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Multimodality eye disease screening is crucial in ophthalmology as it integrates information from diverse sources to complement their respective performances. However, the existing methods are weak in assessing the reliability of each unimodality, and directly fusing an unreliable modality may cause screening errors. To address this issue, we introduce a novel multimodality evidential fusion pipeline for eye disease screening, EyeMoSt, which provides a measure of confidence for unimodality and elegantly integrates the multimodality information from a multi-distribution fusion perspective. Specifically, our model estimates both local uncertainty for unimodality and global uncertainty for the fusion modality to produce reliable classification results. More importantly, the proposed mixture of Student's $t$ distributions adaptively integrates different modalities to endow the model with heavy-tailed properties, increasing robustness and reliability. Our experimental findings on both public and in-house datasets show that our model is more reliable than current methods. Additionally, EyeMost has the potential ability to serve as a data quality discriminator, enabling reliable decision-making for multimodality eye disease screening.

Assessing the robustness of deep neural networks against out-of-distribution inputs is crucial, especially in safety-critical domains like autonomous driving, but also in safety systems where malicious actors can digitally alter inputs to circumvent safety guards. However, designing effective out-of-distribution tests that encompass all possible scenarios while preserving accurate label information is a challenging task. Existing methodologies often entail a compromise between variety and constraint levels for attacks and sometimes even both. In a first step towards a more holistic robustness evaluation of image classification models, we introduce an attack method based on image solarization that is conceptually straightforward yet avoids jeopardizing the global structure of natural images independent of the intensity. Through comprehensive evaluations of multiple ImageNet models, we demonstrate the attack's capacity to degrade accuracy significantly, provided it is not integrated into the training augmentations. Interestingly, even then, no full immunity to accuracy deterioration is achieved. In other settings, the attack can often be simplified into a black-box attack with model-independent parameters. Defenses against other corruptions do not consistently extend to be effective against our specific attack. Project website: //github.com/paulgavrikov/adversarial_solarization

In clinical dictation, utterances after automatic speech recognition (ASR) without explicit punctuation marks may lead to the misunderstanding of dictated reports. To give a precise and understandable clinical report with ASR, automatic punctuation restoration is required. Considering a practical scenario, we propose a fast and light pre-trained model for Chinese medical punctuation restoration based on 'pretraining and fine-tuning' paradigm. In this work, we distill pre-trained models by incorporating supervised contrastive learning and a novel auxiliary pre-training task (Punctuation Mark Prediction) to make it well-suited for punctuation restoration. Our experiments on various distilled models reveal that our model can achieve 95% performance while 10% model size relative to state-of-the-art Chinese RoBERTa.

Precision medicine fundamentally aims to establish causality between dysregulated biochemical mechanisms and cancer subtypes. Omics-based cancer subtyping has emerged as a revolutionary approach, as different level of omics records the biochemical products of multistep processes in cancers. This paper focuses on fully exploiting the potential of multi-omics data to improve cancer subtyping outcomes, and hence developed MoCLIM, a representation learning framework. MoCLIM independently extracts the informative features from distinct omics modalities. Using a unified representation informed by contrastive learning of different omics modalities, we can well-cluster the subtypes, given cancer, into a lower latent space. This contrast can be interpreted as a projection of inter-omics inference observed in biological networks. Experimental results on six cancer datasets demonstrate that our approach significantly improves data fit and subtyping performance in fewer high-dimensional cancer instances. Moreover, our framework incorporates various medical evaluations as the final component, providing high interpretability in medical analysis.

Deep learning models have achieved state-of-the-art results in estimating brain age, which is an important brain health biomarker, from magnetic resonance (MR) images. However, most of these models only provide a global age prediction, and rely on techniques, such as saliency maps to interpret their results. These saliency maps highlight regions in the input image that were significant for the model's predictions, but they are hard to be interpreted, and saliency map values are not directly comparable across different samples. In this work, we reframe the age prediction problem from MR images to an image-to-image regression problem where we estimate the brain age for each brain voxel in MR images. We compare voxel-wise age prediction models against global age prediction models and their corresponding saliency maps. The results indicate that voxel-wise age prediction models are more interpretable, since they provide spatial information about the brain aging process, and they benefit from being quantitative.

Segmenting cells and tracking their motion over time is a common task in biomedical applications. However, predicting accurate instance-wise segmentation and cell motions from microscopy imagery remains a challenging task. Using microstructured environments for analyzing single cells in a constant flow of media adds additional complexity. While large-scale labeled microscopy datasets are available, we are not aware of any large-scale dataset, including both cells and microstructures. In this paper, we introduce the trapped yeast cell (TYC) dataset, a novel dataset for understanding instance-level semantics and motions of cells in microstructures. We release $105$ dense annotated high-resolution brightfield microscopy images, including about $19$k instance masks. We also release $261$ curated video clips composed of $1293$ high-resolution microscopy images to facilitate unsupervised understanding of cell motions and morphology. TYC offers ten times more instance annotations than the previously largest dataset, including cells and microstructures. Our effort also exceeds previous attempts in terms of microstructure variability, resolution, complexity, and capturing device (microscopy) variability. We facilitate a unified comparison on our novel dataset by introducing a standardized evaluation strategy. TYC and evaluation code are publicly available under CC BY 4.0 license.

Instance segmentation in electron microscopy (EM) volumes poses a significant challenge due to the complex morphology of instances and insufficient annotations. Self-supervised learning has recently emerged as a promising solution, enabling the acquisition of prior knowledge of cellular tissue structures that are essential for EM instance segmentation. However, existing pretraining methods often lack the ability to capture complex visual patterns and relationships between voxels, which results in the acquired prior knowledge being insufficient for downstream EM analysis tasks. In this paper, we propose a novel pretraining framework that leverages multiscale visual representations to capture both voxel-level and feature-level consistency in EM volumes. Specifically, our framework enforces voxel-level consistency between the outputs of a Siamese network by a reconstruction function, and incorporates a cross-attention mechanism for soft feature matching to achieve fine-grained feature-level consistency. Moreover, we propose a contrastive learning scheme on the feature pyramid to extract discriminative features across multiple scales. We extensively pretrain our method on four large-scale EM datasets, achieving promising performance improvements in representative tasks of neuron and mitochondria instance segmentation.

Graph transformers need strong inductive biases to derive meaningful attention scores. Yet, current proposals rarely address methods capturing longer ranges, hierarchical structures, or community structures, as they appear in various graphs such as molecules, social networks, and citation networks. In this paper, we propose a hierarchy-distance structural encoding (HDSE), which models a hierarchical distance between the nodes in a graph focusing on its multi-level, hierarchical nature. In particular, this yields a framework which can be flexibly integrated with existing graph transformers, allowing for simultaneous application with other positional representations. Through extensive experiments on 12 real-world datasets, we demonstrate that our HDSE method successfully enhances various types of baseline transformers, achieving state-of-the-art empirical performances on 10 benchmark datasets.

We propose a novel attention gate (AG) model for medical imaging that automatically learns to focus on target structures of varying shapes and sizes. Models trained with AGs implicitly learn to suppress irrelevant regions in an input image while highlighting salient features useful for a specific task. This enables us to eliminate the necessity of using explicit external tissue/organ localisation modules of cascaded convolutional neural networks (CNNs). AGs can be easily integrated into standard CNN architectures such as the U-Net model with minimal computational overhead while increasing the model sensitivity and prediction accuracy. The proposed Attention U-Net architecture is evaluated on two large CT abdominal datasets for multi-class image segmentation. Experimental results show that AGs consistently improve the prediction performance of U-Net across different datasets and training sizes while preserving computational efficiency. The code for the proposed architecture is publicly available.

Object tracking is challenging as target objects often undergo drastic appearance changes over time. Recently, adaptive correlation filters have been successfully applied to object tracking. However, tracking algorithms relying on highly adaptive correlation filters are prone to drift due to noisy updates. Moreover, as these algorithms do not maintain long-term memory of target appearance, they cannot recover from tracking failures caused by heavy occlusion or target disappearance in the camera view. In this paper, we propose to learn multiple adaptive correlation filters with both long-term and short-term memory of target appearance for robust object tracking. First, we learn a kernelized correlation filter with an aggressive learning rate for locating target objects precisely. We take into account the appropriate size of surrounding context and the feature representations. Second, we learn a correlation filter over a feature pyramid centered at the estimated target position for predicting scale changes. Third, we learn a complementary correlation filter with a conservative learning rate to maintain long-term memory of target appearance. We use the output responses of this long-term filter to determine if tracking failure occurs. In the case of tracking failures, we apply an incrementally learned detector to recover the target position in a sliding window fashion. Extensive experimental results on large-scale benchmark datasets demonstrate that the proposed algorithm performs favorably against the state-of-the-art methods in terms of efficiency, accuracy, and robustness.