Evidence map›Paper›PMID 28857494›Full record

ArticleJournal of cellular and molecular medicine2018

DRMDA: deep representations-based miRNA-disease association prediction.

Xing Chen, Yao Gong, De-Hong Zhang, Zhu-Hong You, Zheng-Wei Li

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

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41citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

41 citing papers in PubMed.

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  10. DF-MDA: An effective diffusion-based computational model for predicting miRNA-disease association.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Xing ChenSchool of Information and Control Engineering, China University of Mining and Technology, Xuzhou, China.ORCID 0000-0001-9028-5342
Yao GongSchool of Life Science, Peking University, Beijing, China.
De-Hong ZhangSchool of Information and Control Engineering, China University of Mining and Technology, Xuzhou, China.
Zhu-Hong YouXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Science, Ürümqi, China.
Zheng-Wei LiSchool of Computer Science and Technology, China University of Mining and Technology, Xuzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, microRNAs (miRNAs) are confirmed to be important molecules within many crucial biological processes and therefore related to various complex human diseases. However, previous methods of predicting miRNA-disease associations have their own deficiencies. Under this circumstance, we developed a prediction method called deep representations-based miRNA-disease association (DRMDA) prediction. The original miRNA-disease association data were extracted from HDMM database. Meanwhile, stacked auto-encoder, greedy layer-wise unsupervised pre-training algorithm and support vector machine were implemented to predict potential associations. We compared DRMDA with five previous classical prediction models (HGIMDA, RLSMDA, HDMP, WBSMDA and RWRMDA) in global leave-one-out cross-validation (LOOCV), local LOOCV and fivefold cross-validation, respectively. The AUCs achieved by DRMDA were 0.9177, 08339 and 0.9156 ± 0.0006 in the three tests above, respectively. In further case studies, we predicted the top 50 potential miRNAs for colon neoplasms, lymphoma and prostate neoplasms, and 88%, 90% and 86% of the predicted miRNA can be verified by experimental evidence, respectively. In conclusion, DRMDA is a promising prediction method which could identify potential and novel miRNA-disease associations.

Indexed as

AlgorithmsDeep LearningGenetic Association StudiesComputational BiologyHumansMicroRNAsNeoplasmsMicroRNAsauto-encoderdeep representationdiseasemiRNAmiRNA-disease association

Identifiers

PMID28857494
PMCPMC5742725

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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.