| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cbf4a72441a9802e2698cb95cf6f3949 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2523-301 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B40-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B40-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B25-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B25-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B45-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B5-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G06F19-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G06F19-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G06F19-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G06F19-20 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B45-00 |
| filingDate |
2017-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4cb2b3c1a3dee6111906b2d235baa87b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55e2f42c038191be2188beee272d69d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2050bbbc8e7798c2202344918a149a06 |
| publicationDate |
2018-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
KR-20180128801-A |
| titleOfInvention |
Method for generating distribution of background allele frequency for sequencing data obtained from cell-free nucleic acid and method for detecting mutation from cell-free nucleic acid using the same |
| abstract |
A method for generating a frequency distribution of background alleles for sequence analysis data obtained from a cell-free nucleic acid, a frequency distribution matrix of background alleles by the method, and a method for detecting a mutation from a cell-free nucleic acid using the same. According to this, to eliminate the germ cell mutation, the sequence analysis data obtained from the nucleic acid isolated from the subject's own cells is used to generate the frequency distribution of background alleles for the sequence analysis data obtained from the cell-free nucleic acid There is an advantage of saving cost and time. |
| priorityDate |
2017-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |