| Literature DB >> 33727644 |
Ana-Luisa Silva1, Paulina Klaudyna Powalowska1, Magdalena Stolarek1, Eleanor Ruth Gray1, Rebecca Natalie Palmer1, Bram Herman2, Cameron Alexander Frayling1, Barnaby William Balmforth3.
Abstract
Accurate detection of somatic variants, against a background of wild-type molecules, is essential for clinical decision making in oncology. Existing approaches, such as allele-specific real-time PCR, are typically limited to a single target gene and lack sensitivity. Alternatively, next-generation sequencing methods suffer from slow turnaround time, high costs, and are complex to implement, typically limiting them to single-site use. Here, we report a method, which we term Allele-Specific PYrophosphorolysis Reaction (ASPYRE), for high sensitivity detection of panels of somatic variants. ASPYRE has a simple workflow and is compatible with standard molecular biology reagents and real-time PCR instruments. We show that ASPYRE has single molecule sensitivity and is tolerant of DNA extracted from plasma and formalin fixed paraffin embedded (FFPE) samples. We also demonstrate two multiplex panels, including one for detection of 47 EGFR variants. ASPYRE presents an effective and accessible method that simplifies highly sensitive and multiplexed detection of somatic variants.Entities:
Year: 2021 PMID: 33727644 PMCID: PMC7966381 DOI: 10.1038/s41598-021-85545-3
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379