http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7888024-B2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-34
filingDate 2008-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_537206f7a9d15c0087ff45f3da62157b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51322355dc513b8f3565ab325319efde
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publicationDate 2011-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7888024-B2
titleOfInvention Method of detecting genetic polymorphism
abstract The present invention provides a novel polymorphism detecting method suitable for the detection and identification of copy number variation. n Provided is a method of determining the genotype of a subject in a genomic region comprising an SNP site, comprising a step for performing typing of the SNP site by the invader assay with a DNA-containing sample comprising the genomic region from the subject as the template, wherein fluorescence is measured on a real time basis. The copy number ratio of both alleles is determined using the fluorescence intensity ratio of each allele at a time before saturation of fluorescence intensity. Preferably, the present method further comprises a step for amplifying the genomic region comprising an SNP site prior to the invader step. In this step of amplification, a plurality of regions comprising a plurality of SNP sites can be simultaneously amplified. Furthermore, the present method enables the determination of the copy number of each allele when combined with quantitative PCR.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11251595-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11094398-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018144449-A1
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Total number of triples: 26.