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Author

Chenbin Ma

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Open access Sep 2026

SeaMamba: Frequency-Stabilized Selective State-Space Multiscale Detection for SAR Ships in Complex Maritime Scenes

Ship detection in synthetic aperture radar (SAR) imagery remains challenging because near-shore clutter, coherent speckle noise, dense scattering responses, and large target-scale variations often obscure vessel boundaries and weaken small-ship signatures. Although single-stage detectors provide efficient inference, their predominantly local convolutional modeling and fixed multiscale fusion strategies are insufficient for capturing long-range sea-surface context and adaptively emphasizing discriminative ship responses. To address these limitations, this paper proposes SeaMamba, a frequency-stabilized selective state-space multiscale detector for SAR ship detection in complex maritime scenes. Specifically, a frequency-domain speckle prior is introduced to stabilize SAR inputs while preserving target localization cues. A bidirectional selective state-space modeling module is then used to propagate long-range contextual information with input-adaptive scanning. Furthermore, a gated pyramid reassembly module is designed to refine multiscale features before dense prediction. The proposed method is evaluated on the SAR Ship Detection Dataset (SSDD) and High-Resolution SAR Images Dataset (HRSID) under a unified five-fold cross-validation protocol. SeaMamba achieved mean average precision at an intersection-over-union threshold of 0.5 (mAP@0.5) values of 99.16 ± 0.11% on SSDD and 93.74 ± 0.15% on HRSID. Per-category evaluation, ablation studies, efficiency analysis, and Grad-CAM-based interpretability visualization further demonstrate that SeaMamba improves small-vessel detection, suppresses near-shore false responses, and maintains a practical accuracy-efficiency trade-off.

Xiao-Peng Song, Zhong-Biao Sheng, Shi-Wei Li et al. · 0 citations
Open access Jul 2026

Rethinking pathology image analysis through shuffling

Pathological examination is the current gold standard in cancer diagnosis, yet artificial intelligence (AI) methods still struggle to capture the multi-scale heterogeneity of tumor morphology across patients, tissues, and magnifications. Here, we introduce the PAthoentity Shuffle Strategy (PASS), a principled framework that explicitly models pathoentities, the critical biological structures such as cells, glands, and tissues, and their hierarchical relationships. By controlled shuffling of pathoentities within and across samples, PASS enriches the relational structure available to neural networks, encouraging them to learn both local homogeneity and global heterogeneity. We provide theoretical analysis showing that PASS achieves error bounds comparable to state-of-the-art methods, supporting shuffling as a generalizable computational principle rather than a heuristic. Extensive evaluation on 10 datasets spanning 8 diseases, 9 organs, and 4 magnification levels demonstrates consistent performance gains, robust generalization, and scalability across diverse pathological contexts. Importantly, PASS further shows translational value in a rapid onsite evaluation (ROSE) scenario in gastroenterology, highlighting its potential for clinical deployment. Overall, this study establishes pathoentity shuffling as an effective principle for pathological image analysis, bridging biological insight and computational design to enhance diagnostic modeling and morphological hierarchy learning.

Zeyu Liu, Tianyi Zhang, Brian K. Chen et al. · 0 citations

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