DisSetSim: an online system for calculating similarity between disease sets

Functional similarity between molecules results in similar phenotypes, such as diseases. Therefore, it is an effective way to reveal the function of molecules based on their induced diseases. However, the lack of a tool for obtaining the similarity score of pair-wise disease sets (SSDS) limits this...

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Published inJournal of biomedical semantics Vol. 8; no. S1; pp. 28 - 25
Main Authors Hu, Yang, Zhao, Lingling, Liu, Zhiyan, Ju, Hong, Shi, Hongbo, Xu, Peigang, Wang, Yadong, Cheng, Liang
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 20.09.2017
BioMed Central
BMC
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Summary:Functional similarity between molecules results in similar phenotypes, such as diseases. Therefore, it is an effective way to reveal the function of molecules based on their induced diseases. However, the lack of a tool for obtaining the similarity score of pair-wise disease sets (SSDS) limits this type of application. Here, we introduce DisSetSim, an online system to solve this problem in this article. Five state-of-the-art methods involving Resnik's, Lin's, Wang's, PSB, and SemFunSim methods were implemented to measure the similarity score of pair-wise diseases (SSD) first. And then "pair-wise-best pairs-average" (PWBPA) method was implemented to calculated the SSDS by the SSD. The system was applied for calculating the functional similarity of miRNAs based on their induced disease sets. The results were further used to predict potential disease-miRNA relationships. The high area under the receiver operating characteristic curve AUC (0.9296) based on leave-one-out cross validation shows that the PWBPA method achieves a high true positive rate and a low false positive rate. The system can be accessed from http://www.bio-annotation.cn:8080/DisSetSim/ .
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ISSN:2041-1480
2041-1480
DOI:10.1186/s13326-017-0140-2