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Transcriptome assembly and quantification from Ion Torrent RNA-Seq data

BACKGROUND: High throughput RNA sequencing (RNA-Seq) can generate whole transcriptome information at the single transcript level providing a powerful tool with multiple interrelated applications including transcriptome reconstruction and quantification. The sequences of novel transcripts can be reco...

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Autores principales: Mangul, Serghei, Caciula, Adrian, Al Seesi, Sahar, Brinza, Dumitru, Mӑndoiu, Ion, Zelikovsky, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120146/
https://www.ncbi.nlm.nih.gov/pubmed/25082147
http://dx.doi.org/10.1186/1471-2164-15-S5-S7
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author Mangul, Serghei
Caciula, Adrian
Al Seesi, Sahar
Brinza, Dumitru
Mӑndoiu, Ion
Zelikovsky, Alex
author_facet Mangul, Serghei
Caciula, Adrian
Al Seesi, Sahar
Brinza, Dumitru
Mӑndoiu, Ion
Zelikovsky, Alex
author_sort Mangul, Serghei
collection PubMed
description BACKGROUND: High throughput RNA sequencing (RNA-Seq) can generate whole transcriptome information at the single transcript level providing a powerful tool with multiple interrelated applications including transcriptome reconstruction and quantification. The sequences of novel transcripts can be reconstructed from deep RNA-Seq data, but this is computationally challenging due to sequencing errors, uneven coverage of expressed transcripts, and the need to distinguish between highly similar transcripts produced by alternative splicing. Another challenge in transcriptomic analysis comes from the ambiguities in mapping reads to transcripts. RESULTS: We present MaLTA, a method for simultaneous transcriptome assembly and quantification from Ion Torrent RNA-Seq data. Our approach explores transcriptome structure and incorporates a maximum likelihood model into the assembly and quantification procedure. A new version of the IsoEM algorithm suitable for Ion Torrent RNA-Seq reads is used to accurately estimate transcript expression levels. The MaLTA-IsoEM tool is publicly available at: http://alan.cs.gsu.edu/NGS/?q=malta CONCLUSIONS: Experimental results on both synthetic and real datasets show that Ion Torrent RNA-Seq data can be successfully used for transcriptome analyses. Experimental results suggest increased transcriptome assembly and quantification accuracy of MaLTA-IsoEM solution compared to existing state-of-the-art approaches.
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spelling pubmed-41201462014-08-11 Transcriptome assembly and quantification from Ion Torrent RNA-Seq data Mangul, Serghei Caciula, Adrian Al Seesi, Sahar Brinza, Dumitru Mӑndoiu, Ion Zelikovsky, Alex BMC Genomics Research BACKGROUND: High throughput RNA sequencing (RNA-Seq) can generate whole transcriptome information at the single transcript level providing a powerful tool with multiple interrelated applications including transcriptome reconstruction and quantification. The sequences of novel transcripts can be reconstructed from deep RNA-Seq data, but this is computationally challenging due to sequencing errors, uneven coverage of expressed transcripts, and the need to distinguish between highly similar transcripts produced by alternative splicing. Another challenge in transcriptomic analysis comes from the ambiguities in mapping reads to transcripts. RESULTS: We present MaLTA, a method for simultaneous transcriptome assembly and quantification from Ion Torrent RNA-Seq data. Our approach explores transcriptome structure and incorporates a maximum likelihood model into the assembly and quantification procedure. A new version of the IsoEM algorithm suitable for Ion Torrent RNA-Seq reads is used to accurately estimate transcript expression levels. The MaLTA-IsoEM tool is publicly available at: http://alan.cs.gsu.edu/NGS/?q=malta CONCLUSIONS: Experimental results on both synthetic and real datasets show that Ion Torrent RNA-Seq data can be successfully used for transcriptome analyses. Experimental results suggest increased transcriptome assembly and quantification accuracy of MaLTA-IsoEM solution compared to existing state-of-the-art approaches. BioMed Central 2014-07-14 /pmc/articles/PMC4120146/ /pubmed/25082147 http://dx.doi.org/10.1186/1471-2164-15-S5-S7 Text en Copyright © 2014 Mangul et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 Research
Mangul, Serghei
Caciula, Adrian
Al Seesi, Sahar
Brinza, Dumitru
Mӑndoiu, Ion
Zelikovsky, Alex
Transcriptome assembly and quantification from Ion Torrent RNA-Seq data
title Transcriptome assembly and quantification from Ion Torrent RNA-Seq data
title_full Transcriptome assembly and quantification from Ion Torrent RNA-Seq data
title_fullStr Transcriptome assembly and quantification from Ion Torrent RNA-Seq data
title_full_unstemmed Transcriptome assembly and quantification from Ion Torrent RNA-Seq data
title_short Transcriptome assembly and quantification from Ion Torrent RNA-Seq data
title_sort transcriptome assembly and quantification from ion torrent rna-seq data
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120146/
https://www.ncbi.nlm.nih.gov/pubmed/25082147
http://dx.doi.org/10.1186/1471-2164-15-S5-S7
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