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Targeted high-throughput sequencing of tagged nucleic acid samples

Open access
Meyer, Matthias, Stenzel, Udo, Myles, Sean, Prüfer, Kay, Hofreiter, Michael·2007·Nucleic Acids Research

Abstract

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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Metadata

Authors
Meyer, M., Stenzel, U., Myles, S., Prüfer, K., & Hofreiter, M.
Venue
Nucleic Acids Research
Published
2007-08
Volume
35
Issue
15
Pages
e97
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2095901358
Cited by
194
References
0
FWCI
8.02
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Targeted high-throughput sequencing of tagged nucleic acid samples. https://app.cochat.ai/papers/10.1093/nar/gkm566
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Meyer, M., Stenzel, U., Myles, S., Prüfer, K., & Hofreiter, M. (2007). Targeted high-throughput sequencing of tagged nucleic acid samples. Nucleic Acids Research. https://doi.org/10.1093/nar/gkm566

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