Chengcui Zhang

Dr. Chengcui Zhang


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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5 June 2003 in IEEE Transactions on Geoscience and Remote Sensing
Verified
Journal Article
Closed access
KZKeqi Zhang
Keqi Zhang
SCShu-Ching Chen
Shu-Ching Chen
DWD. Whitman
D. Whitman
MSMei-Ling Shyu
Mei-Ling Shyu
JYJianhua Yan
Jianhua Yan
CZChengcui Zhang
Chengcui Zhang
Recent advances in airborne light detection and ranging (LIDAR) technology allow rapid and inexpensive measurements of topography over large areas. This technology is becoming a primary method for generating high-resolution digital terrain models (DTMs) that are essential to numerous applications such as flood modeling and landslide prediction. Airborne LIDAR systems usually return a three-dimensional cloud of point measurements from reflective objects scanned by the laser beneath the flight path. In order to generate a DTM, measurements from nonground features such as buildings, vehicles, and vegetation have to be classified and removed. In this paper, a progressive morphological filter was developed to detect nonground LIDAR measurements. By gradually increasing the window size of the filter and using elevation difference thresholds, the measurements of vehicles, vegetation, and buildings are removed, while ground data are preserved. Datasets from mountainous and flat urbanized areas were selected to test the progressive morphological filter. The results show that the filter can remove most of the nonground points effectively.

24 April 2024 in ACM Computing Surveys
Verified
Journal Article
Open access
FZFei Zhao
Fei Zhao
CZChengcui Zhang
Chengcui Zhang
BGBaocheng Geng
Baocheng Geng
Multimodal Artificial Intelligence (Multimodal AI), in general, involves various types of data (e.g., images, texts, or data collected from different sensors), feature engineering (e.g., extraction, combination/fusion), and decision-making (e.g., majority vote). As architectures become more and more sophisticated, multimodal neural networks can integrate feature extraction, feature fusion, and decision-making processes into one single model. The boundaries between those processes are increasingly blurred. The conventional multimodal data fusion taxonomy (e.g., early/late fusion), based on which the fusion occurs in, is no longer suitable for the modern deep learning era. Therefore, based on the main-stream techniques used, we propose a new fine-grained taxonomy grouping the state-of-the-art (SOTA) models into five classes: Encoder-Decoder methods, Attention Mechanism methods, Graph Neural Network methods, Generative Neural Network methods, and other Constraint-based methods. Most existing surveys on multimodal data fusion are only focused on one specific task with a combination of two specific modalities. Unlike those, this survey covers a broader combination of modalities, including Vision + Language (e.g., videos, texts), Vision + Sensors (e.g., images, LiDAR), and so on, and their corresponding tasks (e.g., video captioning, object detection). Moreover, a comparison among these methods is provided, as well as challenges and future directions in this area.

7 March 2019 in IEEE Transactions on Knowledge and Data Engineering
Verified
Journal Article
Closed access
ZBZhan Bu
Zhan Bu
HLHuijia Li
Huijia Li
CZChengcui Zhang
Chengcui Zhang
JCJie Cao
Jie Cao
ALAihua Li
Aihua Li
YSYong Shi
Yong Shi
With the explosion of social media networks, many modern applications are concerning about people's connections, which leads to the so-called social computing. An elusive question is to study how opinion communities form and evolve in real-world networks with great individual diversity and complex human connections. In this paper, we attempt to model a realistic social media network as a discrete-time dynamical system, where the opinion matrix and the community structure could mutually affect each other. The community detection in social media networks is naturally formulated as a multi-objective optimization problem, i.e., finding a set of densely connected components with similar opinion vectors. We propose a novel and powerful graph K-means framework, which is composed of three coupled phases in each discrete-time period. Specifically, the first phase uses a fast heuristic approach to identify those opinion leaders who have relatively high local reputation; the second phase adopts a novel dynamic game model to find the locally Pareto-optimal community structure; the final phase employs a robust opinion dynamics model to simulate the evolution of the opinion matrix. We conduct a series of comprehensive experiments on real-world benchmark networks to validate the performance of GK-means through comparisons with the state-of-the-art graph clustering technologies.

18 February 2009 in Information Systems Frontiers
Verified
Journal Article
Closed access
PDF file
WCWei-Bang Chen
Wei-Bang Chen
CZChengcui Zhang
Chengcui Zhang

1 June 2023 in Radiology
Verified
Journal Article
Closed access
PPPraneeth Reddy Amudala Puchakayala
Praneeth Reddy Amudala Puchakayala
VSVenkata L. Sthanam
Venkata L. Sthanam
ANArie Nakhmani
Arie Nakhmani
MCMuhammad F. A. Chaudhary
Muhammad F. A. Chaudhary
APAbhilash Kizhakke Puliyakote
Abhilash Kizhakke Puliyakote
SBSandeep Bodduluri
Sandeep Bodduluri
Background Approximately half of adults with chronic obstructive pulmonary disease (COPD) remain undiagnosed. Chest CT scans are frequently acquired in clinical practice and present an opportunity to detect COPD. Purpose To assess the performance of radiomics features in COPD diagnosis using standard-dose and low-dose CT models. Materials and Methods This secondary analysis included participants enrolled in the Genetic Epidemiology of COPD, or COPDGene, study at baseline (visit 1) and 10 years after baseline (visit 3). COPD was defined by a forced expiratory volume in the 1st second of expiration to forced vital capacity ratio less than 0.70 at spirometry. The performance of demographics, CT emphysema percentage, radiomics features, and a combined feature set derived from inspiratory CT alone was evaluated. CatBoost (Yandex), a gradient boosting algorithm, was used to perform two classification experiments to detect COPD; the two models were trained and tested on standard-dose CT data from visit 1 (model I) and low-dose CT data from visit 3 (model II). Classification performance of the models was evaluated using area under the receiver operating characteristic curve (AUC) and precision-recall curve analysis. Results A total of 8878 participants (mean age, 57 years ± 9 [SD]; 4180 female, 4698 male) were evaluated. Radiomics features in model I achieved an AUC of 0.90 (95% CI: 0.88, 0.91) in the standard-dose CT test cohort versus demographics (AUC, 0.73; 95% CI: 0.71, 0.76; P < .001), emphysema percentage (AUC, 0.82; 95% CI 0.80, 0.84; P < .001), and combined features (AUC, 0.90; 95% CI: 0.89, 0.92; P = .16). Model II, trained on low-dose CT scans, achieved an AUC of 0.87 (95% CI: 0.83, 0.91) on the 20% held-out test set for radiomics features compared with demographics (AUC, 0.70; 95% CI: 0.64, 0.75; P = .001), emphysema percentage (AUC, 0.74; 95% CI: 0.69, 0.79; P = .002), and combined features (AUC, 0.88; 95% CI: 0.85, 0.92; P = .32). Density and texture features were the majority of the top 10 features in the standard-dose model, whereas shape features of lungs and airways were significant contributors in the low-dose CT model. Conclusion A combination of features representing parenchymal texture and lung and airway shape on inspiratory CT scans can be used to accurately detect COPD. ClinicalTrials.gov registration no. NCT00608764 © RSNA, 2023 Supplemental material is available for this article. See also the editorial by Vliegenthart in this issue.

9 July 2020 in JCI Insight
Verified
Journal Article
Open access
PDF file
SBSandeep Bodduluri
Sandeep Bodduluri
ANArie Nakhmani
Arie Nakhmani
JRJoseph M. Reinhardt
Joseph M. Reinhardt
CWCarla G. Wilson
Carla G. Wilson
MMMerry-Lynn McDonald
Merry-Lynn McDonald
SBSurya Bhatt
Surya Bhatt
BACKGROUND: Currently recommended traditional spirometry outputs do not reflect the relative contributions of emphysema and airway disease to airflow obstruction. We hypothesized that machine-learning algorithms can be trained on spirometry data to identify these structural phenotypes. METHODS: Participants enrolled in a large multicenter study (COPDGene) were included. The data points from expiratory flow-volume curves were trained using a deep-learning model to predict structural phenotypes of chronic obstructive pulmonary disease (COPD) on CT, and results were compared with traditional spirometry metrics and an optimized random forest classifier. Area under the receiver operating characteristic curve (AUC) and weighted F-score were used to measure the discriminative accuracy of a fully convolutional neural network, random forest, and traditional spirometry metrics to phenotype CT as normal, emphysema-predominant (>5% emphysema), airway-predominant (Pi10 > median), and mixed phenotypes. Similar comparisons were made for the detection of functional small airway disease phenotype (>20% on parametric response mapping). RESULTS: Among 8980 individuals, the neural network was more accurate in discriminating predominant emphysema/airway phenotypes (AUC 0.80, 95%CI 0.79–0.81) compared with traditional measures of spirometry, FEV 1 /FVC (AUC 0.71, 95%CI 0.69–0.71), FEV 1 % predicted (AUC 0.70, 95%CI 0.68–0.71), and random forest classifier (AUC 0.78, 95%CI 0.77–0.79). The neural network was also more accurate in discriminating predominant emphysema/small airway phenotypes (AUC 0.91, 95%CI 0.90–0.92) compared with FEV 1 /FVC (AUC 0.80, 95%CI 0.78–0.82), FEV 1 % predicted (AUC 0.83, 95%CI 0.80–0.84), and with comparable accuracy with random forest classifier (AUC 0.90, 95%CI 0.88–0.91). CONCLUSIONS: Structural phenotypes of COPD can be identified from spirometry using deep-learning and machine-learning approaches, demonstrating their potential to identify individuals for targeted therapies. TRIAL REGISTRATION: ClinicalTrials.gov NCT00608764. FUNDING: This study was supported by NIH grants K23 HL133438 and R21EB027891 and an American Thoracic Foundation 2018 Unrestricted Research Grant. The COPDGene study is supported by NIH grants NHLBI U01 HL089897 and U01 HL089856. The COPDGene study (NCT00608764) is also supported by the COPD Foundation through contributions made to an Industry Advisory Committee comprising AstraZeneca, Boehringer-Ingelheim, GlaxoSmithKline, Novartis, and Sunovion.