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Review

High-resolution mapping studies of chromatin and gene regulatory elements

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Pages 319-329 | Published online: 03 Dec 2009
 

Abstract

Microarray and high-throughput sequencing technologies have enabled the development of comprehensive assays to identify locations of particular chromatin structures and regulatory elements. It is now possible to create genome-wide maps of DNA methylation, trans-factor binding sites, histone variants and histone tail modifications, nucleosome positions, regions of open chromatin, and chromosome locations and interactions. This review provides a summary of these new assays that are changing the way in which molecular biology research is being performed. While the generation of large amounts of data from these experiments is becoming increasingly easier, the development of corresponding analysis methods has progressed more slowly. It will likely be years before the full extent of the information contained in these data is fully appreciated.

Acknowledgements

We would like to thank Greg Crawford for his discussions and critical review of this manuscript.

Financial & competing interests disclosure

APB and TSF were supported by NIH grant U54-HG004563 and the Institute for Genome Sciences & Policy at Duke University. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

No writing assistance was utilized in the production of this manuscript.

Additional information

Funding

APB and TSF were supported by NIH grant U54-HG004563 and the Institute for Genome Sciences & Policy at Duke University. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. No writing assistance was utilized in the production of this manuscript.

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