| Literature DB >> 28735491 |
Daniel H Wiseman1, Tim C P Somervaille1.
Abstract
Precise quantitation of allelic burden for a pathogenic mutation has diverse clinical and research applications but can be difficult to achieve with conventional qPCR-based techniques, especially at lower mutant allele frequencies. Digital PCR overcomes many of the limitations of qPCR and can be highly quantitative even for single-nucleotide variants, with distinct advantages over next-generation sequencing approaches. Here we describe a method combining the principles of TaqMan®-chemistry SNP genotyping with microfluidic digital PCR to generate a highly sensitive, quantitative allele-specific digital PCR assay for the six most common IDH1 and IDH2 mutations encountered in myeloid malignancy. The concept and approach could easily be applied to other suitable SNVs.Entities:
Keywords: Acute myeloid leukemia; Allelic discrimination; Digital PCR; Isocitrate dehydrogenase; Mutant allele frequency
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Year: 2017 PMID: 28735491 DOI: 10.1007/978-1-4939-7142-8_15
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745