染色体构象捕获
染色质
染色体
计算生物学
生物
DNA
基因组
DNA测序
遗传学
基因
基因表达
增强子
作者
Judith Marsman,Robert C. Day,Grégory Gimenez
标识
DOI:10.1007/978-1-0716-2140-0_16
摘要
The three-dimensional structure of the genome is highly organized and is an important aspect of gene regulation. Chromatin interactions can be identified using chromosome conformation capture-based techniques, which rely on proximity ligation. Of these techniques, circular chromosome conformation capture sequencing (4C-seq) is used to identify all chromatin interactions occurring with a single chromosomal location (one versus all). Here we describe a 4C-seq protocol that has been optimized for primary adherent cells, for which the first digestion step is inefficient using standard 4C-seq protocols. It can, however, also be applied to other cell or tissue types. This protocol utilizes a standard DNA library preparation method using a commercial kit, and includes a description of the data processing steps.
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