VIRTUAL CELLULAR STAINING
    134.
    发明申请
    VIRTUAL CELLULAR STAINING 审中-公开
    虚拟细胞染色

    公开(公告)号:WO2012078796A1

    公开(公告)日:2012-06-14

    申请号:PCT/US2011/063805

    申请日:2011-12-07

    Abstract: Systems and methods are used to display cell structures of a biological cell. A plurality of cell structures of a biological cell is stored and for each cell structure of the plurality of cell structures one or more stain colors are stored. A selected cell structure is received from an input device. One or more stain colors of the selected cell structure are retrieved. The one or more stain colors of the selected cell structure are displayed. A selected stain color is received from the input device. The selected cell structure is displayed in the selected stain color in an exemplary cell image. Further, a three-dimensional image of a biological cell is stored. The three-dimensional image is displayed on a display that includes a touch screen. A movement selection is received from the touch screen. The three-dimensional image is displayed on the display according to the movement selection.

    Abstract translation: 系统和方法用于显示生物细胞的细胞结构。 存储生物细胞的多个细胞结构,并且对于多个细胞结构的每个细胞结构,存储一种或多种染色。 从输入设备接收所选择的单元结构。 检索所选择的细胞结构的一种或多种染色。 显示所选单元结构的一个或多个染色。 从输入装置接收选定的染色。 所选细胞结构以示例性细胞图像中所选择的染色显示。 此外,存储生物细胞的三维图像。 三维图像显示在包括触摸屏的显示器上。 从触摸屏接收移动选择。 根据移动选择,三维图像显示在显示器上。

    SYSTEMS AND METHODS FOR THE ANALYSIS OF PROXIMITY BINDING ASSAY DATA
    135.
    发明申请
    SYSTEMS AND METHODS FOR THE ANALYSIS OF PROXIMITY BINDING ASSAY DATA 审中-公开
    用于分析临时性分析数据的系统和方法

    公开(公告)号:WO2012068276A2

    公开(公告)日:2012-05-24

    申请号:PCT/US2011/061034

    申请日:2011-11-16

    CPC classification number: G06F19/18 G06F19/24

    Abstract: A proximity binding assay (PBA) is performed on at least one test sample, at least one reference sample, a background sample, and one or more calibration samples using a thermal cycler instrument. Ct values are determined for at least one set of test sample data and at least one set of reference sample data. Background corrected Ct values are calculated using a corresponding value in a background sample data set. A linear range is determined for the background corrected Ct values as a function of sample quantity. A linear regression line is calculated for each linear range. One or more parameter values of an exponential model (EM) fold change formula are estimated from the one or more sets of calibration sample data. A target protein quantity and associated confidence interval are calculated using the linear regression lines and the EM fold change formula.

    Abstract translation: 使用热循环仪在至少一个测试样品,至少一个参考样品,背景样品和一个或多个校准样品上进行接近结合测定(PBA)。 对于至少一组测试样本数据和至少一组参考样本数据确定Ct值。 使用背景样本数据集中的对应值计算背景校正的Ct值。 确定背景校正的Ct值作为样品量的函数的线性范围。 对于每个线性范围计算线性回归线。 从一组或多组校准样本数据估计指数模型(EM)倍数变化公式的一个或多个参数值。 使用线性回归线和EM倍数变化公式计算靶蛋白质量和相关置信区间。

    METHODS, WORKFLOWS, KITS, APPARATUSES, AND COMPUTER PROGRAM MEDIA FOR NUCLEIC ACID SAMPLE PREPARATION FOR NUCLEIC ACID SEQUENCING
    137.
    发明申请
    METHODS, WORKFLOWS, KITS, APPARATUSES, AND COMPUTER PROGRAM MEDIA FOR NUCLEIC ACID SAMPLE PREPARATION FOR NUCLEIC ACID SEQUENCING 审中-公开
    用于核酸序列的核酸样品制备的方法,工作流程,工具,设备和计算机程序介质

    公开(公告)号:WO2012006116A2

    公开(公告)日:2012-01-12

    申请号:PCT/US2011/042240

    申请日:2011-06-28

    CPC classification number: C12Q1/6806 C12Q1/6869 C12Q2563/131 C12Q2563/143

    Abstract: A method for preparing a nucleic acid sample for nucleic acid sequencing includes amplifying a nucleic acid target sequence using a primer bound to a first capture substrate; capturing an amplified nucleic acid product by the first capture substrate; generating at least one sequencing ladder from the amplified nucleic acid product using at least one sequencing primer; capturing the at least one sequencing ladder by hybridizing the at least one sequencing ladder to a complementary capture compound on a second capture substrate; and removing the at least one sequencing ladder from the second capture substrate. The first and/or second capture substrate may include a magnetic particle. Other methods, workflows, kits, and computer program media for nucleic acid sample preparation are also disclosed.

    Abstract translation: 用于制备用于核酸测序的核酸样品的方法包括使用与第一捕获底物结合的引物扩增核酸靶序列; 通过第一捕获基质捕获扩增的核酸产物; 使用至少一个测序引物从扩增的核酸产物产生至少一个测序梯; 通过将所述至少一个测序梯度杂交到第二捕获基底上的互补捕获化合物来捕获所述至少一个测序梯; 以及从所述第二捕获基板去除所述至少一个测序梯。 第一和/或第二捕获基板可以包括磁性颗粒。 还公开了用于核酸样品制备的其它方法,工作流程,试剂盒和计算机程序培养基。

    ARRAY COLUMN INTEGRATOR
    139.
    发明申请

    公开(公告)号:WO2012003380A3

    公开(公告)日:2012-01-05

    申请号:PCT/US2011/042683

    申请日:2011-06-30

    Inventor: LEVINE, Peter

    Abstract: The described embodiments may provide a chemical detection circuit with an improved signal-to-noise ration. The chemical detection circuit may include a current source, a chemical detection pixel, an amplifier and a capacitor. The chemical detection pixel may comprise a chemical-sensitive transistor that may have a first and second terminals and a row-select switch coupled between the current source and chemically- sensitive transistor. The amplifier may have a first input and a second input, with the first input coupled to an output of the chemically-sensitive transistor via a switch and the second input coupled to an offset voltage line. The capacitor may be coupled between an output of the amplifier and the first input of the amplifier. The capacitor and amplifier may form an integrator and may be shared by a column of chemical detection pixels.

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