Cargando…
Clustered ChIP-Seq-defined transcription factor binding sites and histone modifications map distinct classes of regulatory elements
BACKGROUND: Transcription factor binding to DNA requires both an appropriate binding element and suitably open chromatin, which together help to define regulatory elements within the genome. Current methods of identifying regulatory elements, such as promoters or enhancers, typically rely on sequenc...
Autores principales: | Rye, Morten, Sætrom, Pål, Håndstad, Tony, Drabløs, Finn |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239327/ https://www.ncbi.nlm.nih.gov/pubmed/22115494 http://dx.doi.org/10.1186/1741-7007-9-80 |
Ejemplares similares
-
A ChIP-Seq Benchmark Shows That Sequence Conservation Mainly Improves Detection of Strong Transcription Factor Binding Sites
por: Håndstad, Tony, et al.
Publicado: (2011) -
Cell-type specificity of ChIP-predicted transcription factor binding sites
por: Håndstad, Tony, et al.
Publicado: (2012) -
The Triform algorithm: improved sensitivity and specificity in ChIP-Seq peak finding
por: Kornacker, Karl, et al.
Publicado: (2012) -
A manually curated ChIP-seq benchmark demonstrates room for improvement in current peak-finder programs
por: Rye, Morten Beck, et al.
Publicado: (2011) -
A comparison of control samples for ChIP-seq of histone modifications
por: Flensburg, Christoffer, et al.
Publicado: (2014)