Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3ca014618e340117bce49debafc4409d http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2a7ebd2ce5ef7e691bd44c48a88a2bfc http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0996f29e4b7edd026efcb9c9e3b24a69 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-158 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/G16B20-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N1-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-00 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N1-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 |
filingDate |
2013-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
2020-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab32b92f7fd686e5416e202885180800 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ffdde250cd6e861ecb9343c8094702f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_146ecdd6887a144311fcafa44fa47e89 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2eec65f5410f581c894597dd1043eaa9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d3d8986a664526a21c5163bab75cc1f6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa44ec69fec5b98ec73d96068ad8e3e4 |
publicationDate |
2020-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-10591391-B2 |
titleOfInvention |
Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats |
abstract |
The present invention provides systems, apparatuses, and methods to detect the presence of fetal cells when mixed with a population of maternal cells in a sample and to test fetal abnormalities, i.e. aneuploidy. In addition, the present invention provides methods to determine when there are insufficient fetal cells for a determination and report a non-informative case. The present invention involves quantifying regions of genomic DNA from a mixed sample. More particularly the invention involves quantifying DNA polymorphisms from the mixed sample. |
priorityDate |
2006-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |