Evidence map›Paper›PMID 30499204›Full record

ArticleJournal of cellular and molecular medicine2019

MCLPMDA: A novel method for miRNA-disease association prediction based on matrix completion and label propagation.

Sheng-Peng Yu, Cheng Liang, Qiu Xiao, Guang-Hui Li, Ping-Jian Ding, Jia-Wei Luo

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

6 authors at 4 institutions in 1 country.

Sheng-Peng YuSchool of Information Science and Engineering, Shandong Normal University, Jinan, China.
Cheng LiangSchool of Information Science and Engineering, Shandong Normal University, Jinan, China.ORCID 0000-0003-3832-0969
Qiu XiaoCollege of Information Science and Engineering, Hunan Normal University, Changsha, China.
Guang-Hui LiSchool of Information Engineering, East China Jiaotong University, Nanchang, China.
Ping-Jian DingCollege of Information Science and Engineering, Hunan University, Changsha, China.
Jia-Wei LuoCollege of Information Science and Engineering, Hunan University, Changsha, China.
Hunan University · CNShandong Normal University · CNEast China Jiaotong University · CNHunan Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiRNAs are a class of small non-coding RNAs that are involved in the development and progression of various complex diseases. Great efforts have been made to discover potential associations between miRNAs and diseases recently. As experimental methods are in general expensive and time-consuming, a large number of computational models have been developed to effectively predict reliable disease-related miRNAs. However, the inherent noise and incompleteness in the existing biological datasets have inevitably limited the prediction accuracy of current computational models. To solve this issue, in this paper, we propose a novel method for miRNA-disease association prediction based on matrix completion and label propagation. Specifically, our method first reconstructs a new miRNA/disease similarity matrix by matrix completion algorithm based on known experimentally verified miRNA-disease associations and then utilizes the label propagation algorithm to reliably predict disease-related miRNAs. As a result, MCLPMDA achieved comparable performance under different evaluation metrics and was capable of discovering greater number of true miRNA-disease associations. Moreover, case study conducted on Breast Neoplasms further confirmed the prediction reliability of the proposed method. Taken together, the experimental results clearly demonstrated that MCLPMDA can serve as an effective and reliable tool for miRNA-disease association prediction.

Indexed as

Genetic Predisposition to DiseaseAlgorithmsBreast NeoplasmsComputational BiologyComputer SimulationFemaleGenetic Association StudiesGenetic Diseases, InbornHumansMicroRNAsMicroRNAslabel propagationmatrix completionmiRNA-disease association prediction

Identifiers

PMID30499204
PMCPMC6349206
OpenAlexW2902400385

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.