Evidence map›Paper›PMID 29297338›Full record

ArticleBMC medical genomics2017

Measuring disease similarity and predicting disease-related ncRNAs by a novel method.

Yang Hu, Meng Zhou, Hongbo Shi, Hong Ju, Qinghua Jiang, Liang Cheng

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

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  13. PWCDA: Path Weighted Method for Predicting circRNA-Disease Associations.International journal of molecular sciences · 2018
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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

6 authors at 3 institutions in 1 country.

Yang HuSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, 150001, People's Republic of China.
Meng ZhouCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150001, China.
Hongbo ShiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150001, China.
Hong JuDepartment of information engineering, Heilongjiang biological science and technology Career Academy, Harbin, 150001, China.
Qinghua JiangSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, 150001, People's Republic of China. qhjiang@hit.edu.cn.
Liang ChengCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150001, China. liangcheng@hrbmu.edu.cn.
Harbin Medical University · CNHarbin Institute of Technology · CNHeilongjiang Academy of Forestry · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSimilar diseases are always caused by similar molecular origins, such as diasease-related protein-coding genes (PCGs). And the molecular associations reflect their similarity. Therefore, current methods for calculating disease similarity often utilized functional interactions of PCGs. Besides, the existing methods have neglected a fact that genes could also be associated in the gene functional network (GFN) based on intermediate nodes.

methodsHere we presented a novel method, InfDisSim, to deduce the similarity of diseases. InfDisSim utilized the whole network based on random walk with damping to model the information flow. A benchmark set of similar disease pairs was employed to evaluate the performance of InfDisSim.

resultsThe region beneath the receiver operating characteristic curve (AUC) was calculated to assess the performance. As a result, InfDisSim reaches a high AUC (0.9786) which indicates a very good performance. Furthermore, after calculating the disease similarity by the InfDisSim, we reconfirmed that similar diseases tend to have common therapeutic drugs (Pearson correlation γ

conclusionsThe high AUC based on benchmark data indicates the method performs well. The method is valuable in the prediction of disease-related lncRNAs and miRNAs.

Indexed as

Computational BiologyDiseaseGene Regulatory NetworksHumansMicroRNAsRNA, Long NoncodingMicroRNAsRNA, Long NoncodingDisease similarityGene functional networkInformation flowlncRNA similarity network

Identifiers

PMID29297338
PMCPMC5751624
OpenAlexW2776616144

What OpenQuestion holds

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LicenceCC BY
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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.