Source:http://linkedlifedata.com/resource/pubmed/id/19736561
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2009-9-18
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pubmed:abstractText |
Chromatin immunoprecipitation followed by sequencing (ChIP-seq) is a technique for genome-wide profiling of DNA-binding proteins, histone modifications or nucleosomes. Owing to the tremendous progress in next-generation sequencing technology, ChIP-seq offers higher resolution, less noise and greater coverage than its array-based predecessor ChIP-chip. With the decreasing cost of sequencing, ChIP-seq has become an indispensable tool for studying gene regulation and epigenetic mechanisms. In this Review, I describe the benefits and challenges in harnessing this technique with an emphasis on issues related to experimental design and data analysis. ChIP-seq experiments generate large quantities of data, and effective computational analysis will be crucial for uncovering biological mechanisms.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1471-0064
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
669-80
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pubmed:dateRevised |
2011-10-12
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pubmed:meshHeading |
pubmed-meshheading:19736561-Animals,
pubmed-meshheading:19736561-Chromatin Immunoprecipitation,
pubmed-meshheading:19736561-Computational Biology,
pubmed-meshheading:19736561-DNA-Binding Proteins,
pubmed-meshheading:19736561-Epigenesis, Genetic,
pubmed-meshheading:19736561-Humans,
pubmed-meshheading:19736561-Nucleosomes,
pubmed-meshheading:19736561-Sequence Analysis, DNA
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pubmed:year |
2009
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pubmed:articleTitle |
ChIP-seq: advantages and challenges of a maturing technology.
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pubmed:affiliation |
Harvard Medical School, 10 Shattuck Street, Boston, MA 02115, USA. peter_park@harvard.edu
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pubmed:publicationType |
Journal Article,
Review,
Research Support, N.I.H., Extramural
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