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Chengqian Zhao

Publications and source records attributed to Chengqian Zhao.

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GMENet: Generative Mixture of Experts Network for Multi-Center Glioma Diagnosis with Incomplete Imaging Sequences

Contemporary glioma diagnosis integrates molecular features with histopathology to guide clinical decision-making. However, in clinical settings, divergent imaging protocols result in incomplete MRI sequences, leading to two primary challenges: forcing existing frameworks to discard a large portion of clinical data during training and consequently limiting their clinical applicability. To address these limitations, we propose GMENet, a Generative Mixture of Experts Network for multi-center glioma diagnosis with incomplete imaging sequences. Firstly, we design a Cross-attention-based Gated Generation Module that synthesizes missing sequence features from available sequences via cross-attention and dynamic gating mechanisms, incorporating a cycle-consistency loss to preserve semantic integrity. Secondly, we introduce a Dynamically Weighted Experts Fusion Module that performs mixture-of-experts interaction and confidence-aware fusion over original and synthesized dual-sequence features for multi-task prediction. We evaluate GMENet on a multi-center cohort of 1,241 subjects from four in-house datasets and two public repositories. Experiments show that GMENet expands clinically usable training data by 97\%, relative to complete-sequence-only data. Furthermore, it consistently outperforms state-of-the-art methods trained on complete data, demonstrating improved robustness under cross-center distribution shifts.

eess.IV

SAMPO-Path: Segmentation Intent-Aligned Preference Optimization for Pathology Foundation Model Segmentation

Foundation models have shown strong performance in multi-object segmentation with visual prompts, yet histopathology images remain challenging due to high cellular density, heterogeneity, and the gap between pixel-level supervision and clinical segmentation intent (e.g., selectively segmenting nuclei of a specific type). In practice, such intents are expressed through diverse and noisy prompts, causing prompt-intent misalignment and inconsistent predictions. We introduce SAMPO (Segmentation Anything Model with Preference Optimization), a preference-aligned fine-tuning framework that explicitly aligns pathology foundation models with clinical segmentation intent. SAMPO is the first to adapt Direct Preference Optimization (DPO) to pure vision foundation models, enabling accurate segmentation from minimal and imperfect prompts. The framework features three key components: (1) online prompt-centric preference mining to synthesize preference pairs across prompt qualities; (2) multi-mask preference learning to leverage output ambiguity for fine-grained ranking supervision; and (3) a hybrid loss combining preference optimization with pixel-level supervision for stable training. Trained on two datasets covering four tasks and evaluated on corresponding test sets and 12 external validation datasets, SAMPO consistently improves segmentation accuracy, robustness to prompt variations, and clinical intent adherence in dense histopathology images.

cs.CV

MindShot: Multi-Shot Video Reconstruction from fMRI with LLM Decoding

Reconstructing dynamic videos from fMRI is important for understanding visual cognition and enabling vivid brain-computer interfaces. However, current methods are critically limited to single-shot clips, failing to address the multi-shot nature of real-world experiences. Multi-shot reconstruction faces fundamental challenges: fMRI signal mixing across shots, the temporal resolution mismatch between fMRI and video obscuring rapid scene changes, and the lack of dedicated multi-shot fMRI-video datasets. To overcome these limitations, we propose a novel divide-and-decode framework for multi-shot fMRI video reconstruction. Our core innovations are: (1) A shot boundary predictor module explicitly decomposing mixed fMRI signals into shot-specific segments. (2) Generative keyframe captioning using LLMs, which decodes robust textual descriptions from each segment, overcoming temporal blur by leveraging high-level semantics. (3) Novel large-scale data synthesis (20k samples) from existing datasets. Experimental results demonstrate our framework outperforms state-of-the-art methods in multi-shot reconstruction fidelity. Ablation studies confirm the critical role of fMRI decomposition and semantic captioning, with decomposition significantly improving decoded caption CLIP similarity by 71.8%. This work establishes a new paradigm for multi-shot fMRI reconstruction, enabling accurate recovery of complex visual narratives through explicit decomposition and semantic prompting.

cs.CV

Cross-Patient Pseudo Bags Generation and Curriculum Contrastive Learning for Imbalanced Multiclassification of Whole Slide Image

Pathology computing has dramatically improved pathologists' workflow and diagnostic decision-making processes. Although computer-aided diagnostic systems have shown considerable value in whole slide image (WSI) analysis, the problem of multi-classification under sample imbalance remains an intractable challenge. To address this, we propose learning fine-grained information by generating sub-bags with feature distributions similar to the original WSIs. Additionally, we utilize a pseudo-bag generation algorithm to further leverage the abundant and redundant information in WSIs, allowing efficient training in unbalanced-sample multi-classification tasks. Furthermore, we introduce an affinity-based sample selection and curriculum contrastive learning strategy to enhance the stability of model representation learning. Unlike previous approaches, our framework transitions from learning bag-level representations to understanding and exploiting the feature distribution of multi-instance bags. Our method demonstrates significant performance improvements on three datasets, including tumor classification and lymph node metastasis. On average, it achieves a 4.39-point improvement in F1 score compared to the second-best method across the three tasks, underscoring its superior performance.

cs.CV

TASL-Net: Tri-Attention Selective Learning Network for Intelligent Diagnosis of Bimodal Ultrasound Video

In the intelligent diagnosis of bimodal (gray-scale and contrast-enhanced) ultrasound videos, medical domain knowledge such as the way sonographers browse videos, the particular areas they emphasize, and the features they pay special attention to, plays a decisive role in facilitating precise diagnosis. Embedding medical knowledge into the deep learning network can not only enhance performance but also boost clinical confidence and reliability of the network. However, it is an intractable challenge to automatically focus on these person- and disease-specific features in videos and to enable networks to encode bimodal information comprehensively and efficiently. This paper proposes a novel Tri-Attention Selective Learning Network (TASL-Net) to tackle this challenge and automatically embed three types of diagnostic attention of sonographers into a mutual transformer framework for intelligent diagnosis of bimodal ultrasound videos. Firstly, a time-intensity-curve-based video selector is designed to mimic the temporal attention of sonographers, thus removing a large amount of redundant information while improving computational efficiency of TASL-Net. Then, to introduce the spatial attention of the sonographers for contrast-enhanced video analysis, we propose the earliest-enhanced position detector based on structural similarity variation, on which the TASL-Net is made to focus on the differences of perfusion variation inside and outside the lesion. Finally, by proposing a mutual encoding strategy that combines convolution and transformer, TASL-Net possesses bimodal attention to structure features on gray-scale videos and to perfusion variations on contrast-enhanced videos. These modules work collaboratively and contribute to superior performance. We conduct a detailed experimental validation of TASL-Net's performance on three datasets, including lung, breast, and liver.

cs.CV