http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111091868-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B40-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B40-10 |
| filingDate | 2019-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2020-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2020-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-111091868-B |
| titleOfInvention | Method and system for analyzing chromosome aneuploidy |
| abstract | The invention provides a chromosome aneuploidy analysis method and a system. The method provided by the invention is used for carrying out statistical analysis on the sequencing depth of the sample based on the Zscore algorithm, and comprehensively judging the chromosome aneuploidy condition by combining the statistical analysis of the SNP allele frequency of the sample. The method has high accuracy, is not influenced by the SNP locus number of the sample to be detected, has high specificity and sensitivity which can reach 100 percent, and can judge whether the abnormal chromosome is deleted or amplified. |
| priorityDate | 2019-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
| Predicate | Subject |
|---|---|
| isDiscussedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID634501 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416046308 |
Total number of triples: 18.