Immunohistochemical (IHC) virtual staining is a task that generates virtual IHC images from H&E images while maintaining pathological semantic consistency with adjacent slices. This task aims to achieve cross-domain mapping between morphological structures and staining patterns through generative models, providing an efficient and cost-effective solution for pathological analysis. However, under weakly paired conditions, spatial heterogeneity between adjacent slices presents significant challenges. This can lead to inaccurate one-to-many mappings and generate results that are inconsistent with the pathological semantics of adjacent slices. To address this issue, we propose a novel unbalanced self-information feature transport for IHC virtual staining, named USIGAN, which extracts global morphological semantics without relying on positional correspondence. By removing weakly paired terms in the joint marginal distribution, we effectively mitigate the impact of weak pairing on joint distributions, thereby significantly improving the content consistency and pathological semantic consistency of the generated results. Moreover, we design the Unbalanced Optimal Transport Consistency Mining (UOT-CTM) mechanism and the Pathology Self-Correspondence Mining (PC-SCM) mechanism to construct correlation matrices between H&E and generated IHC in image-level and real IHC and generated IHC image sets in intra-group level. Experiments conducted on two publicly available datasets demonstrate that our method achieves superior performance across multiple clinically significant metrics, such as IoD and Pearson-R correlation, demonstrating better clinical relevance. The code is available at: https://github.com/MIXAILAB/USIGAN.

Medical image segmentation plays a crucial role in computer-aided diagnosis and treatment planning. Unsupervised segmentation methods that can effectively leverage unlabeled data bring significant promise in clinical application. However, they remain a challenging task in maintaining anatomical structure topological consistency that often produces anatomical structure breaks, connectivity errors, or boundary discontinuities. To address these issues, we propose a novel Unsupervised Topological-Aware Diffusion Condensation Network (UTADC-Net) for medical image segmentation. Specifically, we design a diffusion condensation-based framework that achieves structural consistency in segmentation results by effectively modeling long-range dependencies between pixels and incorporating topological constraints. First, to effectively fuse local details and global semantic information, we employ a pixel-centric patch embedding module by simultaneously modeling local structural features and inter-region interactions. Second, to enhance the topological consistency of segmentation results, we introduce an adaptive topological constraint mechanism that guides the network to learn anatomically aligned structural representations through pixel-level topological relationships and corresponding loss functions. Extensive experiments conducted on three public medical image datasets demonstrate that our proposed UTADC-Net significantly outperforms existing unsupervised methods in terms of segmentation accuracy and topological structure preservation. Notably, our method demonstrates segmentation results with excellent anatomical structural consistency. These results indicate that our framework provides a novel and practical solution for unsupervised medical image segmentation.

Immunohistochemical (IHC) staining enables precise molecular profiling of protein expression, with over 200 clinically available antibody-based tests in modern pathology. However, comprehensive IHC analysis is frequently limited by insufficient tissue quantities in small biopsies. Therefore, virtual multiplex staining emerges as an innovative solution to digitally transform H&E images into multiple IHC representations, yet current methods still face three critical challenges: 1) inadequate semantic guidance for multi-staining, 2) inconsistent distribution of immunochemistry staining, and 3) spatial misalignment across different stain modalities. To overcome these limitations, we present a prompt-guided framework for virtual multiplex IHC staining using only uniplex training data (PGVMS). Our framework introduces three key innovations corresponding to each challenge: First, an adaptive prompt guidance mechanism employing a pathological visual language model dynamically adjusts staining prompts to resolve semantic guidance limitations (Challenge 1). Second, our protein-aware learning strategy (PALS) maintains precise protein expression patterns by direct quantification and constraint of protein distributions (Challenge 2). Third, the prototype-consistent learning strategy (PCLS) establishes cross-image semantic interaction to correct spatial misalignments (Challenge 3). Evaluated on two benchmark datasets, PGVMS demonstrates superior performance in pathological consistency. In general, PGVMS represents a paradigm shift from dedicated single-task models toward unified virtual staining systems.

Virtual staining leverages computer-aided techniques to transfer the style of histochemically stained tissue samples to other staining types. In virtual staining of pathological images, maintaining strict structural consistency is crucial, as these images emphasize structural integrity more than natural images. Even slight structural alterations can lead to deviations in diagnostic semantic information. Furthermore, the unpaired characteristic of virtual staining data may compromise the preservation of pathological diagnostic content. To address these challenges, we propose a dual-path inversion virtual staining method using prompt learning, which optimizes visual prompts to control content and style, while preserving complete pathological diagnostic content. Our proposed inversion technique comprises two key components: (1) Dual Path Prompted Strategy, we utilize a feature adapter function to generate reference images for inversion, providing style templates for input image inversion, called Style Target Path. We utilize the inversion of the input image as the Structural Target path, employing visual prompt images to maintain structural consistency in this path while preserving style information from the style Target path. During the deterministic sampling process, we achieve complete content-style disentanglement through a plug-and-play embedding visual prompt approach. (2) StainPrompt Optimization, where we only optimize the null visual prompt as ``operator'' for dual path inversion, rather than fine-tune pre-trained model. We optimize null visual prompt for structual and style trajectory around pivotal noise on each timestep, ensuring accurate dual-path inversion reconstruction. Extensive evaluations on publicly available multi-domain unpaired staining datasets demonstrate high structural consistency and accurate style transfer results.

Feature-based hardware Trojan (HT) detection method has gained its popularity recently because it does not need any test patterns or golden models. However, HT feature database is to be expanded due to emergence of new HTs. We present in this paper a method based on the structural characteristics of single-triggered HTs. Various structure templates are extracted from gate-level netlists, and a scoring approach and an outlier determination algorithm are proposed. Gates with a high (outlier) score, i.e. highly matched to the templates, are considered as Trojan candidates. Experimental results show that the proposed method can detect 39 out of 40 single-triggered HTs from TrustHub, with low false positive rate (average 0.04%) and a time overhead of 0.02s ~ 2000s. The proposed method makes a good supplement to existing Trojan feature database.