http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2022520794-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6853 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-686 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6869 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6844 |
| filingDate | 2020-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2022520794-A |
| titleOfInvention | How to prepare and analyze a nucleic acid library |
| abstract | Detecting different mutations within the same sample is essential, especially if the sample volume is limited and if a high throughput method is desired for rapid detection of mutations. Methods routinely used in the art require a separate assay to detect different mutations or mutation types in a sample (eg, single nucleotide polymorphism (SNP) or copy number variation (CNV)). And. The present disclosure provides methods for detecting different mutations such as SNPs and CNVs in the same sample. The methods described herein may be useful for preimplantation genetic diagnosis, carrier screening or genotyping. |
| priorityDate | 2019-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 328.