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高分辨率DNA熔解分析:进展与局限

High-resolution DNA melting analysis: advancements and limitations.

作者信息

Wittwer Carl T

机构信息

Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.

出版信息

Hum Mutat. 2009 Jun;30(6):857-9. doi: 10.1002/humu.20951.

Abstract

Recent advances in fluorescent dyes, methods, instruments and software for DNA melting analysis have created versatile new tools for variant scanning and genotyping. High resolution melting analysis (HRM or HRMA) is faster, simpler, and less expensive than alternative approaches requiring separations or labeled probes. With the addition of a saturating dye before PCR followed by rapid melting analysis of the PCR products, the sensitivity of heterozygote scanning approaches 100%. Specificity can be increased by identifying common polymorphisms with small amplicon melting, unlabeled probes or snapback primers to decrease the sequencing burden. However, some homozygotes require mixing for identification. Furthermore, different heterozygotes may produce melting curves so similar to each other that, although they clearly vary from homozygous variants, they are not differentiated from each other. Nevertheless, the experimental return for minimal effort is great. This focus issue of Human Mutation includes a concise, timely review on high resolution melting, a comparison to denaturing gradient gel electrophoresis, integration with qPCR for copy number assessment, combined amplicon scanning and unlabeled probe genotyping from a single melting curve, and applications to the mitochondrial genome and to BRCA1.

摘要

用于DNA熔解分析的荧光染料、方法、仪器及软件的最新进展,为变异扫描和基因分型创造了多功能新工具。高分辨率熔解分析(HRM或HRMA)比需要分离或标记探针的其他方法更快、更简单且成本更低。在PCR前加入饱和染料,随后对PCR产物进行快速熔解分析,杂合子扫描的灵敏度接近100%。通过使用小扩增子熔解、未标记探针或回折引物鉴定常见多态性以减轻测序负担,可提高特异性。然而,一些纯合子需要混合才能鉴定。此外,不同的杂合子可能产生彼此非常相似的熔解曲线,尽管它们与纯合变异明显不同,但彼此之间无法区分。尽管如此,付出最小努力就能获得很大的实验回报。本期《人类突变》聚焦专题包括一篇关于高分辨率熔解的简洁、及时的综述,与变性梯度凝胶电泳的比较,与qPCR整合用于拷贝数评估,从单一熔解曲线进行联合扩增子扫描和未标记探针基因分型,以及在线粒体基因组和BRCA1中的应用。

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