Changli Feng

Dr. Changli Feng

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

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

Representative Publications

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19 May 2021 in Proteomics
Verified
Journal Article
Closed access
PDF file
CFChangli Feng
Changli Feng
HWHaiyan Wei
Haiyan Wei
DYDeyun Yang
Deyun Yang
BFBin Feng
Bin Feng
ZMZhaogui Ma
Zhaogui Ma
HSHua Shi
Hua Shi


1 June 2021 in IEEE/ACM Transactions on Computational Biology and Bioinformatics
Verified
Journal Article
Closed access
CFChangli Feng
Changli Feng
JWJin Wu
Jin Wu
HWHaiyan Wei
Haiyan Wei
LXLei Xu
Lei Xu
Quan ZouQuan Zou
Quan Zou
Malaria is a mosquito-borne disease that results in millions of cases and deaths annually. The development of a fast computational method that identifies secretory proteins of the malaria parasite is important for research on antimalarial drugs and vaccines. Thus, a method was developed to identify the secretory proteins of malaria parasites. In this method, a reduced alphabet was selected to recode the original protein sequence. A feature synthesis method was used to synthesise three different types of feature information. Finally, the random forest method was used as a classifier to identify the secretory proteins. In addition, a web server was developed to share the proposed algorithm. Experiments using the benchmark dataset demonstrated that the overall accuracy achieved by the proposed method was greater than 97.8 percent using the 10-fold cross-validation method. Furthermore, the reduced schemes and characteristic performance analyses are discussed.

29 April 2024 in Computers in Biology and Medicine
Verified
Journal Article
Closed access
CFChangli Feng
Changli Feng
HWHaiyan Wei
Haiyan Wei
XLXin Li
Xin Li
BFBin Feng
Bin Feng
CXChugui Xu
Chugui Xu
RLRuijun Liu
Ruijun Liu

28 February 2023 in PLOS ONE
Verified
Journal Article
Open access
PDF file
XLXin Li
Xin Li
BFBin Feng
Bin Feng
SQSai Qiao
Sai Qiao
HWHaiyan Wei
Haiyan Wei
CFChangli Feng
Changli Feng
Juxtapleural nodules were excluded from the segmented lung region in the Hounsfield unit threshold-based segmentation method. To re-include those regions in the lung region, a new approach was presented using scale-invariant feature transform and gradient vector flow models in this study. First, the scale-invariant feature transform method was utilized to detect all scale-invariant points in the binary lung region. The boundary points in the neighborhood of a scale-invariant point were collected to form the supportive boundary lines. Then, we utilized a Fourier descriptor to obtain a character representation of each supportive boundary line. Spectrum energy recognizes supportive boundaries that must be corrected. Third, the gradient vector flow-snake method was presented to correct the recognized supportive borders with a smooth profile curve, giving an ideal correction edge in those regions. Finally, the performance of the proposed method was evaluated through experiments on multiple authentic computed tomography images. The perfect results and robustness proved that the proposed method could correct the juxtapleural region precisely.

15 July 2024 in IEEE Journal of Biomedical and Health Informatics
Verified
Journal Article
Closed access
CFChangli Feng
Changli Feng
HWHaiyan Wei
Haiyan Wei
CXChugui Xu
Chugui Xu
BFBin FENG
Bin FENG
XZXiaorong Zhu
Xiaorong Zhu
Quan ZouQuan Zou
Quan Zou
Protein classification is a crucial field in bioinformatics. The development of a comprehensive tool that can perform feature evaluation, visualization, automated machine learning, and model interpretation would significantly advance research in protein classification. However, there is a significant gap in the literature regarding tools that integrate all these essential functionalities. This paper presents iProps, a novel Python-based software package, meticulously crafted to fulfill these multifaceted requirements. iProps is distinguished by its proficiency in feature extraction, evaluation, automated machine learning, and interpretation of classification models. Firstly, iProps fully leverages evolutionary information and amino acid reduction information to propose or extend several numerical protein features that are independent of sequence length, including SC-PSSM, ORDip, TRC, CTDC-E, CKSAAGP-E, and so forth; at the same time, it also implements the calculation of 17 other numerical features within the software. iProps also provides feature combination operations for the aforementioned features to generate more hybrid features, and has added data balancing sampling processing as well as built-in classifier settings, among other functionalities. Thus, It can discern the most effective protein class recognition feature from a multitude of candidates, utilizing three automated machine learning algorithms to identify the most optimal classifiers and parameter settings. Furthermore, iProps generates a detailed explanatory report that includes 23 informative graphs derived from three interpretable models. To assess the performance of iProps, a series of numerical experiments were conducted using two well-established datasets. The results demonstrated that our software achieved superior recognition performance in every case. Beyond its contributions to bioinformatics, iProps broadens its applicability by offering robust data analysis tools that are beneficial across various disciplines, capitalizing on its automated machine learning and model interpretation capabilities. As an open-source platform, iProps is readily accessible and features an intuitive user interface, ensuring ease of use for individuals, even those without a background in programming. The source code of the software is available for download at the following website: https://github.com/LigosQ/iProps and https://gitee.com/LigosQ/iProps .