Evidence map›Paper›PMID 31494494›Full record

ArticleiScience2019

A Learning-Based Method for LncRNA-Disease Association Identification Combing Similarity Information and Rotation Forest.

Zhen-Hao Guo, Zhu-Hong You, Yan-Bin Wang, Hai-Cheng Yi, Zhan-Heng Chen

Abstract read
In one paragraph

Article in iScience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

46 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.

Zhen-Hao GuoXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Zhu-Hong YouXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China. Electronic address: zhuhongyou@ms.xjb.ac.cn.
Yan-Bin WangXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China. Electronic address: wangyanbin15@mails.ucas.ac.cn.
Hai-Cheng YiXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.
Zhan-Heng ChenXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNA (lncRNA) play critical roles in the occurrence and development of various diseases. The determination of the lncRNA-disease associations thus would contribute to provide new insights into the pathogenesis of the disease, the diagnosis, and the gene treatments. Considering that traditional experimental approaches are difficult to detect potential human lncRNA-disease associations from the vast amount of biological data, developing computational method could be of significant value. In this paper, we proposed a novel computational method named LDASR to identify associations between lncRNA and disease by analyzing known lncRNA-disease associations. First, the feature vectors of the lncRNA-disease pairs were obtained by integrating lncRNA Gaussian interaction profile kernel similarity, disease semantic similarity, and Gaussian interaction profile kernel similarity. Second, autoencoder neural network was employed to reduce the feature dimension and get the optimal feature subspace from the original feature set. Finally, Rotating Forest was used to carry out prediction of lncRNA-disease association. The proposed method achieves an excellent preference with 0.9502 AUC in leave-one-out cross-validations (LOOCV) and 0.9428 AUC in 5-fold cross-validation, which significantly outperformed previous methods. Moreover, two kinds of case studies on identifying lncRNAs associated with colorectal cancer and glioma further proves the capability of LDASR in identifying novel lncRNA-disease associations. The promising experimental results show that the LDASR can be an excellent addition to the biomedical research in the future.

Indexed as

Biocomputational MethodBioinformaticsComputational Bioinformatics

Identifiers

PMID31494494
PMCPMC6733997

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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.