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Genetic analysis panel kit of NGS (Next generation sequencing) method for simultaneously analyzing sudden cardiac disease and therapeutic drug gene variation

机译:NGS遗传分析面板试剂盒(下一代测序)同时分析突发心脏病和治疗药物基因变化的方法

摘要

The present invention relates to a genetic analysis panel kit of a NGS (Next generation sequencing) method that simultaneously analyzes acute cardiac arrest syndrome and gene mutations in therapeutic drugs, and provides a product for detecting mutations by simultaneously analyzing gene mutations in acute cardiac arrest syndrome and therapeutic drugs. About. More specifically, the present invention uses gene mutations that cause acute cardiac arrest syndrome as an adjuvant therapy for diagnosis of acute cardiac arrest syndrome, and detects mutations in genes used for surgery and drug treatment through drug gene tests to detect individual differences in drug response of patients. And to the use of evaluating the risk of adverse reactions.
机译:本发明涉及一种NGS(下一代测序)方法的遗传分析面板试剂盒,其同时分析治疗药物中的急性心脏骤停综合征和基因突变,并通过同时分析急性心脏骤停综合征中的基因突变来提供用于检测突变的产品和治疗药物。关于。更具体地,本发明使用基因突变导致急性心脏滞留综合征作为辅助治疗,用于诊断急性心脏滞后综合征,并通过药物基因检测来检测用于手术和药物治疗的基因的突变,以检测药物反应的个体差异耐心。并使用评估不良反应的风险。

著录项

  • 公开/公告号KR20210038166A

    专利类型

  • 公开/公告日2021-04-07

    原文格式PDF

  • 申请/专利权人 (주)에스피메드;

    申请/专利号KR1020190120960

  • 发明设计人 신재국;신호정;정혜은;

    申请日2019-09-30

  • 分类号C12Q1/6874;C12N15/10;

  • 国家 KR

  • 入库时间 2022-08-24 18:08:07

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