Evidence map›Paper›PMID 32523330›Full record

ArticleEvolutionary bioinformatics online2020

Deep belief network-Based Matrix Factorization Model for MicroRNA-Disease Associations Prediction.

Yulian Ding, Fei Wang, Xiujuan Lei, Bo Liao, Fang-Xiang Wu

Abstract read
In one paragraph

Article in Evolutionary bioinformatics online, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yulian DingDivision of Biomedical Engineering, University of Saskatchewan, Saskatoon, SK, Canada.
Fei WangDivision of Biomedical Engineering, University of Saskatchewan, Saskatoon, SK, Canada.
Xiujuan LeiSchool of Computer Science, Shaanxi Normal University, Xi'an, China.
Bo LiaoSchool of Mathematics and Statistics, Hainan Normal University, Haikou, China.
Fang-Xiang WuDivision of Biomedical Engineering, University of Saskatchewan, Saskatoon, SK, Canada.ORCID https://orcid.org/0000-0002-4593-9332

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small single-stranded noncoding RNAs that have shown to play a critical role in regulating gene expression. In past decades, cumulative experimental studies have verified that miRNAs are implicated in many complex human diseases and might be potential biomarkers for various types of diseases. With the increase of miRNA-related data and the development of analysis methodologies, some computational methods have been developed for predicting miRNA-disease associations, which are more economical and time-saving than traditional biological experimental approaches. In this study, a novel computational model, deep belief network (DBN)-based matrix factorization (DBN-MF), is proposed for miRNA-disease association prediction. First, the raw interaction features of miRNAs and diseases were obtained from the miRNA-disease adjacent matrix. Second, 2 DBNs were used for unsupervised learning of the features of miRNAs and diseases, respectively, based on the raw interaction features. Finally, a classifier consisting of 2 DBNs and a cosine score function was trained with the initial weights of DBN from the last step. During the training, the miRNA-disease adjacent matrix was factorized into 2 feature matrices for the representation of miRNAs and diseases, and the final prediction label was obtained according to the feature matrices. The experimental results show that the proposed model outperforms the state-of-the-art approaches in miRNA-disease association prediction based on the 10-fold cross-validation. Besides, the effectiveness of our model was further demonstrated by case studies.

Indexed as

deep belief networkdiseasematrix factorizationMicroRNAmicroRNA-disease association

Identifiers

PMID32523330
PMCPMC7235669

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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.