http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1710321-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-566
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78
filingDate 2000-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44883c263a10bba21d8f5d720b189257
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2032f96a5ccf6d00a82921cb4c438cad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a73d8f0cfb869cc00c73f5f7e53cf0c7
publicationDate 2015-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1710321-B1
titleOfInvention Process for high throughput DNA methylation analysis
abstract There is disclosed an improved high-throughput and quantitative process for determining methylation patterns in genomic DNA samples based on amplifying modified nucleic acid, and detecting methylated nucleic acid based on amplification-dependent displacement of specifically annealed hybridization probes. Specifically, the inventive process provides for treating genomic DNA samples with sodium bisulfite to create methylation-dependent sequence differences, followed by detection with fluorescence-based quantitative PCR techniques. The process is particularly well suited for the rapid analysis of a large number of nucleic acid samples, such as those from collections of tumor tissues.
priorityDate 1999-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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