MOLECULAR ASSAY FOR DIAGNOSIS OF HIV TROPISM
    5.
    发明申请
    MOLECULAR ASSAY FOR DIAGNOSIS OF HIV TROPISM 审中-公开
    用于诊断HIV TROPISM的分子测定

    公开(公告)号:US20110262924A1

    公开(公告)日:2011-10-27

    申请号:US13140271

    申请日:2009-12-18

    IPC分类号: C12Q1/68

    CPC分类号: C12Q1/6818

    摘要: The invention is directed to compositions, methods and kits for HIV subtypes in a test sample, wherein target sequence are amplified. The amplified target sequences are then analyzed by any number of mass spectrometric techniques, which data are queried against a database of base composition signatures of HIV subtypes.

    摘要翻译: 本发明涉及测试样品中HIV亚型的组合物,方法和试剂盒,其中靶序列被扩增。 然后通过任何数量的质谱技术分析扩增的靶序列,该数据被查询到HIV亚型的基本组成特征的数据库。

    Capture primers and capture sequence linked solid supports for molecular diagnostic tests
    7.
    发明授权
    Capture primers and capture sequence linked solid supports for molecular diagnostic tests 有权
    捕获引物和捕获序列连接的固体支持物进行分子诊断测试

    公开(公告)号:US09416409B2

    公开(公告)日:2016-08-16

    申请号:US12847788

    申请日:2010-07-30

    申请人: Mark A. Hayden

    发明人: Mark A. Hayden

    IPC分类号: C12Q1/68 C12P19/34 G06F19/22

    摘要: The present invention provides systems, methods, and compositions for performing molecular tests. In particular, the present invention provides methods, compositions and systems for generating target sequence-linked solid supports (e.g., beads) using a solid support linked to a plurality of capture sequences and capture primers composed of a 3′ target-specific portion and a 5′ capture sequence portion. In certain embodiments, the target sequence linked solid support is used in sequencing methods (e.g., pyrosequencing, zero-mode waveguide type sequencing, nanopore sequencing, etc.) to determine the sequence of the target sequence (e.g., in order to detect the identity of a target nucleic acid in sample).

    摘要翻译: 本发明提供用于进行分子测试的系统,方法和组合物。 特别地,本发明提供了使用连接到多个捕获序列的固体支持物并捕获由3'靶标特异性部分组成的引物和用于产生靶序列连接的固体支持物(例如珠粒)的方法,组合物和系统, 5'捕获序列部分。 在某些实施方案中,靶序列连接的固体支持物用于测序方法(例如,焦磷酸测序,零模式波导型测序,纳米孔测序等)以确定靶序列的序列(例如,为了检测身份 的样品中的靶核酸)。

    CAPTURE PRIMERS AND CAPTURE SEQUENCE LINKED SOLID SUPPORTS FOR MOLECULAR DIAGNOSTIC TESTS
    8.
    发明申请
    CAPTURE PRIMERS AND CAPTURE SEQUENCE LINKED SOLID SUPPORTS FOR MOLECULAR DIAGNOSTIC TESTS 有权
    捕获引物和捕获序列链接固体支持分子诊断测试

    公开(公告)号:US20110028334A1

    公开(公告)日:2011-02-03

    申请号:US12847788

    申请日:2010-07-30

    申请人: Mark A. Hayden

    发明人: Mark A. Hayden

    摘要: The present invention provides systems, methods, and compositions for performing molecular tests. In particular, the present invention provides methods, compositions and systems for generating target sequence-linked solid supports (e.g., beads) using a solid support linked to a plurality of capture sequences and capture primers composed of a 3′ target-specific portion and a 5′ capture sequence portion. In certain embodiments, the target sequence linked solid support is used in sequencing methods (e.g., pyrosequencing, zero-mode waveguide type sequencing, nanopore sequencing, etc.) to determine the sequence of the target sequence (e.g., in order to detect the identity of a target nucleic acid in sample).

    摘要翻译: 本发明提供用于进行分子测试的系统,方法和组合物。 特别地,本发明提供了使用连接到多个捕获序列的固体支持物并捕获由3'靶标特异性部分组成的引物和用于产生靶序列连接的固体支持物(例如珠粒)的方法,组合物和系统, 5'捕获序列部分。 在某些实施方案中,靶序列连接的固体支持物用于测序方法(例如,焦磷酸测序,零模式波导型测序,纳米孔测序等)以确定靶序列的序列(例如,为了检测身份 的样品中的靶核酸)。

    DIAGNOSTIC TEST FOR MUTATIONS IN CODONS 12-13 OF HUMAN K-RAS
    9.
    发明申请
    DIAGNOSTIC TEST FOR MUTATIONS IN CODONS 12-13 OF HUMAN K-RAS 审中-公开
    人类K-RAS 12-13号码头突变诊断测试

    公开(公告)号:US20110207143A1

    公开(公告)日:2011-08-25

    申请号:US13126362

    申请日:2009-12-18

    IPC分类号: C12Q1/68

    摘要: The invention is directed to compositions, methods and kits for diagnosing cancers and tumors correlated with mutations in codons 12 and 13 of human K-RAS using primers that amplify target sequences. The amplified target sequences are then analyzed by any number of mass spectrometric techniques, which data are queried against a database of base composition signatures of K-RAS mutations in codons 12 and 13.

    摘要翻译: 本发明涉及使用扩增靶序列的引物来诊断与人K-RAS的密码子12和13的突变相关的癌症和肿瘤的组合物,方法和试剂盒。 然后通过任何数量的质谱技术分析扩增的靶序列,该数据查询密码子12和13中的K-RAS突变的基本组成特征的数据库。

    Assay for prediction of response to Met antagonists
    10.
    发明申请
    Assay for prediction of response to Met antagonists 审中-公开
    测定对Met拮抗剂的反应

    公开(公告)号:US20080160533A1

    公开(公告)日:2008-07-03

    申请号:US11998321

    申请日:2007-11-29

    IPC分类号: C12Q1/68

    摘要: A method for classifying cancer patients as likely to have lower response to MET receptor antagonist therapy comprises assessment of the presence or absence of a single nucleotide polymorphism in the MET promoter in a patient tissue sample. The invention provides more effective identification of patients to receive MET receptor antagonist therapy.

    摘要翻译: 用于对癌症患者进行分类可能对MET受体拮抗剂治疗反应较低的方法包括评估患者组织样品中MET启动子中单核苷酸多态性的存在或不存在。 本发明提供更有效的鉴定患者接受MET受体拮抗剂治疗。