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Targeted Next-Generation Sequencing of Liquid Biopsy Samples from Patients with NSCLC

机译:来自NSCLC患者的液检样本的下一代测序

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摘要

Liquid biopsy tests have become an integral part of the molecular diagnosis of patients with non-small cell lung cancer (NSCLC). We describe a new test panel that uses very low input (20 ng) of cell-free nucleic acids extracted from human plasma, which is designed to yield results in less than 72 h. In this study, we performed novel amplicon-based targeted next-generation sequencing with a semiconductor-based system, the Ion GeneStudio S5 Prime. The analytic performance of the assay was evaluated using contrived and retrospectively collected clinical specimens. The cumulative percent coefficient of variation for the new test process was very precise at 8.4% for inter-day, 4.0% for inter-operator and 3.4% for inter-instrument. We also observed significant agreement (95.7–100%) with an orthogonal, high-sensitivity droplet digital™ Polymerase Chain Reaction (ddPCR) test. This method offers a valuable supplement to assessing targeted mutations from blood while conserving specimens and maintaining sensitivity, with rapid turn-around times to actionable results.
机译:液体活检测试已成为非小细胞肺癌(NSCLC)患者分子诊断的组成部分。我们描述了一种使用从人血浆中提取的极低输入(20ng)的无细胞核酸的新测试面板,其设计成在小于72小时的时间内产生导致的结果。在本研究中,我们进行了基于半导体的系统的新型扩增子基于靶向的下一代测序,即离子基因型S5素。使用学和回顾性收集的临床标本评估测定的分析性能。新试验过程的累积变异系数非常精确,日内为8.4%,互操作员的4.0%,仪器间3.4%。我们还观察到具有正交,高灵敏度液滴数字™聚合酶链反应(DDPCR)试验的重要协议(95.7-100%)。该方法提供了有价值的补充,可评估血液的靶向突变,同时保存标本并保持敏感性,快速转弯时间与可操作的结果。

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