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Unified high-level synthesis and module placement for defect-tolerant microfluidic biochips
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Source Annual ACM IEEE Design Automation Conference archive
Proceedings of the 42nd annual Design Automation Conference table of contents
Anaheim, California, USA
SESSION: Optimization techniques in high-level synthesis table of contents
Pages: 825 - 830  
Year of Publication: 2005
ISBN:1-59593-058-2
Authors
Fei Su  Duke University, Durham, NC
Krishnendu Chakrabarty  Duke University, Durham, NC
Sponsors
ACM: Association for Computing Machinery
SIGDA: ACM Special Interest Group on Design Automation
Publisher
ACM  New York, NY, USA
Bibliometrics
Downloads (6 Weeks): 12,   Downloads (12 Months): 61,   Citation Count: 16
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ABSTRACT

Microfluidic biochips promise to revolutionize biosensing and clinical diagnostics. As more bioassays are executed concurrently on a biochip, system integration and design complexity are expected to increase dramatically. This problem is also identified by the 2003 ITRS document as a major system-level design challenge beyond 2009. We focus here on the automated design of droplet-based microfluidic biochips. We present a synthesis methodology that unifies operation scheduling, resource binding, and module placement for such "digital" biochips. The proposed technique, which is based on parallel recombinative simulated annealing, can also be used after fabrication to bypass defective cells in the microfluidic array. A real-life protein assay is used to evaluate the synthesis methodology.


REFERENCES

Note: OCR errors may be found in this Reference List extracted from the full text article. ACM has opted to expose the complete List rather than only correct and linked references.

 
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2
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T. Zhang et al., Microelectrofluidic Systems: Modeling and Simulation, CRC Press, Boca Raton, FL, 2002.
 
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CITED BY  16

Collaborative Colleagues:
Fei Su: colleagues
Krishnendu Chakrabarty: colleagues