The Core Unit research engineers will be a central resource for devise assembly and testing expertise for all Projects. The research engineers have over 8 years of combined expertise in silicon, glass, and polymer photolithographic fabrication at the Solid State Engineering Laboratory (SSEL). Personnel also have experience in instrumentation design, circuit design, and chemical processing. The research engineers will assures that components are tested and judged consistently, both in isolation and within integrated devices. As a consequence, component testing between projects will references a common benchmark. The Core facility will also allow a pooling of expensive capital resources that are currently held in separate laboratories or are expensive to replicate at several locations. The Core Unit has four Specific Aims: 1) Provide photolithographic fabrication support for all Projects. support will include training and assistance in SSEL procedures as well as large-scale production runs of silicon wafers. Fabrication processes provided by the Core Unit personnel will be backed upon quality control assessment of each fabrication run. 2) Provide deice assembly support for all Projects. The Core will assist in solving assembly and post-fabrication problems for all projects. This will include flow problems, heat and/or mass transport problems, and macro-to-micro scale interfacing. Production level assembly will be available, including wafer dicing, wire bonding, package gluing, and quality assessment. 3) Provide standardized reagents, testing methods, and operation support for all Projects. Core personnel are available for consultation in the design phase of each Project. The Core will assist in the operation of the devices using biological samples, including provision of quality tested common reagents. Computer software support for laboratory instrumentation is also provided. 4) Provide a common platform for testing of devices. The Core will allow students and research engineers from all Projects to use a common set of testing and analysis equipment. Core personnel will develop instrumentation electronics and the uniform test platform for device testing. Test platforms will be constantly improved over the course of the project.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Program Projects (P01)
Project #
5P01HG001984-02
Application #
6318371
Study Section
Project Start
2000-06-05
Project End
2001-03-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2000
Total Cost
$376,377
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Wang, Fang; Burns, Mark A (2009) Performance of nanoliter-sized droplet-based microfluidic PCR. Biomed Microdevices 11:1071-80
Rhee, Minsoung; Burns, Mark A (2009) Microfluidic pneumatic logic circuits and digital pneumatic microprocessors for integrated microfluidic systems. Lab Chip 9:3131-43
Kim, Sung-Jin; Wang, Fang; Burns, Mark A et al. (2009) Temperature-programmed natural convection for micromixing and biochemical reaction in a single microfluidic chamber. Anal Chem 81:4510-6
Wang, Fang; Yang, Ming; Burns, Mark A (2008) Microfabricated valveless devices for thermal bioreactions based on diffusion-limited evaporation. Lab Chip 8:88-97
Zeitoun, Ramsey I; Chen, Zheng; Burns, Mark A (2008) Transverse imaging and simulation of dsDNA electrophoresis in microfabricated glass channels. Electrophoresis 29:4768-74
Rhee, Minsoung; Burns, Mark A (2008) Microfluidic assembly blocks. Lab Chip 8:1365-73
Rhee, Minsoung; Burns, Mark A (2008) Drop mixing in a microchannel for lab-on-a-chip platforms. Langmuir 24:590-601
Srivastava, Nimisha; Burns, Mark A (2007) Microfluidic pressure sensing using trapped air compression. Lab Chip 7:633-7
Chang, Dustin S; Langelier, Sean M; Burns, Mark A (2007) An electronic Venturi-based pressure microregulator. Lab Chip 7:1791-9
Chisa, Jennifer L; Burke, David T (2007) Mammalian mRNA splice-isoform selection is tightly controlled. Genetics 175:1079-87

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