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An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform
BACKGROUND: To take advantage of affordable high-throughput next-generation sequencing technologies to characterize microbial community composition often requires the development of improved methods to overcome technical limitations inherent to the sequencing platforms. Sequencing low sequence diver...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3940169/ https://www.ncbi.nlm.nih.gov/pubmed/24558975 http://dx.doi.org/10.1186/2049-2618-2-6 |
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author | Fadrosh, Douglas W Ma, Bing Gajer, Pawel Sengamalay, Naomi Ott, Sandra Brotman, Rebecca M Ravel, Jacques |
author_facet | Fadrosh, Douglas W Ma, Bing Gajer, Pawel Sengamalay, Naomi Ott, Sandra Brotman, Rebecca M Ravel, Jacques |
author_sort | Fadrosh, Douglas W |
collection | PubMed |
description | BACKGROUND: To take advantage of affordable high-throughput next-generation sequencing technologies to characterize microbial community composition often requires the development of improved methods to overcome technical limitations inherent to the sequencing platforms. Sequencing low sequence diversity libraries such as 16S rRNA amplicons has been problematic on the Illumina MiSeq platform and often generates sequences of suboptimal quality. RESULTS: Here we present an improved dual-indexing amplification and sequencing approach to assess the composition of microbial communities from clinical samples using the V3-V4 region of the 16S rRNA gene on the Illumina MiSeq platform. We introduced a 0 to 7 bp “heterogeneity spacer” to the index sequence that allows an equal proportion of samples to be sequenced out of phase. CONCLUSIONS: Our approach yields high quality sequence data from 16S rRNA gene amplicons using both 250 bp and 300 bp paired-end MiSeq protocols and provides a flexible and cost-effective sequencing option. |
format | Online Article Text |
id | pubmed-3940169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39401692014-03-04 An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform Fadrosh, Douglas W Ma, Bing Gajer, Pawel Sengamalay, Naomi Ott, Sandra Brotman, Rebecca M Ravel, Jacques Microbiome Methodology BACKGROUND: To take advantage of affordable high-throughput next-generation sequencing technologies to characterize microbial community composition often requires the development of improved methods to overcome technical limitations inherent to the sequencing platforms. Sequencing low sequence diversity libraries such as 16S rRNA amplicons has been problematic on the Illumina MiSeq platform and often generates sequences of suboptimal quality. RESULTS: Here we present an improved dual-indexing amplification and sequencing approach to assess the composition of microbial communities from clinical samples using the V3-V4 region of the 16S rRNA gene on the Illumina MiSeq platform. We introduced a 0 to 7 bp “heterogeneity spacer” to the index sequence that allows an equal proportion of samples to be sequenced out of phase. CONCLUSIONS: Our approach yields high quality sequence data from 16S rRNA gene amplicons using both 250 bp and 300 bp paired-end MiSeq protocols and provides a flexible and cost-effective sequencing option. BioMed Central 2014-02-24 /pmc/articles/PMC3940169/ /pubmed/24558975 http://dx.doi.org/10.1186/2049-2618-2-6 Text en Copyright © 2014 Fadrosh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Methodology Fadrosh, Douglas W Ma, Bing Gajer, Pawel Sengamalay, Naomi Ott, Sandra Brotman, Rebecca M Ravel, Jacques An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform |
title | An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform |
title_full | An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform |
title_fullStr | An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform |
title_full_unstemmed | An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform |
title_short | An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform |
title_sort | improved dual-indexing approach for multiplexed 16s rrna gene sequencing on the illumina miseq platform |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3940169/ https://www.ncbi.nlm.nih.gov/pubmed/24558975 http://dx.doi.org/10.1186/2049-2618-2-6 |
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