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SplicingFactory—splicing diversity analysis for transcriptome data
MOTIVATION: Alternative splicing contributes to the diversity of RNA found in biological samples. Current tools investigating patterns of alternative splicing check for coordinated changes in the expression or relative ratio of RNA isoforms where specific isoforms are up- or down-regulated in a cond...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722757/ https://www.ncbi.nlm.nih.gov/pubmed/34499147 http://dx.doi.org/10.1093/bioinformatics/btab648 |
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author | Dankó, Benedek Szikora, Péter Pór, Tamás Szeifert, Alexa Sebestyén, Endre |
author_facet | Dankó, Benedek Szikora, Péter Pór, Tamás Szeifert, Alexa Sebestyén, Endre |
author_sort | Dankó, Benedek |
collection | PubMed |
description | MOTIVATION: Alternative splicing contributes to the diversity of RNA found in biological samples. Current tools investigating patterns of alternative splicing check for coordinated changes in the expression or relative ratio of RNA isoforms where specific isoforms are up- or down-regulated in a condition. However, the molecular process of splicing is stochastic and changes in RNA isoform diversity for a gene might arise between samples or conditions. A specific condition can be dominated by a single isoform, while multiple isoforms with similar expression levels can be present in a different condition. These changes might be the result of mutations, drug treatments or differences in the cellular or tissue environment. Here, we present a tool for the characterization and analysis of RNA isoform diversity using isoform level expression measurements. RESULTS: We developed an R package called SplicingFactory, to calculate various RNA isoform diversity metrics, and compare them across conditions. Using the package, we tested the effect of RNA-seq quantification tools, quantification uncertainty, gene expression levels and isoform numbers on the isoform diversity calculation. We analyzed a set of CD34+ hematopoietic stem cells and myelodysplastic syndrome samples and found a set of genes whose isoform diversity change is associated with SF3B1 mutations. AVAILABILITY AND IMPLEMENTATION: The SplicingFactory package is freely available under the GPL-3.0 license from Bioconductor for the Windows, MacOS and Linux operating systems (https://www.bioconductor.org/packages/release/bioc/html/SplicingFactory.html). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-8722757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87227572022-01-05 SplicingFactory—splicing diversity analysis for transcriptome data Dankó, Benedek Szikora, Péter Pór, Tamás Szeifert, Alexa Sebestyén, Endre Bioinformatics Original Paper MOTIVATION: Alternative splicing contributes to the diversity of RNA found in biological samples. Current tools investigating patterns of alternative splicing check for coordinated changes in the expression or relative ratio of RNA isoforms where specific isoforms are up- or down-regulated in a condition. However, the molecular process of splicing is stochastic and changes in RNA isoform diversity for a gene might arise between samples or conditions. A specific condition can be dominated by a single isoform, while multiple isoforms with similar expression levels can be present in a different condition. These changes might be the result of mutations, drug treatments or differences in the cellular or tissue environment. Here, we present a tool for the characterization and analysis of RNA isoform diversity using isoform level expression measurements. RESULTS: We developed an R package called SplicingFactory, to calculate various RNA isoform diversity metrics, and compare them across conditions. Using the package, we tested the effect of RNA-seq quantification tools, quantification uncertainty, gene expression levels and isoform numbers on the isoform diversity calculation. We analyzed a set of CD34+ hematopoietic stem cells and myelodysplastic syndrome samples and found a set of genes whose isoform diversity change is associated with SF3B1 mutations. AVAILABILITY AND IMPLEMENTATION: The SplicingFactory package is freely available under the GPL-3.0 license from Bioconductor for the Windows, MacOS and Linux operating systems (https://www.bioconductor.org/packages/release/bioc/html/SplicingFactory.html). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2021-09-09 /pmc/articles/PMC8722757/ /pubmed/34499147 http://dx.doi.org/10.1093/bioinformatics/btab648 Text en © The Author(s) 2021. 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 Dankó, Benedek Szikora, Péter Pór, Tamás Szeifert, Alexa Sebestyén, Endre SplicingFactory—splicing diversity analysis for transcriptome data |
title | SplicingFactory—splicing diversity analysis for transcriptome data |
title_full | SplicingFactory—splicing diversity analysis for transcriptome data |
title_fullStr | SplicingFactory—splicing diversity analysis for transcriptome data |
title_full_unstemmed | SplicingFactory—splicing diversity analysis for transcriptome data |
title_short | SplicingFactory—splicing diversity analysis for transcriptome data |
title_sort | splicingfactory—splicing diversity analysis for transcriptome data |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722757/ https://www.ncbi.nlm.nih.gov/pubmed/34499147 http://dx.doi.org/10.1093/bioinformatics/btab648 |
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