Please use this identifier to cite or link to this item: https://doi.org/10.1186/s13059-017-1247-6
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dc.titleNicE-seq: high resolution open chromatin profiling
dc.contributor.authorPONNALURI, VK CHAITHANYA
dc.contributor.authorZHANG, GUOQIANG
dc.contributor.authorESTEVE, PIERRE-OLIVIER
dc.contributor.authorSPRACKLIN, GEORGE
dc.contributor.authorSIAN, STEPHANIE
dc.contributor.authorXU, SHUANG-YONG
dc.contributor.authorBENOUKRAF, TOUATI
dc.contributor.authorPRADHAN, SRIHARSA
dc.date.accessioned2019-06-07T02:09:24Z
dc.date.available2019-06-07T02:09:24Z
dc.date.issued2017-06-28
dc.identifier.citationPONNALURI, 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
dc.identifier.issn1474-760X
dc.identifier.issn1474-760X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/155399
dc.description.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.
dc.language.isoen
dc.publisherBIOMED CENTRAL LTD
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectBiotechnology & Applied Microbiology
dc.subjectGenetics & Heredity
dc.subjectOpen chromatin
dc.subjectNicE-seq
dc.subjectTranscription factor occupancy
dc.subjectDNA methylation
dc.subjectEMBRYONIC STEM-CELLS
dc.subjectGENOME-WIDE
dc.subjectTRANSCRIPTION FACTORS
dc.subjectHYPERSENSITIVE SITES
dc.subjectDNA DEMETHYLATION
dc.subjectMETHYLATION
dc.subjectREGIONS
dc.subjectGENES
dc.subjectACCESSIBILITY
dc.subjectPROMOTER
dc.typeArticle
dc.date.updated2019-06-04T03:53:26Z
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.1186/s13059-017-1247-6
dc.description.sourcetitleGENOME BIOLOGY
dc.description.volume18
dc.description.issue1
dc.published.statePublished
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