数字聚合酶链反应
核酸
表征(材料科学)
计算机科学
计量学
协调
参考值
标准化
计算生物学
纳米技术
生化工程
化学
材料科学
生物
聚合酶链反应
物理
工程类
生物化学
光学
基因
医学
声学
内科学
操作系统
作者
Megan H. Cleveland,Hua‐Jun He,Mojca Milavec,Young‐Kyung Bae,Peter M. Vallone,Jim F. Huggett
标识
DOI:10.1016/j.mam.2024.101256
摘要
Well-characterized reference materials support harmonization and accuracy when conducting nucleic acid-based tests (such as qPCR); digital PCR (dPCR) can measure the absolute concentration of a specific nucleic acid sequence in a background of non-target sequences, making it ideal for the characterization of nucleic acid-based reference materials. National Metrology Institutes are increasingly using dPCR to characterize and certify their reference materials, as it offers several advantages over indirect methods, such as UV-spectroscopy. While dPCR is gaining widespread adoption, it requires optimization and has certain limitations and considerations that users should be aware of when characterizing reference materials. This review highlights the technical considerations of dPCR, as well as its role when developing and characterizing nucleic acid-based reference materials.
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