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Sen-Ching Samson Cheung

Publications and source records attributed to Sen-Ching Samson Cheung.

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Learning Class Difficulty via Dynamic Focal Attention for Histopathology Segmentation

Frequency-based loss reweighting, the standard remedy for imbalanced histopathology segmentation, implicitly assumes that rare classes are difficult. Yet difficulty also arises from morphological variability, boundary ambiguity, and contextual similarity, all largely orthogonal to class frequency. We propose Dynamic Focal Attention (DFA), a simple, efficient mechanism that learns class-specific difficulty directly within the cross-attention of query-based mask decoders. DFA adds a learnable per-class bias to the attention logits, reweighting representations before prediction rather than gradients after it. Initialised from a centred log-frequency prior to prevent gradient starvation and then optimised end-to-end, the bias adapts to difficulty signals as they emerge during training, unifying frequency- and difficulty-aware reweighting in a single attention-bias framework. On three benchmarks (BCSS, BDSA, CRAG), DFA consistently improves Dice and IoU, matching or exceeding a two-stage difficulty-aware baseline without a separate estimator or extra training stage. This shows that encoding difficulty at the representation level is a principled alternative to conventional loss reweighting.

eess.IV

Magnification-Aware Distillation (MAD): A Self-Supervised Framework for Unified Representation Learning in Gigapixel Whole-Slide Images

Whole-slide images (WSIs) contain tissue information distributed across multiple magnification levels, yet most self-supervised methods treat these scales as independent views. This separation prevents models from learning representations that remain stable when resolution changes, a key requirement for practical neuropathology workflows. This study introduces Magnification-Aware Distillation (MAD), a self-supervised strategy that links low-magnification context with spatially aligned high-magnification detail, enabling the model to learn how coarse tissue structure relates to fine cellular patterns. The resulting foundation model, MAD-NP, is trained entirely through this cross-scale correspondence without annotations. A linear classifier trained only on 10x embeddings maintains 96.7% of its performance when applied to unseen 40x tiles, demonstrating strong resolution-invariant representation learning. Segmentation outputs remain consistent across magnifications, preserving anatomical boundaries and minimizing noise. These results highlight the feasibility of scalable, magnification-robust WSI analysis using a unified embedding space

eess.IV