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filingDate 2019-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_45c0669fc1858fe43e7e83140452425a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b8b2387d4266ed185480e1bd698ae4c3
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publicationDate 2020-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110684833-A
titleOfInvention A genetic testing method for evaluating individual sensitivity and side effects of ovulation induction drugs
abstract The invention provides a gene detection method for individual sensitivity and side effects of ovulation induction drugs, comprising the following steps: (1) extracting sample genomic DNA, quantification and quality inspection; (2) performing multiple target gene variants after passing the quality inspection Amplification of sites or enrichment of target genes with specific nucleic acid probes. According to the number of target genes and sites detected, an appropriate amount of amplification products that have passed the quality inspection are taken for first-generation sequencing, and first-generation sequencing is used for specific sites. Amplification and detection; (3) According to the number of target genes and loci to be detected, take an appropriate amount of amplification products that have passed the quality inspection, carry out next-generation sequencing or gene chip analysis, sequence the multiple PCR products, and split the off-machine data. Perform bioinformatics analysis to output SNPs of specific genes; (4) analyze and interpret through the pharmacogenome database and eugenics gene database, and output personalized and precise ovulation induction drug recommendations and programs.
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