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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
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author Buisine, Nicolas
Sachs, Laurent
author_facet Buisine, Nicolas
Sachs, Laurent
author_sort Buisine, Nicolas
collection PubMed
description 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.
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spelling pubmed-28045762010-01-12 Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping Buisine, Nicolas Sachs, Laurent BMC Res Notes Short Report 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. BioMed Central 2009-12-16 /pmc/articles/PMC2804576/ /pubmed/20015379 http://dx.doi.org/10.1186/1756-0500-2-257 Text en Copyright ©2009 Buisine et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Buisine, Nicolas
Sachs, Laurent
Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping
title Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping
title_full Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping
title_fullStr Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping
title_full_unstemmed Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping
title_short Impact of genome assembly status on ChIP-Seq and ChIP-PET data mapping
title_sort impact of genome assembly status on chip-seq and chip-pet data mapping
topic Short Report
url 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
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