arXiv subjects

Shaoliang Peng

Publications and source records attributed to Shaoliang Peng.

At least 19 recordsLinked to original sources

arXiv2026

Global kilometre-scale tropical cyclone inner-core vector winds from sparse scalar CYGNSS observations

Tropical cyclone (TC) inner-core surface wind vectors underpin intensity forecasting and storm-surge prediction, yet direct observations remain scarce: routine aircraft reconnaissance is confined to the North Atlantic and Eastern Pacific and, even there, samples each storm only episodically. CYGNSS is the only satellite that penetrates heavy precipitation to measure inner-core surface winds, but delivers directionless scalar wind speeds and is assimilated by no operational analysis system. Here we show that the full 10 m vector wind field inside the TC inner core can be reconstructed globally at 1.5 km resolution from sparse CYGNSS scalar observations alone, by generalising score-based diffusion assimilation to a nonlinear observation operator and injecting three TC boundary-layer constraints; we further propose a CYGNSS-intrinsic Observation Coverage Sufficiency (OCS) criterion that flags reliable reconstructions without external references. Applied to 4,955 snapshots of 249 TCs across all six active basins (2020-2022), the reconstructions reduce systematic Vmax bias against IBTrACS best-track by ~79% and ~75% relative to ERA5 and CCMP. Independent Tail Doppler Radar validation (47 storms) yields a wind speed RMSE of 6.9 m/s on the 23 coverage-sufficient cases (7.5 m/s overall); ablation across the full sample shows that the physical constraints cut wind-direction RMSE by 60% without degrading speed accuracy. The framework further supports joint assimilation of heterogeneous observations: adding only 11 dropsonde vectors to CYGNSS for TC FIONA (2022) reduces the cross-eye profile RMSE by 42%, outlining a practical pathway for fusing CYGNSS with SFMR, SAR and scatterometer data. The result is a globally consistent, observation-anchored kilometre-scale description of TC inner-core vector winds across all six active basins, including those without routine aircraft reconnaissance.

physics.ao-ph↗

arXiv2026

Diffusion Attention Expert Model for Predicting and Semi-automatic Localizing STAS in Lung Cancer Histopathological Images

Accurate intraoperative and postoperative diagnosis of spread through air spaces (STAS) is essential for guiding surgical decisions and postoperative management in lung cancer. However, histopathological assessment is labor-intensive and is prone to missed or incorrect diagnoses. We propose a Diffusion Attention Expert Model (DAEM) to detect STAS in frozen sections (FSs) and paraffin sections (PSs). Its diffusion attention expert module leverages full attention aggregation to learn multi-scale features from histopathological images, while a dual-branch architecture strengthens multi-scale feature representation. On an internal dataset, DAEM achieves AUCs of 0.8946 for FSs and 0.9112 for PSs. Validation on external multi-center datasets from eight institutions demonstrates strong generalizability and interpretability. Using tumor microenvironment (TME) features in PSs, we further enable semi-automatic measurement of STAS location and its distance from the primary tumor. Several quantitative TME metrics are identified as potential biomarkers for STAS, including micropapillary-type STAS. Overall, DAEM offers a clinically actionable framework for STAS assessment by enabling accurate and interpretable detection on FSs and PSs, supporting postoperative risk stratification through quantitative TME-based analysis.

cs.CV↗

arXiv2025

Annotation-Efficient Active Test-Time Adaptation with Conformal Prediction

Active Test-Time Adaptation (ATTA) improves model robustness under domain shift by selectively querying human annotations at deployment, but existing methods use heuristic uncertainty measures and suffer from low data selection efficiency, wasting human annotation budget. We propose Conformal Prediction Active TTA (CPATTA), which first brings principled, coverage-guaranteed uncertainty into ATTA. CPATTA employs smoothed conformal scores with a top-K certainty measure, an online weight-update algorithm driven by pseudo coverage, a domain-shift detector that adapts human supervision, and a staged update scheme balances human-labeled and model-labeled data. Extensive experiments demonstrate that CPATTA consistently outperforms the state-of-the-art ATTA methods by around 5% in accuracy. Our code and datasets are available at https://github.com/tingyushi/CPATTA.

cs.LG↗

arXiv2025

STAMP: Multi-pattern Attention-aware Multiple Instance Learning for STAS Diagnosis in Multi-center Histopathology Images

Spread through air spaces (STAS) constitutes a novel invasive pattern in lung adenocarcinoma (LUAD), associated with tumor recurrence and diminished survival rates. However, large-scale STAS diagnosis in LUAD remains a labor-intensive endeavor, compounded by the propensity for oversight and misdiagnosis due to its distinctive pathological characteristics and morphological features. Consequently, there is a pressing clinical imperative to leverage deep learning models for STAS diagnosis. This study initially assembled histopathological images from STAS patients at the Second Xiangya Hospital and the Third Xiangya Hospital of Central South University, alongside the TCGA-LUAD cohort. Three senior pathologists conducted cross-verification annotations to construct the STAS-SXY, STAS-TXY, and STAS-TCGA datasets. We then propose a multi-pattern attention-aware multiple instance learning framework, named STAMP, to analyze and diagnose the presence of STAS across multi-center histopathology images. Specifically, the dual-branch architecture guides the model to learn STAS-associated pathological features from distinct semantic spaces. Transformer-based instance encoding and a multi-pattern attention aggregation modules dynamically selects regions closely associated with STAS pathology, suppressing irrelevant noise and enhancing the discriminative power of global representations. Moreover, a similarity regularization constraint prevents feature redundancy across branches, thereby improving overall diagnostic accuracy. Extensive experiments demonstrated that STAMP achieved competitive diagnostic results on STAS-SXY, STAS-TXY and STAS-TCGA, with AUCs of 0.8058, 0.8017, and 0.7928, respectively, surpassing the clinical level.

cs.CV↗

arXiv2025

Generalizable Operating Room Expert with Multimodal Enhancement

Precise spatial modeling in the operating room (OR) is essential for intraoperative awareness, hazard avoidance, and surgical decision-making. Although existing approaches exploit multimodal data to learn spatial relationships, many depend on sensing modalities that are difficult to deploy in real clinical environments and remain limited in explicit 3D reasoning under constrained sensing conditions. Meanwhile, models trained primarily on readily available 2D data often fail to capture the fine-grained geometric and semantic structure of complex OR scenes. To address these limitations, we introduce \textbf{OR-Expert}, a large vision-language framework for 3D spatial reasoning with RGB-only inference. OR-Expert internally derives depth, panoptic segmentation, and point-cloud cues from RGB images and encodes them as structured spatial representations. Its Spatial-Enhanced Feature Fusion Block aligns these pseudo-modalities with RGB and textual features in a shared token space, enabling joint semantic, geometric, and language reasoning. The unified end-to-end MLLM therefore supports detailed spatial understanding without requiring external depth, segmentation, or point-cloud sensors, or additional expert annotations at inference time. Experiments on multiple operating-room benchmarks demonstrate that OR-Expert achieves state-of-the-art performance and generalizes effectively to unseen surgical scenes and downstream spatial reasoning tasks.

cs.CV↗

arXiv2025

PathGene: Benchmarking Driver Gene Mutations and Exon Prediction Using Multicenter Lung Cancer Histopathology Image Dataset

Accurately predicting gene mutations, mutation subtypes and their exons in lung cancer is critical for personalized treatment planning and prognostic assessment. Faced with regional disparities in medical resources and the high cost of genomic assays, using artificial intelligence to infer these mutations and exon variants from routine histopathology images could greatly facilitate precision therapy. Although some prior studies have shown that deep learning can accelerate the prediction of key gene mutations from lung cancer pathology slides, their performance remains suboptimal and has so far been limited mainly to early screening tasks. To address these limitations, we have assembled PathGene, which comprises histopathology images paired with next-generation sequencing reports from 1,576 patients at the Second Xiangya Hospital, Central South University, and 448 TCGA-LUAD patients. This multi-center dataset links whole-slide images to driver gene mutation status, mutation subtypes, exon, and tumor mutational burden (TMB) status, with the goal of leveraging pathology images to predict mutations, subtypes, exon locations, and TMB for early genetic screening and to advance precision oncology. Unlike existing datasets, we provide molecular-level information related to histopathology images in PathGene to facilitate the development of biomarker prediction models. We benchmarked 11 multiple-instance learning methods on PathGene for mutation, subtype, exon, and TMB prediction tasks. These experimental methods provide valuable alternatives for early genetic screening of lung cancer patients and assisting clinicians to quickly develop personalized precision targeted treatment plans for patients. Code and data are available at https://github.com/panliangrui/NIPS2025/.

q-bio.GN↗

arXiv2025

DLiPath: A Benchmark for the Comprehensive Assessment of Donor Liver Based on Histopathological Image Dataset

Pathologists comprehensive evaluation of donor liver biopsies provides crucial information for accepting or discarding potential grafts. However, rapidly and accurately obtaining these assessments intraoperatively poses a significant challenge for pathologists. Features in donor liver biopsies, such as portal tract fibrosis, total steatosis, macrovesicular steatosis, and hepatocellular ballooning are correlated with transplant outcomes, yet quantifying these indicators suffers from substantial inter- and intra-observer variability. To address this, we introduce DLiPath, the first benchmark for comprehensive donor liver assessment based on a histopathology image dataset. We collected and publicly released 636 whole slide images from 304 donor liver patients at the Department of Pathology, the Third Xiangya Hospital, with expert annotations for key pathological features (including cholestasis, portal tract fibrosis, portal inflammation, total steatosis, macrovesicular steatosis, and hepatocellular ballooning). We selected nine state-of-the-art multiple-instance learning (MIL) models based on the DLiPath dataset as baselines for extensive comparative analysis. The experimental results demonstrate that several MIL models achieve high accuracy across donor liver assessment indicators on DLiPath, charting a clear course for future automated and intelligent donor liver assessment research. Data and code are available at https://github.com/panliangrui/ACM_MM_2025.

eess.IV↗

arXiv2025

SMILE: a Scale-aware Multiple Instance Learning Method for Multicenter STAS Lung Cancer Histopathology Diagnosis

Spread through air spaces (STAS) represents a newly identified aggressive pattern in lung cancer, which is known to be associated with adverse prognostic factors and complex pathological features. Pathologists currently rely on time consuming manual assessments, which are highly subjective and prone to variation. This highlights the urgent need for automated and precise diag nostic solutions. 2,970 lung cancer tissue slides are comprised from multiple centers, re-diagnosed them, and constructed and publicly released three lung cancer STAS datasets: STAS CSU (hospital), STAS TCGA, and STAS CPTAC. All STAS datasets provide corresponding pathological feature diagnoses and related clinical data. To address the bias, sparse and heterogeneous nature of STAS, we propose an scale-aware multiple instance learning(SMILE) method for STAS diagnosis of lung cancer. By introducing a scale-adaptive attention mechanism, the SMILE can adaptively adjust high attention instances, reducing over-reliance on local regions and promoting consistent detection of STAS lesions. Extensive experiments show that SMILE achieved competitive diagnostic results on STAS CSU, diagnosing 251 and 319 STAS samples in CPTAC andTCGA,respectively, surpassing clinical average AUC. The 11 open baseline results are the first to be established for STAS research, laying the foundation for the future expansion, interpretability, and clinical integration of computational pathology technologies. The datasets and code are available at https://anonymous.4open.science/r/IJCAI25-1DA1.

cs.CV↗

arXiv2024

Feature-interactive Siamese graph encoder-based image analysis to predict STAS from histopathology images in lung cancer

Spread through air spaces (STAS) is a distinct invasion pattern in lung cancer, crucial for prognosis assessment and guiding surgical decisions. Histopathology is the gold standard for STAS detection, yet traditional methods are subjective, time-consuming, and prone to misdiagnosis, limiting large-scale applications. We present VERN, an image analysis model utilizing a feature-interactive Siamese graph encoder to predict STAS from lung cancer histopathological images. VERN captures spatial topological features with feature sharing and skip connections to enhance model training. Using 1,546 histopathology slides, we built a large single-cohort STAS lung cancer dataset. VERN achieved an AUC of 0.9215 in internal validation and AUCs of 0.8275 and 0.8829 in frozen and paraffin-embedded test sections, respectively, demonstrating clinical-grade performance. Validated on a single-cohort and three external datasets, VERN showed robust predictive performance and generalizability, providing an open platform (http://plr.20210706.xyz:5000/) to enhance STAS diagnosis efficiency and accuracy.

eess.IV↗

arXiv2024

FedDP: Privacy-preserving method based on federated learning for histopathology image segmentation

Hematoxylin and Eosin (H&E) staining of whole slide images (WSIs) is considered the gold standard for pathologists and medical practitioners for tumor diagnosis, surgical planning, and post-operative assessment. With the rapid advancement of deep learning technologies, the development of numerous models based on convolutional neural networks and transformer-based models has been applied to the precise segmentation of WSIs. However, due to privacy regulations and the need to protect patient confidentiality, centralized storage and processing of image data are impractical. Training a centralized model directly is challenging to implement in medical settings due to these privacy concerns.This paper addresses the dispersed nature and privacy sensitivity of medical image data by employing a federated learning framework, allowing medical institutions to collaboratively learn while protecting patient privacy. Additionally, to address the issue of original data reconstruction through gradient inversion during the federated learning training process, differential privacy introduces noise into the model updates, preventing attackers from inferring the contributions of individual samples, thereby protecting the privacy of the training data.Experimental results show that the proposed method, FedDP, minimally impacts model accuracy while effectively safeguarding the privacy of cancer pathology image data, with only a slight decrease in Dice, Jaccard, and Acc indices by 0.55%, 0.63%, and 0.42%, respectively. This approach facilitates cross-institutional collaboration and knowledge sharing while protecting sensitive data privacy, providing a viable solution for further research and application in the medical field.

cs.CV↗

arXiv2024

FORESEE: Multimodal and Multi-view Representation Learning for Robust Prediction of Cancer Survival

Integrating the different data modalities of cancer patients can significantly improve the predictive performance of patient survival. However, most existing methods ignore the simultaneous utilization of rich semantic features at different scales in pathology images. When collecting multimodal data and extracting features, there is a likelihood of encountering intra-modality missing data, introducing noise into the multimodal data. To address these challenges, this paper proposes a new end-to-end framework, FORESEE, for robustly predicting patient survival by mining multimodal information. Specifically, the cross-fusion transformer effectively utilizes features at the cellular level, tissue level, and tumor heterogeneity level to correlate prognosis through a cross-scale feature cross-fusion method. This enhances the ability of pathological image feature representation. Secondly, the hybrid attention encoder (HAE) uses the denoising contextual attention module to obtain the contextual relationship features and local detail features of the molecular data. HAE's channel attention module obtains global features of molecular data. Furthermore, to address the issue of missing information within modalities, we propose an asymmetrically masked triplet masked autoencoder to reconstruct lost information within modalities. Extensive experiments demonstrate the superiority of our method over state-of-the-art methods on four benchmark datasets in both complete and missing settings.

cs.CV↗

arXiv2024

Opportunities and challenges in the application of large artificial intelligence models in radiology

Influenced by ChatGPT, artificial intelligence (AI) large models have witnessed a global upsurge in large model research and development. As people enjoy the convenience by this AI large model, more and more large models in subdivided fields are gradually being proposed, especially large models in radiology imaging field. This article first introduces the development history of large models, technical details, workflow, working principles of multimodal large models and working principles of video generation large models. Secondly, we summarize the latest research progress of AI large models in radiology education, radiology report generation, applications of unimodal and multimodal radiology. Finally, this paper also summarizes some of the challenges of large AI models in radiology, with the aim of better promoting the rapid revolution in the field of radiography.

cs.CV↗

arXiv2024

SELECTOR: Heterogeneous graph network with convolutional masked autoencoder for multimodal robust prediction of cancer survival

Accurately predicting the survival rate of cancer patients is crucial for aiding clinicians in planning appropriate treatment, reducing cancer-related medical expenses, and significantly enhancing patients' quality of life. Multimodal prediction of cancer patient survival offers a more comprehensive and precise approach. However, existing methods still grapple with challenges related to missing multimodal data and information interaction within modalities. This paper introduces SELECTOR, a heterogeneous graph-aware network based on convolutional mask encoders for robust multimodal prediction of cancer patient survival. SELECTOR comprises feature edge reconstruction, convolutional mask encoder, feature cross-fusion, and multimodal survival prediction modules. Initially, we construct a multimodal heterogeneous graph and employ the meta-path method for feature edge reconstruction, ensuring comprehensive incorporation of feature information from graph edges and effective embedding of nodes. To mitigate the impact of missing features within the modality on prediction accuracy, we devised a convolutional masked autoencoder (CMAE) to process the heterogeneous graph post-feature reconstruction. Subsequently, the feature cross-fusion module facilitates communication between modalities, ensuring that output features encompass all features of the modality and relevant information from other modalities. Extensive experiments and analysis on six cancer datasets from TCGA demonstrate that our method significantly outperforms state-of-the-art methods in both modality-missing and intra-modality information-confirmed cases. Our codes are made available at https://github.com/panliangrui/Selector.

cs.CV↗

arXiv2024

MGTUNet: An new UNet for colon nuclei instance segmentation and quantification

Colorectal cancer (CRC) is among the top three malignant tumor types in terms of morbidity and mortality. Histopathological images are the gold standard for diagnosing colon cancer. Cellular nuclei instance segmentation and classification, and nuclear component regression tasks can aid in the analysis of the tumor microenvironment in colon tissue. Traditional methods are still unable to handle both types of tasks end-to-end at the same time, and have poor prediction accuracy and high application costs. This paper proposes a new UNet model for handling nuclei based on the UNet framework, called MGTUNet, which uses Mish, Group normalization and transposed convolution layer to improve the segmentation model, and a ranger optimizer to adjust the SmoothL1Loss values. Secondly, it uses different channels to segment and classify different types of nucleus, ultimately completing the nuclei instance segmentation and classification task, and the nuclei component regression task simultaneously. Finally, we did extensive comparison experiments using eight segmentation models. By comparing the three evaluation metrics and the parameter sizes of the models, MGTUNet obtained 0.6254 on PQ, 0.6359 on mPQ, and 0.8695 on R2. Thus, the experiments demonstrated that MGTUNet is now a state-of-the-art method for quantifying histopathological images of colon cancer.

cs.CV↗

arXiv2023

ESM-NBR: fast and accurate nucleic acid-binding residue prediction via protein language model feature representation and multi-task learning

Protein-nucleic acid interactions play a very important role in a variety of biological activities. Accurate identification of nucleic acid-binding residues is a critical step in understanding the interaction mechanisms. Although many computationally based methods have been developed to predict nucleic acid-binding residues, challenges remain. In this study, a fast and accurate sequence-based method, called ESM-NBR, is proposed. In ESM-NBR, we first use the large protein language model ESM2 to extract discriminative biological properties feature representation from protein primary sequences; then, a multi-task deep learning model composed of stacked bidirectional long short-term memory (BiLSTM) and multi-layer perceptron (MLP) networks is employed to explore common and private information of DNA- and RNA-binding residues with ESM2 feature as input. Experimental results on benchmark data sets demonstrate that the prediction performance of ESM2 feature representation comprehensively outperforms evolutionary information-based hidden Markov model (HMM) features. Meanwhile, the ESM-NBR obtains the MCC values for DNA-binding residues prediction of 0.427 and 0.391 on two independent test sets, which are 18.61 and 10.45% higher than those of the second-best methods, respectively. Moreover, by completely discarding the time-cost multiple sequence alignment process, the prediction speed of ESM-NBR far exceeds that of existing methods (5.52s for a protein sequence of length 500, which is about 16 times faster than the second-fastest method). A user-friendly standalone package and the data of ESM-NBR are freely available for academic use at: https://github.com/wwzll123/ESM-NBR.

q-bio.QM↗

arXiv2023

LDCSF: Local depth convolution-based Swim framework for classifying multi-label histopathology images

Histopathological images are the gold standard for diagnosing liver cancer. However, the accuracy of fully digital diagnosis in computational pathology needs to be improved. In this paper, in order to solve the problem of multi-label and low classification accuracy of histopathology images, we propose a locally deep convolutional Swim framework (LDCSF) to classify multi-label histopathology images. In order to be able to provide local field of view diagnostic results, we propose the LDCSF model, which consists of a Swin transformer module, a local depth convolution (LDC) module, a feature reconstruction (FR) module, and a ResNet module. The Swin transformer module reduces the amount of computation generated by the attention mechanism by limiting the attention to each window. The LDC then reconstructs the attention map and performs convolution operations in multiple channels, passing the resulting feature map to the next layer. The FR module uses the corresponding weight coefficient vectors obtained from the channels to dot product with the original feature map vector matrix to generate representative feature maps. Finally, the residual network undertakes the final classification task. As a result, the classification accuracy of LDCSF for interstitial area, necrosis, non-tumor and tumor reached 0.9460, 0.9960, 0.9808, 0.9847, respectively. Finally, we use the results of multi-label pathological image classification to calculate the tumor-to-stromal ratio, which lays the foundation for the analysis of the microenvironment of liver cancer histopathological images. Second, we released a multilabel histopathology image of liver cancer, our code and data are available at https://github.com/panliangrui/LSF.

cs.CV↗

arXiv2023

CVFC: Attention-Based Cross-View Feature Consistency for Weakly Supervised Semantic Segmentation of Pathology Images

Histopathology image segmentation is the gold standard for diagnosing cancer, and can indicate cancer prognosis. However, histopathology image segmentation requires high-quality masks, so many studies now use imagelevel labels to achieve pixel-level segmentation to reduce the need for fine-grained annotation. To solve this problem, we propose an attention-based cross-view feature consistency end-to-end pseudo-mask generation framework named CVFC based on the attention mechanism. Specifically, CVFC is a three-branch joint framework composed of two Resnet38 and one Resnet50, and the independent branch multi-scale integrated feature map to generate a class activation map (CAM); in each branch, through down-sampling and The expansion method adjusts the size of the CAM; the middle branch projects the feature matrix to the query and key feature spaces, and generates a feature space perception matrix through the connection layer and inner product to adjust and refine the CAM of each branch; finally, through the feature consistency loss and feature cross loss to optimize the parameters of CVFC in co-training mode. After a large number of experiments, An IoU of 0.7122 and a fwIoU of 0.7018 are obtained on the WSSS4LUAD dataset, which outperforms HistoSegNet, SEAM, C-CAM, WSSS-Tissue, and OEEM, respectively.

cs.CV↗

arXiv2023

PACS: Prediction and analysis of cancer subtypes from multi-omics data based on a multi-head attention mechanism model

Due to the high heterogeneity and clinical characteristics of cancer, there are significant differences in multi-omic data and clinical characteristics among different cancer subtypes. Therefore, accurate classification of cancer subtypes can help doctors choose the most appropriate treatment options, improve treatment outcomes, and provide more accurate patient survival predictions. In this study, we propose a supervised multi-head attention mechanism model (SMA) to classify cancer subtypes successfully. The attention mechanism and feature sharing module of the SMA model can successfully learn the global and local feature information of multi-omics data. Second, it enriches the parameters of the model by deeply fusing multi-head attention encoders from Siamese through the fusion module. Validated by extensive experiments, the SMA model achieves the highest accuracy, F1 macroscopic, F1 weighted, and accurate classification of cancer subtypes in simulated, single-cell, and cancer multiomics datasets compared to AE, CNN, and GNN-based models. Therefore, we contribute to future research on multiomics data using our attention-based approach.

q-bio.QM↗