Evidence map›Paper›PMID 27323856›Full record

ArticleOncotarget2016

IntNetLncSim: an integrative network analysis method to infer human lncRNA functional similarity.

Liang Cheng, Hongbo Shi, Zhenzhen Wang, Yang Hu, Haixiu Yang, Chen Zhou, Jie Sun, Meng Zhou

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Identification ofComputational and mathematical methods in medicine · 2022
    Article
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  7. Review
  8. Article
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  13. Comprehensive Analysis Revealed thatFrontiers in cell and developmental biology · 2021
    Article
  14. Review
  15. Article
  16. Article
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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

8 authors.

Liang ChengCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, PR China.
Hongbo ShiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, PR China.
Zhenzhen WangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, PR China.
Yang HuSchool of Life Science and Technology, Harbin Institute of Technology, Harbin 150001, PR China.
Haixiu YangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, PR China.
Chen ZhouCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, PR China.
Jie SunCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, PR China.
Meng ZhouCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence indicated that long non-coding RNAs (lncRNAs) were involved in various biological processes and complex diseases by communicating with mRNAs/miRNAs each other. Exploiting interactions between lncRNAs and mRNA/miRNAs to lncRNA functional similarity (LFS) is an effective method to explore function of lncRNAs and predict novel lncRNA-disease associations. In this article, we proposed an integrative framework, IntNetLncSim, to infer LFS by modeling the information flow in an integrated network that comprises both lncRNA-related transcriptional and post-transcriptional information. The performance of IntNetLncSim was evaluated by investigating the relationship of LFS with the similarity of lncRNA-related mRNA sets (LmRSets) and miRNA sets (LmiRSets). As a result, LFS by IntNetLncSim was significant positively correlated with the LmRSet (Pearson correlation γ2=0.8424) and LmiRSet (Pearson correlation γ2=0.2601). Particularly, the performance of IntNetLncSim is superior to several previous methods. In the case of applying the LFS to identify novel lncRNA-disease relationships, we achieved an area under the ROC curve (0.7300) in experimentally verified lncRNA-disease associations based on leave-one-out cross-validation. Furthermore, highly-ranked lncRNA-disease associations confirmed by literature mining demonstrated the excellent performance of IntNetLncSim. Finally, a web-accessible system was provided for querying LFS and potential lncRNA-disease relationships: http://www.bio-bigdata.com/IntNetLncSim.

Indexed as

Gene Regulatory NetworksModels, GeneticCarrier ProteinsHumansMicroRNAsNuclear ProteinsRNA, Long NoncodingCarrier ProteinsMicroRNAsMRNIP protein, humanNuclear ProteinsRNA, Long Noncodingintegrated networklncRNA-disease associationslncRNA functional similaritylong non-coding RNAs

Identifiers

PMID27323856
PMCPMC5216984

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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.