Please use this identifier to cite or link to this item: https://doi.org/10.1186/s13059-017-1247-6
Title: NicE-seq: high resolution open chromatin profiling
Authors: PONNALURI, VK CHAITHANYA
ZHANG, GUOQIANG
ESTEVE, PIERRE-OLIVIER
SPRACKLIN, GEORGE
SIAN, STEPHANIE 
XU, SHUANG-YONG
BENOUKRAF, TOUATI 
PRADHAN, SRIHARSA
Keywords: Science & Technology
Life Sciences & Biomedicine
Biotechnology & Applied Microbiology
Genetics & Heredity
Open chromatin
NicE-seq
Transcription factor occupancy
DNA methylation
EMBRYONIC STEM-CELLS
GENOME-WIDE
TRANSCRIPTION FACTORS
HYPERSENSITIVE SITES
DNA DEMETHYLATION
METHYLATION
REGIONS
GENES
ACCESSIBILITY
PROMOTER
Issue Date: 28-Jun-2017
Publisher: BIOMED CENTRAL LTD
Citation: PONNALURI, VK CHAITHANYA, ZHANG, GUOQIANG, ESTEVE, PIERRE-OLIVIER, SPRACKLIN, GEORGE, SIAN, STEPHANIE, XU, SHUANG-YONG, BENOUKRAF, TOUATI, PRADHAN, SRIHARSA (2017-06-28). NicE-seq: high resolution open chromatin profiling. GENOME BIOLOGY 18 (1). ScholarBank@NUS Repository. https://doi.org/10.1186/s13059-017-1247-6
Abstract: © 2017 The Author(s). Open chromatin profiling integrates information across diverse regulatory elements to reveal the transcriptionally active genome. Tn5 transposase and DNase I sequencing-based methods prefer native or high cell numbers. Here, we describe NicE-seq (nicking enzyme assisted sequencing) for high-resolution open chromatin profiling on both native and formaldehyde-fixed cells. NicE-seq captures and reveals open chromatin sites (OCSs) and transcription factor occupancy at single nucleotide resolution, coincident with DNase hypersensitive and ATAC-seq sites at a low sequencing burden. OCSs correlate with RNA polymerase II occupancy and active chromatin marks, while displaying a contrasting pattern to CpG methylation. Decitabine-mediated hypomethylation of HCT116 displays higher numbers of OCSs.
Source Title: GENOME BIOLOGY
URI: https://scholarbank.nus.edu.sg/handle/10635/155399
ISSN: 1474-760X
1474-760X
DOI: 10.1186/s13059-017-1247-6
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