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DeeReCT-PolyA: a robust and generic deep learning method for PAS identification
MOTIVATION: Polyadenylation is a critical step for gene expression regulation during the maturation of mRNA. An accurate and robust method for poly(A) signals (PASs) identification is not only desired for the purpose of better transcripts’ end annotation, but can also help us gain a deeper insight o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612895/ https://www.ncbi.nlm.nih.gov/pubmed/30500881 http://dx.doi.org/10.1093/bioinformatics/bty991 |
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author | Xia, Zhihao Li, Yu Zhang, Bin Li, Zhongxiao Hu, Yuhui Chen, Wei Gao, Xin |
author_facet | Xia, Zhihao Li, Yu Zhang, Bin Li, Zhongxiao Hu, Yuhui Chen, Wei Gao, Xin |
author_sort | Xia, Zhihao |
collection | PubMed |
description | MOTIVATION: Polyadenylation is a critical step for gene expression regulation during the maturation of mRNA. An accurate and robust method for poly(A) signals (PASs) identification is not only desired for the purpose of better transcripts’ end annotation, but can also help us gain a deeper insight of the underlying regulatory mechanism. Although many methods have been proposed for PAS recognition, most of them are PAS motif- and human-specific, which leads to high risks of overfitting, low generalization power, and inability to reveal the connections between the underlying mechanisms of different mammals. RESULTS: In this work, we propose a robust, PAS motif agnostic, and highly interpretable and transferrable deep learning model for accurate PAS recognition, which requires no prior knowledge or human-designed features. We show that our single model trained over all human PAS motifs not only outperforms the state-of-the-art methods trained on specific motifs, but can also be generalized well to two mouse datasets. Moreover, we further increase the prediction accuracy by transferring the deep learning model trained on the data of one species to the data of a different species. Several novel underlying poly(A) patterns are revealed through the visualization of important oligomers and positions in our trained models. Finally, we interpret the deep learning models by converting the convolutional filters into sequence logos and quantitatively compare the sequence logos between human and mouse datasets. AVAILABILITY AND IMPLEMENTATION: https://github.com/likesum/DeeReCT-PolyA SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6612895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66128952019-07-12 DeeReCT-PolyA: a robust and generic deep learning method for PAS identification Xia, Zhihao Li, Yu Zhang, Bin Li, Zhongxiao Hu, Yuhui Chen, Wei Gao, Xin Bioinformatics Original Papers MOTIVATION: Polyadenylation is a critical step for gene expression regulation during the maturation of mRNA. An accurate and robust method for poly(A) signals (PASs) identification is not only desired for the purpose of better transcripts’ end annotation, but can also help us gain a deeper insight of the underlying regulatory mechanism. Although many methods have been proposed for PAS recognition, most of them are PAS motif- and human-specific, which leads to high risks of overfitting, low generalization power, and inability to reveal the connections between the underlying mechanisms of different mammals. RESULTS: In this work, we propose a robust, PAS motif agnostic, and highly interpretable and transferrable deep learning model for accurate PAS recognition, which requires no prior knowledge or human-designed features. We show that our single model trained over all human PAS motifs not only outperforms the state-of-the-art methods trained on specific motifs, but can also be generalized well to two mouse datasets. Moreover, we further increase the prediction accuracy by transferring the deep learning model trained on the data of one species to the data of a different species. Several novel underlying poly(A) patterns are revealed through the visualization of important oligomers and positions in our trained models. Finally, we interpret the deep learning models by converting the convolutional filters into sequence logos and quantitatively compare the sequence logos between human and mouse datasets. AVAILABILITY AND IMPLEMENTATION: https://github.com/likesum/DeeReCT-PolyA SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-07 2018-11-30 /pmc/articles/PMC6612895/ /pubmed/30500881 http://dx.doi.org/10.1093/bioinformatics/bty991 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Papers Xia, Zhihao Li, Yu Zhang, Bin Li, Zhongxiao Hu, Yuhui Chen, Wei Gao, Xin DeeReCT-PolyA: a robust and generic deep learning method for PAS identification |
title | DeeReCT-PolyA: a robust and generic deep learning method for PAS identification |
title_full | DeeReCT-PolyA: a robust and generic deep learning method for PAS identification |
title_fullStr | DeeReCT-PolyA: a robust and generic deep learning method for PAS identification |
title_full_unstemmed | DeeReCT-PolyA: a robust and generic deep learning method for PAS identification |
title_short | DeeReCT-PolyA: a robust and generic deep learning method for PAS identification |
title_sort | deerect-polya: a robust and generic deep learning method for pas identification |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612895/ https://www.ncbi.nlm.nih.gov/pubmed/30500881 http://dx.doi.org/10.1093/bioinformatics/bty991 |
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