Evidence map›Paper›PMID 35428965›Full record

ArticleInterdisciplinary sciences, computational life sciences2022

DNRLCNN: A CNN Framework for Identifying MiRNA-Disease Associations Using Latent Feature Matrix Extraction with Positive Samples.

Jiancheng Zhong, Wubin Zhou, Jiedong Kang, Zhuo Fang, Minzhu Xie, Qiu Xiao, Wei Peng

Abstract read
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In one paragraph

Article in Interdisciplinary sciences, computational life sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 37% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

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

7 authors at 3 institutions in 1 country.

Jiancheng ZhongCollege of Information Science and Engineering, Hunan Normal University, Changsha, 410083, China.
Wubin ZhouCollege of Information Science and Engineering, Hunan Normal University, Changsha, 410083, China.
Jiedong KangCollege of Information Science and Engineering, Hunan Normal University, Changsha, 410083, China.
Zhuo FangCollege of Information Science and Engineering, Hunan Normal University, Changsha, 410083, China.
Minzhu XieCollege of Information Science and Engineering, Hunan Normal University, Changsha, 410083, China.
Qiu XiaoCollege of Information Science and Engineering, Hunan Normal University, Changsha, 410083, China. xiaoqiu@hunnu.edu.cn.
Wei PengFaculty of Information Engineering and Automation, Kunming University of Science and Technology, Kunming, 650500, China. weipeng1980@gmail.com.
Hunan Normal University · CNChangsha Normal University · CNKunming University of Science and Technology · CN

Funding

Chinese Government Scholarship 201906725017Hunan Provincial Science and Technology Department No.2018WK4001National Natural Science Foundation of China 61972185National Natural Science Foundation of China No. 62002116Natural Science Foundation of Hunan Province 2020JJ5373Natural Science Foundation of Hunan Province Nos.2018JJ2262Scientific Research Fund of Hunan Provincial Education Department 19A316Scientific Research Fund of Hunan Provincial Education Department 20B348Scientific Research Fund of Hunan Provincial Education Department Nos.15CY007
6 · The paper itself

Abstract

Emerging evidence indicates that miRNAs have strong relationships with many human diseases. Investigating the associations will contribute to elucidating the activities of miRNAs and pathogenesis mechanisms, and providing new opportunities for disease diagnosis and drug discovery. Therefore, it is of significance to identify potential associations between miRNAs and diseases. The existing databases about the miRNA-disease associations (MDAs) only provide the known MDAs, which can be regarded as positive samples. However, the unknown MDAs are not sufficient to regard as reliable negative samples. To deal with this uncertainty, we proposed a convolutional neural network (CNN) framework, named DNRLCNN, based on a latent feature matrix extracted by only positive samples to predict MDAs. First, by only considering the positive samples into the calculation process, we captured the latent feature matrix for complex interactions between miRNAs and diseases in low-dimensional space. Then, we constructed a feature vector for each miRNA and disease pair based on the feature representation. Finally, we adopted a modified CNN for the feature vector to predict MDAs. As a result, our model achieves better performance than other state-of-the-art methods which based CNN in fivefold cross-validation on both miRNA-disease association prediction task (average AUC of 0.9030) and miRNA-phenotype association prediction task (average AUC of 0. 9442). In addition, we carried out case studies on two human diseases, and all the top-50 predicted miRNAs for lung neoplasms are confirmed by HMDD v3.2 and dbDEMC 2.0 databases, 98% of the top-50 predicted miRNAs for heart failure are confirmed. The experiment results show that our model has the capability of inferring potential disease-related miRNAs.

Indexed as

MicroRNAsAlgorithmsComputational BiologyGenetic Predisposition to DiseaseHumansNeural Networks, ComputerMicroRNAsConvolutional neural networkDisease–gene associationLatent feature extractionPositive samplesSimilarity networks

Identifiers

PMID35428965
OpenAlexW4223916839

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.