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    • 5. 发明申请
    • SYSTEMS AND METHODS FOR DETECTING THE PRESENCE OF A BIOLOGICAL STATUS USING CLUSTERING
    • 用于检测使用聚类的生物状态存在的系统和方法
    • WO2011060222A2
    • 2011-05-19
    • PCT/US2010056455
    • 2010-11-12
    • BECKMAN COULTER INCLU JIULIUWANG ZIHUAREYES ANTONIO AREVALOGUSTAFSON ERIK ALANRILEY JOHN STEVEN
    • LU JIULIUWANG ZIHUAREYES ANTONIO AREVALOGUSTAFSON ERIK ALANRILEY JOHN STEVEN
    • G06F19/24
    • G06F19/24C12Q1/689C12Q2600/112G06F19/12G06F19/18
    • A method for determining the presence of a biological entity. The method may include entering into a digital computer, at least a plurality of first input values associated with a first genetic element (e.g., mecA), a plurality of second input values associated with a second genetic element (femA), and a plurality of third input values associated with a third genetic element (e.g., orfX) associated with a plurality of samples. Each sample includes a first input value in the plurality of first input values, a second input value in the plurality of second input values, and a third input value in the plurality of third input values. The method also includes determining a threshold value associated with the third genetic element, separating the samples using the threshold value into a first set of samples and a second set of samples, clustering the first set of samples in a feature space defined by the first genetic element and the second genetic element, defining a first boundary space using the first set of samples, and defining a second boundary space using the second set of samples. The first and second boundary spaces differentiate a biological entity from other biological statuses. Other embodiments may also include the use of a genetic element such as SCCmec.
    • 用于确定生物实体的存在的方法。 该方法可以包括进入数字计算机,与第一遗传元素(例如,mecA)相关联的至少多个第一输入值,与第二遗传元件(femA)相关联的多个第二输入值,以及多个 与与多个样本相关联的第三遗传元素(例如,orfX)相关联的第三输入值。 每个样本包括多个第一输入值中的第一输入值,多个第二输入值中的第二输入值和多个第三输入值中的第三输入值。 该方法还包括确定与第三遗传元件相关联的阈值,使用阈值将样本分离成第一组样本和第二组样本,将第一组样本聚集在由第一遗传学定义的特征空间中 元素和第二遗传元素,使用第一组样本定义第一边界空间,以及使用第二组样本定义第二边界空间。 第一和第二边界空间将生物体与其他生物状态区分开来。 其他实施方案还可以包括遗传元件如SCCmec的使用。
    • 6. 发明申请
    • DETECTING AND HANDLING COINCIDENCE IN PARTICLE ANALYSIS
    • 检测和处理粒子分析中的相关性
    • WO2010042401A1
    • 2010-04-15
    • PCT/US2009/059363
    • 2009-10-02
    • BECKMAN COULTER, INC.BRITTON, Ted, W.LU, JiuliuROSE, Jeffrey, L.
    • BRITTON, Ted, W.LU, JiuliuROSE, Jeffrey, L.
    • G01N21/00
    • G01N15/1429G01N15/1459G01N2015/1037G01N2015/1461
    • Methods and systems substantially eliminate data representative of coincident events from particle analyzer data. A fluid sample containing particles for analysis is prepared. Using an electrical or optical measurement device, signals are sensed. Each signal corresponds to events detected in a sub-sample of the fluid sample flowing through a measurement region in the particle analyzer. The existence of coincidence in the events is determined based on measuring a peak and first and second points of each of the signals. The first and second points have a signal value corresponding to a predetermined portion of the peak. Results data based upon the coincident events and non-coincident events is generated. The results data is then analyzed. In various examples, the method is applicable to a variety of particle types, and may be implemented on different types of particle analyzers including hematology analyzer and flow cytometers.
    • 方法和系统基本上消除了代表颗粒分析仪数据的重合事件的数据。 制备含有用于分析的颗粒的流体样品。 使用电气或光学测量设备,感测到信号。 每个信号对应于在流过粒子分析仪中的测量区域的流体样品的子样本中检测到的事件。 基于测量每个信号的峰值和第一和第二点来确定事件中的一致性的存在。 第一和第二点具有对应于峰值的预定部分的信号值。 生成基于一致事件和非重合事件的结果数据。 然后分析结果数据。 在各种实施例中,该方法适用于各种粒子类型,并且可以在包括血液分析仪和流式细胞仪在内的不同类型的粒子分析仪上实施。