ChIP-seq: a New Technique for Genome-wide Profiling of Protein-DNA Interaction

被引:5
|
作者
Liang Fang [1 ]
Xu Keo [1 ]
Gong Zhao-Jian [1 ]
Li Qiao [1 ]
Ma Jian [1 ,2 ]
Xiong Wei [1 ,2 ]
Zeng Zhao-Yang [1 ]
Li Gui-Yuan [1 ,2 ]
机构
[1] Cent S Univ, Key Lab Carcinogenesis & Canc Invas, Key Lab Carcinogenesis, Minist Hlth,Minist Educ,Canc Res Inst, Changsha 410078, Hunan, Peoples R China
[2] Cent S Univ, Dis Genome Res Ctr, Hunan Key Lab Nonresolving Inflammat & Canc, Changsha 410013, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
ChIP-seq; next generation sequencing; gene regulation; epigenetics; data analysis; INTEGRATED SOFTWARE-SYSTEM; FACTOR-BINDING SITES; HIGH-RESOLUTION; IN-VIVO; CHROMATIN-STRUCTURE; GENE-EXPRESSION; HISTONE; IMMUNOPRECIPITATION; METHYLATION; CANCER;
D O I
10.3724/SP.J.1206.2012.00305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chromatin immunoprecipitation followed by sequencing (ChIP-seq) is a burgeoning technique which combines Chromatin immunoprecipitation (ChIP) with massively parallel DNA sequencing to detect protein-DNA binding events, histone modifications, nucleosomes positioning and DNA methylation on a genome-wide scale. Motivated by the tremendous progress in next-generation sequencing (NGS) technology, ChIP-seq offers higher resolution, less noise, and broader coverage than conventional microarray based ChIP-chip. With the decreasing cost of sequencing, ChIP-seq has become an indispensable tool for studying gene regulation and epigenetic mechanisms. In this review, we describe its latest advances, with an emphasis on issues related to data analysis and its application.
引用
收藏
页码:216 / 227
页数:12
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