Evidence map›Paper›PMID 30744078›Full record

ArticleGenes2019

A Probabilistic Matrix Factorization Method for Identifying lncRNA-disease Associations.

Zhanwei Xuan, Jiechen Li, Jingwen Yu, Xiang Feng, Bihai Zhao, Lei Wang

Open access · goldAbstract read
In one paragraph

Article in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 64 citations in OpenAlex.

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  18. LLCLPLDA: a novel model for predicting lncRNA-disease associations.Molecular genetics and genomics : MGG · 2019
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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 1 institution in 1 country.

Zhanwei XuanCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, China. Zhanwei_xuan@163.com.
Jiechen LiCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, China. lijiechen39555@163.com.
Jingwen YuCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, China. jingwen.yu18@gmail.com.
Xiang FengCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, China. fengxiang@xtu.edu.cn.
Bihai ZhaoCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, China. bihaizhao@163.com.
Lei WangCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, China. wanglei@xtu.edu.cn.ORCID 0000-0002-5065-8447
Changsha University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, an increasing number of studies have indicated that long-non-coding RNAs (lncRNAs) can participate in various crucial biological processes and can also be used as the most promising biomarkers for the treatment of certain diseases such as coronary artery disease and various cancers. Due to costs and time complexity, the number of possible disease-related lncRNAs that can be verified by traditional biological experiments is very limited. Therefore, in recent years, it has been very popular to use computational models to predict potential disease-lncRNA associations. In this study, we constructed three kinds of association networks, namely the lncRNA-miRNA association network, the miRNA-disease association network, and the lncRNA-disease correlation network firstly. Then, through integrating these three newly constructed association networks, we constructed an lncRNA-disease weighted association network, which would be further updated by adopting the KNN algorithm based on the semantic similarity of diseases and the similarity of lncRNA functions. Thereafter, according to the updated lncRNA-disease weighted association network, a novel computational model called PMFILDA was proposed to infer potential lncRNA-disease associations based on the probability matrix decomposition. Finally, to evaluate the superiority of the new prediction model PMFILDA, we performed Leave One Out Cross-Validation (LOOCV) based on strongly validated data filtered from MNDR and the simulation results indicated that the performance of PMFILDA was better than some state-of-the-art methods. Moreover, case studies of breast cancer, lung cancer, and colorectal cancer were implemented to further estimate the performance of PMFILDA, and simulation results illustrated that PMFILDA could achieve satisfying prediction performance as well.

Indexed as

Genetic Predisposition to DiseaseSoftwareGenome-Wide Association StudyHumansRNA, Long NoncodingRNA, Long Noncodingdiseaseidentifying disease-related lncRNAlncRNAlncRNA-disease associationsmiRNA

Identifiers

PMID30744078
PMCPMC6410097
OpenAlexW2912626494

What OpenQuestion holds

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LicenceCC BY
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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.