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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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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. |
format | Text |
id | pubmed-2804576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT buisinenicolas impactofgenomeassemblystatusonchipseqandchippetdatamapping AT sachslaurent impactofgenomeassemblystatusonchipseqandchippetdatamapping |