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Automated high throughput nucleic acid purification from formalin-fixed paraffin-embedded tissue samples for next generation sequence analysis

机译:从福尔马林固定石蜡包埋的组织样品中自动进行高通量核酸纯化用于下一代序列分析

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摘要

Curation and storage of formalin-fixed, paraffin-embedded (FFPE) samples are standard procedures in hospital pathology laboratories around the world. Many thousands of such samples exist and could be used for next generation sequencing analysis. Retrospective analyses of such samples are important for identifying molecular correlates of carcinogenesis, treatment history and disease outcomes. Two major hurdles in using FFPE material for sequencing are the damaged nature of the nucleic acids and the labor-intensive nature of nucleic acid purification. These limitations and a number of other issues that span multiple steps from nucleic acid purification to library construction are addressed here. We optimized and automated a 96-well magnetic bead-based extraction protocol that can be scaled to large cohorts and is compatible with automation. Using sets of 32 and 91 individual FFPE samples respectively, we generated libraries from 100 ng of total RNA and DNA starting amounts with 95–100% success rate. The use of the resulting RNA in micro-RNA sequencing was also demonstrated. In addition to offering the potential of scalability and rapid throughput, the yield obtained with lower input requirements makes these methods applicable to clinical samples where tissue abundance is limiting.
机译:福尔马林固定,石蜡包埋(FFPE)样品的处理和储存是世界各地医院病理实验室的标准程序。存在成千上万的此类样本,可用于下一代测序分析。此类样品的回顾性分析对于确定癌变,治疗史和疾病结局的分子相关性很重要。使用FFPE材料进行测序的两个主要障碍是核酸的受损性质和核酸纯化的劳动密集型性质。这些限制和许多其他问题涵盖了从核酸纯化到文库构建的多个步骤。我们优化并自动化了基于96孔磁珠的提取协议,该协议可扩展至大型队列,并且与自动化兼容。我们分别使用32个和91个单独的FFPE样品,从100 ng总RNA和DNA起始量生成文库,成功率为95–100%。还证明了所得RNA在微RNA测序中的用途。除了提供可扩展性和快速通量的潜力外,以较低的输入要求获得的产量还使这些方法适用于组织丰度受到限制的临床样品。

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