首页> 外国专利> Brief description of the selection of at least one screen of mutations, its application to a method of rapid identification of the alleles of systems polymorphic and device for its óoeuvre.

Brief description of the selection of at least one screen of mutations, its application to a method of rapid identification of the alleles of systems polymorphic and device for its óoeuvre.

机译:简要介绍至少一个突变筛选的选择,将其应用于快速识别多态系统等位基因及其方法的方法。

摘要

Methods for the selection of at least one mutation screen from a set of allelic sequences of a polymorphic gene and for the rapid identification of alleles of polymorphic genes, nucleotide probes obtained from the said mutation screens, especially consisting of a data bank and device for implementing the said methods. The method for the identification of alleles comprises: (a) the selection of all or part of a known consensus sequence of the said polymorphic gene; (b) the creation of a template for the mutations of the corresponding sequences of known alleles; (c) the identification of the indiscernible sequences by comparison in pairs (alleles having the same mutation profile in the sequence selected in (a)) and the exclusion of one of the members of the said pairs; (e) the identification and the enumeration of the obligatory mutations or the so-called allele marker mutations, that is to say those which are required or sufficient for distinguishing two alleles which are otherwise identical (set O of obligatory mutations); and (f) the production of the said minimum mutation screen(s) comprising at least the obligatory mutations of step (e); and then (g) the selection, among the screens selected in step (f) of the said method for the selection of mutation screens, of the mutation screen which is most suitable for the preparation of oligonucleotide probes suitable for use in the differentiation of all the alleles; (h) an appropriate hybridisation of an allele X to be identified with the oligonucleotide probes selected from the mutation screen(s) established in steps (a) to (g); and (i) identification of the allele X by detecting the said hybrid(s) optionally formed in step (h).
机译:从一组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,特别是由数据库和用于实施的装置组成所述方法。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的突变创建模板; (c)通过成对比较(在(a)中选择的序列中具有相同突变谱的等位基因)进行比较鉴定并排除所述成对成员之一; (e)鉴定和枚举强制性突变或所谓的等位基因标记突变,也就是说,区分两个相同的等位基因是必需的或足够的,以区分两个相同的等位基因(强制性突变的集合O); (f)产生至少包含步骤(e)的强制性突变的所述最小突变筛选;然后(g)在所述用于选择突变筛选的方法的步骤(f)中选择的筛选中,选择最适合于制备适用于所有分化的寡核苷酸探针的突变筛选等位基因(h)待鉴定的等位基因X与选自步骤(a)至(g)中建立的突变筛选的寡核苷酸探针的适当杂交; (i)通过检测任选在步骤(h)中形成的所述杂种来鉴定等位基因X。

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