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Genome-wide scanning of genetic polymorphisms

机译:全基因组遗传多态性扫描

摘要

A method and compositions are provided for analyzing whole genomes, or representations thereof, to determine associations between traits and genotypes. Sets of hybridization probes (referred to herein as “isostringency probes”) are provided that are complementary to sites uniformly spaced throughout unique sequence regions a genome, or target polynucleotide, and that are designed for facile isolation of subsets that form perfectly matched duplexes with the genome or target polynucleotide being analyzed. The nucleotide sequences of the isostringency probes are selected to ensure that the probes have substantially identical duplex stabilities. In accordance with tie method of the invention, representations of a genome are attached to solid phase supports and are used to capture isostringency probes forming perfectly matched duplexes. The captured probes are then released and applied to an array of complementary sequences for detection.
机译:提供了一种用于分析整个基因组或其表示以确定性状和基因型之间的关联的方法和组合物。提供了杂交探针组(在本文中称为“等严格性探针”),其与在基因组或靶多核苷酸的整个独特序列区域中均匀间隔的位点互补,并且被设计用于容易地分离形成与之完美匹配的双链体的子集。被分析的基因组或目标多核苷酸。选择等严格性探针的核苷酸序列以确保探针具有基本相同的双链体稳定性。根据本发明的结合方法,基因组的代表物附着于固相支持物,并用于捕获形成完全匹配的双链体的等严格性探针。然后释放捕获的探针并将其应用于互补序列阵列以进行检测。

著录项

  • 公开/公告号US2004110166A1

    专利类型

  • 公开/公告日2004-06-10

    原文格式PDF

  • 申请/专利权人 MACEVICZ STEPHEN C.;

    申请/专利号US20030383371

  • 发明设计人 STEPHEN C. MACEVICZ;

    申请日2003-03-06

  • 分类号C12Q1/68;C12M1/34;

  • 国家 US

  • 入库时间 2022-08-21 23:18:42

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