An integrated system for sample preparation and DNA sequencing is proposed. The computer controlled system will automate all steps from picking recombinant clones from agar plates to production of primary sequence data. The DNA sequencing system will eliminate all bottle necks that occur between subcloning and obtaining raw sequence data, significantly reduce both labor and reagent costs, and have a throughput of up to 250 megabases of raw DNA sequence per machine per year - more than an order-of-magnitude increase in throughput over existing technologies. The DNA sequencing system will consist of four basic hardware components - a clone picker, a microextraction module (MEM), a device for processing small volume polymerase chain reaction and cycle sequencing reactions (PCR/CS), and a capillary array electrophoresis (CAE) DNA sequencer. The DNA sequencing system will leverage the capabilities of both an existing prototype CAE instrument, which is a high throughput capillary array DNA sequencing instrument, and a colony picker, which is a functional high throughput device. In addition, major modules of the operating software have already been developed. The goals of the project are to: 1) design and construct a flow process PCR/CS device, 2) design and construct a micro-extraction module and integrate it with the clone picker, 3) evaluate improved amplification and sequencing chemistry to simplify the proposed system, and 4) integrate the chemistry and hardware and test the DNA sequencing system within a large-scale sequencing project. Development of the integrated DNA sequencing system will facilitate the completion of the DNA sequence acquisition phase of the Human Genome Project and enable the application of DNA sequencing to clinical settings for the diagnosis of human genetic diseases and the development of biopharmaceuticals.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
3R01HG001775-02S1
Application #
6136596
Study Section
Ethical, Legal, Social Implications Review Committee (GNOM)
Program Officer
Schloss, Jeffery
Project Start
1997-07-01
Project End
2000-06-30
Budget Start
1999-08-27
Budget End
2000-06-30
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Molecular Dynamics, Inc.
Department
Type
DUNS #
City
Sunnyvale
State
CA
Country
United States
Zip Code
94085
Thomas, R S; Rank, D R; Penn, S G et al. (2001) Identification of toxicologically predictive gene sets using cDNA microarrays. Mol Pharmacol 60:1189-94
Liu, S; Ren, H; Gao, Q et al. (2000) Automated parallel DNA sequencing on multiple channel microchips. Proc Natl Acad Sci U S A 97:5369-74
Beja, O; Aravind, L; Koonin, E V et al. (2000) Bacterial rhodopsin: evidence for a new type of phototrophy in the sea. Science 289:1902-6
Hadd, A G; Goard, M P; Rank, D R et al. (2000) Sub-microliter DNA sequencing for capillary array electrophoresis. J Chromatogr A 894:191-201
Dolnik, V; Liu, S; Jovanovich, S (2000) Capillary electrophoresis on microchip. Electrophoresis 21:41-54
Simpson, P C; Roach, D; Woolley, A T et al. (1998) High-throughput genetic analysis using microfabricated 96-sample capillary array electrophoresis microplates. Proc Natl Acad Sci U S A 95:2256-61