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Mining disease genes using integrated protein-protein interaction and gene-gene co-regulation information

  • Jin Li*
  • , Limei Wang
  • , Maozu Guo
  • , Ruijie Zhang
  • , Qiguo Dai
  • , Xiaoyan Liu
  • , Chunyu Wang
  • , Zhixia Teng
  • , Ping Xuan
  • , Mingming Zhang
  • *Corresponding author for this work
  • School of Computer Science and Technology, Harbin Institute of Technology
  • School of Life Science and Technology, Harbin Institute of Technology
  • Harbin Medical University

Research output: Contribution to journalArticlepeer-review

Abstract

In humans, despite the rapid increase in disease-associated gene discovery, a large proportion of disease-associated genes are still unknown. Many network-based approaches have been used to prioritize disease genes. Many networks, such as the protein-protein interaction (PPI), KEGG, and gene co-expression networks, have been used. Expression quantitative trait loci (eQTLs) have been successfully applied for the determination of genes associated with several diseases. In this study, we constructed an eQTL-based gene-gene co-regulation network (GGCRN) and used it to mine for disease genes. We adopted the random walk with restart (RWR) algorithm to mine for genes associated with Alzheimer disease. Compared to the Human Protein Reference Database (HPRD) PPI network alone, the integrated HPRD PPI and GGCRN networks provided faster convergence and revealed new disease-related genes. Therefore, using the RWR algorithm for integrated PPI and GGCRN is an effective method for disease-associated gene mining.

Original languageEnglish
Pages (from-to)251-256
Number of pages6
JournalFEBS Open Bio
Volume5
DOIs
StatePublished - 1 Mar 2015
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Co-regulation network
  • Disease gene mining
  • EQTL
  • Protein-protein interaction
  • Random walk with restart

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