An interactive environment for agile analysis and visualization of ChIP-sequencing data

EaSeq, a user-friendly and freely available software tool, offers fast and comprehensive ChIP-sequencing data analyses, enabling experimentalists to easily extract information and generate hypotheses from genome-wide datasets. To empower experimentalists with a means for fast and comprehensive chrom...

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Bibliographic Details
Published inNature structural & molecular biology Vol. 23; no. 4; pp. 349 - 357
Main Authors Lerdrup, Mads, Johansen, Jens Vilstrup, Agrawal-Singh, Shuchi, Hansen, Klaus
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.04.2016
Nature Publishing Group
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Summary:EaSeq, a user-friendly and freely available software tool, offers fast and comprehensive ChIP-sequencing data analyses, enabling experimentalists to easily extract information and generate hypotheses from genome-wide datasets. To empower experimentalists with a means for fast and comprehensive chromatin immunoprecipitation sequencing (ChIP-seq) data analyses, we introduce an integrated computational environment, EaSeq. The software combines the exploratory power of genome browsers with an extensive set of interactive and user-friendly tools for genome-wide abstraction and visualization. It enables experimentalists to easily extract information and generate hypotheses from their own data and public genome-wide datasets. For demonstration purposes, we performed meta-analyses of public Polycomb ChIP-seq data and established a new screening approach to analyze more than 900 datasets from mouse embryonic stem cells for factors potentially associated with Polycomb recruitment. EaSeq, which is freely available and works on a standard personal computer, can substantially increase the throughput of many analysis workflows, facilitate transparency and reproducibility by automatically documenting and organizing analyses, and enable a broader group of scientists to gain insights from ChIP-seq data.
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ISSN:1545-9993
1545-9985
1545-9985
DOI:10.1038/nsmb.3180