Evidence map›Paper›PMID 28177900›Full record

ArticleOncotarget2017

MCMDA: Matrix completion for MiRNA-disease association prediction.

Jian-Qiang Li, Zhi-Hao Rong, Xing Chen, Gui-Ying Yan, Zhu-Hong You

Abstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

92 citing papers in PubMed.

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32 more citing papers are in PubMed but not listed here.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jian-Qiang LiCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, 518060, China.
Zhi-Hao RongSchool of Software, Beihang University, Beijing, 100191, China.
Xing ChenSchool of Information and Control Engineering, China University of Mining and Technology, Xuzhou, 221116, China.
Gui-Ying YanAcademy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, 100190, China.
Zhu-Hong YouXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Science, ürümqi, 830011, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nowadays, researchers have realized that microRNAs (miRNAs) are playing a significant role in many important biological processes and they are closely connected with various complex human diseases. However, since there are too many possible miRNA-disease associations to analyze, it remains difficult to predict the potential miRNAs related to human diseases without a systematic and effective method. In this study, we developed a Matrix Completion for MiRNA-Disease Association prediction model (MCMDA) based on the known miRNA-disease associations in HMDD database. MCMDA model utilized the matrix completion algorithm to update the adjacency matrix of known miRNA-disease associations and furthermore predict the potential associations. To evaluate the performance of MCMDA, we performed leave-one-out cross validation (LOOCV) and 5-fold cross validation to compare MCMDA with three previous classical computational models (RLSMDA, HDMP, and WBSMDA). As a result, MCMDA achieved AUCs of 0.8749 in global LOOCV, 0.7718 in local LOOCV and average AUC of 0.8767+/-0.0011 in 5-fold cross validation. Moreover, the prediction results associated with colon neoplasms, kidney neoplasms, lymphoma and prostate neoplasms were verified. As a consequence, 84%, 86%, 78% and 90% of the top 50 potential miRNAs for these four diseases were respectively confirmed by recent experimental discoveries. Therefore, MCMDA model is superior to the previous models in that it improves the prediction performance although it only depends on the known miRNA-disease associations.

Indexed as

AlgorithmsArea Under CurveColonic NeoplasmsComputational BiologyComputer SimulationGenetic Association StudiesGenetic Predisposition to DiseaseHumansKidney NeoplasmsLymphomaMicroRNAsROC CurveSensitivity and SpecificityMicroRNAsdiseasematrix completionmiRNAmiRNA-disease association

Identifiers

PMID28177900
PMCPMC5400576

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.