Beilun Wang

Dr. Beilun Wang


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 January 2025 in Nature Microbiology
Verified
Journal Article
Closed access
PDF file
BWBeilun Wang
Beilun Wang
PLPeijun Lin
Peijun Lin
YZYuwei Zhong
Yuwei Zhong
XTXiao Tan
Xiao Tan
YSYangyang Shen
Yangyang Shen
YWYihan Wu
Yihan Wu

30 April 2023
Verified
Conference Paper
Open access
YWYuchen Wang
Yuchen Wang
JZJinghui Zhang
Jinghui Zhang
ZHZhengjie Huang
Zhengjie Huang
WLWeibin Li
Weibin Li
SFShikun Feng
Shikun Feng
JLJunzhou Luo
Junzhou Luo
Node classification is a substantial problem in graph-based fraud detection. Many existing works adopt Graph Neural Networks (GNNs) to enhance fraud detectors. While promising, currently most GNN-based fraud detectors fail to generalize to the low homophily setting. Besides, label utilization has been proved to be significant factor for node classification problem. But we find they are less effective in fraud detection tasks due to the low homophily in graphs. In this work, we propose GAGA, a novel Group AGgregation enhanced TrAnsformer, to tackle the above challenges. Specifically, the group aggregation provides a portable method to cope with the low homophily issue. Such an aggregation explicitly integrates the label information to generate distinguishable neighborhood information. Along with group aggregation, an attempt towards end-to-end trainable group encoding is proposed which augments the original feature space with the class labels. Meanwhile, we devise two additional learnable encodings to recognize the structural and relational context. Then, we combine the group aggregation and the learnable encodings into a Transformer encoder to capture the semantic information. Experimental results clearly show that GAGA outperforms other competitive graph-based fraud detectors by up to 24.39% on two trending public datasets and a real-world industrial dataset from Baidu. Even more, the group aggregation is demonstrated to outperform other label utilization methods (e.g., C&S, BoT/UniMP) in the low homophily setting.

19 September 2022 in Knowledge-Based Systems
Verified
Journal Article
Closed access
BWBeilun Wang
Beilun Wang
HXHaoqing Xu
Haoqing Xu
CLChunshu Li
Chunshu Li
YLYuchen Li
Yuchen Li
MWMeng Wang
Meng Wang

24 June 2021 in JMIR Medical Informatics
Verified
Journal Article
Open access
MWMeng Wang
Meng Wang
Haofen WangHaofen Wang
Haofen Wang
XLXing Liu
Xing Liu
XMXinyu Ma
Xinyu Ma
BWBeilun Wang
Beilun Wang
Background: Minimizing adverse reactions caused by drug-drug interactions (DDIs) has always been a prominent research topic in clinical pharmacology. Detecting all possible interactions through clinical studies before a drug is released to the market is a demanding task. The power of big data is opening up new approaches to discovering various DDIs. However, these data contain a huge amount of noise and provide knowledge bases that are far from being complete or used with reliability. Most existing studies focus on predicting binary DDIs between drug pairs and ignore other interactions. Objective: Leveraging both drug knowledge graphs and biomedical text is a promising pathway for rich and comprehensive DDI prediction, but it is not without issues. Our proposed model seeks to address the following challenges: data noise and incompleteness, data sparsity, and computational complexity. Methods: We propose a novel framework, Predicting Rich DDI, to predict DDIs. The framework uses graph embedding to overcome data incompleteness and sparsity issues to make multiple DDI label predictions. First, a large-scale drug knowledge graph is generated from different sources. The knowledge graph is then embedded with comprehensive biomedical text into a common low-dimensional space. Finally, the learned embeddings are used to efficiently compute rich DDI information through a link prediction process. Results: To validate the effectiveness of the proposed framework, extensive experiments were conducted on real-world data sets. The results demonstrate that our model outperforms several state-of-the-art baseline methods in terms of capability and accuracy. Conclusions: We propose a novel framework, Predicting Rich DDI, to predict DDIs. Using rich DDI information, it can competently predict multiple labels for a pair of drugs across numerous domains, ranging from pharmacological mechanisms to side effects. To the best of our knowledge, this framework is the first to provide a joint translation-based embedding model that learns DDIs by integrating drug knowledge graphs and biomedical text simultaneously in a common low-dimensional space. The model also predicts DDIs using multiple labels rather than single or binary labels. Extensive experiments were conducted on real-world data sets to demonstrate the effectiveness and efficiency of the model. The results show our proposed framework outperforms several state-of-the-art baselines.

13 August 2021 in Sensors
Verified
Journal Article
Open access
PDF file
KHkaihong huang
kaihong huang
CLChunshu Li
Chunshu Li
JZJiaQi Zhang
JiaQi Zhang
BWBeilun Wang
Beilun Wang
The demand for the sensor-based detection of camouflage objects widely exists in biological research, remote sensing, and military applications. However, the performance of traditional object detection algorithms is limited, as they are incapable of extracting informative parts from low signal-to-noise ratio features. To address this problem, we propose Camouflaged Object Detection with Cascade and Feedback Fusion (CODCEF), a deep learning framework based on an RGB optical sensor that leverages a cascaded structure with Feedback Partial Decoders (FPD) instead of a traditional encoder–decoder structure. Through a selective fusion strategy and feedback loop, FPD reduces the loss of information and the interference of noises in the process of feature interweaving. Furthermore, we introduce Pixel Perception Fusion (PPF) loss, which aims to pay more attention to local pixels that might become the edges of an object. Experimental results on an edge device show that CODCEF achieved competitive results compared with 10 state-of-the-art methods.

3 August 2020 in IEEE Access
Verified
Journal Article
Open access
BWBeilun Wang
Beilun Wang
RMRui Ma
Rui Ma
JKJingyu Kuang
Jingyu Kuang
YZYan Zhang
Yan Zhang
The convolutional neural network (CNN) is widely used in various computer vision problems such as image recognition and image classification because of its powerful ability to process image data. However, it is an end-to-end model that remains a “block box” for users. The internal logic of CNN is not explicitly known. Interpreting CNN can help us better understand neural networks and the various ways they benefit us as users. In this paper, we explain the contributions of the convolutional layer of CNN with a neuroscience experiment paradigm: the Ms. Pac-Man video game. Ms. Pac-Man is a popular game that provides a complex yet natural decision-making task rather than a laboratory artifact. An analysis of the game can thus intuitively reveal the complicated decision-making process in animal brains. We sought to (1) elucidate the role of the CNN convolutional layer and (2) analyze the low-level strategies in animal brains based on high-level decisions. We use recorded videos of monkeys playing the Ms. Pac-Man game to empirically demonstrate that our network is able to predict the moving direction of the Pac-Man at every time step. We further find that the decision-making process at work during gameplay is high-reward-driven. A heatmap of the weighted feature map at each convolutional layer shows that CNN makes predictions based on the most important input pattern, which in this case is the high reward entities in the game.