IMC-MDA: Prediction of miRNA-disease association based on induction matrix completion

被引:3
|
作者
Li, Zejun [1 ]
Zhang, Yuxiang [2 ]
Bai, Yuting [3 ]
Xie, Xiaohui [1 ]
Zeng, Lijun [1 ]
机构
[1] Hunan Inst Technol, Sch Comp & Informat Sci, Hengyang 412002, Peoples R China
[2] Zhengzhou Univ, Sch Comp & Artificial Intelligence, Zhengzhou 450001, Henan, Peoples R China
[3] Hunan Univ, Coll Informat Sci & Engn, Changsha 410082, Hunan, Peoples R China
基金
湖南省自然科学基金;
关键词
miRNA-disease; miRNAs; disease; matrix completion; directed acyclic graphs; MICRORNA; COVID-19; NETWORK; SIMILARITY; IMPACT;
D O I
10.3934/mbe.2023471
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To comprehend the etiology and pathogenesis of many illnesses, it is essential to iden-tify disease-associated microRNAs (miRNAs). However, there are a number of challenges with cur-rent computational approaches, such as the lack of "negative samples", that is, confirmed irrelevant miRNA-disease pairs, and the poor performance in terms of predicting miRNAs related with "iso-lated diseases", i.e. illnesses with no known associated miRNAs, which presents the need for novel computational methods. In this study, for the purpose of predicting the connection between disease and miRNA, an inductive matrix completion model was designed, referred to as IMC-MDA. In the model of IMC-MDA, for each miRNA-disease pair, the predicted marks are calculated by combining the known miRNA-disease connection with the integrated disease similarities and miRNA similarities. Based on LOOCV, IMC-MDA had an AUC of 0.8034, which shows better performance than previous methods. Furthermore, experiments have validated the prediction of disease-related miRNAs for three major human diseases: colon cancer, kidney cancer, and lung cancer.
引用
收藏
页码:10659 / 10674
页数:16
相关论文
共 50 条
  • [1] MCMDA: Matrix completion for MiRNA-disease association prediction
    Li, Jian-Qiang
    Rong, Zhi-Hao
    Chen, Xing
    Yan, Gui-Ying
    You, Zhu-Hong
    ONCOTARGET, 2017, 8 (13) : 21187 - 21199
  • [2] Prediction of miRNA-disease association based on multisource inductive matrix completion
    Wang, Yawei
    Yin, Zhixiang
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [3] Predicting miRNA-disease association based on inductive matrix completion
    Chen, Xing
    Wang, Lei
    Qu, Jia
    Guan, Na-Na
    Li, Jian-Qiang
    BIOINFORMATICS, 2018, 34 (24) : 4256 - 4265
  • [4] Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction
    Zhu, Rongxiang
    Ji, Chaojie
    Wang, Yingying
    Cai, Yunpeng
    Wu, Hongyan
    FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY, 2020, 8
  • [5] MiRNA-Disease association prediction via non-negative matrix factorization based matrix completion
    Zheng, Xiao
    Zhang, Chujie
    Wan, Cheng
    SIGNAL PROCESSING, 2022, 190
  • [6] NCMCMDA: miRNA-disease association prediction through neighborhood constraint matrix completion
    Chen, Xing
    Sun, Lian-Gang
    Zhao, Yan
    BRIEFINGS IN BIOINFORMATICS, 2021, 22 (01) : 485 - 496
  • [7] MCLPMDA: A novel method for miRNA-disease association prediction based on matrix completion and label propagation
    Yu, Sheng-Peng
    Liang, Cheng
    Xiao, Qiu
    Li, Guang-Hui
    Ding, Ping-Jian
    Luo, Jia-Wei
    JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2019, 23 (02) : 1427 - 1438
  • [8] SNFIMCMDA: Similarity Network Fusion and Inductive Matrix Completion for miRNA-Disease Association Prediction
    Li, Lei
    Gao, Zhen
    Zheng, Chun-Hou
    Wang, Yu
    Wang, Yu-Tian
    Ni, Jian-Cheng
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
  • [9] Neural inductive matrix completion with graph convolutional networks for miRNA-disease association prediction
    Li, Jin
    Zhang, Sai
    Liu, Tao
    Ning, Chenxi
    Zhang, Zhuoxuan
    Zhou, Wei
    BIOINFORMATICS, 2020, 36 (08) : 2538 - 2546
  • [10] QIMCMDA: MiRNA-Disease Association Prediction by q-Kernel Information and Matrix Completion
    Wang, Lin
    Chen, Yaguang
    Zhang, Naiqian
    Chen, Wei
    Zhang, Yusen
    Gao, Rui
    FRONTIERS IN GENETICS, 2020, 11