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Development of a Multi-State Decoding Framework

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R43HG003096-01
Agency Tracking Number: HG003096
Amount: $141,830.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Solicitation Year: N/A
Award Year: 2003
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
United States
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 (858) 202-4630
Business Contact
Phone: (858) 202-4502
Research Institution

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.

* Information listed above is at the time of submission. *

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