Disease biomarker identification based on sample network optimization

被引:2
|
作者
Wei, Pi-Jing [1 ]
Ma, Wenwen [3 ]
Li, Yanxin [4 ]
Su, Yansen [2 ,5 ]
机构
[1] Anhui Univ, Inst Phys Sci & Informat Technol, Informat Mat & Intelligent Sensing Lab Anhui Prov, 111 Jiulong Rd, Hefei 230601, Anhui, Peoples R China
[2] Hefei Comprehens Natl Sci Ctr, Inst Artificial Intelligence, 5089 Wangjiang West Rd, Hefei 230088, Peoples R China
[3] Anhui Univ, Sch Comp Sci & Technol, Key Lab Intelligent Comp & Signal Proc, 111 Jiulong Rd, Hefei 230601, Peoples R China
[4] Third Hosp Xingtai, Dept Cardiol, Xingtai 054000, Hebei, Peoples R China
[5] Anhui Univ, Sch Artificial Intelligence, 111 Jiulong Rd, Hefei 230601, Peoples R China
基金
中国国家自然科学基金;
关键词
Disease biomarker identification; Sample similarity network; Multi-objective evolution algorithm; Sample classification; PARTICLE SWARM OPTIMIZATION; FEATURE-SELECTION; PARAGANGLIOMA; CLASSIFICATION; PHEOCHROMOCYTOMA;
D O I
10.1016/j.ymeth.2023.03.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A large amount of evidence shows that biomarkers are discriminant features related to disease development. Thus, the identification of disease biomarkers has become a basic problem in the analysis of complex diseases in the medical fields, such as disease stage judgment, disease diagnosis and treatment. Research based on networks have become one of the most popular methods. Several algorithms based on networks have been proposed to identify biomarkers, however the networks of genes or molecules ignored the similarities and associations among the samples. It is essential to further understand how to construct and optimize the networks to make the identified biomarkers more accurate. On this basis, more effective strategies can be developed to improve the performance of biomarkers identification. In this study, a multi-objective evolution algorithm based on sample similarity networks has been proposed for disease biomarker identification. Specifically, we design the sample similarity networks to extract the structural characteristic information among samples, which used to calculate the influence of the sample to each class. Besides, based on the networks and the group of biomarkers we choose in every iteration, we can divide samples into different classes by the importance for each class. Then, in the process of evolution algorithm population iteration, we develop the elite guidance strategy and fusion selection strategy to select the biomarkers which make the sample classification more accurate. The experiment results on the five gene expression datasets suggests that the algorithm we proposed is superior over some state-of-the-art disease biomarker identification methods.
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页码:42 / 49
页数:8
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