumour segmentation results than other competing methods.

Prototypical part network (ProtoPNet) methods have been designed to achieve interpretable classification by associating predictions with a set of training prototypes, which we refer to as trivial prototypes because they are trained to lie far from the classification boundary in the feature space. Note that it is possible to make an analogy between ProtoPNet and support vector machine (SVM) given that the classification from both methods relies on computing similarity with a set of training points (i.e., trivial prototypes in ProtoPNet, and support vectors in SVM). However, while trivial prototypes are located far from the classification boundary, support vectors are located close to this boundary, and we argue that this discrepancy with the well-established SVM theory can result in ProtoPNet models with inferior classification accuracy. In this paper, we aim to improve the classification of ProtoPNet with a new method to learn support prototypes that lie near the classification boundary in the feature space, as suggested by the SVM theory. In addition, we target the improvement of classification results with a new model, named ST-ProtoPNet, which exploits our support prototypes and the trivial prototypes to provide more effective classification. Experimental results on CUB-200-2011, Stanford Cars, and Stan-ford Dogs datasets demonstrate that ST-ProtoPNet achieves state-of-the-art classification accuracy and interpretability results. We also show that the proposed support prototypes tend to be better localised in the object of interest rather than in the background region.