COMPOSITIONS AND METHODS FOR MOLECULAR LABELING
    23.
    发明申请
    COMPOSITIONS AND METHODS FOR MOLECULAR LABELING 审中-公开
    用于分子标记的组合物和方法

    公开(公告)号:US20160201125A1

    公开(公告)日:2016-07-14

    申请号:US14995744

    申请日:2016-01-14

    Abstract: The invention provides barcode libraries and methods of making and using them including obtaining a plurality of nucleic acid constructs in which each construct comprises a unique N-mer and a functional N-mer and segregating the constructs into a fluid compartments such that each compartment contains one or more copies of a unique construct. The invention further provides methods for digital PCR and for use of barcode libraries in digital PCR.

    Abstract translation: 本发明提供条形码文件库及其制备和使用方法,包括获得多个核酸构建体,其中每个构建体包含独特的N-聚体和功能性N-聚体,并将构建体分离成流体隔室,使得每个隔室含有一个 或更多的独特构造的副本。 本发明还提供数字PCR和数字PCR中条形码库的使用方法。

    DIGITAL ANALYSIS OF NUCLEIC ACID MODIFICATION
    25.
    发明申请
    DIGITAL ANALYSIS OF NUCLEIC ACID MODIFICATION 审中-公开
    核酸修饰的数字分析

    公开(公告)号:US20150099266A1

    公开(公告)日:2015-04-09

    申请号:US14505974

    申请日:2014-10-03

    CPC classification number: G16B20/00

    Abstract: In certain aspects, methods of the invention involve performing modification state specific enzymatic reaction of nucleic acid in a sample, determining a value associated with efficiency of the modification state specific enzymatic reaction based on a control, determining an amount of target nucleic acid in the sample, and normalizing the amount of target nucleic acid based on the efficiency value. Based on the normalized amount of target nucleic acid, the method further includes determining whether the normalized amount of target nucleic acid is indicative of a condition.

    Abstract translation: 在某些方面,本发明的方法涉及在样品中进行核酸的修饰状态特异性酶反应,基于对照确定与修饰状态特异性酶促反应的效率相关的值,确定样品中靶核酸的量 ,并根据效率值使目标核酸的量归一化。 基于目标核酸的归一化量,该方法还包括确定目标核酸的归一化量是否指示条件。

    METHODS FOR ANALYZING DNA
    29.
    发明申请

    公开(公告)号:US20180100185A1

    公开(公告)日:2018-04-12

    申请号:US15835697

    申请日:2017-12-08

    Inventor: Michael Samuels

    Abstract: The invention generally relates to methods for increasing the amount of DNA available for analysis when using partitioned samples and parallel processing. For example, double-stranded DNA can be dissociated into two single-stranded components, and the single strands partitioned into different droplets prior to analysis. The disclosed methods are useful for performing digital PCR analysis on samples where the target DNA is not in abundance, for example when the sample originates from a body fluid or an FFPE sample.

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