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Evaluation and application of RNA-Seq by MinION
The current RNA-Seq method analyses fragments of mRNAs, from which it is occasionally difficult to reconstruct the entire transcript structure. Here, we performed and evaluated the recent procedure for full-length cDNA sequencing using the Nanopore sequencer MinION. We applied MinION RNA-Seq for var...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379022/ https://www.ncbi.nlm.nih.gov/pubmed/30462165 http://dx.doi.org/10.1093/dnares/dsy038 |
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author | Seki, Masahide Katsumata, Eri Suzuki, Ayako Sereewattanawoot, Sarun Sakamoto, Yoshitaka Mizushima-Sugano, Junko Sugano, Sumio Kohno, Takashi Frith, Martin C Tsuchihara, Katsuya Suzuki, Yutaka |
author_facet | Seki, Masahide Katsumata, Eri Suzuki, Ayako Sereewattanawoot, Sarun Sakamoto, Yoshitaka Mizushima-Sugano, Junko Sugano, Sumio Kohno, Takashi Frith, Martin C Tsuchihara, Katsuya Suzuki, Yutaka |
author_sort | Seki, Masahide |
collection | PubMed |
description | The current RNA-Seq method analyses fragments of mRNAs, from which it is occasionally difficult to reconstruct the entire transcript structure. Here, we performed and evaluated the recent procedure for full-length cDNA sequencing using the Nanopore sequencer MinION. We applied MinION RNA-Seq for various applications, which would not always be easy using the usual RNA-Seq by Illumina. First, we examined and found that even though the sequencing accuracy was still limited to 92.3%, practically useful RNA-Seq analysis is possible. Particularly, taking advantage of the long-read nature of MinION, we demonstrate the identification of splicing patterns and their combinations as a form of full-length cDNAs without losing precise information concerning their expression levels. Transcripts of fusion genes in cancer cells can also be identified and characterized. Furthermore, the full-length cDNA information can be used for phasing of the SNPs detected by WES on the transcripts, providing essential information to identify allele-specific transcriptional events. We constructed a catalogue of full-length cDNAs in seven major organs for two particular individuals and identified allele-specific transcription and splicing. Finally, we demonstrate that single-cell sequencing is also possible. RNA-Seq on the MinION platform should provide a novel approach that is complementary to the current RNA-Seq. |
format | Online Article Text |
id | pubmed-6379022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63790222019-02-22 Evaluation and application of RNA-Seq by MinION Seki, Masahide Katsumata, Eri Suzuki, Ayako Sereewattanawoot, Sarun Sakamoto, Yoshitaka Mizushima-Sugano, Junko Sugano, Sumio Kohno, Takashi Frith, Martin C Tsuchihara, Katsuya Suzuki, Yutaka DNA Res Full Papers The current RNA-Seq method analyses fragments of mRNAs, from which it is occasionally difficult to reconstruct the entire transcript structure. Here, we performed and evaluated the recent procedure for full-length cDNA sequencing using the Nanopore sequencer MinION. We applied MinION RNA-Seq for various applications, which would not always be easy using the usual RNA-Seq by Illumina. First, we examined and found that even though the sequencing accuracy was still limited to 92.3%, practically useful RNA-Seq analysis is possible. Particularly, taking advantage of the long-read nature of MinION, we demonstrate the identification of splicing patterns and their combinations as a form of full-length cDNAs without losing precise information concerning their expression levels. Transcripts of fusion genes in cancer cells can also be identified and characterized. Furthermore, the full-length cDNA information can be used for phasing of the SNPs detected by WES on the transcripts, providing essential information to identify allele-specific transcriptional events. We constructed a catalogue of full-length cDNAs in seven major organs for two particular individuals and identified allele-specific transcription and splicing. Finally, we demonstrate that single-cell sequencing is also possible. RNA-Seq on the MinION platform should provide a novel approach that is complementary to the current RNA-Seq. Oxford University Press 2019-02 2018-11-20 /pmc/articles/PMC6379022/ /pubmed/30462165 http://dx.doi.org/10.1093/dnares/dsy038 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. 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 | Full Papers Seki, Masahide Katsumata, Eri Suzuki, Ayako Sereewattanawoot, Sarun Sakamoto, Yoshitaka Mizushima-Sugano, Junko Sugano, Sumio Kohno, Takashi Frith, Martin C Tsuchihara, Katsuya Suzuki, Yutaka Evaluation and application of RNA-Seq by MinION |
title | Evaluation and application of RNA-Seq by MinION |
title_full | Evaluation and application of RNA-Seq by MinION |
title_fullStr | Evaluation and application of RNA-Seq by MinION |
title_full_unstemmed | Evaluation and application of RNA-Seq by MinION |
title_short | Evaluation and application of RNA-Seq by MinION |
title_sort | evaluation and application of rna-seq by minion |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379022/ https://www.ncbi.nlm.nih.gov/pubmed/30462165 http://dx.doi.org/10.1093/dnares/dsy038 |
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