Jie Sun

Xudong Mou, Rui Wang, Tiejun Wang et al.

Time series anomaly detection (TSAD) is a vital yet challenging task, particularly in scenarios where labeled anomalies are scarce and temporal dependencies are complex. Recent anomaly assumption (AA) approaches alleviate the lack of anomalies by injecting synthetic samples and training discriminative models. Despite promising results, these methods often suffer from two fundamental limitations: patchy generation, where scattered anomaly knowledge leads to overly simplistic or incoherent anomaly injection, and Anomaly Shift, where synthetic anomalies either resemble normal data too closely or diverge unrealistically from real anomalies, thereby distorting classification boundaries. In this paper, we propose CAPMix, a controllable anomaly augmentation framework that addresses both issues. First, we design a CutAddPaste mechanism to inject diverse and complex anomalies in a targeted manner, avoiding patchy generation. Second, we introduce a label revision strategy to adaptively refine anomaly labels, reducing the risk of anomaly shift. Finally, we employ dual-space mixup within a temporal convolutional network to enforce smoother and more robust decision boundaries. Extensive experiments on five benchmark datasets, including AIOps, UCR, SWaT, WADI, and ESA, demonstrate that CAPMix achieves significant improvements over state-of-the-art baselines, with enhanced robustness against contaminated training data. The code is available at https://github.com/alsike22/CAPMix.

Kai Yao, Zhaorui Tan, Zixian Su et al.

Open compound domain adaptation (OCDA) aims to transfer knowledge from a labeled source domain to a mix of unlabeled homogeneous compound target domains while generalizing to open unseen domains. Existing OCDA methods solve the intra-domain gaps by a divide-and-conquer strategy, which divides the problem into several individual and parallel domain adaptation (DA) tasks. Such approaches often contain multiple sub-networks or stages, which may constrain the model's performance. In this work, starting from the general DA theory, we establish the generalization bound for the setting of OCDA. Built upon this, we argue that conventional OCDA approaches may substantially underestimate the inherent variance inside the compound target domains for model generalization. We subsequently present Stochastic Compound Mixing (SCMix), an augmentation strategy with the primary objective of mitigating the divergence between source and mixed target distributions. We provide theoretical analysis to substantiate the superiority of SCMix and prove that the previous methods are sub-groups of our methods. Extensive experiments show that our method attains a lower empirical risk on OCDA semantic segmentation tasks, thus supporting our theories. Combining the transformer architecture, SCMix achieves a notable performance boost compared to the SoTA results.

Kai Yao, Kaizhu Huang, Jie Sun et al.

Automatic nuclei segmentation and classification play a vital role in digital pathology. However, previous works are mostly built on data with limited diversity and small sizes, making the results questionable or misleading in actual downstream tasks. In this paper, we aim to build a reliable and robust method capable of dealing with data from the 'the clinical wild'. Specifically, we study and design a new method to simultaneously detect, segment, and classify nuclei from Haematoxylin and Eosin (H&E) stained histopathology data, and evaluate our approach using the recent largest dataset: PanNuke. We address the detection and classification of each nuclei as a novel semantic keypoint estimation problem to determine the center point of each nuclei. Next, the corresponding class-agnostic masks for nuclei center points are obtained using dynamic instance segmentation. Meanwhile, we proposed a novel Joint Pyramid Fusion Module (JPFM) to model the cross-scale dependencies, thus enhancing the local feature for better nuclei detection and classification. By decoupling two simultaneous challenging tasks and taking advantage of JPFM, our method can benefit from class-aware detection and class-agnostic segmentation, thus leading to a significant performance boost. We demonstrate the superior performance of our proposed approach for nuclei segmentation and classification across 19 different tissue types, delivering new benchmark results.

Kai Yao, Kaizhu Huang, Jie Sun et al.

We consider unsupervised cell nuclei segmentation in this paper. Exploiting the recently-proposed unpaired image-to-image translation between cell nuclei images and randomly synthetic masks, existing approaches, e.g., CycleGAN, have achieved encouraging results. However, these methods usually take a two-stage pipeline and fail to learn end-to-end in cell nuclei images. More seriously, they could lead to the lossy transformation problem, i.e., the content inconsistency between the original images and the corresponding segmentation output. To address these limitations, we propose a novel end-to-end unsupervised framework called Aligned Disentangling Generative Adversarial Network (AD-GAN). Distinctively, AD-GAN introduces representation disentanglement to separate content representation (the underling spatial structure) from style representation (the rendering of the structure). With this framework, spatial structure can be preserved explicitly, enabling a significant reduction of macro-level lossy transformation. We also propose a novel training algorithm able to align the disentangled content in the latent space to reduce micro-level lossy transformation. Evaluations on real-world 2D and 3D datasets show that AD-GAN substantially outperforms the other comparison methods and the professional software both quantitatively and qualitatively. Specifically, the proposed AD-GAN leads to significant improvement over the current best unsupervised methods by an average 17.8% relatively (w.r.t. the metric DICE) on four cell nuclei datasets. As an unsupervised method, AD-GAN even performs competitive with the best supervised models, taking a further leap towards end-to-end unsupervised nuclei segmentation.