Publications by authors named "Suyu Dong"

The development of large, high-quality ECG datasets is essential for advancing automated cardiac disease diagnosis. However, challenges such as limited access to data, small dataset sizes, and class imbalances persist. Deep generative models offer an effective solution by generating synthetic ECG data, which not only addresses data scarcity but also enhances data privacy.

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Diffusion models, as a class of generative models, have demonstrated significant performance in image generation since their inception. The fundamental principle behind diffusion models is the definition of a forward process and a reverse process. The input data is progressively perturbed by adding random noise during the forward process, and the expected noise distribution is learned.

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Purpose: In order to automate the centerline extraction of the coronary tree, three challenges must be addressed: tracking branches automatically, passing through plaques successfully, and detecting endpoints accurately. This study aims to develop a method to solve the three challenges.

Methods: We propose a branch-endpoint-aware coronary centerline extraction framework.

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In domain continual medical image segmentation, distillation-based methods mitigate catastrophic forgetting by continuously reviewing old knowledge. However, these approaches often exhibit biases towards both new and old knowledge simultaneously due to confounding factors, which can undermine segmentation performance. To address these biases, we propose the Causality-Adjusted Data Augmentation (CauAug) framework, introducing a novel causal intervention strategy called the Texture-Domain Adjustment Hybrid-Scheme (TDAHS) alongside two causality-targeted data augmentation approaches: the Cross Kernel Network (CKNet) and the Fourier Transformer Generator (FTGen).

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In recent years, semi-supervised methods have been rapidly developed for three-dimensional (3D) medical image analysis. However, previous semi-supervised methods for three-dimensional medical images usually focused on single-view information and required a large number of annotated datasets. In this paper, we innovatively propose a multi-view (coronal and transverse) attention network for semi-supervised 3D cardiac image segmentation.

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Medical vision-language pretraining (VLP) that leverages naturally-paired medical image-report data is crucial for medical image analysis. However, existing methods struggle to accurately characterize associations between images and diseases, leading to inaccurate or incomplete diagnostic results. In this work, we propose MedFILIP, a fine-grained VLP model, introduces medical image-specific knowledge through contrastive learning, specifically: 1) An information extractor based on a large language model is proposed to decouple comprehensive disease details from reports, which excels in extracting disease deals through flexible prompt engineering, thereby effectively reducing text complexity while retaining rich information at a tiny cost.

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The lumen centerline of the coronary artery allows vessel reconstruction used to detect stenoses and plaques. Discrete-action-based centerline extraction methods suffer from artifacts and plaques. This study aimed to develop a continuous-action-based method which performs more effectively in cases involving artifacts or plaques.

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Introduction: In clinical, the echocardiogram is the most widely used for diagnosing heart diseases. Different heart diseases are diagnosed based on different views of the echocardiogram images, so efficient echocardiogram view classification can help cardiologists diagnose heart disease rapidly. Echocardiogram view classification is mainly divided into supervised and semi-supervised methods.

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A generic and versatile CT Image Reconstruction (CTIR) scheme can efficiently mitigate imaging noise resulting from inherent physical limitations, substantially bolstering the dependability of CT imaging diagnostics across a wider spectrum of patient cases. Current CTIR techniques often concentrate on distinct areas such as Low-Dose CT denoising (LDCTD), Sparse-View CT reconstruction (SVCTR), and Metal Artifact Reduction (MAR). Nevertheless, due to the intricate nature of multi-scenario CTIR, these techniques frequently narrow their focus to specific tasks, resulting in limited generalization capabilities for diverse scenarios.

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Accurate prediction of binding between human leukocyte antigen (HLA) class I molecules and antigenic peptide segments is a challenging task and a key bottleneck in personalized immunotherapy for cancer. Although existing prediction tools have demonstrated significant results using established datasets, most can only predict the binding affinity of antigenic peptides to HLA and do not enable the immunogenic interpretation of new antigenic epitopes. This limitation results from the training data for the computational models relying heavily on a large amount of peptide-HLA (pHLA) eluting ligand data, in which most of the candidate epitopes lack immunogenicity.

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While significant strides have been made in predicting neoepitopes that trigger autologous CD4+ T cell responses, accurately identifying the antigen presentation by human leukocyte antigen (HLA) class II molecules remains a challenge. This identification is critical for developing vaccines and cancer immunotherapies. Current prediction methods are limited, primarily due to a lack of high-quality training epitope datasets and algorithmic constraints.

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Motivation: Understanding the intermolecular interactions of ligand-target pairs is key to guiding the optimization of drug research on cancers, which can greatly mitigate overburden workloads for wet labs. Several improved computational methods have been introduced and exhibit promising performance for these identification tasks, but some pitfalls restrict their practical applications: (i) first, existing methods do not sufficiently consider how multigranular molecule representations influence interaction patterns between proteins and compounds; and (ii) second, existing methods seldom explicitly model the binding sites when an interaction occurs to enable better prediction and interpretation, which may lead to unexpected obstacles to biological researchers.

Results: To address these issues, we here present DrugMGR, a deep multigranular drug representation model capable of predicting binding affinities and regions for each ligand-target pair.

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Domain continual medical image segmentation plays a crucial role in clinical settings. This approach enables segmentation models to continually learn from a sequential data stream across multiple domains. However, it faces the challenge of catastrophic forgetting.

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Motivation: Accurate identification of target proteins that interact with drugs is a vital step , which can significantly foster the development of drug repurposing and drug discovery. In recent years, numerous deep learning-based methods have been introduced to treat drug-target interaction (DTI) prediction as a classification task. The output of this task is binary identification suggesting the absence or presence of interactions.

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Objective: Existing methods for automated coronary artery branch labeling in cardiac CT angiography face two limitations: 1) inability to model overall correlation of branches, since differences between branches cannot be captured directly. 2) a serious class imbalance between main and side branches.

Methods And Procedures: Inspired by the application of Transformer in sequence data, we propose a topological Transformer network (TTN), which solves the vessel branch labeling from a novel perspective of sequence labeling learning.

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Cardiac diseases have high mortality rates and are a significant threat to human health. Echocardiography is a commonly used imaging technique to diagnose cardiac diseases because of its portability, non-invasiveness and low cost. Precise segmentation of basic cardiac structures is crucial for cardiologists to efficiently diagnose cardiac diseases, but this task is challenging due to several reasons, such as: (1) low image contrast, (2) incomplete structures of cardiac, and (3) unclear border between the ventricle and the atrium in some echocardiographic images.

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The heart is a relatively complex non-rigid motion organ in the human body. Quantitative motion analysis of the heart takes on a critical significance to help doctors with accurate diagnosis and treatment. Moreover, cardiovascular magnetic resonance imaging (CMRI) can be used to perform a more detailed quantitative analysis evaluation for cardiac diagnosis.

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Intelligent three-dimensional (3D) reconstruction technology plays an important role in the diagnosis and treatment of diseases. It has been widely used in assisted liver surgery. At present, the 3D reconstruction information of liver is mainly obtained based on CT enhancement data.

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We proposed a novel efficient method for 3D left ventricle (LV) segmentation on echocardiography, which is important for cardiac disease diagnosis. The proposed method effectively overcame the 3D echocardiography's challenges: high dimensional data, complex anatomical environments, and limited annotation data. First, we proposed a deep atlas network, which integrated LV atlas into the deep learning framework to address the 3D LV segmentation problem on echocardiography for the first time, and improved the performance based on limited annotation data.

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Accurate and automated cardiac bi-ventricle quantification based on cardiac magnetic resonance (CMR) image is a very crucial procedure for clinical cardiac disease diagnosis. Two traditional and commensal tasks, i.e.

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Segmentation of the left ventricle (LV) from three-dimensional echocardiography (3DE) plays a key role in the clinical diagnosis of the LV function. In this work, we proposed a new automatic method for the segmentation of LV, based on the fully convolutional networks (FCN) and deformable model. This method implemented a coarse-to-fine framework.

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Functional analysis of the L-type calcium channel has shown that the R858H mutation associated with severe QT interval prolongation may lead to ventricular fibrillation (VF). This study investigated multiple potential mechanisms by which the R858H mutation facilitates and perpetuates VF. The Ten Tusscher-Panfilov (TP06) human ventricular cell models incorporating the experimental data on the kinetic properties of L-type calcium channels were integrated into one-dimensional (1D) fiber, 2D sheet, and 3D ventricular models to investigate the pro-arrhythmic effects of mutations by quantifying changes in intracellular calcium handling, action potential profiles, action potential duration restitution (APDR) curves, dispersion of repolarization (DOR), QT interval and spiral wave dynamics.

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Objective: Left ventricular (LV) volume estimation is a critical procedure for cardiac disease diagnosis. The objective of this paper is to address a direct LV volume prediction task.

Methods: In this paper, we propose a direct volume prediction method based on the end-to-end deep convolutional neural networks.

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