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An expectation–maximization framework for comprehensive prediction of isoform-specific functions

MOTIVATION: Advances in RNA sequencing technologies have achieved an unprecedented accuracy in the quantification of mRNA isoforms, but our knowledge of isoform-specific functions has lagged behind. There is a need to understand the functional consequences of differential splicing, which could be su...

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Autores principales: Karlebach, Guy, Carmody, Leigh, Sundaramurthi, Jagadish Chandrabose, Casiraghi, Elena, Hansen, Peter, Reese, Justin, Mungall, Christopher J, Valentini, Giorgio, Robinson, Peter N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079350/
https://www.ncbi.nlm.nih.gov/pubmed/36929917
http://dx.doi.org/10.1093/bioinformatics/btad132
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author Karlebach, Guy
Carmody, Leigh
Sundaramurthi, Jagadish Chandrabose
Casiraghi, Elena
Hansen, Peter
Reese, Justin
Mungall, Christopher J
Valentini, Giorgio
Robinson, Peter N
author_facet Karlebach, Guy
Carmody, Leigh
Sundaramurthi, Jagadish Chandrabose
Casiraghi, Elena
Hansen, Peter
Reese, Justin
Mungall, Christopher J
Valentini, Giorgio
Robinson, Peter N
author_sort Karlebach, Guy
collection PubMed
description MOTIVATION: Advances in RNA sequencing technologies have achieved an unprecedented accuracy in the quantification of mRNA isoforms, but our knowledge of isoform-specific functions has lagged behind. There is a need to understand the functional consequences of differential splicing, which could be supported by the generation of accurate and comprehensive isoform-specific gene ontology annotations. RESULTS: We present isoform interpretation, a method that uses expectation–maximization to infer isoform-specific functions based on the relationship between sequence and functional isoform similarity. We predicted isoform-specific functional annotations for 85 617 isoforms of 17 900 protein-coding human genes spanning a range of 17 430 distinct gene ontology terms. Comparison with a gold-standard corpus of manually annotated human isoform functions showed that isoform interpretation significantly outperforms state-of-the-art competing methods. We provide experimental evidence that functionally related isoforms predicted by isoform interpretation show a higher degree of domain sharing and expression correlation than functionally related genes. We also show that isoform sequence similarity correlates better with inferred isoform function than with gene-level function. AVAILABILITY AND IMPLEMENTATION: Source code, documentation, and resource files are freely available under a GNU3 license at https://github.com/TheJacksonLaboratory/isopretEM and https://zenodo.org/record/7594321.
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spelling pubmed-100793502023-04-07 An expectation–maximization framework for comprehensive prediction of isoform-specific functions Karlebach, Guy Carmody, Leigh Sundaramurthi, Jagadish Chandrabose Casiraghi, Elena Hansen, Peter Reese, Justin Mungall, Christopher J Valentini, Giorgio Robinson, Peter N Bioinformatics Original Paper MOTIVATION: Advances in RNA sequencing technologies have achieved an unprecedented accuracy in the quantification of mRNA isoforms, but our knowledge of isoform-specific functions has lagged behind. There is a need to understand the functional consequences of differential splicing, which could be supported by the generation of accurate and comprehensive isoform-specific gene ontology annotations. RESULTS: We present isoform interpretation, a method that uses expectation–maximization to infer isoform-specific functions based on the relationship between sequence and functional isoform similarity. We predicted isoform-specific functional annotations for 85 617 isoforms of 17 900 protein-coding human genes spanning a range of 17 430 distinct gene ontology terms. Comparison with a gold-standard corpus of manually annotated human isoform functions showed that isoform interpretation significantly outperforms state-of-the-art competing methods. We provide experimental evidence that functionally related isoforms predicted by isoform interpretation show a higher degree of domain sharing and expression correlation than functionally related genes. We also show that isoform sequence similarity correlates better with inferred isoform function than with gene-level function. AVAILABILITY AND IMPLEMENTATION: Source code, documentation, and resource files are freely available under a GNU3 license at https://github.com/TheJacksonLaboratory/isopretEM and https://zenodo.org/record/7594321. Oxford University Press 2023-03-17 /pmc/articles/PMC10079350/ /pubmed/36929917 http://dx.doi.org/10.1093/bioinformatics/btad132 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (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 Original Paper
Karlebach, Guy
Carmody, Leigh
Sundaramurthi, Jagadish Chandrabose
Casiraghi, Elena
Hansen, Peter
Reese, Justin
Mungall, Christopher J
Valentini, Giorgio
Robinson, Peter N
An expectation–maximization framework for comprehensive prediction of isoform-specific functions
title An expectation–maximization framework for comprehensive prediction of isoform-specific functions
title_full An expectation–maximization framework for comprehensive prediction of isoform-specific functions
title_fullStr An expectation–maximization framework for comprehensive prediction of isoform-specific functions
title_full_unstemmed An expectation–maximization framework for comprehensive prediction of isoform-specific functions
title_short An expectation–maximization framework for comprehensive prediction of isoform-specific functions
title_sort expectation–maximization framework for comprehensive prediction of isoform-specific functions
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079350/
https://www.ncbi.nlm.nih.gov/pubmed/36929917
http://dx.doi.org/10.1093/bioinformatics/btad132
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