http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2022301656-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_916075766043ce900399a4c2eee9f054 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 |
| filingDate | 2022-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efeb95b0c0297ddb6937f820c18efe20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ad88bdd5bcd7212896fb331c8e122bb |
| publicationDate | 2022-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-2022301656-A1 |
| titleOfInvention | Genome sequencing as an alternative to cytogenetic analysis |
| abstract | A computer-implemented method for the identification of clinically relevant structural variants in a subject with AML or MDS from whole genome sequencing data is disclosed that includes providing a whole-genome sequencing dataset, performing a structural variant analysis on the whole-genome sequencing dataset and producing a report that includes clinically relevant CNAs, SVs, and gene-level variants identified by the structural variant analysis. |
| priorityDate | 2021-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 302.