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    • 6. 发明申请
    • SYSTEMS AND METHODS FOR METHYLATION PREDICTION
    • 用于甲基化预测的系统和方法
    • WO2007095493A3
    • 2007-10-04
    • PCT/US2007061982
    • 2007-02-12
    • APPLERA CORPKARGER ACHIMBOYD VICKI
    • KARGER ACHIMBOYD VICKI
    • C12Q1/68
    • C12Q1/6827Y10T436/143333C12Q2565/125C12Q2545/114C12Q2523/125
    • A method is provided for predicting an amount of methylation of at least one target region. The method includes establishing an observed size of a plurality of oligonucleotides relative to a size standard and correlating the observed size to a number of each of nucleotide base in each of the plurality of oligonucleotides. A mobility coefficient can be determined for each base of each respective oligonucleotide and the determined mobility coefficients can be applied to a predetermined number of polynucleotides subjected to methylation detection analysis. The plurality of oligonucleotides are treated with a modifying agent to obtain amplicons in methylated and unmethylated target regions and amplicons derived from methylated and unmethylated target regions are distinguished based on their relative mobilities. The degree of methylation can be predicted based on distinguished methylated regions.
    • 提供了用于预测至少一个目标区域的甲基化量的方法。 该方法包括相对于大小标准建立多个寡核苷酸的观察大小,并将观察到的大小与多个寡核苷酸中的每一个中的每个核苷酸碱基的数量相关联。 可以针对每个相应的寡核苷酸的每个碱基确定迁移系数,并且可以将确定的迁移系数应用于进行甲基化检测分析的预定数量的多核苷酸。 用修饰剂处理多个寡核苷酸以获得甲基化和非甲基化靶区域中的扩增子,并且基于其相对迁移率区分源自甲基化和未甲基化靶标区域的扩增子。 甲基化程度可根据区分的甲基化区域预测。
    • 9. 发明申请
    • METHODS REACTION MIXTURES AND KITS FOR LIGATING POLYNUCLEOTIDES
    • 方法反应混合物和用于引发多核苷酸的试剂盒
    • WO2006005055A3
    • 2006-03-16
    • PCT/US2005023737
    • 2005-06-30
    • APPLERA CORPANDERSEN MARKWENZ MICHAEL HCHEN CAIFUKARGER ACHIM
    • ANDERSEN MARKWENZ MICHAEL HCHEN CAIFUKARGER ACHIM
    • C12Q1/48C12Q1/527C12Q1/68
    • C12Q1/6855C12P19/34
    • The present teachings pertain to methods, reaction mixtures, and kits for ligating polynucleotides. In some embodiments, a heat-activatable ligation agent, a phosphorylation agent, and a decontamination agent are included in the same ligation reaction mixture with at least one probe set, at least one linker set, and at least one target polynucleotide. A reaction at a first temperature results in hybridization of the probes to the target, phosphorylation of the probes, and decontamination of unwanted reaction components. A reaction at a second temperature results in the ligation of the probes together. In some embodiments, the present teachings are applied in highly multi-plexed ligation reactions in which a plurality of single nucleotide polymorphisms in a plurality of target polynucleotides are queried, and eventually detected using a mobility dependent analysis technique.
    • 本教导涉及用于连接多核苷酸的方法,反应混合物和试剂盒。 在一些实施方案中,与至少一个探针组,至少一个接头组和至少一个靶多核苷酸在相同的连接反应混合物中包括可热激活的连接剂,磷酸化剂和去污剂。 在第一温度下的反应导致探针与靶的杂交,探针的磷酸化,以及不期望的反应成分的去污。 在第二温度下的反应导致探头连接在一起。 在一些实施方案中,本教导应用于高多重连接的连接反应中,其中查询多个目标多核苷酸中的多个单核苷酸多态性,并且最终使用迁移率依赖性分析技术检测。