MicroRNA Prediction Based on 3D Graphical Representation of RNA Secondary Structures

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Date

2019

Journal Title

Journal ISSN

Volume Title

Publisher

Tubitak Scientific & Technological Research Council Turkey

Open Access Color

GOLD

Green Open Access

Yes

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93

OpenAIRE Views

175

Publicly Funded

No
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Average
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Average
Popularity
Top 10%

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Abstract

MicroRNAs (miRNAs) are posttranscriptional regulators of gene expression. While a miRNA can target hundreds of messenger RNA (mRNAs), an mRNA can be targeted by different miRNAs, not to mention that a single miRNA might have various binding sites in an mRNA sequence. Therefore, it is quite involved to investigate miRNAs experimentally. Thus, machine learning (ML) is frequently used to overcome such challenges. The key parts of a ML analysis largely depend on the quality of input data and the capacity of the features describing the data. Previously, more than 1000 features were suggested for miRNAs. Here, it is shown that using 36 features representing the RNA secondary structure and its dynamic 3D graphical representation provides up to 98% accuracy values. In this study, a new approach for ML-based miRNA prediction is proposed. Thousands of models are generated through classification of known human miRNAs and pseudohairpins with 3 classifiers: decision tree, naive Bayes, and random forest. Although the method is based on human data, the best model was able to correctly assign 96% of nonhuman hairpins from MirGeneDB, suggesting that this approach might be useful for the analysis of miRNAs from other species.

Description

Sacar Demirci, Muserref Duygu/0000-0003-2012-0598;

Keywords

MicroRNA, RNA Structure, Machine Learning, Random Forest, Decision Tree, Naive Bayes, machine learning, decision tree, MicroRNA, RNA structure, random forest, Article, naive Bayes

Fields of Science

0301 basic medicine, 03 medical and health sciences

Citation

WoS Q

Q3

Scopus Q

Q4
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OpenCitations Citation Count
4

Source

Turkish Journal of Biology

Volume

43

Issue

4

Start Page

274

End Page

280
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CrossRef : 2

Scopus : 3

PubMed : 2

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3

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3

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1

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4

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