Gansen Zhao

Dr. Gansen Zhao


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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11 February 2014 in Multimedia Tools and Applications
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Fatos XhafaFatos Xhafa
Fatos Xhafa
JLJingwei Li
Jingwei Li
GZGansen Zhao
Gansen Zhao
JLJin Li
Jin Li
XCXiaofeng Chen
Xiaofeng Chen
DWDuncan S. Wong
Duncan S. Wong

18 June 2020 in IEEE/ACM Transactions on Computational Biology and Bioinformatics
Verified
Journal Article
Closed access
CLChengchuang Lin
Chengchuang Lin
GZGansen Zhao
Gansen Zhao
ZYZhirong Yang
Zhirong Yang
AYAihua Yin
Aihua Yin
XWXinming Wang
Xinming Wang
QCQiren Chen
Qiren Chen
Method: This paper focuses on chromosome classification because it is critical for chromosome karyotyping. In recent years, deep learning-based methods are the most promising methods for solving the tasks of chromosome classification. Although the deep learning-based Inception architecture has yielded state-of-the-art performance in the 2015 ILSVRC challenge, it has not been used in chromosome classification tasks so far. Therefore, we develop an automatic chromosome classification approach named CIR-Net based on Inception-ResNet which is an optimized version of Inception. However, the classification performance of origin Inception-ResNet on the insufficient chromosome dataset still has a lot of capacity for improvement. Further, we propose a simple but effective augmentation method called CDA for improving the performance of CIR-Net. Results: The experimental results show that our proposed method achieves 95.98% classification accuracy on the clinical G-band chromosome dataset whose training dataset is insufficient. Moreover, the proposed augmentation method CDA improves more than 8.5% (from 87.46% to 95.9%) classification accuracy compared to other methods. In this paper, the experimental results demonstrate that our proposed method is recent the most effective solution for solving clinical chromosome classification problems in chromosome auto-karyotyping on the condition of the insufficient training dataset. Code and Dataset are available at https://github.com/CloudDataLab/CIR-Net.

6 August 2022 in BMC Medical Informatics and Decision Making
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YLYujie Li
Yujie Li
YSYingShan Shen
YingShan Shen
XFXiaomao Fan
Xiaomao Fan
XHXingxian Huang
Xingxian Huang
HYHaibo Yu
Haibo Yu
WMWenjun Ma
Wenjun Ma
Background: Major depressive disorder (MDD) is a common mental illness, characterized by persistent depression, sadness, despair, etc., troubling people’s daily life and work seriously. Methods: In this work, we present a novel automatic MDD detection framework based on EEG signals. First of all, we derive highly MDD-correlated features, calculating the ratio of extracted features from EEG signals at frequency bands between $$\beta$$ β and $$\alpha$$ α . Then, a two-stage feature selection method named PAR is presented with the sequential combination of Pearson correlation coefficient (PCC) and recursive feature elimination (RFE), where the advantages lie in minimizing the feature searching space. Finally, we employ widely used machine learning methods of support vector machine (SVM), logistic regression (LR), and linear regression (LNR) for MDD detection with the merit of feature interpretability. Results: Experiment results show that our proposed MDD detection framework achieves competitive results. The accuracy and $$F_{1}$$ F 1 score are up to 0.9895 and 0.9846, respectively. Meanwhile, the regression determination coefficient $$R^2$$ R 2 for MDD severity assessment is up to 0.9479. Compared with existing MDD detection methods with the best accuracy of 0.9840 and $$F_1$$ F 1 score of 0.97, our proposed framework achieves the state-of-the-art MDD detection performance. Conclusions: Development of this MDD detection framework can be potentially deployed into a medical system to aid physicians to screen out MDD patients.

1 January 2022 in Computers in Biology and Medicine
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Journal Article
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HLHongtuo Lin
Hongtuo Lin
CJChufan Jian
Chufan Jian
YCYang Cao
Yang Cao
XMXiaoguang Ma
Xiaoguang Ma
Hailiang WangHailiang Wang
Hailiang Wang
HZHui Zhou
Hui Zhou

1 April 2021 in Medical Image Analysis
Verified
Journal Article
Closed access
CLChengchuang Lin
Chengchuang Lin
GZGansen Zhao
Gansen Zhao
AYAihua Yin
Aihua Yin
ZYZhirong Yang
Zhirong Yang
LGLi Guo
Li Guo
ZMZhaohui Ma
Zhaohui Ma

27 November 2017 in Scientific Reports
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GLGuangjian Liu
Guangjian Liu
YXYi Xu
Yi Xu
XWXinming Wang
Xinming Wang
XZXutian Zhuang
Xutian Zhuang
HLHuiying Liang
Huiying Liang
HXHuimin Xia
Huimin Xia
Children of severe hand, foot, and mouth disease (HFMD) often present with same clinical features as those of mild HFMD during the early stage, yet later deteriorate rapidly with a fulminant disease course. Our goal was to: (1) develop a machine learning system to automatically identify cases with high risk of severe HFMD at the time of admission; (2) compare the effectiveness of the new system with the existing risk scoring system. Data on 2,532 HFMD children admitted between March 2012 and July 2015, were collected retrospectively from a medical center in China. By applying a holdout strategy and a 10-fold cross validation method, we developed four models with the random forest algorithm using different variable sets. The prediction system HFMD-RF based on the model of 16 variables from both the structured and unstructured data, achieved 0.824 sensitivity, 0.931 specificity, 0.916 accuracy, and 0.916 area under the curve in the independent test set. Most remarkably, HFMD-RF offers significant gains with respect to the commonly used pediatric critical illness score in clinical practice. As all the selected risk factors can be easily obtained, HFMD-RF might prove to be useful for reductions in mortality and complications of severe HFMD.