Fast DNA Sequencing via Transverse Electronic Transport

A rapid and low-cost method to sequence DNA would usher in a revolution in medicine. We propose and theoretically show the feasibility of a protocol for sequencing based on the distributions of transverse electrical currents of single-stranded DNA while it translocates through a nanopore. Our estima...

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Published in:Nano letters Vol. 6; no. 4; pp. 779 - 782
Main Authors: Lagerqvist, Johan, Zwolak, Michael, Di Ventra, Massimiliano
Format: Journal Article
Language:English
Published: Washington, DC American Chemical Society 01.04.2006
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ISSN:1530-6984, 1530-6992
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Abstract A rapid and low-cost method to sequence DNA would usher in a revolution in medicine. We propose and theoretically show the feasibility of a protocol for sequencing based on the distributions of transverse electrical currents of single-stranded DNA while it translocates through a nanopore. Our estimates, based on the statistics of these distributions, reveal that sequencing of an entire human genome could be done with very high accuracy in a matter of hours without parallelization, that is, orders of magnitude faster than present techniques. The practical implementation of our approach would represent a substantial advancement in our ability to study, predict, and cure diseases from the perspective of the genetic makeup of each individual.
AbstractList A rapid and low-cost method to sequence DNA would usher in a revolution in medicine. We propose and theoretically show the feasibility of a protocol for sequencing based on the distributions of transverse electrical currents of single-stranded DNA while it translocates through a nanopore. Our estimates, based on the statistics of these distributions, reveal that sequencing of an entire human genome could be done with very high accuracy in a matter of hours without parallelization, that is, orders of magnitude faster than present techniques. The practical implementation of our approach would represent a substantial advancement in our ability to study, predict, and cure diseases from the perspective of the genetic makeup of each individual.
A rapid and low-cost method to sequence DNA would usher in a revolution in medicine. We propose and theoretically show the feasibility of a protocol for sequencing based on the distributions of transverse electrical currents of single-stranded DNA while it translocates through a nanopore. Our estimates, based on the statistics of these distributions, reveal that sequencing of an entire human genome could be done with very high accuracy in a matter of hours without parallelization, that is, orders of magnitude faster than present techniques. The practical implementation of our approach would represent a substantial advancement in our ability to study, predict, and cure diseases from the perspective of the genetic makeup of each individual.A rapid and low-cost method to sequence DNA would usher in a revolution in medicine. We propose and theoretically show the feasibility of a protocol for sequencing based on the distributions of transverse electrical currents of single-stranded DNA while it translocates through a nanopore. Our estimates, based on the statistics of these distributions, reveal that sequencing of an entire human genome could be done with very high accuracy in a matter of hours without parallelization, that is, orders of magnitude faster than present techniques. The practical implementation of our approach would represent a substantial advancement in our ability to study, predict, and cure diseases from the perspective of the genetic makeup of each individual.
A rapid and low-cost method to sequence DNA would usher in a revolution in medicine. We propose and theoretically show the feasibility of a protocol for sequencing based on the distributions of transverse electrical currents of single-stranded DNA while it translocates through a nanopore. Our estimates, based on the statistics of these distributions, reveal that sequencing of an entire human genome could be done with very high accuracy in a matter of hours without parallelization, e.g., orders of magnitude faster than present techniques. The practical implementation of our approach would represent a substantial advancement in our ability to study, predict and cure diseases from the perspective of the genetic makeup of each individual.
Author Lagerqvist, Johan
Di Ventra, Massimiliano
Zwolak, Michael
AuthorAffiliation 2 Physics Department, California Institute of Technology, Pasadena, CA 91125
1 Department of Physics, University of California, San Diego, La Jolla, CA 92093-0319
AuthorAffiliation_xml – name: 1 Department of Physics, University of California, San Diego, La Jolla, CA 92093-0319
– name: 2 Physics Department, California Institute of Technology, Pasadena, CA 91125
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  surname: Zwolak
  fullname: Zwolak, Michael
– sequence: 3
  givenname: Massimiliano
  surname: Di Ventra
  fullname: Di Ventra, Massimiliano
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Nucleotide sequence
DNA
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Nanopore
Genome
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Nanoporosity
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Snippet A rapid and low-cost method to sequence DNA would usher in a revolution in medicine. We propose and theoretically show the feasibility of a protocol for...
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SubjectTerms Biological and medical sciences
Biosensing Techniques - instrumentation
Biosensing Techniques - methods
Computer Simulation
Computer-Aided Design
Conformational dynamics in molecular biology
DNA - analysis
DNA - chemistry
DNA - radiation effects
Electrochemistry - instrumentation
Electrochemistry - methods
Electrodes
Electron Transport
Feasibility Studies
Fundamental and applied biological sciences. Psychology
Models, Chemical
Molecular biophysics
Oligonucleotide Array Sequence Analysis - instrumentation
Oligonucleotide Array Sequence Analysis - methods
Sequence Analysis, DNA - instrumentation
Sequence Analysis, DNA - methods
Title Fast DNA Sequencing via Transverse Electronic Transport
URI http://dx.doi.org/10.1021/nl0601076
https://www.ncbi.nlm.nih.gov/pubmed/16608283
https://www.proquest.com/docview/67856581
https://pubmed.ncbi.nlm.nih.gov/PMC2556950
Volume 6
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