Analyzing Multiplexed Amplicons for Advanced Sequencing

Information

  • Research Project
  • 6992217
  • ApplicationId
    6992217
  • Core Project Number
    R43HG003796
  • Full Project Number
    1R43HG003796-01
  • Serial Number
    3796
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/12/2005 - 19 years ago
  • Project End Date
    3/31/2007 - 17 years ago
  • Program Officer Name
    SCHLOSS, JEFFERY
  • Budget Start Date
    9/12/2005 - 19 years ago
  • Budget End Date
    3/31/2007 - 17 years ago
  • Fiscal Year
    2005
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/12/2005 - 19 years ago

Analyzing Multiplexed Amplicons for Advanced Sequencing

Although the sequence of the human genome was substantially completed in 2002, there is still a huge need for the production of DMA sequence data. The number of organisms and individuals which may be sequenced is still significantly constrained by the lengthy time, high complexity and exorbitant costs of today's Sanger sequencing methods. Significant effort is currently going into the creation of new chemistries to read out the bases of DMA strands without the use of electrophoresis; however, the sample preparation processes to feed these sequencing systems has yet to be fully worked out and optimized. Many of the advanced sequencing methods require many millions of sets of amplified DNA fragments, with each set being comprised of millions of identical fragments. These sets are attached to a solid support which is then processed to read out the sequence. We propose the use of novel ultra-high-density micromachined plates as the vessels for preparing nanoliter-scale reactions for sequencing. This preparation generally includes DNA fragmentation, amplification, enrichment and solid-support-attachment steps which result in a chip with a large number of samples ready to be sequenced. Currently proposed sample preparation methods using polonies or beads may require a large number of steps to succeed and researchers may not have the freedom to practice certain protected bead-based technologies. The proposed Phase I project will include the demonstration of DNA amplification of several fragment species and a determination of how many different fragments may be reasonably analyzed from a single spot of an advanced sequencing by synthesis system. The ability to analyze multiple species in each spot could improve throughput and significantly simplify-sample preparation steps. Successful accomplishment of the Phase I milestones and completion of a subsequent Phase II and Phase III projects will result in the development of an ultra-high throughput prototype system which can produce cost-effective high-density chips for use in conjunction with advanced DNA sequencing instruments. Ultimately, this next generation of sample preparation and sequencing technologies, which can produce DNA sequence several orders of magnitude cheaper and faster than existing systems, can help to make the promise of individualized therapeutics a reality.

IC Name
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
  • Activity
    R43
  • Administering IC
    HG
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    79993
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    172
  • Ed Inst. Type
  • Funding ICs
    NHGRI:79993\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    INTELLIGENT BIO-SYSTEMS, INC.
  • Organization Department
  • Organization DUNS
    170777770
  • Organization City
    Waltham
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    02451
  • Organization District
    UNITED STATES