http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013163935-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_698be06221ddfa3a53412e98829d4c6a |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2013-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89bb585e5e4a218815c7ea347111afa6 |
publicationDate | 2013-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | WO-2013163935-A1 |
titleOfInvention | Method for isolating and obtaining pure and complete fetus genome dna |
abstract | Provided is a method for isolating and obtaining pure and complete fetus genome DNA, comprising the following steps: isolating a nucleated erythrocyte from the maternal (pregnant woman) peripheral blood, identifying the individual hereditary feature subtype of the mother and/or father of the fetus; conducting high fidelity whole genome DNA amplification on the signal cell isolated from the nucleated erythrocyte; identifying the individual hereditary feature subtype of the fetus according to the laws of hereditary, and determining a fetus-originating genome DNA. The fetus-originating pure whole genome DNA provided by the present invention lays a material foundation for prenatal heredity diagnosis. |
priorityDate | 2012-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.