HUMAN IDENTIFIATION USING A PANEL OF SNPS
    1.
    发明申请
    HUMAN IDENTIFIATION USING A PANEL OF SNPS 审中-公开
    使用SNPS的面板进行人体识别

    公开(公告)号:WO2014012107A2

    公开(公告)日:2014-01-16

    申请号:PCT/US2013050531

    申请日:2013-07-15

    Inventor: LAGACE ROBERT

    CPC classification number: C12Q1/6853 C12Q1/6855 C12Q2525/131

    Abstract: The present invention provides methods, compositions, kits, systems and apparatus that are useful for multiplex PCR of one or more nucleic acids which belong to a panel of single nucleotide polymorphisms (SNPs) useful to identify a human. In particular, various target-specific primers are provided that allow for the selective amplification of one or more target sequences in the panel. In some aspects, amplified target sequences obtained using the disclosed methods, kits, systems and apparatuses can be used in various downstream processes including nucleic acid sequencing and used to identify a human.

    Abstract translation: 本发明提供了可用于多属性PCR的多属性的方法,组合物,试剂盒,系统和装置,所述核酸属于用于鉴定人的单核苷酸多态性(SNP)的一组。 特别地,提供允许在面板中选择性扩增一个或多个靶序列的各种靶特异性引物。 在一些方面,使用所公开的方法,试剂盒,系统和装置获得的扩增靶序列可用于包括核酸测序在内的各种下游过程并用于鉴定人。

    AMELOGENIN SNP ON CHROMOSOME X
    3.
    发明申请
    AMELOGENIN SNP ON CHROMOSOME X 审中-公开
    AMELOGENIN SNP染色体X

    公开(公告)号:WO2011020075A3

    公开(公告)日:2011-04-14

    申请号:PCT/US2010045544

    申请日:2010-08-13

    CPC classification number: C07H21/04 C12Q1/6879 C12Q2600/156

    Abstract: Disclosed are methods for gender determination in the intron 1 region of the amelogenin locus and a newly discovered single nucleotide polymorphism (SNP) within the X chromosome of the amelogenin locus which can cause allelic dropout. Also disclosed are kits useful in gender determination.

    Abstract translation: 公开了用于在釉原蛋白基因座的内含子1区域中确定性别的方法以及可能导致等位基因辍学的釉原蛋白基因座的X染色体内新发现的单核苷酸多态性(SNP)的方法。 还公开了用于性别决定的试剂盒。

Patent Agency Ranking