PCR Methodology

Ian Carter, Catriona Halliday, Theo P Sloots, Todd M Pryce, Ian Kay, Gerry Harnett, Glenys R Chidlow, Philip Giffard

    Research output: Chapter in Book/Report/Conference proceedingChapter

    Abstract

    PCR methodologies have become firmly entrenched in many clinical laboratories for the detection of a wide range of organisms, because they offer major advantages of improved sensitivity and rapidity over traditional diagnostic methods. However, many variables need to be considered in performing a reliable PCR assay, ranging from nucleic acid extraction, storage, composition of the PCR reaction mix used, to the dynamics of the amplification reaction. To control for these variables, there is an obvious need for standardised reagents and quality assurance programmes to obtain reproducible and clinically significant results. The diagnostic potential of the PCR technology has been greatly enhanced with the development of multiplex, real-time, and quantitative PCR methods, and these are now routinely performed in many diagnostic laboratories. More recently, PCR has been applied to bacterial typing, and a reasonable prediction is that in the near future, bacterial typing will be performed by either some variant of next-generation sequencing, or by HRM analysis of selected markers, depending on the amount of information required. � 2010 Springer Science+Business Media B.V.
    Original languageEnglish
    Title of host publicationPCR for Clinical Mircrobiology
    Place of PublicationNew York
    PublisherSpringer
    Pages11-48
    Number of pages38
    ISBN (Print)978-90-481-9038-6
    Publication statusPublished - 2010

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  • Cite this

    Carter, I., Halliday, C., Sloots, T. P., Pryce, T. M., Kay, I., Harnett, G., Chidlow, G. R., & Giffard, P. (2010). PCR Methodology. In PCR for Clinical Mircrobiology (pp. 11-48). Springer.