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 |
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| Main Authors: | , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Washington, DC
American Chemical Society
01.04.2006
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| Subjects: | |
| ISSN: | 1530-6984, 1530-6992 |
| Online Access: | Get full text |
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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. |
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| 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 |
| Author_xml | – sequence: 1 givenname: Johan surname: Lagerqvist fullname: Lagerqvist, Johan – sequence: 2 givenname: Michael surname: Zwolak fullname: Zwolak, Michael – sequence: 3 givenname: Massimiliano surname: Di Ventra fullname: Di Ventra, Massimiliano |
| BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17682777$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/16608283$$D View this record in MEDLINE/PubMed |
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| Keywords | Human Nucleotide sequence DNA DNA sequence Nanopore Genome Implementation 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 |
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