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dc.contributor.authorKodzius, Rimantas*
dc.contributor.authorChang, Donald Choy*
dc.contributor.authorSheng, Ping*
dc.contributor.authorWen, Weijia*
dc.contributor.authorWu, Jinbo*
dc.contributor.authorXiao, Kang*
dc.contributor.authorYu, Vivian*
dc.date.accessioned2013-10-30T06:13:04Z
dc.date.available2013-10-30T06:13:04Z
dc.date.issued2010-05-01en
dc.identifier.urihttp://hdl.handle.net/10754/304732en
dc.description.abstractSince its invention in 1983, polymerase chain reaction (PCR) has been the method of choice for DNA amplification. Successful PCR depends on the optimization of several parameters, which is a cumbersome task due to the many variables (conditions and componen
dc.description.sponsorshipHong Kong Research Grants Council (Grant No. HKUST 603208 and 660207); Award No. SA-C0040/UK-C0016 made by King Abdullah University of Science and Technology (KAUST).en
dc.language.isoenen
dc.publisherHong Kong University of Science and Technologyen
dc.relation.urlhttp://pgworkshop.ust.hk/en
dc.subjectMicrofludicsen
dc.subjectPCR (polymerase chain reaction)en
dc.subjectTwo temperature PCRen
dc.subjectDNA amplificationen
dc.subjectDNA detectionen
dc.titleTwo-temperature PCR for Microfluidicsen
dc.typePresentationen
dc.contributor.departmentComputational Bioscience Research Center (CBRC)*
dc.identifier.journalHong Kong University of Science and Technologyen
dc.eprint.versionPublisher's Version/PDFen
dc.contributor.institutionThe Hong Kong University of Science and Technology (HKUST)*
refterms.dateFOA2018-06-14T06:36:48Z


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