http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112885410-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_faffff5fef7b07b9c3a8381822a726e3 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B30-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B40-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G06F18-23 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G06K9-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B40-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B30-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 |
| filingDate | 2021-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82654d4e560fb7a1a35cff94f64f2c75 |
| publicationDate | 2021-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-112885410-A |
| titleOfInvention | Genotyping microarray for CNV structural variant detection |
| abstract | The invention provides a genotyping chip for CNV structural variation detection, comprising a first sequence reading circuit, a second sequence splitting circuit, a third end pairing circuit, a fourth shunt detection circuit and an array density probe group; The probe group includes a first array density probe and a second array density probe; the first array density probe generates a first density level sequence probe signal; the second sequence splitting circuit generates a second density level sequence split signal; The second density-level sequence splitting signal performs end monitoring to obtain multiple end monitoring signals; the third end matching circuit outputs multiple matching results based on the multiple end monitoring signals, and the fourth shunt detection circuit performs shunt detection on the multiple matching results, thereby outputting the gene Sequence structural variation information. The present invention also proposes a corresponding genotyping method. The invention improves the application range and detection performance of the existing classical CNV structure variation detection algorithm. |
| priorityDate | 2021-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.