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    • 6. 发明申请
    • Systems and Methods for Data Aggregation and Prioritization
    • 数据汇总和优先排序的系统和方法
    • US20120105471A1
    • 2012-05-03
    • US13345939
    • 2012-01-09
    • John P. FordLiying Huang
    • John P. FordLiying Huang
    • G09G5/00
    • G06F19/3487G06F3/04817G06F3/0482G06F17/30994G06F19/00G16H15/00
    • Computer-enabled systems and methods aggregate data related to a particular subject or field and present the data in a simplified display. The data is divided into predetermined categories, which are graphically displayed in a predetermined arrangement. Systems and methods differentiate and visually display critical data abnormalities separately from non-critical data. The systems and methods enable an observer to identify the critical deviations or anomalies of data with respect to a predetermined base line by an intuitive visual display of all of the data from any sized data universe on a single screen. The data is indexed at multiple display levels such as a stack of one patient's data, a stack of all patient data for the universe of patients of a single practitioner, or a group of practitioners of any size. A portion of the display preferably may be selected and expanded to show only that portion in greater detail.
    • 计算机启用的系统和方法聚合与特定主题或字段相关的数据,并以简化的显示呈现数据。 数据被分成预定的类别,其以预定的布置图形地显示。 系统和方法与非关键数据分开区分并可视地显示关键数据异常。 系统和方法使得观察者能够通过在单个屏幕上来自任何尺寸的数据空间的所有数据的直观可视显示来识别数据相对于预定基线的关键偏差或异常。 数据以多个显示级别进行索引,例如一个患者数据的堆叠,单个从业者的患者的全部患者数据的堆叠或任何大小的一组从业者。 优选地,可以选择和扩展显示器的一部分,以更详细地仅显示该部分。
    • 10. 发明授权
    • Process and apparatus for purifying and concentrating DNA from crude
mixtures containing DNA
    • 用于从含有DNA的粗混合物中纯化和浓缩DNA的方法和装置
    • US4750982A
    • 1988-06-14
    • US878822
    • 1986-06-26
    • Graham J. TomblinKaren B. WexlerJohn P. FordStuart G. Fischer
    • Graham J. TomblinKaren B. WexlerJohn P. FordStuart G. Fischer
    • B01D57/02G01N27/447G01N27/26
    • G01N27/447B01D57/02
    • A process and apparatus for purifying and concentrating DNA, which has relatively high molecular weight, from test samples containing DNA, for example from human whole blood samples; the collected DNA is of usable volume and concentration, and is of such purity as to permit conventional restriction by a number of enzymes without the need for further purification. The apparatus consists essentially of an agarose gel disc, typically 5 mm. thick by 31 mm. in diameter, immersed in an electrophoresis buffer solution and supported between two 8 micrometer polycarbonate filters in an electric field. Further, the method involves the loading of a suitably treated sample such as blood lysate onto the top face of the agarose gel disc and then applying an electric field. Of the constituent parts of the treated blood, the DNA molecules are the largest with regard to molecular weight. Consequently, their passage through the agarose gel disc, under the force of the electric field, is impeded. All other constituent parts of the treated blood pass relatively rapidly through the disc and are removed, being swept away by flow of the buffer solution. The DNA is then eluted and collected, in concentrated form by application of the electric field, while the normal flow of buffer solution between the bottom of the gel matrix and a collection chamber is prevented.
    • 用于从含有DNA的测试样品中纯化和浓缩具有相对较高分子量的DNA的方法和装置,例如来自人全血样品; 所收集的DNA具有可用的体积和浓度,并且具有如下纯度:允许常规的许多酶的限制,而不需要进一步纯化。 该装置基本上由通常为5mm的琼脂糖凝胶盘组成。 厚31毫米。 浸入电泳缓冲溶液中,并在电场下支撑在两个8微米的聚碳酸酯过滤器之间。 此外,该方法包括将适当处理的样品如血液裂解物加载到琼脂糖凝胶盘的顶面上,然后施加电场。 在处理血液的组成部分中,DNA分子在分子量方面是最大的。 因此,它们在电场的作用下通过琼脂糖凝胶盘被阻止。 经处理的血液的所有其他组成部分相对快速地通过椎间盘,并被除去,被缓冲溶液的流动扫除。 然后通过施加电场以浓缩形式洗脱和收集DNA,同时防止凝胶基质的底部和收集室之间的缓冲溶液的正常流动。