Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-Seq

<p>Abstract</p> <p>Background</p> <p><it>In vivo </it>positioning and covalent modifications of nucleosomes play an important role in epigenetic regulation, but genome-wide studies of positioned nucleosomes and their modifications in human still remain limit...

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Main Authors: Lei Ying, Song Jun S, Shin Hyunjin, Zhang Yong, Liu X Shirley
Format: Article
Language:English
Published: BMC 2008-11-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/9/537
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spelling doaj-569282fac4184658a068db166284784d2020-11-24T21:44:38ZengBMCBMC Genomics1471-21642008-11-019153710.1186/1471-2164-9-537Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-SeqLei YingSong Jun SShin HyunjinZhang YongLiu X Shirley<p>Abstract</p> <p>Background</p> <p><it>In vivo </it>positioning and covalent modifications of nucleosomes play an important role in epigenetic regulation, but genome-wide studies of positioned nucleosomes and their modifications in human still remain limited.</p> <p>Results</p> <p>This paper describes a novel computational framework to efficiently identify positioned nucleosomes and their histone modification profiles from nucleosome-resolution histone modification ChIP-Seq data. We applied the algorithm to histone methylation ChIP-Seq data in human CD4<sup>+ </sup>T cells and identified over 438,000 positioned nucleosomes, which appear predominantly at functionally important regions such as genes, promoters, DNase I hypersensitive regions, and transcription factor binding sites. Our analysis shows the identified nucleosomes play a key role in epigenetic gene regulation within those functionally important regions via their positioning and histone modifications.</p> <p>Conclusion</p> <p>Our method provides an effective framework for studying nucleosome positioning and epigenetic marks in mammalian genomes. The algorithm is open source and available at <url>http://liulab.dfci.harvard.edu/NPS/</url>.</p> http://www.biomedcentral.com/1471-2164/9/537
collection DOAJ
language English
format Article
sources DOAJ
author Lei Ying
Song Jun S
Shin Hyunjin
Zhang Yong
Liu X Shirley
spellingShingle Lei Ying
Song Jun S
Shin Hyunjin
Zhang Yong
Liu X Shirley
Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-Seq
BMC Genomics
author_facet Lei Ying
Song Jun S
Shin Hyunjin
Zhang Yong
Liu X Shirley
author_sort Lei Ying
title Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-Seq
title_short Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-Seq
title_full Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-Seq
title_fullStr Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-Seq
title_full_unstemmed Identifying Positioned Nucleosomes with Epigenetic Marks in Human from ChIP-Seq
title_sort identifying positioned nucleosomes with epigenetic marks in human from chip-seq
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2008-11-01
description <p>Abstract</p> <p>Background</p> <p><it>In vivo </it>positioning and covalent modifications of nucleosomes play an important role in epigenetic regulation, but genome-wide studies of positioned nucleosomes and their modifications in human still remain limited.</p> <p>Results</p> <p>This paper describes a novel computational framework to efficiently identify positioned nucleosomes and their histone modification profiles from nucleosome-resolution histone modification ChIP-Seq data. We applied the algorithm to histone methylation ChIP-Seq data in human CD4<sup>+ </sup>T cells and identified over 438,000 positioned nucleosomes, which appear predominantly at functionally important regions such as genes, promoters, DNase I hypersensitive regions, and transcription factor binding sites. Our analysis shows the identified nucleosomes play a key role in epigenetic gene regulation within those functionally important regions via their positioning and histone modifications.</p> <p>Conclusion</p> <p>Our method provides an effective framework for studying nucleosome positioning and epigenetic marks in mammalian genomes. The algorithm is open source and available at <url>http://liulab.dfci.harvard.edu/NPS/</url>.</p>
url http://www.biomedcentral.com/1471-2164/9/537
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