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CRBPDL: Identification of circRNA-RBP interaction sites using an ensemble neural network approach
by
Zou, Quan
, Lin, Chen
, Niu, Mengting
in
Algorithms
/ Animals
/ Binding sites
/ Binding Sites - genetics
/ Biology and life sciences
/ Circular RNA
/ Computational Biology
/ Computer and Information Sciences
/ Datasets
/ Deep learning
/ Feature extraction
/ Machine Learning
/ Methods
/ Models, Biological
/ Neural networks
/ Neural Networks, Computer
/ Nucleotide sequence
/ Physical Sciences
/ Post-transcription
/ Research and Analysis Methods
/ RNA sequencing
/ RNA Splicing - genetics
/ RNA, Circular - chemistry
/ RNA, Circular - genetics
/ RNA, Circular - metabolism
/ RNA-binding protein
/ RNA-Binding Proteins - chemistry
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ RNA-protein interactions
/ Splicing
2022
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CRBPDL: Identification of circRNA-RBP interaction sites using an ensemble neural network approach
by
Zou, Quan
, Lin, Chen
, Niu, Mengting
in
Algorithms
/ Animals
/ Binding sites
/ Binding Sites - genetics
/ Biology and life sciences
/ Circular RNA
/ Computational Biology
/ Computer and Information Sciences
/ Datasets
/ Deep learning
/ Feature extraction
/ Machine Learning
/ Methods
/ Models, Biological
/ Neural networks
/ Neural Networks, Computer
/ Nucleotide sequence
/ Physical Sciences
/ Post-transcription
/ Research and Analysis Methods
/ RNA sequencing
/ RNA Splicing - genetics
/ RNA, Circular - chemistry
/ RNA, Circular - genetics
/ RNA, Circular - metabolism
/ RNA-binding protein
/ RNA-Binding Proteins - chemistry
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ RNA-protein interactions
/ Splicing
2022
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CRBPDL: Identification of circRNA-RBP interaction sites using an ensemble neural network approach
by
Zou, Quan
, Lin, Chen
, Niu, Mengting
in
Algorithms
/ Animals
/ Binding sites
/ Binding Sites - genetics
/ Biology and life sciences
/ Circular RNA
/ Computational Biology
/ Computer and Information Sciences
/ Datasets
/ Deep learning
/ Feature extraction
/ Machine Learning
/ Methods
/ Models, Biological
/ Neural networks
/ Neural Networks, Computer
/ Nucleotide sequence
/ Physical Sciences
/ Post-transcription
/ Research and Analysis Methods
/ RNA sequencing
/ RNA Splicing - genetics
/ RNA, Circular - chemistry
/ RNA, Circular - genetics
/ RNA, Circular - metabolism
/ RNA-binding protein
/ RNA-Binding Proteins - chemistry
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ RNA-protein interactions
/ Splicing
2022
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CRBPDL: Identification of circRNA-RBP interaction sites using an ensemble neural network approach
Journal Article
CRBPDL: Identification of circRNA-RBP interaction sites using an ensemble neural network approach
2022
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Overview
Circular RNAs (circRNAs) are non-coding RNAs with a special circular structure produced formed by the reverse splicing mechanism. Increasing evidence shows that circular RNAs can directly bind to RNA-binding proteins (RBP) and play an important role in a variety of biological activities. The interactions between circRNAs and RBPs are key to comprehending the mechanism of posttranscriptional regulation. Accurately identifying binding sites is very useful for analyzing interactions. In past research, some predictors on the basis of machine learning (ML) have been presented, but prediction accuracy still needs to be ameliorated. Therefore, we present a novel calculation model, CRBPDL, which uses an Adaboost integrated deep hierarchical network to identify the binding sites of circular RNA-RBP. CRBPDL combines five different feature encoding schemes to encode the original RNA sequence, uses deep multiscale residual networks (MSRN) and bidirectional gating recurrent units (BiGRUs) to effectively learn high-level feature representations, it is sufficient to extract local and global context information at the same time. Additionally, a self-attention mechanism is employed to train the robustness of the CRBPDL. Ultimately, the Adaboost algorithm is applied to integrate deep learning (DL) model to improve prediction performance and reliability of the model. To verify the usefulness of CRBPDL, we compared the efficiency with state-of-the-art methods on 37 circular RNA data sets and 31 linear RNA data sets. Moreover, results display that CRBPDL is capable of performing universal, reliable, and robust. The code and data sets are obtainable at https://github.com/nmt315320/CRBPDL.git .
Publisher
Public Library of Science,Public Library of Science (PLoS)
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