| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b7b2d4990735732e51fa59d7c320a5ae |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-112
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-118 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6874
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6886 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6874
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 |
| filingDate |
2018-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_159a4d25e9ba31758d8e765c9dc95df7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79d0b47fc4f400da54a664b5be03d481
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6084a6480746fb6475514fe7f1a4861c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79485005dfe5b91679cc24fa4f709199
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c945aa69092b153b0eabd55ee3b4e833
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9efe11f7cb91b3f1188a9930240b4fa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae40cf9ff17dc23c9edf610cbd8d0d14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_222d817b302cc997e5b68d07975ed0d3 |
| publicationDate |
2021-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-2021147937-A1 |
| titleOfInvention |
Target-enriched multiplexed parallel analysis for assessment of risk for genetic conditions |
| abstract |
The invention provides methods for assessment of risk for genetic conditions using target-enriched multiplexed parallel analysis, for example fetal risk for genetic conditions in prenatal testing. The methods of the invention utilize Target Capture Sequences (TACS) to thereby enrich for target sequences of interest, followed by massive parallel sequencing and statistical analysis of the enriched population. The methods of the disclosure can be used to determine carrier status of inheritable genetic abnormalities associated with genetic conditions and from this information the fetal risk of inheriting the genetic condition can be determined. Kits for carrying out the methods of the invention are also provided. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114990202-A |
| priorityDate |
2017-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |