http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007537762-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6823 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6837 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6841 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6825 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N37-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-543 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2005-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2007-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2007537762-A |
| titleOfInvention | Single label comparative hybridization |
| abstract | The present invention provides methods for detecting and mapping chromosomal or genetic abnormalities associated with various diseases, or trends for various diseases, or methods for detecting the phenomenon of large scale copy number variation. In particular, the present invention performs array-based comparative hybridization that allows reproducibility between samples and improves sensitivity by using the same detectable label for both test and reference sample nucleic acids. Provides an advanced way for The methods of the present invention are useful for detecting or diagnosing specific medical conditions such as cancer and detecting cancer trends based on detection of chromosomal or genetic abnormalities and gene expression levels. The methods of the present invention are also particularly useful for detecting or diagnosing genetic disorders in or predisposition to prenatal samples. Furthermore, the methods of the present invention are also useful for detecting or diagnosing novel genetic abnormalities associated with postnatal developmental abnormalities. |
| priorityDate | 2004-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 298.