http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20190095531-A

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filingDate 2012-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_300245a846536b77857048a0bf6a5102
publicationDate 2019-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20190095531-A
titleOfInvention Methods for detecting nucleic acid sequence variants
abstract The present invention provides a method for detecting the presence or absence of nucleic acid variants in a target region. These methods include amplifying the target region with forward primers and reverse primers in the presence of selector blockers. The selector blocker comprises a sequence complementary to the target region in the absence of the nucleic acid variant. The method further comprises detecting the amplification of the target region, wherein the amplification of the target region indicates the presence of the nucleic acid variant in the target region. Such nucleic acid variants may include deletions, mutations or insertions.
priorityDate 2011-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ59800
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ1KVQ9
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410493926

Total number of triples: 316.