多路复用
体细胞
周转时间
液体活检
计算生物学
工作流程
分子诊断学
生物
基因
计算机科学
遗传学
癌症
数据库
操作系统
作者
Ana-Luisa Silva,Paulina Klaudyna Powalowska,Magdalena Stolarek,Eleanor R. Gray,Rebecca N Palmer,Bram Herman,Cameron A Frayling,Barnaby W Balmforth
标识
DOI:10.1038/s41598-021-85545-3
摘要
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.
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