http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2021536612-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16H50-20 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/G16B30-20 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B30-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-00 |
| filingDate | 2019-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2021536612-A |
| titleOfInvention | Detection of genetic variants based on merged and unmerged reads |
| abstract | Gene sequence reads with the same molecular bar code and sequence from sequence reads from nucleic acid sequencers are identified, the gene reads are grouped into families, and the families containing split reads are processed into samples of polynucleotide molecules. Methods and systems for improving the identification of nucleic acid variants by detecting variants of. The present disclosure relates to computer technology that provides accurate diagnosis based on determination of various states of nucleic acids such as DNA or RNA derived from a genome, chromosome, or other genetic part sequenced from a sample. |
| priorityDate | 2018-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 298.