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Targeted high-throughput sequencing of tagged nucleic acid samples

High-throughput 454 DNA sequencing technology allows much faster and more cost-effective sequencing than traditional Sanger sequencing. However, the technology imposes inherent limitations on the number of samples that can be processed in parallel. Here we introduce parallel tagged sequencing (PTS),...

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Detalles Bibliográficos
Autores principales: Meyer, Matthias, Stenzel, Udo, Myles, Sean, Prüfer, Kay, Hofreiter, Michael
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976447/
https://www.ncbi.nlm.nih.gov/pubmed/17670798
http://dx.doi.org/10.1093/nar/gkm566
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author Meyer, Matthias
Stenzel, Udo
Myles, Sean
Prüfer, Kay
Hofreiter, Michael
author_facet Meyer, Matthias
Stenzel, Udo
Myles, Sean
Prüfer, Kay
Hofreiter, Michael
author_sort Meyer, Matthias
collection PubMed
description High-throughput 454 DNA sequencing technology allows much faster and more cost-effective sequencing than traditional Sanger sequencing. However, the technology imposes inherent limitations on the number of samples that can be processed in parallel. Here we introduce parallel tagged sequencing (PTS), a simple, inexpensive and flexible barcoding technique that can be used for parallel sequencing any number and type of double-stranded nucleic acid samples. We demonstrate that PTS is particularly powerful for sequencing contiguous DNA fragments such as mtDNA genomes: in theory as many as 250 mammalian mtDNA genomes can be sequenced in a single GS FLX run. PTS dramatically increases the sequencing throughput of samples in parallel and thus fully mobilizes the resources of the 454 technology for targeted sequencing.
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spelling pubmed-19764472007-09-26 Targeted high-throughput sequencing of tagged nucleic acid samples Meyer, Matthias Stenzel, Udo Myles, Sean Prüfer, Kay Hofreiter, Michael Nucleic Acids Res Methods Online High-throughput 454 DNA sequencing technology allows much faster and more cost-effective sequencing than traditional Sanger sequencing. However, the technology imposes inherent limitations on the number of samples that can be processed in parallel. Here we introduce parallel tagged sequencing (PTS), a simple, inexpensive and flexible barcoding technique that can be used for parallel sequencing any number and type of double-stranded nucleic acid samples. We demonstrate that PTS is particularly powerful for sequencing contiguous DNA fragments such as mtDNA genomes: in theory as many as 250 mammalian mtDNA genomes can be sequenced in a single GS FLX run. PTS dramatically increases the sequencing throughput of samples in parallel and thus fully mobilizes the resources of the 454 technology for targeted sequencing. Oxford University Press 2007-08 2007-08-01 /pmc/articles/PMC1976447/ /pubmed/17670798 http://dx.doi.org/10.1093/nar/gkm566 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Meyer, Matthias
Stenzel, Udo
Myles, Sean
Prüfer, Kay
Hofreiter, Michael
Targeted high-throughput sequencing of tagged nucleic acid samples
title Targeted high-throughput sequencing of tagged nucleic acid samples
title_full Targeted high-throughput sequencing of tagged nucleic acid samples
title_fullStr Targeted high-throughput sequencing of tagged nucleic acid samples
title_full_unstemmed Targeted high-throughput sequencing of tagged nucleic acid samples
title_short Targeted high-throughput sequencing of tagged nucleic acid samples
title_sort targeted high-throughput sequencing of tagged nucleic acid samples
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976447/
https://www.ncbi.nlm.nih.gov/pubmed/17670798
http://dx.doi.org/10.1093/nar/gkm566
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