http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010136691-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f4d9f5df19923c7dde908e31cf70e982 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2008-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb6ab2b81a28c7ae49142ed1bedba878 |
| publicationDate | 2010-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2010136691-A |
| titleOfInvention | Method and apparatus for detecting chromosomal structural abnormalities |
| abstract | In a method for detecting a gene translocation having an abnormal chromosome structure, a mixture of a plurality of nucleic acid probes, a probe that crosses a predetermined breakpoint region, A first probe straddling the cut point from upstream of the cut point; A method for detecting a structural abnormality of a chromosome, characterized in that a second probe from the downstream of a breakpoint before or before the breakpoint is labeled with a different label. [Effects] When detecting a structural abnormality of a chromosome by combining a probe labeled with a nucleic acid or a nucleic acid analog with a complementary chromosomal region, the frequency of false positives decreases, and even a fine structural abnormality can be detected. . [Selection] Figure 2 |
| priorityDate | 2008-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.