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ATAC-seq: A Method for Assaying Chromatin Accessibility Genome-Wide.

作者信息

Buenrostro Jason D, Wu Beijing, Chang Howard Y, Greenleaf William J

机构信息

Department of Genetics, Stanford University School of Medicine, Stanford, California.

Program in Epithelial Biology and the Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California.

出版信息

Curr Protoc Mol Biol. 2015 Jan 5;109:21.29.1-21.29.9. doi: 10.1002/0471142727.mb2129s109.


DOI:10.1002/0471142727.mb2129s109
PMID:25559105
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4374986/
Abstract

This unit describes Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq), a method for mapping chromatin accessibility genome-wide. This method probes DNA accessibility with hyperactive Tn5 transposase, which inserts sequencing adapters into accessible regions of chromatin. Sequencing reads can then be used to infer regions of increased accessibility, as well as to map regions of transcription-factor binding and nucleosome position. The method is a fast and sensitive alternative to DNase-seq for assaying chromatin accessibility genome-wide, or to MNase-seq for assaying nucleosome positions in accessible regions of the genome.

摘要

相似文献

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ATAC-seq: A Method for Assaying Chromatin Accessibility Genome-Wide.

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[10]
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本文引用的文献

[1]
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Nat Rev Genet. 2013-12-24

[2]
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Nat Methods. 2013-10-6

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Genome Res. 2012-9

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Nature. 2012-9-6

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Nature. 2012-9-6

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Nature. 2012-9-6

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Annu Rev Biochem. 2012

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Nat Rev Genet. 2011-7-12

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Genome Biol. 2010-12-8

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