Rescue of Low-Yield DNA Samples for Next-Generation Sequencing Using Vacuum Centrifugal Concentration in a Clinical Workflow

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
L. K. Vestergaard, Nicolai S. Mikkelsen, Douglas N P Oliveira, T. Poulsen, E. Hoegdall
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Abstract

The implementation of next-generation sequencing (NGS) in clinical oncology has enabled the analysis of multiple cancer-associated genes for diagnostics and treatment purposes. The detection of pathogenic and likely pathogenic mutations is crucial to manage the disease. Obtaining the mutational profile may be challenging in samples with low yields of DNA—reflected by the type of biological material, such as formalin-fixed paraffin-embedded tissue (FFPE), needle biopsies, and circulating free/tumor DNA, as well as a sparse tumor content. Moreover, standardized strict procedures for the extraction of DNA in a clinical setting might contribute to lower amounts of DNA per µL. The detection of variants in low-yield DNA samples remains a challenge in clinical diagnostics, where molecular analyses such as NGS are needed. Here, we performed vacuum centrifugation on DNA extracted from five FFPE tissue blocks, with concentrations below 0.2 ng/µL. Through NGS analysis, we found that low-yield DNA samples could be concentrated to sufficient levels, without compromising the mutational profile.
在临床工作流程中使用真空离心浓缩拯救低产量DNA样品用于下一代测序
下一代测序(NGS)在临床肿瘤学中的实施使多种癌症相关基因的分析能够用于诊断和治疗目的。检测致病性和可能的致病性突变对控制疾病至关重要。在DNA产量低的样本中,获得突变谱可能具有挑战性——这反映在生物材料的类型上,如福尔马林固定石蜡包埋组织(FFPE)、针活检、循环游离/肿瘤DNA以及稀疏的肿瘤含量。此外,在临床环境中提取DNA的标准化严格程序可能有助于降低每µL的DNA量。在需要NGS等分子分析的临床诊断中,检测低产量DNA样本中的变异仍然是一个挑战。在这里,我们对从五个FFPE组织块中提取的DNA进行了真空离心,其浓度低于0.2纳克/µL。通过NGS分析,我们发现低产量的DNA样本可以浓缩到足够的水平,而不会影响突变谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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