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Real-time selective sequencing using nanopore technology
The Oxford Nanopore MinION sequences DNA by sensing changes in electrical current flow in real-time as molecules traverse nanopores. Optionally, the voltage across specific nanopores can be reversed, ejecting the DNA molecule. This enables “Read Until”, the selection of specific DNA molecules for se...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008457/ https://www.ncbi.nlm.nih.gov/pubmed/27454285 http://dx.doi.org/10.1038/nmeth.3930 |
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author | Loose, Matthew Malla, Sunir Stout, Michael |
author_facet | Loose, Matthew Malla, Sunir Stout, Michael |
author_sort | Loose, Matthew |
collection | PubMed |
description | The Oxford Nanopore MinION sequences DNA by sensing changes in electrical current flow in real-time as molecules traverse nanopores. Optionally, the voltage across specific nanopores can be reversed, ejecting the DNA molecule. This enables “Read Until”, the selection of specific DNA molecules for sequencing. We use dynamic time warping to match reads to reference, selecting regions of small genomes, individual amplicons, or normalization of the amplicon set. This first demonstration of direct selection of specific DNA molecules in real-time enables many novel future applications. |
format | Online Article Text |
id | pubmed-5008457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-50084572017-01-25 Real-time selective sequencing using nanopore technology Loose, Matthew Malla, Sunir Stout, Michael Nat Methods Article The Oxford Nanopore MinION sequences DNA by sensing changes in electrical current flow in real-time as molecules traverse nanopores. Optionally, the voltage across specific nanopores can be reversed, ejecting the DNA molecule. This enables “Read Until”, the selection of specific DNA molecules for sequencing. We use dynamic time warping to match reads to reference, selecting regions of small genomes, individual amplicons, or normalization of the amplicon set. This first demonstration of direct selection of specific DNA molecules in real-time enables many novel future applications. 2016-07-25 2016-09 /pmc/articles/PMC5008457/ /pubmed/27454285 http://dx.doi.org/10.1038/nmeth.3930 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Loose, Matthew Malla, Sunir Stout, Michael Real-time selective sequencing using nanopore technology |
title | Real-time selective sequencing using nanopore technology |
title_full | Real-time selective sequencing using nanopore technology |
title_fullStr | Real-time selective sequencing using nanopore technology |
title_full_unstemmed | Real-time selective sequencing using nanopore technology |
title_short | Real-time selective sequencing using nanopore technology |
title_sort | real-time selective sequencing using nanopore technology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008457/ https://www.ncbi.nlm.nih.gov/pubmed/27454285 http://dx.doi.org/10.1038/nmeth.3930 |
work_keys_str_mv | AT loosematthew realtimeselectivesequencingusingnanoporetechnology AT mallasunir realtimeselectivesequencingusingnanoporetechnology AT stoutmichael realtimeselectivesequencingusingnanoporetechnology |