生物
亚硫酸氢盐测序
DNA甲基化
计算生物学
人类基因组
基因组
遗传学
染色质
DNA
增强子
DNA测序
表观遗传学
基因
转录因子
基因表达
作者
Anna Křepelová,Francesco Neri
出处
期刊:Methods in molecular biology
日期:2021-01-01
卷期号:: 353-368
标识
DOI:10.1007/978-1-0716-1597-3_20
摘要
DNA methylation can regulate gene expression by modulating chromatin accessibility and transcription factor binding on promoter and enhancer regions. Whole-genome bisulfite sequencing (WGBS) represents the most informative and comprehensive analysis to profile the DNA methylation status of all the cytosines at single-base resolution. However, most of the available protocols recommend an amount of input DNA (50 ng-5μg) that makes the WGBS unsuitable for limited samples and cell populations. In this chapter, we provide complete protocol to perform WGBS libraries from very low-input DNA. This protocol is recommended for the analysis of the whole-genome DNA methylation pattern in rare cell populations, like a defined stem cell population isolated from animal models or human samples.
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