| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_af92759c928daeb7f0daabbb0499f059 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-118 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16H15-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B30-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B30-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G06F40-174
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6886 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6869 |
| filingDate |
2020-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f36a09aa00bd2f4e27bc2c8013c72fb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c911ab50b286de5f4f8439ec9e469984
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_110c1e093247684c77440dc03df78662
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0b9e938473d9c2ba5f1070e338f4611
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1426ead2fa4b5f8145efa70516f0a216 |
| publicationDate |
2021-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-2021000082-A |
| titleOfInvention |
Nucleic acid sequence analysis method of patient sample, presentation method of analysis result, presentation device, presentation program, and nucleic acid sequence analysis system of patient sample |
| abstract |
PROBLEM TO BE SOLVED: To facilitate consideration in disclosure of information on germline mutations found in a nucleic acid test to patients, their relatives, doctors in charge, and the like. A method of analyzing a nucleic acid sequence of a patient sample by a computer, wherein a first nucleic acid sequence data derived from a tumor cell collected from a patient and a first nucleic acid sequence data derived from a non-tumor cell collected from the same patient are obtained. 2 nucleic acid sequence data and 2 are acquired, somatic cell mutations are detected based on the first nucleic acid sequence data, germ cell mutations are detected based on the second nucleic acid sequence data, and information on the germ cell mutations. The problem is solved by an analysis method in which the presentation style for presenting is selected from a plurality of candidates and an analysis report is generated by the selected presentation style. [Selection diagram] Fig. 1 |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2023181370-A1 |
| priorityDate |
2019-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |