Development of a Multi-State Decoding Framework

Information

  • Research Project
  • 6737095
  • ApplicationId
    6737095
  • Core Project Number
    R43HG003096
  • Full Project Number
    1R43HG003096-01
  • Serial Number
    3096
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/2003 - 20 years ago
  • Project End Date
    3/29/2004 - 20 years ago
  • Program Officer Name
    HEATH, ANNE K
  • Budget Start Date
    9/30/2003 - 20 years ago
  • Budget End Date
    3/29/2004 - 20 years ago
  • Fiscal Year
    2003
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/26/2003 - 20 years ago
Organizations

Development of a Multi-State Decoding Framework

DESCRIPTION (provided by applicant): This proposal aims to increase the capability and decrease the cost of decoding the Illumina bead array platform by adding decode states. DNA probes attached to microbeads are randomly loaded onto fiber optic bundles. A decoding process of sequential hybridization stages is necessary to determine the locus correspondence of each bead. Decoders (sequences complementary to the DNA probes on the beads) that are either unlabeled, or labeled with a dye are hybridized to the array. Images are taken after each hybridization, and the experiment is designed so that the hybridization signature of each bead through the decode process, uniquely determines the identity of the bead. The cost and time of decoding is proportional to the number of decode stages. The number of stages is determined by the number of loci represented on the array and the number of distinguishable labels, or decode states, used in the decode process (e.g. ON in dye 1). The current availability of 3 states allows the decoding of 1,500 probes in 8 stages. The successful execution of this project would extend the number of states to at least 8. With 8 states, the number of stages for the 1,500-probe product would become 4. The number of probes that could be decoded in 8 stages would increase by 3 orders of magnitude. The main components of the project are wet lab chemistry and algorithm development. Wet lab chemistry will be used to determine the optimal mixture of dye labeled and unlabeled oligonucleotides that will lead to distinguishable intensity states. Beads will have signal levels in FAM and CY3 dye. Variability in the process will need to be sufficiently low to reliably distinguish different concentrations of dye labeled oligonucleo tides. Three levels of FAM and CY3 signal would lead to 9 states. It is likely that 8 of these will be reliably distinguishable. Pattern matching algorithms will be developed to decode the beads. Decision tree methods based on expected signal will be applied. Arrays will be decoded twice -- first with the current 3-state decoding, and then with the multi-state decoding -- to enable training and machine learning algorithms. Achieving 8 state decoding will decrease the cost of the array and dramatically increase the number of loci explored and the number of probes per locus.

IC Name
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
  • Activity
    R43
  • Administering IC
    HG
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    141830
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    172
  • Ed Inst. Type
  • Funding ICs
    NHGRI:141830\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ILLUMINA, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    SAN DIEGO
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    921211975
  • Organization District
    UNITED STATES