Principles of ChIP-seq Data Analysis Illustrated with Examples

被引:0
|
作者
Ambrosini, Giovanna [1 ]
Dreos, Rene [1 ]
Bucher, Philipp [1 ]
机构
[1] Swiss Fed Inst Technol Lausanne EPFL, Swiss Inst Expt Canc Res ISREC, CH-1015 Lausanne, Switzerland
来源
PROCEEDINGS IWBBIO 2014: INTERNATIONAL WORK-CONFERENCE ON BIOINFORMATICS AND BIOMEDICAL ENGINEERING, VOLS 1 AND 2 | 2014年
关键词
ChIP-seq; DNase I hypersensitive sites; transcription factor binding sites; histone marks; bioinformatics analysis; PROTEIN-DNA INTERACTIONS; PROFILES;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chromatin immunoprecipitation (ChIP) followed by high-throughput sequencing (ChIP-seq) is a powerful method to determine how transcription factors and other chromatin-associated proteins interact with DNA in order to regulate gene transcription. A single ChIP-seq experiment produces large amounts of highly reproducible data. The challenge is to extract knowledge from the data by thoughtful application of appropriate bioinformatics tools. Here we present a concise introduction into ChIP-seq data analysis in the form of a tutorial based on tools developed by our group. We expose biological questions, explain methods and provide guidelines for the interpretation of the results. While this article focuses on ChIP-seq, most of the algorithms and tools we present are applicable to other chromatin profiling assays based on next generation sequencing (NGS) technology as well.
引用
收藏
页码:682 / 694
页数:13
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