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Single-cell RNAseq for the study of isoforms—how is that possible?

Single-cell RNAseq and alternative splicing studies have recently become two of the most prominent applications of RNAseq. However, the combination of both is still challenging, and few research efforts have been dedicated to the intersection between them. Cell-level insight on isoform expression is...

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Detalles Bibliográficos
Autores principales: Arzalluz-Luque, Ángeles, Conesa, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085759/
https://www.ncbi.nlm.nih.gov/pubmed/30097058
http://dx.doi.org/10.1186/s13059-018-1496-z
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author Arzalluz-Luque, Ángeles
Conesa, Ana
author_facet Arzalluz-Luque, Ángeles
Conesa, Ana
author_sort Arzalluz-Luque, Ángeles
collection PubMed
description Single-cell RNAseq and alternative splicing studies have recently become two of the most prominent applications of RNAseq. However, the combination of both is still challenging, and few research efforts have been dedicated to the intersection between them. Cell-level insight on isoform expression is required to fully understand the biology of alternative splicing, but it is still an open question to what extent isoform expression analysis at the single-cell level is actually feasible. Here, we establish a set of four conditions that are required for a successful single-cell-level isoform study and evaluate how these conditions are met by these technologies in published research.
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spelling pubmed-60857592018-08-16 Single-cell RNAseq for the study of isoforms—how is that possible? Arzalluz-Luque, Ángeles Conesa, Ana Genome Biol Review Single-cell RNAseq and alternative splicing studies have recently become two of the most prominent applications of RNAseq. However, the combination of both is still challenging, and few research efforts have been dedicated to the intersection between them. Cell-level insight on isoform expression is required to fully understand the biology of alternative splicing, but it is still an open question to what extent isoform expression analysis at the single-cell level is actually feasible. Here, we establish a set of four conditions that are required for a successful single-cell-level isoform study and evaluate how these conditions are met by these technologies in published research. BioMed Central 2018-08-10 /pmc/articles/PMC6085759/ /pubmed/30097058 http://dx.doi.org/10.1186/s13059-018-1496-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Arzalluz-Luque, Ángeles
Conesa, Ana
Single-cell RNAseq for the study of isoforms—how is that possible?
title Single-cell RNAseq for the study of isoforms—how is that possible?
title_full Single-cell RNAseq for the study of isoforms—how is that possible?
title_fullStr Single-cell RNAseq for the study of isoforms—how is that possible?
title_full_unstemmed Single-cell RNAseq for the study of isoforms—how is that possible?
title_short Single-cell RNAseq for the study of isoforms—how is that possible?
title_sort single-cell rnaseq for the study of isoforms—how is that possible?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085759/
https://www.ncbi.nlm.nih.gov/pubmed/30097058
http://dx.doi.org/10.1186/s13059-018-1496-z
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