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Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations
To assess the performance of the Oxford Nanopore Technologies MinION sequencing platform, cDNAs from the External RNA Controls Consortium (ERCC) RNA Spike-In mix were sequenced. This mix mimics mammalian mRNA species and consists of 92 polyadenylated transcripts with known concentration. cDNA librar...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995519/ https://www.ncbi.nlm.nih.gov/pubmed/27554526 http://dx.doi.org/10.1038/srep31602 |
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author | Oikonomopoulos, Spyros Wang, Yu Chang Djambazian, Haig Badescu, Dunarel Ragoussis, Jiannis |
author_facet | Oikonomopoulos, Spyros Wang, Yu Chang Djambazian, Haig Badescu, Dunarel Ragoussis, Jiannis |
author_sort | Oikonomopoulos, Spyros |
collection | PubMed |
description | To assess the performance of the Oxford Nanopore Technologies MinION sequencing platform, cDNAs from the External RNA Controls Consortium (ERCC) RNA Spike-In mix were sequenced. This mix mimics mammalian mRNA species and consists of 92 polyadenylated transcripts with known concentration. cDNA libraries were generated using a template switching protocol to facilitate the direct comparison between different sequencing platforms. The MinION performance was assessed for its ability to sequence the cDNAs directly with good accuracy in terms of abundance and full length. The abundance of the ERCC cDNA molecules sequenced by MinION agreed with their expected concentration. No length or GC content bias was observed. The majority of cDNAs were sequenced as full length. Additionally, a complex cDNA population derived from a human HEK-293 cell line was sequenced on an Illumina HiSeq 2500, PacBio RS II and ONT MinION platforms. We observed that there was a good agreement in the measured cDNA abundance between PacBio RS II and ONT MinION (r(pearson) = 0.82, isoforms with length more than 700bp) and between Illumina HiSeq 2500 and ONT MinION (r(pearson) = 0.75). This indicates that the ONT MinION can sequence quantitatively both long and short full length cDNA molecules. |
format | Online Article Text |
id | pubmed-4995519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49955192016-08-30 Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations Oikonomopoulos, Spyros Wang, Yu Chang Djambazian, Haig Badescu, Dunarel Ragoussis, Jiannis Sci Rep Article To assess the performance of the Oxford Nanopore Technologies MinION sequencing platform, cDNAs from the External RNA Controls Consortium (ERCC) RNA Spike-In mix were sequenced. This mix mimics mammalian mRNA species and consists of 92 polyadenylated transcripts with known concentration. cDNA libraries were generated using a template switching protocol to facilitate the direct comparison between different sequencing platforms. The MinION performance was assessed for its ability to sequence the cDNAs directly with good accuracy in terms of abundance and full length. The abundance of the ERCC cDNA molecules sequenced by MinION agreed with their expected concentration. No length or GC content bias was observed. The majority of cDNAs were sequenced as full length. Additionally, a complex cDNA population derived from a human HEK-293 cell line was sequenced on an Illumina HiSeq 2500, PacBio RS II and ONT MinION platforms. We observed that there was a good agreement in the measured cDNA abundance between PacBio RS II and ONT MinION (r(pearson) = 0.82, isoforms with length more than 700bp) and between Illumina HiSeq 2500 and ONT MinION (r(pearson) = 0.75). This indicates that the ONT MinION can sequence quantitatively both long and short full length cDNA molecules. Nature Publishing Group 2016-08-24 /pmc/articles/PMC4995519/ /pubmed/27554526 http://dx.doi.org/10.1038/srep31602 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Oikonomopoulos, Spyros Wang, Yu Chang Djambazian, Haig Badescu, Dunarel Ragoussis, Jiannis Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations |
title | Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations |
title_full | Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations |
title_fullStr | Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations |
title_full_unstemmed | Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations |
title_short | Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations |
title_sort | benchmarking of the oxford nanopore minion sequencing for quantitative and qualitative assessment of cdna populations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995519/ https://www.ncbi.nlm.nih.gov/pubmed/27554526 http://dx.doi.org/10.1038/srep31602 |
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