Show simple item record

dc.date.accessioned2018-06-28T08:45:42Z
dc.date.issued2017-01-01
dc.identifierhttps://academic.oup.com/nar/article-lookup/doi/10.1093/nar/gkw1015
dc.identifier.citationNUCLEIC ACIDS RESEARCH, 2017, 45 (4)
dc.identifier.issn0305-1048
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1958
dc.description.abstractPromoters and enhancers regulate the initiation of gene expression and maintenance of expression levels in spatial and temporal manner. Recent findings stemming from the Cap Analysis of Gene Expression (CAGE) demonstrate that promoters and enhancers, based on their expression profiles after stimulus, belong to different transcription response subclasses. One of the most promising biological features that might explain the difference in transcriptional response between subclasses is the local chromatin environment. We introduce a novel computational framework, PEDAL, for distinguishing effectively transcriptional profiles of promoters and enhancers using solely histone modification marks, chromatin accessibility and binding sites of transcription factors and co-activators. A case study on data from MCF-7 cell-line reveals that PEDAL can identify successfully the transcription response subclasses of promoters and enhancers from two different stimulations. Moreover, we report subsets of input markers that discriminate with minimized classification error MCF-7 promoter and enhancer transcription response subclasses. Our work provides a general computational approach for identifying effectively cell-specific and stimulation-specific promoter and enhancer transcriptional profiles, and thus, contributes to improve our understanding of transcriptional activation in human.
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectUNIFIED ARCHITECTURE FEATURE-SELECTION ACTIVE ENHANCERS GENOME EXPRESSION PROVIDES REGIONS CANCER ATLAS CELLS
dc.titleDiscriminative identification of transcriptional responses of promoters and enhancers after stimulus
dc.typeJournal Article
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfNUCLEIC ACIDS RESEARCH
pubs.issue4
pubs.notesISI Document Delivery No.: EN5OO Times Cited: 0 Cited Reference Count: 34 Kleftogiannis, Dimitrios Kalnis, Panos Arner, Erik Bajic, Vladimir B. King Abdullah University of Science and Technology (KAUST); MEXT King Abdullah University of Science and Technology (KAUST); Research Grant from MEXT [to the RIKEN Center for Life Science Technologies]. Funding for open access charge: King Abdullah University of Science and Technology (KAUST). 0 OXFORD UNIV PRESS OXFORD NUCLEIC ACIDS RES none Promoters and enhancers regulate the initiation of gene expression and maintenance of expression levels in spatial and temporal manner. Recent findings stemming from the Cap Analysis of Gene Expression (CAGE) demonstrate that promoters and enhancers, based on their expression profiles after stimulus, belong to different transcription response subclasses. One of the most promising biological features that might explain the difference in transcriptional response between subclasses is the local chromatin environment. We introduce a novel computational framework, PEDAL, for distinguishing effectively transcriptional profiles of promoters and enhancers using solely histone modification marks, chromatin accessibility and binding sites of transcription factors and co-activators. A case study on data from MCF-7 cell-line reveals that PEDAL can identify successfully the transcription response subclasses of promoters and enhancers from two different stimulations. Moreover, we report subsets of input markers that discriminate with minimized classification error MCF-7 promoter and enhancer transcription response subclasses. Our work provides a general computational approach for identifying effectively cell-specific and stimulation-specific promoter and enhancer transcriptional profiles, and thus, contributes to improve our understanding of transcriptional activation in human.
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR
pubs.volume45
pubs.embargo.termsNot known
dc.contributor.icrauthorKleftogiannis, Dimitrios


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0