首页> 外国专利> METHOD OF SELECTING AT LEAST ONE MUTATION SCREEN, ITS APPLICATION TO A METHOD FOR RAPID IDENTIFICATION OF ALLELES OF POLYMORPHOUS SYSTEMS AND DEVICE FOR IMPLEMENTATION THEREOF

METHOD OF SELECTING AT LEAST ONE MUTATION SCREEN, ITS APPLICATION TO A METHOD FOR RAPID IDENTIFICATION OF ALLELES OF POLYMORPHOUS SYSTEMS AND DEVICE FOR IMPLEMENTATION THEREOF

机译:至少一个突变屏幕的选择方法及其在多态系统等位基因快速鉴定方法中的应用及其实现方法

摘要

2123789 9311262 PCTABS00022 Methods of selecting at least one mutation screen from a series of allele sequences of a polymorphous gene and for rapid identification of alleles of polymorphous genes, nucleotide probes obtained from the said mutation screens, placed specifically in data bank form, and a device for implementing the said method are disclosed. The method for identifying alleles consists of: (a) selecting all or part of a known consensus sequence of the said polymorphous gene; (b) creating a mutation matrix for the corresponding sequences of known alleles; (c) identifying indiscernable sequences by comparison in twos (alleles having the same mutation profile in the sequence selected in (a)) and excluding one of the members of the said pairs; (d) identifying and counting the obligatory mutations or allele marker mutations, i.e. those which are necessary and adequate for distinguishing between two alleles which are otherwise identical (set O of obligatory mutations); and (f) obtaining the said minimum mutation screen(s), comprising at least the obligatory mutations of step (e); then (g) selecting from the screen selected in step (f) of the said mutation screen selection process the most suitable mutation screen for preparing oligonucleotide probes suitable for use in differenciating all the alleles; (h) appropriately hybridizing an allele X to be identified with the oligonucleotide probes selected from the mutation screen(s) obtained in steps (a) to (g); and (i) identifying the allele X by detection of the said hybrid(s) which may have been formed in step (h).
机译:2123789 9311262 PCTABS00022从一系列多态基因的等位基因序列中选择至少一个突变筛选并快速鉴定该多态基因的等位基因的方法,从所述突变筛选获得的核苷酸探针,特别是以数据库形式放置,以及一种装置公开了用于实现所述方法的方法。鉴定等位基因的方法包括:(a)选择所述多态性基因的全部或部分已知共有序列; (b)为已知等位基因的相应序列创建一个突变矩阵; (c)通过比较(在(a)中选择的序列中具有相同突变谱的等位基因)进行比较来鉴定难以区分的序列,并且排除所述对中的一个成员; (d)鉴定和计数强制性突变或等位基因标记突变,即区分两个在其他方面相同的等位基因所必需和充分的突变(强制性突变的集合O); (f)获得至少包括步骤(e)的强制性突变的所述最小突变筛选;然后(g)从所述突变筛选选择过程的步骤(f)中选择的筛选中选择最合适的突变筛选,以制备适合用于区分所有等位基因的寡核苷酸探针; (h)将待鉴定的等位基因X与选自步骤(a)至(g)中获得的突变筛选的寡核苷酸探针适当杂交; (i)通过检测可能在步骤(h)中形成的所述杂种来鉴定等位基因X。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号