Evidence map›Paper›PMID 31555320›Full record

ArticleFrontiers in genetics2019

Predicting lncRNA-miRNA Interaction

Yu-An Huang, Zhi-An Huang, Zhu-Hong You, Zexuan Zhu, Wen-Zhun Huang, Jian-Xin Guo, Chang-Qing Yu

Abstract read
In one paragraph

Article in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

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

21 citing papers in PubMed.

  1. Bioinformatics Approaches in Noncoding RNAs Research.Experientia supplementum (2012) · 2026
    Review
  2. Review
  3. lncRNA TUG1 and kidney diseases.BMC nephrology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Role of miR-424 in the carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  8. Article
  9. PmliHFM: Predicting Plant miRNA-lncRNA Interactions with Hybrid Feature Mining Network.Interdisciplinary sciences, computational life sciences · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Bioinformatic Tools for the Analysis and Prediction of ncRNA Interactions.International journal of molecular sciences · 2021
    Review
  15. Review
  16. Review
  17. Article
  18. A Compressive Review about TaxolMolecules (Basel, Switzerland) · 2020
    Review
  19. Application of deep learning in genomics.Science China. Life sciences · 2020
    Review
  20. Review
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.

Yu-An HuangCollege of Electronics and Information Engineering, Xijing University, Xi'an, China.
Zhi-An HuangDepartment of Computer Science, City University of Hong Kong, Kowloon, Hong Kong.
Zhu-Hong YouCollege of Electronics and Information Engineering, Xijing University, Xi'an, China.
Zexuan ZhuCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, China.
Wen-Zhun HuangCollege of Electronics and Information Engineering, Xijing University, Xi'an, China.
Jian-Xin GuoCollege of Electronics and Information Engineering, Xijing University, Xi'an, China.
Chang-Qing YuCollege of Electronics and Information Engineering, Xijing University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interaction of miRNA and lncRNA is known to be important for gene regulations. However, the number of known lncRNA-miRNA interactions is still very limited and there are limited computational tools available for predicting new ones. Considering that lncRNAs and miRNAs share internal patterns in the partnership between each other, the underlying lncRNA-miRNA interactions could be predicted by utilizing the known ones, which could be considered as a semi-supervised learning problem. It is shown that the attributes of lncRNA and miRNA have a close relationship with the interaction between each other. Effective use of side information could be helpful for improving the performance especially when the training samples are limited. In view of this, we proposed an end-to-end prediction model called GCLMI (Graph Convolution for novel lncRNA-miRNA Interactions) by combining the techniques of graph convolution and auto-encoder. Without any preprocessing process on the feature information, our method can incorporate raw data of node attributes with the topology of the interaction network. Based on a real dataset collected from a public database, the results of experiments conducted on k-fold cross validations illustrate the robustness and effectiveness of the prediction performance of the proposed prediction model. We prove the graph convolution layer as designed in the proposed model able to effectively integrate the input data by filtering the graph with node features. The proposed model is anticipated to yield highly potential lncRNA-miRNA interactions in the scenario that different types of numerical features describing lncRNA or miRNA are provided by users, serving as a useful computational tool.

Indexed as

computational prediction modelgraph convolution networkLncRNA–miRNA interactionsregulation networksystem biology model

Identifiers

PMID31555320
PMCPMC6727066

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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.