http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111172248-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6851 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6851 |
| filingDate | 2020-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-111172248-B |
| titleOfInvention | A universal kit for verification of copy number variation based on fragment analysis technology |
| abstract | The invention discloses a universal kit for verifying copy number variation based on fragment analysis technology, comprising a primer composition for genetic markers of length polymorphism and quality control sites, Taq DNA polymerase, buffer for PCR amplification, and a control genome DNA, pure water, wherein, the primer composition of polymorphic genetic marker and quality control site includes a single primer containing fluorescein-labeled primer pairs shown in SEQ.ID.No.1 to SEQ.ID.No.20 . The universal kit provided by the present invention can accurately determine the CNV copy number of the target region is 0, 1, 2, 3 or more, and is suitable for both copy number increase and copy number reduction, effectively overcoming the need for first-generation sequencing and real-time The shortcomings of the fluorescence scheme, and no need to prepare a standard curve, the operation is simple and the accuracy is high. |
| priorityDate | 2020-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 52.