Discovering disease-associated genes in weighted protein-protein interaction networks

被引:8
|
作者
Cui, Ying [1 ,2 ,4 ,5 ]
Cai, Meng [3 ,4 ,5 ]
Stanley, H. Eugene [4 ,5 ]
机构
[1] Xidian Univ, Sch Mechanoelect Engn, Xian 710071, Shaanxi, Peoples R China
[2] Xidian Univ, Key Lab Elect Equipment Struct Design, Minist Educ, Xian 710071, Shaanxi, Peoples R China
[3] Xidian Univ, Sch Econ & Management, Xian 710071, Shaanxi, Peoples R China
[4] Boston Univ, Ctr Polymer Studies, Boston, MA 02215 USA
[5] Boston Univ, Dept Phys, Boston, MA 02215 USA
基金
中国国家自然科学基金;
关键词
Disease gene discovering; Topological properties; Weighted PPI network; Machine learning; INTERACTION DATABASE; IDENTIFICATION; CENTRALITY; POWER;
D O I
10.1016/j.physa.2017.12.080
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Although there have been many network-based attempts to discover disease-associated genes, most of them have not taken edge weight - which quantifies their relative strength - into consideration. We use connection weights in a protein-protein interaction (PPI) network to locate disease-related genes. We analyze the topological properties of both weighted and unweighted PPI networks and design an improved random forest classifier to distinguish disease genes from non-disease genes. We use a cross-validation test to confirm that weighted networks are better able to discover disease-associated genes than unweighted networks, which indicates that including link weight in the analysis of network properties provides a better model of complex genotype-phenotype associations. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 61
页数:9
相关论文
共 50 条
  • [1] Discovering functional interaction patterns in protein-protein interaction networks
    Turanalp, Mehmet E.
    Can, Tolga
    BMC BIOINFORMATICS, 2008, 9 (1)
  • [2] Discovering functional interaction patterns in protein-protein interaction networks
    Mehmet E Turanalp
    Tolga Can
    BMC Bioinformatics, 9
  • [3] Prediction of protein-protein interaction networks and druggable genes associated with parkinson's disease
    Varadharajan, Venkatramanan
    Ganapathi, Sri Thatchayani
    Mandal, Sanjeeb Kumar
    INDIAN JOURNAL OF BIOCHEMISTRY & BIOPHYSICS, 2022, 59 (01): : 39 - 49
  • [4] DIGNiFI: Discovering causative genes for orphan diseases using protein-protein interaction networks
    Liu, Xiaoxia
    Yang, Zhihao
    Lin, Hongfei
    Simmons, Michael
    Lu, Zhiyong
    PROCEEDINGS OF THE 7TH ACM INTERNATIONAL CONFERENCE ON BIOINFORMATICS, COMPUTATIONAL BIOLOGY, AND HEALTH INFORMATICS, 2016, : 527 - 527
  • [5] DIGNiFI: Discovering causative genes for orphan diseases using protein-protein interaction networks
    Liu, Xiaoxia
    Yang, Zhihao
    Lin, Hongfei
    Simmons, Michael
    Lu, Zhiyong
    BMC SYSTEMS BIOLOGY, 2017, 11
  • [6] Discovering disease-genes by topological features in human protein-protein interaction network
    Xu, Jianzhen
    Li, Yongjin
    BIOINFORMATICS, 2006, 22 (22) : 2800 - 2805
  • [7] Protein-Protein Interaction Sites are Hot Spots for Disease-Associated Nonsynonymous SNPs
    David, Alessia
    Razali, Rozami
    Wass, Mark N.
    Sternberg, Michael J. E.
    HUMAN MUTATION, 2012, 33 (02) : 359 - 363
  • [8] Identifying influential genes in protein-protein interaction networks
    Sun, Peng Gang
    Quan, Yi Ning
    Miao, Qi Guang
    Chi, Juan
    INFORMATION SCIENCES, 2018, 454 : 229 - 241
  • [9] Discovering frequent subgraph patterns from protein-protein interaction networks
    Liu, Mingxing
    Ma, Wubin
    Deng, Su
    Huang, Hongbin
    Journal of Computational Information Systems, 2014, 10 (12): : 5329 - 5337
  • [10] Complexes discovery from weighted protein-protein interaction networks
    Liu, Lizhen
    Cheng, Miaomiao
    Wang, Hanshi
    Song, Wei
    Journal of Bionanoscience, 2015, 9 (01): : 55 - 62