http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112126677-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-172 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B25-20 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6827 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B25-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-50 |
| filingDate | 2020-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-112126677-B |
| titleOfInvention | Noninvasive deafness haplotype gene mutation detection method |
| abstract | The application provides a noninvasive detection method for detecting fetal deafness haplotype gene mutation by using genome DNA of leucocytes of a pregnant woman and a husband thereof and plasma free DNA of the pregnant woman, wherein a GemCode platform is used for preparing a second-generation sequencing library from the genome DNA of the pregnant woman and the husband thereof and preparing a library from the plasma free DNA of the pregnant woman; capturing and hybridizing by using a specific probe; performing high-throughput sequencing on the captured library through a second-generation sequencing platform to obtain sequencing original data; after the original data is filtered and the low-quality and linker sequences are removed to obtain clean data, the genotype of the fetus is determined by analyzing the haplotypes of both parents and the genetic information of the fetus. |
| priorityDate | 2020-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 48.