InTAD: chromosome conformation guided analysis of enhancer target genes

High-throughput technologies for analyzing chromosome conformation at a genome scale have revealed that chromatin is organized in topologically associated domains (TADs). While TADs are relatively stable across cell types, intra-TAD activities are cell type specific. Epigenetic profiling of differen...

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Hauptverfasser: Okonechnikov, Konstantin (VerfasserIn) , Pfister, Stefan (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 31 January 2019
In: BMC bioinformatics
Year: 2019, Jahrgang: 20
ISSN:1471-2105
DOI:10.1186/s12859-019-2655-2
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1186/s12859-019-2655-2
Verlag, Volltext: https://doi.org/10.1186/s12859-019-2655-2
Volltext
Verfasserangaben:Konstantin Okonechnikov, Serap Erkek, Jan O. Korbel, Stefan M. Pfister and Lukas Chavez

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520 |a High-throughput technologies for analyzing chromosome conformation at a genome scale have revealed that chromatin is organized in topologically associated domains (TADs). While TADs are relatively stable across cell types, intra-TAD activities are cell type specific. Epigenetic profiling of different tissues and cell-types has identified a large number of non-coding epigenetic regulatory elements (‘enhancers’) that can be located far away from coding genes. Linear proximity is a commonly chosen criterion for associating enhancers with their potential target genes. While enhancers frequently regulate the closest gene, unambiguous identification of enhancer regulated genes remains to be a challenge in the absence of sample matched chromosome conformation data. 
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