Deep cross-modal hashing has become an essential tool for supervised multimodal search. These models tend to be optimized with large, curated multimodal datasets, where most labels have been manually verified. Unfortunately, in many scenarios, such accurate labeling may not be avail-able. In contrast, datasets with low-quality annotations may be acquired, which inevitably introduce numerous mis-takes or label noise and therefore degrade the search per-formance. To address the challenge, we present a general robust cross-modal hashing framework to correlate distinct modalities and combat noisy labels simultaneously. More specifically, we propose a proxy-based contrastive (PC) loss to mitigate the gap between different modalities and train networks for different modalities Jointly with small-loss samples that are selected with the PC loss and a mu-tual quantization loss. The small-loss sample selection from such Joint loss can help choose confident examples to guide the model training, and the mutual quantization loss can maximize the agreement between different modalities and is beneficial to improve the effectiveness of sample selection. Experiments on three widely-used multimodal datasets show that our method significantly outperforms existing state-of-the-arts.

Multi-modal neuroimage retrieval has greatly facilitated the efficiency and accuracy of decision making in clinical practice by providing physicians with previous cases (with visually similar neuroimages) and corresponding treatment records. However, existing methods for image retrieval usually fail when applied directly to multi-modal neuroimage databases, since neuroimages generally have smaller inter-class variation and larger inter-modal discrepancy compared to natural images. To this end, we propose a deep Bayesian hash learning framework, called CenterHash, which can map multi-modal data into a shared Hamming space and learn discriminative hash codes from imbalanced multi-modal neuroimages. The key idea to tackle the small inter-class variation and large inter-modal discrepancy is to learn a common center representation for similar neuroimages from different modalities and encourage hash codes to be explicitly close to their corresponding center representations. Specifically, we measure the similarity between hash codes and their corresponding center representations and treat it as a center prior in the proposed Bayesian learning framework. A weighted contrastive likelihood loss function is also developed to facilitate hash learning from imbalanced neuroimage pairs. Comprehensive empirical evidence shows that our method can generate effective hash codes and yield state-of-the-art performance in cross-modal retrieval on three multi-modal neuroimage datasets.

Brain connectivity alterations associated with mental disorders have been widely reported in both functional MRI (fMRI) and diffusion MRI (dMRI). However, extracting useful information from the vast amount of information afforded by brain networks remains a great challenge. Capturing network topology, graph convolutional networks (GCNs) have demonstrated to be superior in learning network representations tailored for identifying specific brain disorders. Existing graph construction techniques generally rely on a specific brain parcellation to define regions-of-interest (ROIs) to construct networks, often limiting the analysis into a single spatial scale. In addition, most methods focus on the pairwise relationships between the ROIs and ignore high-order associations between subjects. In this letter, we propose a mutual multi-scale triplet graph convolutional network (MMTGCN) to analyze functional and structural connectivity for brain disorder diagnosis. We first employ several templates with different scales of ROI parcellation to construct coarse-to-fine brain connectivity networks for each subject. Then, a triplet GCN (TGCN) module is developed to learn functional/structural representations of brain connectivity networks at each scale, with the triplet relationship among subjects explicitly incorporated into the learning process. Finally, we propose a template mutual learning strategy to train different scale TGCNs collaboratively for disease classification. Experimental results on 1,160 subjects from three datasets with fMRI or dMRI data demonstrate that our MMTGCN outperforms several state-of-the-art methods in identifying three types of brain disorders.