Source:http://linkedlifedata.com/resource/pubmed/id/21204035
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2011-1-4
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pubmed:abstractText |
Formalin fixation has been used to preserve tissues for more than a hundred years, and there are currently more than 300 million archival samples in the United States alone. The application of genomic protocols such as high-density oligonucleotide array Comparative Genomic Hybridization (aCGH) to formalin-fixed, paraffin-embedded (FFPE) tissues, therefore, opens an untapped resource of available tissues for research and facilitates utilization of existing clinical data in a research sample set. However, formalin fixation results in cross-linking of proteins and DNA, typically leading to such a significant degradation of DNA template that little is available for use in molecular applications. Here, we describe a protocol to circumvent formalin fixation artifact by utilizing enzymatic reactions to obtain quality DNA from a wide range of FFPE tissues for successful genome-wide discovery of gene dosage alterations in archival clinical samples.
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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:issn |
1940-6029
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
700
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
185-98
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pubmed:meshHeading | |
pubmed:year |
2011
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pubmed:articleTitle |
Genomic analysis by oligonucleotide array Comparative Genomic Hybridization utilizing formalin-fixed, paraffin-embedded tissues.
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pubmed:affiliation |
Integrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
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pubmed:publicationType |
Journal Article
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