seqMINER: an integrated ChIP-seq data interpretation platform

被引:328
作者
Ye, Tao [1 ]
Krebs, Arnaud R. [1 ]
Choukrallah, Mohamed-Amin [1 ]
Keime, Celine
Plewniak, Frederic
Davidson, Irwin [1 ]
Tora, Laszlo [1 ]
机构
[1] Univ Strasbourg, CNRS UMR 7104, INSERM U596, Dept Funct Genom & Canc,IGBMC, Illkirch Graffenstaden, Cu Strasbourg, France
关键词
EMBRYONIC STEM-CELLS; DEVELOPMENTAL REGULATORS; HUMAN GENOME; GENES; ENHANCERS; SOFTWARE; POLYCOMB; BROWSER; SYSTEM; STATE;
D O I
10.1093/nar/gkq1287
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
In a single experiment, chromatin immunoprecipitation combined with high throughput sequencing (ChIP-seq) provides genome-wide information about a given covalent histone modification or transcription factor occupancy. However, time efficient bioinformatics resources for extracting biological meaning out of these gigabyte-scale datasets are often a limiting factor for data interpretation by biologists. We created an integrated portable ChIP-seq data interpretation platform called seqMINER, with optimized performances for efficient handling of multiple genome-wide datasets. seqMINER allows comparison and integration of multiple ChIP-seq datasets and extraction of qualitative as well as quantitative information. seqMINER can handle the biological complexity of most experimental situations and proposes methods to the user for data classification according to the analysed features. In addition, through multiple graphical representations, seqMINER allows visualization and modelling of general as well as specific patterns in a given dataset. To demonstrate the efficiency of seqMINER, we have carried out a comprehensive analysis of genome-wide chromatin modification data in mouse embryonic stem cells to understand the global epigenetic landscape and its change through cellular differentiation.
引用
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页数:10
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