http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2011329373-B2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6886
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filingDate 2011-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81419f9321812daa768c8a16cb56a3fb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2a94c409f8ec1834c08d034c7fa09f6
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publicationDate 2014-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2011329373-B2
titleOfInvention Mutation detection assay
abstract A method of sample analysis is provided. In certain embodiments, the method involves: a) amplifying a product from a sample that comprises both wild type copies of a genomic locus and mutant copies of the genomic locus that have a point mutation relative to said wild type copies of the genomic locus, to produce an amplified sample, where: i. the amplifying is done using a first primer and a second primer; and ii. the first primer comprises a 3' terminal nucleotide that base pairs with the point mutation and also comprises a nucleotide sequence that is fully complementary to a sequence in the locus with the exception of a single base mismatch within 6 bases of the 3' terminal nucleotide; and b) detecting the presence of said product in said amplified sample using a flap assay that employs an invasive oligonucleotide. A kit for performing the method is also provided.
priorityDate 2010-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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