V-FIND: Revealing the Intrinsic Forgery Knowledge Encoded in Video Forgery Detectors

As generated videos become increasingly realistic, reliable video forgery detection is increasingly important. Existing studies typically optimize and use video forgery detectors as black boxes, while the latent forgery-discriminative knowledge inside them remains largely unexplored. Instead of continuing to rely on resource-intensive full-model retraining to steadily improve detection performance, we ask whether video forgery detection can also be achieved by uncovering and activating sparse forensic knowledge within the detector. We find that forgery-discriminative knowledge is not uniformly distributed across the full representation space, but is concentrated in a sparse set of functionally specialized neurons. Based on this insight, we propose a video forgery-intrinsic neuron discovery (V-FIND) framework. V-FIND first localizes critical layers that exhibit pronounced discrepancies between real and forged videos, and then identifies latent anchor neurons that consistently carry forgery-discriminative signals, organizing them into a compact forensic subspace. With the original backbone frozen and only a lightweight linear classifier trained, this subspace still delivers strong detection performance across multiple external benchmarks for generated videos. Further neuron intervention experiments provide direct evidence for the functional specificity of the discovered neurons. Overall, these results suggest that video forgery detectors contain sparse, extractable, and reusable forgery-discriminative knowledge, offering a new perspective on understanding and exploiting their intrinsic forensic capability.

MSD-Score: Multi-Scale Distributional Scoring for Reference-Free Image Caption Evaluation

Evaluating image captions without references remains challenging because global embedding similarity often misses fine-grained mismatches such as hallucinated objects, missing attributes, or incorrect relations. We propose MSD-Score, a reference-free metric that models image patch and text token embeddings as von Mises-Fisher mixtures on the unit hypersphere. Instead of treating each modality as a single point, MSD-Score formulates image-text matching as a multi-scale distributional scoring problem. Semantic discrepancies are quantified via a weighted bi-directional KL divergence and combined with global similarity in a multi-scale framework for both single- and multi-candidate evaluations. Extensive experiments show that MSD-Score achieves state-of-the-art correlation with human judgments among reference-free metrics. Beyond accuracy, its probabilistic formulation yields transparent and decomposable diagnostics of local grounding errors, providing a deterministic complementary signal to holistic similarity metrics and judge-based evaluators.

Dynamic Residual Encoding with Slide-Level Contrastive Learning for End-to-End Whole Slide Image Representation

Whole Slide Image (WSI) representation is critical for cancer subtyping, cancer recognition and mutation prediction.Training an end-to-end WSI representation model poses significant challenges, as a standard gigapixel slide can contain tens of thousands of image tiles, making it difficult to compute gradients of all tiles in a single mini-batch due to current GPU limitations. To address this challenge, we propose a method of dynamic residual encoding with slide-level contrastive learning (DRE-SLCL) for end-to-end WSI representation. Our approach utilizes a memory bank to store the features of tiles across all WSIs in the dataset. During training, a mini-batch usually contains multiple WSIs. For each WSI in the batch, a subset of tiles is randomly sampled and their features are computed using a tile encoder. Then, additional tile features from the same WSI are selected from the memory bank. The representation of each individual WSI is generated using a residual encoding technique that incorporates both the sampled features and those retrieved from the memory bank. Finally, the slide-level contrastive loss is computed based on the representations and histopathology reports ofthe WSIs within the mini-batch. Experiments conducted over cancer subtyping, cancer recognition, and mutation prediction tasks proved the effectiveness of the proposed DRE-SLCL method.

HRDecoder: High-Resolution Decoder Network for Fundus Image Lesion Segmentation

High resolution is crucial for precise segmentation in fundus images, yet handling high-resolution inputs incurs considerable GPU memory costs, with diminishing performance gains as overhead increases. To address this issue while tackling the challenge of segmenting tiny objects, recent studies have explored local-global fusion methods. These methods preserve fine details using local regions and capture long-range context information from downscaled global images. However, the necessity of multiple forward passes inevitably incurs significant computational overhead, adversely affecting inference speed. In this paper, we propose HRDecoder, a simple High-Resolution Decoder network for fundus lesion segmentation. It integrates a high-resolution representation learning module to capture fine-grained local features and a high-resolution fusion module to fuse multi-scale predictions. Our method effectively improves the overall segmentation accuracy of fundus lesions while consuming reasonable memory and computational overhead, and maintaining satisfying inference speed. Experimental results on the IDRID and DDR datasets demonstrate the effectiveness of our method. Code is available at https://github.com/CVIU-CSU/HRDecoder.

An efficient framework based on large foundation model for cervical cytopathology whole slide image screening

Current cervical cytopathology whole slide image (WSI) screening primarily relies on detection-based approaches, which are limited in performance due to the expense and time-consuming annotation process. Multiple Instance Learning (MIL), a weakly supervised approach that relies solely on bag-level labels, can effectively alleviate these challenges. Nonetheless, MIL commonly employs frozen pretrained models or self-supervised learning for feature extraction, which suffers from low efficacy or inefficiency. In this paper, we propose an efficient framework for cervical cytopathology WSI classification using only WSI-level labels through unsupervised and weakly supervised learning. Given the sparse and dispersed nature of abnormal cells within cytopathological WSIs, we propose a strategy that leverages the pretrained foundation model to filter the top$k$ high-risk patches. Subsequently, we suggest parameter-efficient fine-tuning (PEFT) of a large foundation model using contrastive learning on the filtered patches to enhance its representation ability for task-specific signals. By training only the added linear adapters, we enhance the learning of patch-level features with substantially reduced time and memory consumption. Experiments conducted on the CSD and FNAC 2019 datasets demonstrate that the proposed method enhances the performance of various MIL methods and achieves state-of-the-art (SOTA) performance. The code and trained models are publicly available at https://github.com/CVIU-CSU/TCT-InfoNCE.

Unsupervised Collaborative Metric Learning with Mixed-Scale Groups for General Object Retrieval

The task of searching for visual objects in a large image dataset is difficult because it requires efficient matching and accurate localization of objects that can vary in size. Although the segment anything model (SAM) offers a potential solution for extracting object spatial context, learning embeddings for local objects remains a challenging problem. This paper presents a novel unsupervised deep metric learning approach, termed unsupervised collaborative metric learning with mixed-scale groups (MS-UGCML), devised to learn embeddings for objects of varying scales. Following this, a benchmark of challenges is assembled by utilizing COCO 2017 and VOC 2007 datasets to facilitate the training and evaluation of general object retrieval models. Finally, we conduct comprehensive ablation studies and discuss the complexities faced within the domain of general object retrieval. Our object retrieval evaluations span a range of datasets, including BelgaLogos, Visual Genome, LVIS, in addition to a challenging evaluation set that we have individually assembled for open-vocabulary evaluation. These comprehensive evaluations effectively highlight the robustness of our unsupervised MS-UGCML approach, with an object level and image level mAPs improvement of up to 6.69% and 10.03%, respectively. The code is publicly available at https://github.com/dengyuhai/MS-UGCML.

Coded Residual Transform for Generalizable Deep Metric Learning

A fundamental challenge in deep metric learning is the generalization capability of the feature embedding network model since the embedding network learned on training classes need to be evaluated on new test classes. To address this challenge, in this paper, we introduce a new method called coded residual transform (CRT) for deep metric learning to significantly improve its generalization capability. Specifically, we learn a set of diversified prototype features, project the feature map onto each prototype, and then encode its features using their projection residuals weighted by their correlation coefficients with each prototype. The proposed CRT method has the following two unique characteristics. First, it represents and encodes the feature map from a set of complimentary perspectives based on projections onto diversified prototypes. Second, unlike existing transformer-based feature representation approaches which encode the original values of features based on global correlation analysis, the proposed coded residual transform encodes the relative differences between the original features and their projected prototypes. Embedding space density and spectral decay analysis show that this multi-perspective projection onto diversified prototypes and coded residual representation are able to achieve significantly improved generalization capability in metric learning. Finally, to further enhance the generalization performance, we propose to enforce the consistency on their feature similarity matrices between coded residual transforms with different sizes of projection prototypes and embedding dimensions. Our extensive experimental results and ablation studies demonstrate that the proposed CRT method outperform the state-of-the-art deep metric learning methods by large margins and improving upon the current best method by up to 4.28% on the CUB dataset.

Exploring Contextual Relationships for Cervical Abnormal Cell Detection

Cervical abnormal cell detection is a challenging task as the morphological discrepancies between abnormal and normal cells are usually subtle. To determine whether a cervical cell is normal or abnormal, cytopathologists always take surrounding cells as references to identify its abnormality. To mimic these behaviors, we propose to explore contextual relationships to boost the performance of cervical abnormal cell detection. Specifically, both contextual relationships between cells and cell-to-global images are exploited to enhance features of each region of interest (RoI) proposals. Accordingly, two modules, dubbed as RoI-relationship attention module (RRAM) and global RoI attention module (GRAM), are developed and their combination strategies are also investigated. We establish a strong baseline by using Double-Head Faster R-CNN with feature pyramid network (FPN) and integrate our RRAM and GRAM into it to validate the effectiveness of the proposed modules. Experiments conducted on a large cervical cell detection dataset reveal that the introduction of RRAM and GRAM both achieves better average precision (AP) than the baseline methods. Moreover, when cascading RRAM and GRAM, our method outperforms the state-of-the-art (SOTA) methods. Furthermore, we also show the proposed feature enhancing scheme can facilitate both image-level and smear-level classification. The code and trained models are publicly available at https://github.com/CVIU-CSU/CR4CACD.

M2MRF: Many-to-Many Reassembly of Features for Tiny Lesion Segmentation in Fundus Images

Feature reassembly is an essential component in modern CNNs-based segmentation approaches, which includes feature downsampling and upsampling operators. Existing feature reassembly operators reassemble multiple features from a small predefined region into one for each target location independently. This may result in loss of spatial information, which could vanish activations of tiny lesions particularly when they cluster together. In this paper, we propose a many-to-many reassembly of features (M2MRF). It reassembles features in a dimension-reduced feature space and simultaneously aggregates multiple features inside a large predefined region into multiple target features. In this way, long range spatial dependencies are captured to maintain activations on tiny lesions, particularly when multiple lesions coexist. Experimental results on two lesion segmentation benchmarks, i.e. DDR and IDRiD, show that our M2MRF outperforms existing feature reassembly operators.

Dual-Branch Network with Dual-Sampling Modulated Dice Loss for Hard Exudate Segmentation from Colour Fundus Images

Automated segmentation of hard exudates in colour fundus images is a challenge task due to issues of extreme class imbalance and enormous size variation. This paper aims to tackle these issues and proposes a dual-branch network with dual-sampling modulated Dice loss. It consists of two branches: large hard exudate biased learning branch and small hard exudate biased learning branch. Both of them are responsible for their own duty separately. Furthermore, we propose a dual-sampling modulated Dice loss for the training such that our proposed dual-branch network is able to segment hard exudates in different sizes. In detail, for the first branch, we use a uniform sampler to sample pixels from predicted segmentation mask for Dice loss calculation, which leads to this branch naturally be biased in favour of large hard exudates as Dice loss generates larger cost on misidentification of large hard exudates than small hard exudates. For the second branch, we use a re-balanced sampler to oversample hard exudate pixels and undersample background pixels for loss calculation. In this way, cost on misidentification of small hard exudates is enlarged, which enforces the parameters in the second branch fit small hard exudates well. Considering that large hard exudates are much easier to be correctly identified than small hard exudates, we propose an easy-to-difficult learning strategy by adaptively modulating the losses of two branches. We evaluate our proposed method on two public datasets and results demonstrate that ours achieves state-of-the-art performances.