Evidence map›Paper›PMID 38408987›Full record

ArticleBMC biology2024

CircRNA identification and feature interpretability analysis.

Mengting Niu, Chunyu Wang, Yaojia Chen, Quan Zou, Ren Qi, Lei Xu

Abstract read
In one paragraph

Article in BMC biology, 2024. 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.

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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.

Mengting NiuSchool of Electronic and Communication Engineering, Shenzhen Polytechnic University, Shenzhen, 518055, China.ORCID http://orcid.org/0000-0001-9175-4649
Chunyu WangFaculty of Computing, Harbin Institute of Technology, Harbin, 150000, Heilongjiang, China.
Yaojia ChenInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, No.4 Block 2 North Jianshe Road, Chengdu, 610054, China.
Quan ZouInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, No.4 Block 2 North Jianshe Road, Chengdu, 610054, China.
Ren QiSchool of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China. qiren@tju.edu.cn.
Lei XuSchool of Electronic and Communication Engineering, Shenzhen Polytechnic University, Shenzhen, 518055, China. csleixu@szpu.edu.cn.

Funding

Key Field of Department of Education of Guangdong Province 2022ZDZX2082Municipal Government of Quzhou under Grant Number 2022D023National Natural Science Foundation of China 61872114National Natural Science Foundation of China 61922020National Natural Science Foundation of China 62131004National Natural Science Foundation of China 62201129National Natural Science Foundation of China 62231013National Natural Science Foundation of China 62271329National Natural Science Foundation of China 62302341National Natural Science Foundation of China 62303328National Natural Science Foundation of China 62372332Research fund of Shenzhen Polytechnic University 6022310036KResearch fund of Shenzhen Polytechnic University 6023310037KShenzhen Fundamental Research and Discipline Layout project 6022331007KSichuan Provincial Science Fund for Distinguished Young Scholars 2021JDJQ0025Special Science Foundation of Quzhou 2023D036Zhejiang Provincial Post-doctor Excellent Scientific Research Project Fund ZJ2022038
6 · The paper itself

Abstract

backgroundCircular RNAs (circRNAs) can regulate microRNA activity and are related to various diseases, such as cancer. Functional research on circRNAs is the focus of scientific research. Accurate identification of circRNAs is important for gaining insight into their functions. Although several circRNA prediction models have been developed, their prediction accuracy is still unsatisfactory. Therefore, providing a more accurate computational framework to predict circRNAs and analyse their looping characteristics is crucial for systematic annotation.

resultsWe developed a novel framework, CircDC, for classifying circRNAs from other lncRNAs. CircDC uses four different feature encoding schemes and adopts a multilayer convolutional neural network and bidirectional long short-term memory network to learn high-order feature representation and make circRNA predictions. The results demonstrate that the proposed CircDC model is more accurate than existing models. In addition, an interpretable analysis of the features affecting the model is performed, and the computational framework is applied to the extended application of circRNA identification.

conclusionsCircDC is suitable for the prediction of circRNA. The identification of circRNA helps to understand and delve into the related biological processes and functions. Feature importance analysis increases model interpretability and uncovers significant biological properties. The relevant code and data in this article can be accessed for free at https://github.com/nmt315320/CircDC.git .

Indexed as

MicroRNAsNeoplasmsComputational BiologyHumansNeural Networks, ComputerRNA, CircularMicroRNAsRNA, CircularCircRNADeep learningFeatureInterpretationSHAP

Identifiers

PMID38408987
PMCPMC10898045

What OpenQuestion holds

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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.