SE33 MUTATIONS IMPACTING GENOTYPE CONCORDANCE
    6.
    发明申请
    SE33 MUTATIONS IMPACTING GENOTYPE CONCORDANCE 审中-公开
    SE33突变影响基因型的意义

    公开(公告)号:US20160010146A1

    公开(公告)日:2016-01-14

    申请号:US14809418

    申请日:2015-07-27

    Abstract: Disclosed are primer set compositions, methods and kits for human identification using the highly complex sequence locus, SE33 (ACTBP2) in single and multiplex PCR reactions. Additionally, disclosed are three newly discovered single nucleotide polymorphisms (SNPs) within the SE33 locus that can cause discordance seen as mobility shift or allelic dropout. Also disclosed are kits useful in human identification.

    Abstract translation: 公开了使用高度复杂的序列位点SE33(ACTBP2)在单次和多重PCR反应中进行人类鉴定的引物组合物,方法和试剂盒。 另外,所公开的是在SE33基因座内的三种新发现的单核苷酸多态性(SNP),其可以导致视为移动性偏移或等位基因缺失的不一致。 还公开了可用于人类鉴定的试剂盒。

    HUMAN IDENTIFICATION USING A PANEL OF SNPs
    8.
    发明申请
    HUMAN IDENTIFICATION USING A PANEL OF SNPs 审中-公开
    使用单核苷酸多态性面板进行人体鉴定

    公开(公告)号:US20150167068A1

    公开(公告)日:2015-06-18

    申请号:US14414532

    申请日:2013-07-15

    Inventor: Robert Lagace

    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的一种或多种核酸的方法,组合物,试剂盒,系统和装置,所述核酸属于可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。

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