| Literature DB >> 30320738 |
Charles Decraene1, Amanda Bortolini Silveira2, Marc Michel2, François-Clément Bidard3, Jean-Yves Pierga4, Marc-Henri Stern5, Charlotte Proudhon6.
Abstract
Droplet digital polymerase chain reaction (ddPCR) is a highly sensitive quantitative polymerase chain reaction (PCR) method based on sample fractionation into thousands of nano-sized water-in-oil individual reactions. Recently, ddPCR has become one of the most accurate and sensitive tools for circulating tumor DNA (ctDNA) detection. One of the major limitations of the standard ddPCR technique is the restricted number of mutations that can be screened per reaction, as specific hydrolysis probes recognizing each possible allelic version are required. An alternative methodology, the drop-off ddPCR, increases throughput, since it requires only a single pair of probes to detect and quantify potentially all genetic alterations in the targeted region. Drop-off ddPCR displays comparable sensitivity to conventional ddPCR assays with the advantage of detecting a greater number of mutations in a single reaction. It is cost-effective, conserves precious sample material, and can also be used as a discovery tool when mutations are not known a priori.Entities:
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Year: 2018 PMID: 30320738 PMCID: PMC6235282 DOI: 10.3791/58051
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355