Evidence map›Paper›PMID 30514298›Full record

ArticleBiomedical engineering online2018

Imbalanced biomedical data classification using self-adaptive multilayer ELM combined with dynamic GAN.

Liyuan Zhang, Huamin Yang, Zhengang Jiang

Abstract read
In one paragraph

Article in Biomedical engineering online, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Liyuan ZhangSchool of Computer Science and Technology, Medical Imaging Engineering Laboratory, Changchun University of Science and Technology, No.7089, Weixing Road, Changchun, China.ORCID http://orcid.org/0000-0002-5382-3030
Huamin YangSchool of Computer Science and Technology, Medical Imaging Engineering Laboratory, Changchun University of Science and Technology, No.7089, Weixing Road, Changchun, China. yhm@cust.edu.cn.
Zhengang JiangSchool of Computer Science and Technology, Medical Imaging Engineering Laboratory, Changchun University of Science and Technology, No.7089, Weixing Road, Changchun, China.

Funding

National Key Research and Development Program of China No.2017YFC0108303
6 · The paper itself

Abstract

backgroundImbalanced data classification is an inevitable problem in medical intelligent diagnosis. Most of real-world biomedical datasets are usually along with limited samples and high-dimensional feature. This seriously affects the classification performance of the model and causes erroneous guidance for the diagnosis of diseases. Exploring an effective classification method for imbalanced and limited biomedical dataset is a challenging task.

methodsIn this paper, we propose a novel multilayer extreme learning machine (ELM) classification model combined with dynamic generative adversarial net (GAN) to tackle limited and imbalanced biomedical data. Firstly, principal component analysis is utilized to remove irrelevant and redundant features. Meanwhile, more meaningful pathological features are extracted. After that, dynamic GAN is designed to generate the realistic-looking minority class samples, thereby balancing the class distribution and avoiding overfitting effectively. Finally, a self-adaptive multilayer ELM is proposed to classify the balanced dataset. The analytic expression for the numbers of hidden layer and node is determined by quantitatively establishing the relationship between the change of imbalance ratio and the hyper-parameters of the model. Reducing interactive parameters adjustment makes the classification model more robust.

resultsTo evaluate the classification performance of the proposed method, numerical experiments are conducted on four real-world biomedical datasets. The proposed method can generate authentic minority class samples and self-adaptively select the optimal parameters of learning model. By comparing with W-ELM, SMOTE-ELM, and H-ELM methods, the quantitative experimental results demonstrate that our method can achieve better classification performance and higher computational efficiency in terms of ROC, AUC, G-mean, and F-measure metrics.

conclusionsOur study provides an effective solution for imbalanced biomedical data classification under the condition of limited samples and high-dimensional feature. The proposed method could offer a theoretical basis for computer-aided diagnosis. It has the potential to be applied in biomedical clinical practice.

Indexed as

Biomedical ResearchData AnalysisMachine LearningDynamic GANHigh-dimensional featureImbalanced data classificationLimited biomedical samplesMultilayer ELM

Identifiers

PMID30514298
PMCPMC6280414

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.