http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014531208-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2563-107 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2527-107 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6886 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
| filingDate | 2012-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2014-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2014531208-A |
| titleOfInvention | Gene copy number polymorphism testing method |
| abstract | The present invention relates to the field of genetic testing, and particularly to a method for testing gene copy number polymorphism. In this method, an endogenous or exogenous similar sequence that is not similar to the sequence of the gene to be tested is selected, the corresponding primer is designed, the sequence of the gene to be tested and the similar sequence are simultaneously amplified, and then a melting curve Analyze. When a copy number variation occurs in a gene waiting for testing, the analysis result of the melting curve thereof can be clearly distinguished from the analysis result of the gene waiting for wild-type testing, thereby achieving the purpose of the test. The method of the present invention is used not only for examination of gene copy number polymorphism but also for examination of chromosome aneuploid. Further, the method of the present invention is applied not only to screening of gene copy number polymorphism patients and chromosomal aneuploid patients, to normal prenatal testing, but also to noninvasive prenatal diagnosis. The method of the present invention has advantages such as high speed, accuracy, high sensitivity, high specificity, high throughput, low cost, and no contamination. [Selection] Figure 1 |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-7235315-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2019074004-A1 |
| priorityDate | 2011-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.