http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114134213-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_85d452bb6cb8798de973c8ffb8a9073c |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858 |
filingDate | 2021-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb58aa2161b60c501891990b542f4bd0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc5e1655c6eae42cbad7abf11e5d3804 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e41422bf23d071b1df6451f989f51817 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ef5cadf99c6f2941f7a62688ba8409f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_180b26c97ee081e4d2984768e100ab95 |
publicationDate | 2022-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-114134213-A |
titleOfInvention | A kind of gene amplification detection method based on nucleic acid mass spectrometry technology |
abstract | The invention discloses a gene amplification detection method based on nucleic acid mass spectrometry technology, comprising the following steps: setting a target gene region, configuring a reference gene, confirming experimental primers based on the target gene region and the reference gene; Perform the primer reaction processing operation on the sample to obtain the sample to be analyzed; set the interpretation interval, configure the spotter and the nucleic acid mass spectrometer, perform the data analysis and interpretation operation based on the sample to be analyzed, the interpretation interval, the spotter and the nucleic acid mass spectrometer, and obtain the gene amplification Interpretation results; the present invention can achieve higher detection accuracy than fluorescence in situ hybridization technology and immunohistochemical technology in the prior art, and higher detection throughput than fluorescence quantitative PCR technology and digital PCR technology, and lower than fluorescence quantitative PCR technology Compared with the detection cost of digital PCR technology, it also has the level of shorter detection time compared with next-generation sequencing NGS technology. |
priorityDate | 2021-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 197.