http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2364833-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ac316c4307d2a84add2bae0328f607bd
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-702
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70
filingDate 2010-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff67acc1bd5c837589ab586bc794be6e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_529187f3420c157af426b1b5acc976fa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dbd7f92f698ce7a18a4efdd03d43aeb
publicationDate 2011-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2364833-A1
titleOfInvention VIRUS WEST NILE GENOMIC AMPLIFICATION METHOD.
abstract West genomic genomic amplification methodnNile The method is based on the amplification of an area of the regionn3 'non-coding virus, preferably by Time PCRnReal, thanks to the use of a pair of primers minimallyndegenerates, allowing West Nile virus amplificationnpresent in a sample of any of the known lineages. Henamplified fragment is preferably detected with a probenspecific to the area, also minimally degenerated. The couple ofnDegenerate primers chosen, as well as the preferred probe, givenleading to high sensitivity in the detection of all lineages andnalso at a high specificity for West Nile virus.
priorityDate 2010-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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