首页> 外国专利> METHOD FOR SCREENING MULTIPLE SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH SUSCEPTIBILITY OF SPECIFIC DISEASE OR DRUG

METHOD FOR SCREENING MULTIPLE SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH SUSCEPTIBILITY OF SPECIFIC DISEASE OR DRUG

机译:筛查与特定疾病或药物敏感性相关的多个单核苷酸多态性的方法

摘要

The present invention in each case group and control group the following steps are included: a) select one or more mononucleotide sequences of SNP; B) selection generates one or more of all possible combination by two or more list SNP multiple SNP Genotypings modes formed: single SNP from following steps; C the frequency e genetic patterns of case group and control group) are extracted; And the genotype and institute's lectotype with statistical significance d) are determined in the group of frequency of use; It is related to the multiplex screening method of the meaningful single nucleotide polymorphism in the case where including following group. By the multiplex screening method of single nucleotide polymorphism according to the present invention, it can be securely related to the multiple single nucleotide polymorphism for screening specified disease or drug sensitivity from the whole gene group of individual. ;Multiple single nucleotide polymorphism, Genotyping mode (genetic pattern), odds ratio (odds ratio), verify Fisher(Fisher's precision tests) accuracy
机译:在每种情况下的组和对照组中,本发明包括以下步骤:a)选择一个或多个SNP的单核苷酸序列; B)选择通过两个或多个列表SNP产生所有可能组合中的一个或多个,形成多个SNP基因分型模式:来自以下步骤的单个SNP; C提取病例组和对照组的频率遗传模式;在使用频率组中确定具有统计学意义d)的基因型和研究所的选型。与包括以下基团的情况下的有意义的单核苷酸多态性的多重筛选方法有关。通过根据本发明的单核苷酸多态性的多重筛选方法,它可以与多单核苷酸多态性牢固地相关,以从个体的整个基因组中筛选特定的疾病或药物敏感性。 ;多个单核苷酸多态性,基因分型模式(遗传模式),比值比(几率),验证Fisher(Fisher精度测试)的准确性

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