Evidence map›Paper›PMID 31510011›Full record

ArticleInternational journal of molecular sciences2019

LDAPred: A Method Based on Information Flow Propagation and a Convolutional Neural Network for the Prediction of Disease-Associated lncRNAs.

Ping Xuan, Lan Jia, Tiangang Zhang, Nan Sheng, Xiaokun Li, Jinbao Li

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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.

Ping XuanSchool of Computer Science and Technology, Heilongjiang University, Harbin 150080, China. xuanping@hlju.edu.cn.
Lan JiaSchool of Computer Science and Technology, Heilongjiang University, Harbin 150080, China. jialan_yee@163.com.
Tiangang ZhangSchool of Mathematical Science, Heilongjiang University, Harbin 150080, China. zhang@hlju.edu.cn.
Nan ShengSchool of Computer Science and Technology, Heilongjiang University, Harbin 150080, China. shengnanwangyi@163.com.
Xiaokun LiPostdoctoral Program of Heilongjiang Hengxun Technology Co., Ltd., Harbin 150090, China. xiaokun_li_hx_hlju@163.com.
Jinbao LiSchool of Computer Science and Technology, Heilongjiang University, Harbin 150080, China. jbli@hlju.edu.cn.

Funding

China Postdoctoral Science Foundation 2019M650069Fundamental Research Foundation of Universities in Heilongjiang Province for Technology Innovation KJCX201805Fundamental Research Foundation of Universities in Heilongjiang Province for Youth Innovation Team RCYJTD201805Heilongjiang Postdoctoral Scientific Research Staring Foundation BHL-Q18104National Natural Science Foundation of China 61702296, 61302139Natural Science Foundation of Heilongjiang Province LH2019F049, LH2019A029
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) play a crucial role in the pathogenesis and development of complex diseases. Predicting potential lncRNA-disease associations can improve our understanding of the molecular mechanisms of human diseases and help identify biomarkers for disease diagnosis, treatment, and prevention. Previous research methods have mostly integrated the similarity and association information of lncRNAs and diseases, without considering the topological structure information among these nodes, which is important for predicting lncRNA-disease associations. We propose a method based on information flow propagation and convolutional neural networks, called LDAPred, to predict disease-related lncRNAs. LDAPred not only integrates the similarities, associations, and interactions among lncRNAs, diseases, and miRNAs, but also exploits the topological structures formed by them. In this study, we construct a dual convolutional neural network-based framework that comprises the left and right sides. The embedding layer on the left side is established by utilizing lncRNA, miRNA, and disease-related biological premises. On the right side of the frame, multiple types of similarity, association, and interaction relationships among lncRNAs, diseases, and miRNAs are calculated based on information flow propagation on the bi-layer networks, such as the lncRNA-disease network. They contain the network topological structure and they are learned by the right side of the framework. The experimental results based on five-fold cross-validation indicate that LDAPred performs better than several state-of-the-art methods. Case studies on breast cancer, colon cancer, and osteosarcoma further demonstrate LDAPred's ability to discover potential lncRNA-disease associations.

Indexed as

AlgorithmsNeural Networks, ComputerComputational BiologyGenetic Predisposition to DiseaseHumansMicroRNAsNeoplasmsReproducibility of ResultsRNA, Long NoncodingSensitivity and SpecificityMicroRNAsRNA, Long Noncodingconvolutional neural networkdeep learninginformation flow propagationlncRNA–disease associationnetwork topological structure

Identifiers

PMID31510011
PMCPMC6771133

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.