| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bd81debf9c36d0a66f6a6b61aeae297f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f11cdde3c30b9e333d9c463c22d6a48c |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2521-101 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6811
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate |
2010-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_12621e3738499f98cda8f851748608f3 |
| publicationDate |
2010-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
WO-2010093552-A1 |
| titleOfInvention |
Method of amplification of gc-rich dna templates |
| abstract |
Methods are provided for increasing the processivity of DNA polymerases on GC-rich templates. The methods relate to providing enhancers and biased ratios of dNTPs, and may be used in DNA amplification reactions. The methods are useful for detecting genotypes associated with GC-rich repeats, including Fragile X Syndrome. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9469872-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2539464-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2539464-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9371560-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10428363-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2539464-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8759037-B2 |
| priorityDate |
2009-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |