Evidence map›Paper›PMID 32736513›Full record

ArticleBMC bioinformatics2020

IDSSIM: an lncRNA functional similarity calculation model based on an improved disease semantic similarity method.

Wenwen Fan, Junliang Shang, Feng Li, Yan Sun, Shasha Yuan, Jin-Xing Liu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

6 authors.

Wenwen FanSchool of Information Science and Engineering, Qufu Normal University, Rizhao, 276826, China.
Junliang ShangSchool of Information Science and Engineering, Qufu Normal University, Rizhao, 276826, China. shangjunliang110@163.com.ORCID http://orcid.org/0000-0002-8488-2228
Feng LiSchool of Information Science and Engineering, Qufu Normal University, Rizhao, 276826, China.
Yan SunSchool of Information Science and Engineering, Qufu Normal University, Rizhao, 276826, China.
Shasha YuanSchool of Information Science and Engineering, Qufu Normal University, Rizhao, 276826, China.
Jin-Xing LiuSchool of Information Science and Engineering, Qufu Normal University, Rizhao, 276826, China.

Funding

China Postdoctoral Science Foundation 2018M642635National Science Foundation of China 61701279National Science Foundation of China 61872220National Science Foundation of China 61902216National Science Foundation of China 61972226
6 · The paper itself

Abstract

backgroundIt has been widely accepted that long non-coding RNAs (lncRNAs) play important roles in the development and progression of human diseases. Many association prediction models have been proposed for predicting lncRNA functions and identifying potential lncRNA-disease associations. Nevertheless, among them, little effort has been attempted to measure lncRNA functional similarity, which is an essential part of association prediction models.

resultsIn this study, we presented an lncRNA functional similarity calculation model, IDSSIM for short, based on an improved disease semantic similarity method, highlight of which is the introduction of information content contribution factor into the semantic value calculation to take into account both the hierarchical structures of disease directed acyclic graphs and the disease specificities. IDSSIM and three state-of-the-art models, i.e., LNCSIM1, LNCSIM2, and ILNCSIM, were evaluated by applying their disease semantic similarity matrices and the lncRNA functional similarity matrices, as well as corresponding matrices of human lncRNA-disease associations coming from either lncRNADisease database or MNDR database, into an association prediction method WKNKN for lncRNA-disease association prediction. In addition, case studies of breast cancer and adenocarcinoma were also performed to validate the effectiveness of IDSSIM.

conclusionsResults demonstrated that in terms of ROC curves and AUC values, IDSSIM is superior to compared models, and can improve accuracy of disease semantic similarity effectively, leading to increase the association prediction ability of the IDSSIM-WKNKN model; in terms of case studies, most of potential disease-associated lncRNAs predicted by IDSSIM can be confirmed by databases and literatures, implying that IDSSIM can serve as a promising tool for predicting lncRNA functions, identifying potential lncRNA-disease associations, and pre-screening candidate lncRNAs to perform biological experiments. The IDSSIM code, all experimental data and prediction results are available online at https://github.com/CDMB-lab/IDSSIM .

Indexed as

AlgorithmsModels, GeneticSemanticsAdenocarcinomaArea Under CurveBreast NeoplasmsComputational BiologyDatabases, GeneticDiseaseFemaleHumansRNA, Long NoncodingROC CurveRNA, Long NoncodingDisease semantic similaritylncRNA-disease associationsLncRNA functional similarity

Identifiers

PMID32736513
PMCPMC7430881

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.