Decoding long nanopore sequencing reads of natural DNA

Andrew H. Laszlo, Ian M. Derrington, Brian C. Ross, Henry Brinkerhoff, Andrew Adey, Ian C. Nova, Jonathan M. Craig, Kyle W. Langford, Jenny Mae Samson, Riza Daza, Kenji Doering, Jay Shendure, Jens H. Gundlach

Research output: Contribution to journalArticle

221 Scopus citations

Abstract

Nanopore sequencing of DNA is a single-molecule technique that may achieve long reads, low cost and high speed with minimal sample preparation and instrumentation. Here, we build on recent progress with respect to nanopore resolution and DNA control to interpret the procession of ion current levels observed during the translocation of DNA through the pore MspA. As approximately four nucleotides affect the ion current of each level, we measured the ion current corresponding to all 256 four-nucleotide combinations (quadromers). This quadromer map is highly predictive of ion current levels of previously unmeasured sequences derived from the bacteriophage phi X 174 genome. Furthermore, we show nanopore sequencing reads of phi X 174 up to 4,500 bases in length, which can be unambiguously aligned to the phi X 174 reference genome, and demonstrate proof-of-concept utility with respect to hybrid genome assembly and polymorphism detection. This work provides a foundation for nanopore sequencing of long, natural DNA strands.

Original languageEnglish (US)
Pages (from-to)829-833
Number of pages5
JournalNature biotechnology
Volume32
Issue number8
DOIs
StatePublished - Aug 2014

ASJC Scopus subject areas

  • Biotechnology
  • Bioengineering
  • Applied Microbiology and Biotechnology
  • Molecular Medicine
  • Biomedical Engineering

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  • Cite this

    Laszlo, A. H., Derrington, I. M., Ross, B. C., Brinkerhoff, H., Adey, A., Nova, I. C., Craig, J. M., Langford, K. W., Samson, J. M., Daza, R., Doering, K., Shendure, J., & Gundlach, J. H. (2014). Decoding long nanopore sequencing reads of natural DNA. Nature biotechnology, 32(8), 829-833. https://doi.org/10.1038/nbt.2950