Real-time Multiplex Single-Molecule DNA Sequencing

Information

  • Research Project
  • 7921327
  • ApplicationId
    7921327
  • Core Project Number
    R01HG003710
  • Full Project Number
    3R01HG003710-03S1
  • Serial Number
    3710
  • FOA Number
    RFA-HG-04-003
  • Sub Project Id
  • Project Start Date
    9/30/2009 - 15 years ago
  • Project End Date
    8/31/2010 - 14 years ago
  • Program Officer Name
    SCHLOSS, JEFFERY
  • Budget Start Date
    9/30/2009 - 15 years ago
  • Budget End Date
    8/31/2010 - 14 years ago
  • Fiscal Year
    2009
  • Support Year
    3
  • Suffix
    S1
  • Award Notice Date
    9/30/2009 - 15 years ago

Real-time Multiplex Single-Molecule DNA Sequencing

DESCRIPTION (provided by applicant): Genome sequencing has revolutionized biology and medicine. A 5-fold decrease in sequencing cost over the past 10 years has fueled an explosive growth in the availability of genome sequence data for numerous organisms. Despite these advances, the vast majority of the value from sequence data has yet to be realized, as the cost of routine sequencing is prohibitive. Current sequencing technologies based on capillary electrophoresis will likely not allow order-of-magnitude decreases in cost. Alternative sequencing technologies are required. Here we propose to use DNA polymerase enzyme as a fast and frugal sequencing engine by monitoring DNA polymerization in real-time. Nanofluidics, Inc. was established as a spin-out from Cornell University explicitly to leverage 2 technological advances that enable real-time single-molecule sequencing system. The first is an optical confinement technology, the zero-mode waveguide (ZMW), which allows detection of single nucleotide incorporation in real-time during processive DNA polymerization. The second, terminal-phosphate fluorescent labeling, is a method of attaching fluorophores to nucleotides such that they are automatically removed from the DNA strand after incorporation. By leaving the DNA structure un-hindered with fluorophores, this method allows highly processive incorporation even using 100% replacement with labeled nucleotides. The combination of these technologies eliminates the need for slow and expensive washing of the reaction or un-blocking of the polymerase. Because the polymerase is free-running, the sequence read can proceed as long as the polymerase continues synthesizing, which can be as long as hundreds of thousands of bases. Both the ZMW and the polymerase are small, and the system has no fluidics or moving parts, making the technology amenable to high degrees of multiplexing. The goal of this program is to deploy these technologies in a 4-color, real-time, multiplex single-molecule DNA sequencing system that will enable sequencing of a mammalian genome for $50,000 by 2008, and $1000 by 2010.

IC Name
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
  • Activity
    R01
  • Administering IC
    HG
  • Application Type
    3
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    714406
  • Sub Project Total Cost
  • ARRA Funded
    True
  • CFDA Code
    701
  • Ed Inst. Type
  • Funding ICs
    NHGRI:714406\
  • Funding Mechanism
    Research Projects
  • Study Section
    ZHG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    PACIFIC BIOSCIENCES OF CALIFORNIA, INC.
  • Organization Department
  • Organization DUNS
    149130325
  • Organization City
    MENLO PARK
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    94025
  • Organization District
    UNITED STATES