Abstract
Chromatin immunoprecipitation coupled with massive parallel sequencing (ChIP-seq) is a powerful technology to identify the genome-wide locations of DNA binding proteins such as transcription factors or modified histones. As more and more experimental laboratories are adopting ChIP-seq to unravel the transcriptional and epigenetic regulatory mechanisms, computational analyses of ChIP-seq also become increasingly comprehensive and sophisticated. In this article, we review current computational methodology for ChIP-seq analysis, recommend useful algorithms and workflows, and introduce quality control measures at different analytical steps. We also discuss how ChIP-seq could be integrated with other types of genomic assays, such as gene expression profiling and genome-wide association studies, to provide a more comprehensive view of gene regulatory mechanisms in important physiological and pathological processes.
| Original language | English |
|---|---|
| Pages (from-to) | 54-70 |
| Number of pages | 17 |
| Journal | Quantitative Biology |
| Volume | 1 |
| Issue number | 1 |
| DOIs | |
| State | Published - Mar 1 2013 |
Keywords
- Chromatin Signature
- Histone Mark
- Nucleosome Occupancy
- Peak Calling
- Target Gene Prediction
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