| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1cb98082561173e3872367ac6ed34be6 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B50-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B30-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B40-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B50-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-00 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B50-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48 |
| filingDate |
2017-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
2021-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb9beb8e250dd4cf150ed1ea62b30f56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6679596ac8f662375198e70af33ca8da
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_618c3216733671c88b0f0aebc1fb3ec2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16d35c4e5054f2ebec5ab218784f1138
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec98adedce9099abac5849c3b9ead9c6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1c49a5dcea698c4c76f8c2a22f94a35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99e47bfb13fec49a774bc77523dfba44 |
| publicationDate |
2021-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
RU-2750706-C2 |
| titleOfInvention |
Bioinformatic systems, devices and methods for performing secondary and/or tertiary processing |
| abstract |
FIELD: biotechnology. n SUBSTANCE: invention relates to the field of biotechnology. A computer-implemented method for the joint determination of variants in homologous regions is proposed. The method includes identifying one or more homologous regions to be co-processed, loading a co-cluster for the regions to be co-processed, creating a list of candidate variants from the co-cluster and creating a connectivity matrix that determines the order of processing the positions of candidate variants, determining the position of the candidate variant from the final genotype matrix, and outputting a variant definition file. n EFFECT: invention provides improved accuracy of the data obtained from the sequence. n 9 cl, 80 dwg |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2020327377-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11676685-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11783917-B2 |
| priorityDate |
2016-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |