| Literature DB >> 26484710 |
Nirmal Rajasekaran1, Myung Ryurl Oh2, Sung-Su Kim1, Si Eun Kim2, Young Deug Kim3, Hyun-Jeung Choi4, Bohyun Byun4, Young Kee Shin5.
Abstract
ddPCR is a highly sensitive PCR method that utilizes a water-oil emulsion system. Using a droplet generator, an extracted nucleic acid sample is partitioned into ~20,000 nano-sized, water-in-oil droplets, and PCR amplification occurs in individual droplets. The ddPCR approach is in identifying sequence mutations, copy number alterations, and select structural rearrangements involving targeted genes. Here, we demonstrate the use of ddPCR as a powerful technique for precisely quantitating rare BRAF V600E mutations in FFPE reference standard cell lines, which is helpful in identifying individuals with cancer. In conclusion, ddPCR technique offers the potential to precisely profile the specific rare mutations in different genes in various types of FFPE samples.Entities:
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Year: 2015 PMID: 26484710 PMCID: PMC4692650 DOI: 10.3791/53190
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355