亚硫酸氢盐
故障排除
DNA甲基化
甲基化
计算生物学
亚硫酸氢盐测序
协议(科学)
亚硫酸氢钠
化学
生物
表观遗传学
计算机科学
DNA
医学
基因
基因表达
遗传学
病理
操作系统
有机化学
替代医学
作者
João Lobo,Ad Gillis,Leendert H. J. Looijenga
出处
期刊:Methods in molecular biology
日期:2020-08-27
卷期号:: 167-180
被引量:2
标识
DOI:10.1007/978-1-0716-0860-9_12
摘要
DNA methylation constitutes the most studied epigenetic mechanism, regulating gene expression in several physiological and pathological states. Targeted methylation polymerase chain reaction (PCR)-based analyses are among the most universal and commonly used techniques in research. They can be of use for validating methylation-based biomarkers to include in clinical practice. Optimal execution and interpretation of data is fundamental for achieving accurate and reproducible results.In this chapter we describe the backbone procedures behind targeted methylation analyses: bisulfite conversion and downstream PCR-based techniques, including real-time quantitative methylation-specific PCR (qMSP) and high-resolution melting (HRM) methylation-sensitive analyses. Specifically, we give details about the protocol, discuss the pros and cons of these methodologies, and give practical tips for achieving optimal results and for troubleshooting.
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