Integrating random walk and binary regression to identify novel miRNA-disease association

Abstract Background In the last few decades, cumulative experimental researches have witnessed and verified the important roles of microRNAs (miRNAs) in the development of human complex diseases. Benefitting from the rapid growth both in the availability of miRNA-related data and the development of...

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Main Authors: Ya-Wei Niu, Guang-Hui Wang, Gui-Ying Yan, Xing Chen
Format: Article
Language:English
Published: BMC 2019-01-01
Series:BMC Bioinformatics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12859-019-2640-9
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author Ya-Wei Niu
Guang-Hui Wang
Gui-Ying Yan
Xing Chen
author_facet Ya-Wei Niu
Guang-Hui Wang
Gui-Ying Yan
Xing Chen
author_sort Ya-Wei Niu
collection DOAJ
description Abstract Background In the last few decades, cumulative experimental researches have witnessed and verified the important roles of microRNAs (miRNAs) in the development of human complex diseases. Benefitting from the rapid growth both in the availability of miRNA-related data and the development of various analysis methodologies, up until recently, some computational models have been developed to predict human disease related miRNAs, efficiently and quickly. Results In this work, we proposed a computational model of Random Walk and Binary Regression-based MiRNA-Disease Association prediction (RWBRMDA). RWBRMDA extracted features for each miRNA from random walk with restart on the integrated miRNA similarity network for binary logistic regression to predict potential miRNA-disease associations. RWBRMDA obtained AUC of 0.8076 in the leave-one-out cross validation. Additionally, we carried out three different patterns of case studies on four human complex diseases. Specifically, Esophageal cancer and Prostate cancer were conducted as one kind of case study based on known miRNA-disease associations in HMDD v2.0 database. Out of the top 50 predicted miRNAs, 94 and 90% were respectively confirmed by recent experimental reports. To simulate new disease without known related miRNAs, the information of known Breast cancer related miRNAs was removed. As a result, 98% of the top 50 predicted miRNAs for Breast cancer were confirmed. Lymphoma, the verified ratio of which was 88%, was used to assess the prediction robustness of RWBRMDA based on the association records in HMDD v1.0 database. Conclusions We anticipated that RWBRMDA could benefit the future experimental investigations about the relation between human disease and miRNAs by generating promising and testable top-ranked miRNAs, and significantly reducing the effort and cost of identification works.
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spelling doaj.art-486bf5e042ce4cc3b7cdcbbe2794228a2022-12-22T01:46:21ZengBMCBMC Bioinformatics1471-21052019-01-0120111310.1186/s12859-019-2640-9Integrating random walk and binary regression to identify novel miRNA-disease associationYa-Wei Niu0Guang-Hui Wang1Gui-Ying Yan2Xing Chen3School of Mathematics, Shandong UniversitySchool of Mathematics, Shandong UniversityAcademy of Mathematics and Systems Science, Chinese Academy of SciencesSchool of Information and Control Engineering, China University of Mining and TechnologyAbstract Background In the last few decades, cumulative experimental researches have witnessed and verified the important roles of microRNAs (miRNAs) in the development of human complex diseases. Benefitting from the rapid growth both in the availability of miRNA-related data and the development of various analysis methodologies, up until recently, some computational models have been developed to predict human disease related miRNAs, efficiently and quickly. Results In this work, we proposed a computational model of Random Walk and Binary Regression-based MiRNA-Disease Association prediction (RWBRMDA). RWBRMDA extracted features for each miRNA from random walk with restart on the integrated miRNA similarity network for binary logistic regression to predict potential miRNA-disease associations. RWBRMDA obtained AUC of 0.8076 in the leave-one-out cross validation. Additionally, we carried out three different patterns of case studies on four human complex diseases. Specifically, Esophageal cancer and Prostate cancer were conducted as one kind of case study based on known miRNA-disease associations in HMDD v2.0 database. Out of the top 50 predicted miRNAs, 94 and 90% were respectively confirmed by recent experimental reports. To simulate new disease without known related miRNAs, the information of known Breast cancer related miRNAs was removed. As a result, 98% of the top 50 predicted miRNAs for Breast cancer were confirmed. Lymphoma, the verified ratio of which was 88%, was used to assess the prediction robustness of RWBRMDA based on the association records in HMDD v1.0 database. Conclusions We anticipated that RWBRMDA could benefit the future experimental investigations about the relation between human disease and miRNAs by generating promising and testable top-ranked miRNAs, and significantly reducing the effort and cost of identification works.http://link.springer.com/article/10.1186/s12859-019-2640-9microRNADiseasemiRNA-disease associationRandom walkBinary regression
spellingShingle Ya-Wei Niu
Guang-Hui Wang
Gui-Ying Yan
Xing Chen
Integrating random walk and binary regression to identify novel miRNA-disease association
BMC Bioinformatics
microRNA
Disease
miRNA-disease association
Random walk
Binary regression
title Integrating random walk and binary regression to identify novel miRNA-disease association
title_full Integrating random walk and binary regression to identify novel miRNA-disease association
title_fullStr Integrating random walk and binary regression to identify novel miRNA-disease association
title_full_unstemmed Integrating random walk and binary regression to identify novel miRNA-disease association
title_short Integrating random walk and binary regression to identify novel miRNA-disease association
title_sort integrating random walk and binary regression to identify novel mirna disease association
topic microRNA
Disease
miRNA-disease association
Random walk
Binary regression
url http://link.springer.com/article/10.1186/s12859-019-2640-9
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