http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018101375-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cbd7eb2e3a76b55013b3156a0375ecd5 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-68 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2017-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f12fac081714769db721f880ac6d2d39 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3c35a54a45ca0346d7e107850cefe65 |
publicationDate | 2018-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | WO-2018101375-A1 |
titleOfInvention | Method for detecting human genomic dna |
abstract | Provided is a method for detecting and/or assaying human genomic DNA in a test sample at high sensitivity. One "human Alu model sequence" representing the consensus sequence of 46 human Alu subfamilies is identified, and PCR primer-probe candidates for Alu detection are selected using this human Alu model sequence. Next, a primer-probe set that is an oligonucleotide sequence which hybridizes specifically with the human Alu sequence and that comprises an oligonucleotide sequence capable of minimizing dimer formation is selected using proprietary criteria. The human genomic DNA in the test sample can be detected and/or assayed at high sensitivity by conducting quantitative real-time PCR using the PCR primer-probe for Alu detection obtained in this manner. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021136559-A1 |
priorityDate | 2016-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 83.