| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4bd24d0edc441a277cf5d128b2c97b31 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B15-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G06F17-10
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/G16B20-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B5-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B5-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B40-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B30-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B15-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 |
| filingDate |
2018-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ccdf5fe940141ebeda143eb07fb4d6a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3a614c1e9377874e58d1b1f061eb82a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9311872c925a517064ba990f878be237
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f686b6d094a6f32575ccf42a37850e67 |
| publicationDate |
2019-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-2019164627-A1 |
| titleOfInvention |
Models for Targeted Sequencing |
| abstract |
A processing system uses a Bayesian inference based model for targeted sequencing or variant calling. In an embodiment, the processing system generates candidate variants of a cell free nucleic acid sample. The processing system determines likelihoods of true alternate frequencies for each of the candidate variants in the cell free nucleic acid sample and in a corresponding genomic nucleic acid sample. The processing system filters or scores the candidate variants by the model using at least the likelihoods of true alternate frequencies. The processing system outputs the filtered candidate variants, which may be used to generate features for a predictive cancer or disease model. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2023317052-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11482303-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021041968-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11783915-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021016441-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11581062-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2020132151-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2799778-C1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2799778-C9
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021064365-A1 |
| priorityDate |
2017-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |