亚硫酸氢盐测序
亚硫酸氢盐
CpG站点
照明菌甲基化试验
DNA甲基化
甲基化DNA免疫沉淀
生物
DNA测序
甲基化
计算生物学
基因组DNA
聚合酶链反应
限制性酶
DNA
遗传学
分子生物学
基因
基因表达
作者
Kazuhiko Nakabayashi,Michihiro Yamamura,Keita Haseagawa,Kenichiro Hata
出处
期刊:Methods in molecular biology
日期:2022-09-30
卷期号:: 39-51
被引量:9
标识
DOI:10.1007/978-1-0716-2724-2_3
摘要
Reduced representation bisulfite sequencing (RRBS) enriches CpG-rich genomic regions using the MspI restriction enzyme-which cuts DNA at all CCGG sites, regardless of their DNA methylation status at the CG site-and enables the measurement of DNA methylation levels at 5% ~ 10% of all CpG sites in the mammalian genome. RRBS has been utilized in a large number of studies as a cost-effective method to investigate DNA methylation patterns, mainly at gene promoters and CpG islands. Here, we describe protocols for gel-free preparation of RRBS libraries, quality control, sequencing, and data analysis. Our protocols typically require nine cycles of polymerase chain reaction (PCR) amplification to obtain a sufficient amount of library for sequencing when 100 ng of genomic DNA is used as a starting material; moreover, it takes 3 days to complete library preparation and quality control procedures for up to eight samples.
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