Hangjun Che

Liang Peng, Yixuan Ye, Cheng Liu et al.

Multi-view clustering has been empirically shown to improve learning performance by leveraging the inherent complementary information across multiple views of data. However, in real-world scenarios, collecting strictly aligned views is challenging, and learning from both aligned and unaligned data becomes a more practical solution. Partially View-aligned Clustering aims to learn correspondences between misaligned view samples to better exploit the potential consistency and complementarity across views, including both aligned and unaligned data. However, most existing PVC methods fail to leverage unaligned data to capture the shared semantics among samples from the same cluster. Moreover, the inherent heterogeneity of multi-view data induces distributional shifts in representations, leading to inaccuracies in establishing meaningful correspondences between cross-view latent features and, consequently, impairing learning effectiveness. To address these challenges, we propose a Semantic MAtching contRasTive learning model (SMART) for PVC. The main idea of our approach is to alleviate the influence of cross-view distributional shifts, thereby facilitating semantic matching contrastive learning to fully exploit semantic relationships in both aligned and unaligned data. Extensive experiments on eight benchmark datasets demonstrate that our method consistently outperforms existing approaches on the PVC problem.

Hongzong Li, Jiahao Ma, Zhanpeng Shi et al.

Antibody binding site prediction plays a pivotal role in computational immunology and therapeutic antibody design. Existing sequence or structure methods rely on single-view features and fail to identify antibody-specific binding sites on the antigens. In this paper, we propose \textbf{CAME-AB}, a novel Cross-modality Attention framework with a Mixture-of-Experts (MoE) backbone for robust antibody binding site prediction. CAME-AB integrates five biologically grounded modalities, including raw amino acid encodings, BLOSUM substitution profiles, pretrained language model embeddings, structure-aware features, and GCN-refined biochemical graphs, into a unified multimodal representation. To enhance adaptive cross-modal reasoning, we propose an \emph{adaptive modality fusion} module that learns to dynamically weight each modality based on its global relevance and input-specific contribution. A Transformer encoder combined with an MoE module further promotes feature specialization and capacity expansion. We additionally incorporate a supervised contrastive learning objective to explicitly shape the latent space geometry, encouraging intra-class compactness and inter-class separability. To improve optimization stability and generalization, we apply stochastic weight averaging during training. Extensive experiments on benchmark antibody-antigen datasets demonstrate that CAME-AB consistently outperforms strong baselines on multiple metrics, including Precision, Recall, F1-score, AUC-ROC, and MCC. Ablation studies further validate the effectiveness of each architectural component and the benefit of multimodal feature integration. The model implementation details and the codes are available on https://anonymous.4open.science/r/CAME-AB-C525