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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...

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Autores principales: Fadrosh, Douglas W, Ma, Bing, Gajer, Pawel, Sengamalay, Naomi, Ott, Sandra, Brotman, Rebecca M, Ravel, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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.
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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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