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COSSMO: predicting competitive alternative splice site selection using deep learning
MOTIVATION: Alternative splice site selection is inherently competitive and the probability of a given splice site to be used also depends on the strength of neighboring sites. Here, we present a new model named the competitive splice site model (COSSMO), which explicitly accounts for these competit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022534/ https://www.ncbi.nlm.nih.gov/pubmed/29949959 http://dx.doi.org/10.1093/bioinformatics/bty244 |
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author | Bretschneider, Hannes Gandhi, Shreshth Deshwar, Amit G Zuberi, Khalid Frey, Brendan J |
author_facet | Bretschneider, Hannes Gandhi, Shreshth Deshwar, Amit G Zuberi, Khalid Frey, Brendan J |
author_sort | Bretschneider, Hannes |
collection | PubMed |
description | MOTIVATION: Alternative splice site selection is inherently competitive and the probability of a given splice site to be used also depends on the strength of neighboring sites. Here, we present a new model named the competitive splice site model (COSSMO), which explicitly accounts for these competitive effects and predicts the percent selected index (PSI) distribution over any number of putative splice sites. We model an alternative splicing event as the choice of a 3′ acceptor site conditional on a fixed upstream 5′ donor site or the choice of a 5′ donor site conditional on a fixed 3′ acceptor site. We build four different architectures that use convolutional layers, communication layers, long short-term memory and residual networks, respectively, to learn relevant motifs from sequence alone. We also construct a new dataset from genome annotations and RNA-Seq read data that we use to train our model. RESULTS: COSSMO is able to predict the most frequently used splice site with an accuracy of 70% on unseen test data, and achieve an R(2) of 0.6 in modeling the PSI distribution. We visualize the motifs that COSSMO learns from sequence and show that COSSMO recognizes the consensus splice site sequences and many known splicing factors with high specificity. AVAILABILITY AND IMPLEMENTATION: Model predictions, our training dataset, and code are available from http://cossmo.genes.toronto.edu. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6022534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60225342018-07-10 COSSMO: predicting competitive alternative splice site selection using deep learning Bretschneider, Hannes Gandhi, Shreshth Deshwar, Amit G Zuberi, Khalid Frey, Brendan J Bioinformatics Ismb 2018–Intelligent Systems for Molecular Biology Proceedings MOTIVATION: Alternative splice site selection is inherently competitive and the probability of a given splice site to be used also depends on the strength of neighboring sites. Here, we present a new model named the competitive splice site model (COSSMO), which explicitly accounts for these competitive effects and predicts the percent selected index (PSI) distribution over any number of putative splice sites. We model an alternative splicing event as the choice of a 3′ acceptor site conditional on a fixed upstream 5′ donor site or the choice of a 5′ donor site conditional on a fixed 3′ acceptor site. We build four different architectures that use convolutional layers, communication layers, long short-term memory and residual networks, respectively, to learn relevant motifs from sequence alone. We also construct a new dataset from genome annotations and RNA-Seq read data that we use to train our model. RESULTS: COSSMO is able to predict the most frequently used splice site with an accuracy of 70% on unseen test data, and achieve an R(2) of 0.6 in modeling the PSI distribution. We visualize the motifs that COSSMO learns from sequence and show that COSSMO recognizes the consensus splice site sequences and many known splicing factors with high specificity. AVAILABILITY AND IMPLEMENTATION: Model predictions, our training dataset, and code are available from http://cossmo.genes.toronto.edu. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2018-07-01 2018-06-27 /pmc/articles/PMC6022534/ /pubmed/29949959 http://dx.doi.org/10.1093/bioinformatics/bty244 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 | Ismb 2018–Intelligent Systems for Molecular Biology Proceedings Bretschneider, Hannes Gandhi, Shreshth Deshwar, Amit G Zuberi, Khalid Frey, Brendan J COSSMO: predicting competitive alternative splice site selection using deep learning |
title | COSSMO: predicting competitive alternative splice site selection using deep learning |
title_full | COSSMO: predicting competitive alternative splice site selection using deep learning |
title_fullStr | COSSMO: predicting competitive alternative splice site selection using deep learning |
title_full_unstemmed | COSSMO: predicting competitive alternative splice site selection using deep learning |
title_short | COSSMO: predicting competitive alternative splice site selection using deep learning |
title_sort | cossmo: predicting competitive alternative splice site selection using deep learning |
topic | Ismb 2018–Intelligent Systems for Molecular Biology Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022534/ https://www.ncbi.nlm.nih.gov/pubmed/29949959 http://dx.doi.org/10.1093/bioinformatics/bty244 |
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