DNA甲基化
表观遗传学
生物
甲基化
基因
遗传学
5-甲基胞嘧啶
基因表达
基因沉默
照明菌甲基化试验
计算生物学
作者
Manoj K. Singh,John E. Edwards
出处
期刊:Methods in molecular biology
日期:2021-01-01
被引量:1
标识
DOI:10.1007/978-1-0716-0876-0_34
摘要
There is increasing interest in understanding the pathological role of DNA methylation changes in disease by profiling genome-wide methylation changes. This includes both 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC). The typical profiling study is designed to measure 5mC and/or 5hmC levels alongside gene expression in a set of samples and controls to determine a list of candidate genes whose 5mC and/or 5hmC changes are associated with expression changes. We recently showed that ME-Class2 substantially outperforms other bioinformatic approaches at accurately identify genes with highly associated methylation and expression changes. ME-Class2 further illuminated how synergistic changes in 5mC and 5hmC potentially contribute to gene silencing and activation. Here we present a detailed protocol for using ME-Class2 to analyze genome-wide methylation (5mC and/or 5hmC) and expression data. Further, we provide advice about extending ME-Class2 to study the relationships between other epigenetic marks.
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