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Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping

BACKGROUND: ChIP-Seq and ChIP-PET can potentially be used with any genome for genome wide profiling of protein-DNA interaction sites. Unfortunately, it is probable that most genome assemblies will never reach the quality of the human genome assembly. Therefore, it remains to be determined whether Ch...

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Detalles Bibliográficos
Autores principales: Buisine, Nicolas, Sachs, Laurent
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804576/
https://www.ncbi.nlm.nih.gov/pubmed/20015379
http://dx.doi.org/10.1186/1756-0500-2-257
Descripción
Sumario:BACKGROUND: ChIP-Seq and ChIP-PET can potentially be used with any genome for genome wide profiling of protein-DNA interaction sites. Unfortunately, it is probable that most genome assemblies will never reach the quality of the human genome assembly. Therefore, it remains to be determined whether ChIP-Seq and ChIP-PET are practicable with genome sequences other than a few (e.g. human and mouse). FINDINGS: Here, we used in silico simulations to assess the impact of completeness or fragmentation of genome assemblies on ChIP-Seq and ChIP-PET data mapping. CONCLUSIONS: Most currently published genome assemblies are suitable for mapping the short sequence tags produced by ChIP-Seq or ChIP-PET.