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RNAProt: an efficient and feature-rich RNA binding protein binding site predictor

BACKGROUND: Cross-linking and immunoprecipitation followed by next-generation sequencing (CLIP-seq) is the state-of-the-art technique used to experimentally determine transcriptome-wide binding sites of RNA-binding proteins (RBPs). However, it relies on gene expression, which can be highly variable...

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Autores principales: Uhl, Michael, Tran, Van Dinh, Heyl, Florian, Backofen, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372218/
https://www.ncbi.nlm.nih.gov/pubmed/34406415
http://dx.doi.org/10.1093/gigascience/giab054
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author Uhl, Michael
Tran, Van Dinh
Heyl, Florian
Backofen, Rolf
author_facet Uhl, Michael
Tran, Van Dinh
Heyl, Florian
Backofen, Rolf
author_sort Uhl, Michael
collection PubMed
description BACKGROUND: Cross-linking and immunoprecipitation followed by next-generation sequencing (CLIP-seq) is the state-of-the-art technique used to experimentally determine transcriptome-wide binding sites of RNA-binding proteins (RBPs). However, it relies on gene expression, which can be highly variable between conditions and thus cannot provide a complete picture of the RBP binding landscape. This creates a demand for computational methods to predict missing binding sites. Although there exist various methods using traditional machine learning and lately also deep learning, we encountered several problems: many of these are not well documented or maintained, making them difficult to install and use, or are not even available. In addition, there can be efficiency issues, as well as little flexibility regarding options or supported features. RESULTS: Here, we present RNAProt, an efficient and feature-rich computational RBP binding site prediction framework based on recurrent neural networks. We compare RNAProt with 1 traditional machine learning approach and 2 deep-learning methods, demonstrating its state-of-the-art predictive performance and better run time efficiency. We further show that its implemented visualizations capture known binding preferences and thus can help to understand what is learned. Since RNAProt supports various additional features (including user-defined features, which no other tool offers), we also present their influence on benchmark set performance. Finally, we show the benefits of incorporating additional features, specifically structure information, when learning the binding sites of an hairpin loop binding RBP. CONCLUSIONS: RNAProt provides a complete framework for RBP binding site predictions, from data set generation over model training to the evaluation of binding preferences and prediction. It offers state-of-the-art predictive performance, as well as superior run time efficiency, while at the same time supporting more features and input types than any other tool available so far. RNAProt is easy to install and use, comes with comprehensive documentation, and is accompanied by informative statistics and visualizations. All this makes RNAProt a valuable tool to apply in future RBP binding site research.
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spelling pubmed-83722182021-08-18 RNAProt: an efficient and feature-rich RNA binding protein binding site predictor Uhl, Michael Tran, Van Dinh Heyl, Florian Backofen, Rolf Gigascience Technical Note BACKGROUND: Cross-linking and immunoprecipitation followed by next-generation sequencing (CLIP-seq) is the state-of-the-art technique used to experimentally determine transcriptome-wide binding sites of RNA-binding proteins (RBPs). However, it relies on gene expression, which can be highly variable between conditions and thus cannot provide a complete picture of the RBP binding landscape. This creates a demand for computational methods to predict missing binding sites. Although there exist various methods using traditional machine learning and lately also deep learning, we encountered several problems: many of these are not well documented or maintained, making them difficult to install and use, or are not even available. In addition, there can be efficiency issues, as well as little flexibility regarding options or supported features. RESULTS: Here, we present RNAProt, an efficient and feature-rich computational RBP binding site prediction framework based on recurrent neural networks. We compare RNAProt with 1 traditional machine learning approach and 2 deep-learning methods, demonstrating its state-of-the-art predictive performance and better run time efficiency. We further show that its implemented visualizations capture known binding preferences and thus can help to understand what is learned. Since RNAProt supports various additional features (including user-defined features, which no other tool offers), we also present their influence on benchmark set performance. Finally, we show the benefits of incorporating additional features, specifically structure information, when learning the binding sites of an hairpin loop binding RBP. CONCLUSIONS: RNAProt provides a complete framework for RBP binding site predictions, from data set generation over model training to the evaluation of binding preferences and prediction. It offers state-of-the-art predictive performance, as well as superior run time efficiency, while at the same time supporting more features and input types than any other tool available so far. RNAProt is easy to install and use, comes with comprehensive documentation, and is accompanied by informative statistics and visualizations. All this makes RNAProt a valuable tool to apply in future RBP binding site research. Oxford University Press 2021-08-18 /pmc/articles/PMC8372218/ /pubmed/34406415 http://dx.doi.org/10.1093/gigascience/giab054 Text en © The Author(s) 2021. Published by Oxford University Press GigaScience. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Note
Uhl, Michael
Tran, Van Dinh
Heyl, Florian
Backofen, Rolf
RNAProt: an efficient and feature-rich RNA binding protein binding site predictor
title RNAProt: an efficient and feature-rich RNA binding protein binding site predictor
title_full RNAProt: an efficient and feature-rich RNA binding protein binding site predictor
title_fullStr RNAProt: an efficient and feature-rich RNA binding protein binding site predictor
title_full_unstemmed RNAProt: an efficient and feature-rich RNA binding protein binding site predictor
title_short RNAProt: an efficient and feature-rich RNA binding protein binding site predictor
title_sort rnaprot: an efficient and feature-rich rna binding protein binding site predictor
topic Technical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372218/
https://www.ncbi.nlm.nih.gov/pubmed/34406415
http://dx.doi.org/10.1093/gigascience/giab054
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