Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.

<h4>Background</h4>The identification of human disease-related microRNAs (disease miRNAs) is important for further investigating their involvement in the pathogenesis of diseases. More experimentally validated miRNA-disease associations have been accumulated recently. On the basis of the...

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Main Authors: Ping Xuan, Ke Han, Maozu Guo, Yahong Guo, Jinbao Li, Jian Ding, Yong Liu, Qiguo Dai, Jin Li, Zhixia Teng, Yufei Huang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23950912/?tool=EBI
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spelling doaj-065252b329b546a5b742ca3fe8994d0c2021-03-04T12:07:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7020410.1371/journal.pone.0070204Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.Ping XuanKe HanMaozu GuoYahong GuoJinbao LiJian DingYong LiuQiguo DaiJin LiZhixia TengYufei Huang<h4>Background</h4>The identification of human disease-related microRNAs (disease miRNAs) is important for further investigating their involvement in the pathogenesis of diseases. More experimentally validated miRNA-disease associations have been accumulated recently. On the basis of these associations, it is essential to predict disease miRNAs for various human diseases. It is useful in providing reliable disease miRNA candidates for subsequent experimental studies.<h4>Methodology/principal findings</h4>It is known that miRNAs with similar functions are often associated with similar diseases and vice versa. Therefore, the functional similarity of two miRNAs has been successfully estimated by measuring the semantic similarity of their associated diseases. To effectively predict disease miRNAs, we calculated the functional similarity by incorporating the information content of disease terms and phenotype similarity between diseases. Furthermore, the members of miRNA family or cluster are assigned higher weight since they are more probably associated with similar diseases. A new prediction method, HDMP, based on weighted k most similar neighbors is presented for predicting disease miRNAs. Experiments validated that HDMP achieved significantly higher prediction performance than existing methods. In addition, the case studies examining prostatic neoplasms, breast neoplasms, and lung neoplasms, showed that HDMP can uncover potential disease miRNA candidates.<h4>Conclusions</h4>The superior performance of HDMP can be attributed to the accurate measurement of miRNA functional similarity, the weight assignment based on miRNA family or cluster, and the effective prediction based on weighted k most similar neighbors. The online prediction and analysis tool is freely available at http://nclab.hit.edu.cn/hdmpred.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23950912/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Ping Xuan
Ke Han
Maozu Guo
Yahong Guo
Jinbao Li
Jian Ding
Yong Liu
Qiguo Dai
Jin Li
Zhixia Teng
Yufei Huang
spellingShingle Ping Xuan
Ke Han
Maozu Guo
Yahong Guo
Jinbao Li
Jian Ding
Yong Liu
Qiguo Dai
Jin Li
Zhixia Teng
Yufei Huang
Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.
PLoS ONE
author_facet Ping Xuan
Ke Han
Maozu Guo
Yahong Guo
Jinbao Li
Jian Ding
Yong Liu
Qiguo Dai
Jin Li
Zhixia Teng
Yufei Huang
author_sort Ping Xuan
title Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.
title_short Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.
title_full Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.
title_fullStr Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.
title_full_unstemmed Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors.
title_sort prediction of micrornas associated with human diseases based on weighted k most similar neighbors.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description <h4>Background</h4>The identification of human disease-related microRNAs (disease miRNAs) is important for further investigating their involvement in the pathogenesis of diseases. More experimentally validated miRNA-disease associations have been accumulated recently. On the basis of these associations, it is essential to predict disease miRNAs for various human diseases. It is useful in providing reliable disease miRNA candidates for subsequent experimental studies.<h4>Methodology/principal findings</h4>It is known that miRNAs with similar functions are often associated with similar diseases and vice versa. Therefore, the functional similarity of two miRNAs has been successfully estimated by measuring the semantic similarity of their associated diseases. To effectively predict disease miRNAs, we calculated the functional similarity by incorporating the information content of disease terms and phenotype similarity between diseases. Furthermore, the members of miRNA family or cluster are assigned higher weight since they are more probably associated with similar diseases. A new prediction method, HDMP, based on weighted k most similar neighbors is presented for predicting disease miRNAs. Experiments validated that HDMP achieved significantly higher prediction performance than existing methods. In addition, the case studies examining prostatic neoplasms, breast neoplasms, and lung neoplasms, showed that HDMP can uncover potential disease miRNA candidates.<h4>Conclusions</h4>The superior performance of HDMP can be attributed to the accurate measurement of miRNA functional similarity, the weight assignment based on miRNA family or cluster, and the effective prediction based on weighted k most similar neighbors. The online prediction and analysis tool is freely available at http://nclab.hit.edu.cn/hdmpred.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23950912/?tool=EBI
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