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游离 DNA 提取:效率、数量和质量评估。

Extraction of Cell-Free DNA: Evaluation of Efficiency, Quantity, and Quality.

机构信息

Department of Molecular Diagnostics, Aalborg University Hospital, Aalborg, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Department of Molecular Diagnostics, Aalborg University Hospital, Aalborg, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

出版信息

J Mol Diagn. 2024 Apr;26(4):310-319. doi: 10.1016/j.jmoldx.2024.01.008. Epub 2024 Feb 2.

Abstract

Cell-free DNA (cfDNA) serves as a valuable biomarker for early disease detection and monitoring. However, the use of cfDNA for analysis faces challenges owing to general low but variable abundance and fragmentation. Preanalytical factors, including cfDNA extraction, impact cfDNA quality and quantity. Efficient and robust cfDNA extraction is essential for reliable results in downstream applications, and various commercial extraction methods exist, each with trade-offs. To aid researchers and clinicians in choosing the proper cfDNA extraction method, manual, semiautomated, and automated methods were evaluated, including the QIAamp Circulating Nucleic Acid Kit (manual and QIAcube), QIAamp MinElute ccfDNA Kit (QIAcube), and QIAsymphony DSP Circulating DNA Kit (QIAsymphony). For each extraction method, cfDNA was extracted on two separate days, using samples obtained from 18 healthy donors. This study assessed extraction efficiency, quantity, and quality using droplet digital PCR and TapeStation. The QIAamp Circulating Nucleic Acid Kit, both manual and semiautomated, outperformed the QIAamp MinElute ccfDNA Kit (QIAcube) and QIAsymphony DSP Circulating DNA Kit (QIAsymphony), showing higher recovery rates and cfDNA quantity. All methods were reproducible, with no day-to-day variability and no contamination by high-molecular-weight DNA. The QIAamp Circulating Nucleic Acid Kit offers high yield without compromising quality. Implementation of the method should consider specific study and clinical needs, taking into account each method's advantages and limitations for optimal outcomes.

摘要

无细胞游离 DNA(cfDNA)可作为早期疾病检测和监测的有价值的生物标志物。然而,由于其普遍含量低且存在变异性,cfDNA 分析的应用存在挑战。包括 cfDNA 提取在内的分析前因素会影响 cfDNA 的质量和数量。高效且稳健的 cfDNA 提取对于下游应用的可靠结果至关重要,并且存在各种商业提取方法,每种方法都有其优缺点。为了帮助研究人员和临床医生选择合适的 cfDNA 提取方法,对手动、半自动和自动化方法进行了评估,包括 QIAamp Circulating Nucleic Acid 试剂盒(手动和 QIAcube)、QIAamp MinElute ccfDNA 试剂盒(QIAcube)和 QIAsymphony DSP Circulating DNA 试剂盒(QIAsymphony)。对于每种提取方法,在两天内使用从 18 位健康供体获得的样本提取 cfDNA。本研究使用液滴数字 PCR 和 TapeStation 评估了提取效率、数量和质量。QIAamp Circulating Nucleic Acid 试剂盒(手动和半自动)均优于 QIAamp MinElute ccfDNA 试剂盒(QIAcube)和 QIAsymphony DSP Circulating DNA 试剂盒(QIAsymphony),显示出更高的回收率和 cfDNA 数量。所有方法均具有重现性,没有日间变异性,也没有高分子量 DNA 的污染。QIAamp Circulating Nucleic Acid 试剂盒在不影响质量的情况下提供高产量。该方法的实施应考虑具体的研究和临床需求,同时考虑每种方法的优缺点,以获得最佳结果。

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