Evidence map›Paper›PMID 32241268›Full record

ArticleBMC medical genomics2020

Prediction of circRNA-disease associations based on inductive matrix completion.

Menglu Li, Mengya Liu, Yannan Bin, Junfeng Xia

Abstract read
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Article in BMC medical genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

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22citing papers in PubMed
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1 · What the graph read from it

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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

22 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Menglu LiKey Laboratory of Intelligent Computing and Signal Processing of Ministry of Education, School of Computer Science and Technology, Anhui University, Hefei, 230601, Anhui, China.
Mengya LiuInstitutes of Physical Science and Information Technology, Anhui University, Hefei, 230601, Anhui, China.
Yannan BinKey Laboratory of Intelligent Computing and Signal Processing of Ministry of Education, School of Computer Science and Technology, Anhui University, Hefei, 230601, Anhui, China.
Junfeng XiaKey Laboratory of Intelligent Computing and Signal Processing of Ministry of Education, School of Computer Science and Technology, Anhui University, Hefei, 230601, Anhui, China. jfxia@ahu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrently, numerous studies indicate that circular RNA (circRNA) is associated with various human complex diseases. While identifying disease-related circRNAs in vivo is time- and labor-consuming, a feasible and effective computational method to predict circRNA-disease associations is worthy of more studies.

resultsHere, we present a new method called SIMCCDA (Speedup Inductive Matrix Completion for CircRNA-Disease Associations prediction) to predict circRNA-disease associations. Based on known circRNA-disease associations, circRNA sequence similarity, disease semantic similarity, and the computed Gaussian interaction profile kernel similarity, we used speedup inductive matrix completion to construct the model. The proposed SIMCCDA method obtains an area under ROC curve (AUC) of 0.8465 with leave-one-out cross validation in the dataset, which is obtained by the combination of the three databases (circRNA disease, circ2Disease and circR2Disease). Our method surpasses other state-of-art models in predicting circRNA-disease associations. Furthermore, we conducted case studies in breast cancer, stomach cancer and colorectal cancer for further performance evaluation.

conclusionAll the results show reliable prediction ability of SIMCCDA. We anticipate that SIMCCDA could be utilized to facilitate further developments in the field and follow-up investigations by biomedical researchers.

Indexed as

AlgorithmsGene Expression Regulation, NeoplasticBiomarkers, TumorComputational BiologyGene Regulatory NetworksHumansNeoplasmsPrognosisRNA, CircularRNA-SeqTranscriptomeBiomarkers, TumorRNA, CircularCircRNA-disease associationsCircRNA sequence similarityDisease semantic similarityInductive matrix completion

Identifiers

PMID32241268
PMCPMC7118830

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LicenceCC BY
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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.