http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2844768-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_05105424d52fe459531dba0304906c0f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2013-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f015857181c8df6049f50b3628d9f935
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a1718ef5dda3ab7ff6de7ff95096760
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42038725c3789a0f89cae70efdbbe4be
publicationDate 2015-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2844768-A1
titleOfInvention Digital analyte analysis
abstract The invention generally relates to droplet based digital PCR and methods for analyzing a target nucleic acid using the same. In certain embodiments, a method for determining the nucleic acid make-up of a sample is provided. In one aspect, the invention provides a droplet that contains a single nucleic acid template and a plurality of primer pairs specific for multiple target sites on the template. The single nucleic acid template can be DNA or RNA. The template is amplified in the droplet for detection; and may preferably be amplified using a plurality of primer pairs as described herein. The ability to amplify and detect single nucleic acids in droplets enables digital PCR, detection, counting, and differentiation among nucleic acids, especially those present in heterogeneous samples. Thus, the invention applies to digital amplification techniques and, in specific embodiments enables multiplex PCR in droplets.
priorityDate 2012-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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