Methods for Amplifying Fragmented Target Nucleic Acids Utilizing an Assembler Sequence
    41.
    发明申请
    Methods for Amplifying Fragmented Target Nucleic Acids Utilizing an Assembler Sequence 审中-公开
    使用汇编序列扩增分离的靶核酸的方法

    公开(公告)号:US20160068900A1

    公开(公告)日:2016-03-10

    申请号:US14773366

    申请日:2014-03-15

    IPC分类号: C12Q1/68

    摘要: The present invention provides methods of amplifying a fragmented target nucleic acid containing short target nucleic acid fragments utilizing an assembler sequence to convert these short fragments into longer sequences enabling their identification and interrogation. This is particularly important when attempting to identify small genetic variations, such as SNVs, present in highly fragmented nucleic acid samples. Amplification is accomplished by hybridizing the short target nucleic acid sequences to the assembler sequence, where these short sequences serve as primers for extension. Since the fragmented target nucleic acids that contain SNVs are utilized as primers on the assembler sequence they are preserved during amplification and can be detected.

    摘要翻译: 本发明提供了利用汇编序列扩增含有短靶核酸片段的片段化靶核酸的方法,以将这些短片段转化成更长的序列,使其能够进行鉴定和询问。 当试图鉴定存在于高度片段化的核酸样品中的小的遗传变异(例如SNV)时,这尤其重要。 通过将短目标核酸序列杂交到汇编序列来完成扩增,其中这些短序列用作扩增的引物。 由于含有SNV的片段化靶核酸作为汇编序列上的引物,因此在扩增过程中被保留并可以被检测。

    Composition kits and methods for performing amplification reactions
    48.
    发明授权
    Composition kits and methods for performing amplification reactions 有权
    用于进行扩增反应的组合物试剂盒和方法

    公开(公告)号:US07696337B2

    公开(公告)日:2010-04-13

    申请号:US11574307

    申请日:2005-08-26

    IPC分类号: C07H21/04 C12Q1/68

    摘要: The present invention is directed to novel methods of synthesizing multiple copies of a target nucleic acid sequence which are autocatalytic (i.e., able to cycle automatically without the need to modify reaction conditions such as temperature, pH, or ionic strength and using the product of one cycle in the next one). In particular, the present invention discloses a method of nucleic acid amplification which is robust and efficient, while reducing the appearance of side products. The method uses only one primer, the “priming oligonucleotide,” a 3′blocked promoter oligonucleotide and optionally, a means for terminating a primer extension reaction, to amplify RNA or DNA molecules in vitro, while reducing or eliminating the formation of side products. The method of the present invention minimizes or eliminates the emergence of side products, thus providing a high level of specificity. Furthermore, the appearance of side products can complicate the analysis of the amplification reaction by various molecular detection techniques. The present invention minimizes or eliminates this problem, thus providing an enhanced level of sensitivity.

    摘要翻译: 本发明涉及合成目标核酸序列的多个拷贝的新型方法,所述目标核酸序列是自动催化的(即,能够自动循环而不需要修饰诸如温度,pH或离子强度的反应条件,并且使用一种 循环在下一个)。 特别地,本发明公开了一种鲁棒有效的核酸扩增方法,同时减少了副产物的外观。 该方法仅使用一种引物,即引物寡核苷酸,3'封闭的启动子寡核苷酸和任选的终止引物延伸反应的手段,以体外扩增RNA或DNA分子,同时减少或消除副产物的形成。 本发明的方法使副产物的出现最小化或消除,从而提供高水平的特异性。 此外,副产物的出现可能通过各种分子检测技术使扩增反应的分析复杂化。 本发明使这个问题最小化或消除了这一点,从而提供了增强的灵敏度。

    Extended dynamic range assays
    50.
    发明授权
    Extended dynamic range assays 有权
    扩展动态范围测定

    公开(公告)号:US06350579B1

    公开(公告)日:2002-02-26

    申请号:US09649636

    申请日:2000-08-28

    申请人: Norman C. Nelson

    发明人: Norman C. Nelson

    IPC分类号: G01N33533

    摘要: A method and compositions for the detection and/or quantification of an analyte through the use of a plurality of labeled probes, with two or more said probes targeted to different regions of said analyte. In specific embodiments, the labels are separately distinguishable, and/or are present at different specific activities on the labels.

    摘要翻译: 一种用于通过使用多个标记探针来检测和/或定量分析物的方法和组合物,其中两个或多个所述探针靶向所述分析物的不同区域。 在具体实施方案中,标签是分开区分的,和/或以不同的特定活性存在于标签上。