Predicting MicroRNA-Disease Associations Using Network Topological Similarity Based on DeepWalk
Author(s) -
Guanghui Li,
Jiawei Luo,
Qiu Xiao,
Cheng Liang,
Pingjian Ding,
Buwen Cao
Publication year - 2017
Publication title -
ieee access
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 127
ISSN - 2169-3536
DOI - 10.1109/access.2017.2766758
Subject(s) - aerospace , bioengineering , communication, networking and broadcast technologies , components, circuits, devices and systems , computing and processing , engineered materials, dielectrics and plasmas , engineering profession , fields, waves and electromagnetics , general topics for engineers , geoscience , nuclear engineering , photonics and electrooptics , power, energy and industry applications , robotics and control systems , signal processing and analysis , transportation
Recently, increasing experimental studies have shown that microRNAs (miRNAs) involved in multiple physiological processes are connected with several complex human diseases. Identifying human disease-related miRNAs will be useful in uncovering novel prognostic markers for cancer. Currently, several computational approaches have been developed for miRNA-disease association prediction based on the integration of additional biological information of diseases and miRNAs, such as disease semantic similarity and miRNA functional similarity. However, these methods do not work well when this information is unavailable. In this paper, we present a similarity-based miRNA-disease prediction method that enhances the existing association discovery methods through a topology-based similarity measure. DeepWalk, a deep learning method, is utilized in this paper to calculate similarities within a miRNA-disease association network. It shows superior predictive performance for 22 complex diseases, with area under the ROC curve scores ranging from 0.805 to 0.937 by using five-fold cross-validation. In addition, case studies on breast cancer, lung cancer, and prostatic cancer further justify the use of our method to discover latent miRNA-disease pairs.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom