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    • 1. 发明授权
    • Multimedia communication method using virtual world interface in mobile personal computers
    • 在移动个人电脑中使用虚拟世界界面的多媒体通信方法
    • US07464337B2
    • 2008-12-09
    • US10344080
    • 2001-02-26
    • Kyungsook HanSangrae Lee
    • Kyungsook HanSangrae Lee
    • G06F3/00G06F3/048
    • H04L51/04
    • A method for communication of multimedia data using virtual world interface in a mobile personal computers is disclosed. The method comprises logging in to the server; displaying an initial menu picture on a screen of the mobile personal computer, the initial menu picture including a plurality of menu items for transmission or retrieval of the multimedia data; and performing a subroutine associated with a selected one of the menu items in the initial menu picture to transmit or retrieve the multimedia data. According to this invention, information can rapidly and accurately be exchanged at any time or place. Further, desired media data can conveniently be transmitted or retrieved by merely a clicking operation of a stylus pen or a drag operation of a mouse without executing a multiplicity of individual programs for transmission and/or retrieval of different media data.
    • 公开了一种在移动个人计算机中使用虚拟世界界面来传送多媒体数据的方法。 该方法包括登录到服务器; 在移动个人计算机的屏幕上显示初始菜单图像,初始菜单图片包括用于传输或检索多媒体数据的多个菜单项; 以及执行与所述初始菜单图像中的所述菜单项中的所选择的一个相关联的子程序,以发送或检索所述多媒体数据。 根据本发明,可以在任何时间或地点快速,准确地交换信息。 此外,期望的媒体数据可以通过仅触摸笔的点击操作或鼠标的拖动操作而被方便地发送或检索,而不执行用于传输和/或检索不同媒体数据的多个单独的节目。
    • 3. 发明授权
    • Visualization method of RNA pseudoknot structures
    • RNA pseudoknot结构的可视化方法
    • US07974786B2
    • 2011-07-05
    • US10852872
    • 2004-05-24
    • Kyungsook HanYan A. Byun
    • Kyungsook HanYan A. Byun
    • G06F19/00G06F17/60G01N33/48
    • G06F19/26
    • The present invention relates to a visualization method of RNA pseudoknot structures for more efficiently and clearly visualizing all types of RNA pseudoknot structures including H-types in the form of a planar graph without edge-crossing so that the structures can be easily examined. The visualization method comprises reading the structure data in bracket view, identifying stem-loops and pseudoknots enclosed in bracket pairs from the input structure data, first computing the position and shape of a stem-loop contained in an identified pseudoknot to visualize the stem-loop, second computing the position and shape of the pseudoknot containing the calculated stem-loop to visualize the pseudoknot, third computing the position and shape of a stem-loop outside the computed pseudoknot, and inserting or connecting the visualized stem-loops into or to the pseudoknots to complete an RNA pseudoknot structure drawing.
    • 本发明涉及一种RNA伪鸟结构的可视化方法,用于更有效和清晰地可视化所有类型的RNA伪鸟结构,包括无边缘交叉的平面图形式的H型,使得可以容易地检查结构。 可视化方法包括从括号视图中读取结构数据,从输入结构数据中识别包围在支架对中的茎环和假鸟,首先计算包含在识别的假动物中的茎环的位置和形状,以可视化茎环 第二次计算包含计算出的茎 - 环的伪距的位置和形状,以便可视化伪距,第三次计算在计算的伪距之外的茎环的位置和形状,以及将可视化茎环插入或连接到 pseudoknots完成RNA假结构图。
    • 4. 发明授权
    • Method for visualizing large-scale protein interaction data
    • 用于可视化大规模蛋白质相互作用数据的方法
    • US07280921B2
    • 2007-10-09
    • US10290432
    • 2002-11-07
    • Kyungsook HanByong-Hyon Ju
    • Kyungsook HanByong-Hyon Ju
    • G06F17/11G06F17/50
    • C40B30/04G01N33/6845G06F19/18G06F19/26
    • Disclosed is a method of visualizing large-scale protein interaction data, comprising the steps of (1) producing an initial layout by placing all nodes of protein interaction data on the surface of a sphere by increasing horizontal and vertical angles of polar coordinates; and (2) yielding a graph by iterating a process moving each node of the initial layout to an equilibrium position considering global spring forces between non-adjacent nodes as well as local spring forces between adjacent nodes on a predetermined number of times, by which large-scale protein interaction data is effectively visualized in a three-dimensional space. The method for visualization of the present invention, which is much faster than the conventional algorithms, can be used for interactive analysis, as well as provide an integrated system capable of directly visualizing query results from a protein-protein interaction database.
    • 公开了一种可视化大规模蛋白质相互作用数据的方法,包括以下步骤:(1)通过增加极坐标的水平和垂直角度将蛋白质相互作用数据的所有节点放置在球体的表面上来产生初始布局; 和(2)通过迭代将初始布局的每个节点移动到平衡位置的过程来产生图形,考虑非相邻节点之间的全局弹簧力以及预定次数的相邻节点之间的局部弹簧力,由此, 尺度蛋白质相互作用数据在三维空间中有效地可视化。 本发明的可视化方法比常规算法快得多,可用于交互式分析,并且提供能够直接从蛋白质 - 蛋白质相互作用数据库可视化查询结果的集成系统。
    • 5. 发明申请
    • System for predicting programmed ribosomal frameshift sites in genome sequences
    • 用于预测基因组序列中编程的核糖体移码位点的系统
    • US20080103745A1
    • 2008-05-01
    • US11680178
    • 2007-02-28
    • Kyungsook HanSanghoon MoonYanga Byun
    • Kyungsook HanSanghoon MoonYanga Byun
    • G06G7/48
    • G16B30/00G16B20/00
    • Disclosed is a system for predicting programmed ribosomal frameshift sites in genome sequences, in which programmed frameshifts, which are difficult to detect because of their variation with gene types, are classified into −1 frameshifts and +1 frameshifts as basic frameshift models, each consisting of four types of modules, and the modules are combined in various ways, whereby the system can predict frameshifts of various user-defined modules and computationally detect frameshifts at high efficiency. Also, the present invention provides related web service which is accessible regardless of the operating system of the user's computer. Request messages for frameshifts and response messages to the search results of frameshifts are sent and received in XML format, so that they can be flexibly applied to programs using various languages.
    • 公开了一种用于预测基因组序列中编程的核糖体移码位点的系统,其中由于它们与基因类型的变化而难以检测的编程的帧序列被分类为基本移码模型的-1个帧和1个帧,每个载体由 四种类型的模块和模块以各种方式组合,由此系统可以预测各种用户定义的模块的帧移动,并以高效率计算检测帧跳。 此外,本发明提供了无论用户计算机的操作系统如何都可访问的相关web服务。 以帧格式发送和接收对帧移动的搜索结果的请求消息,以便将它们发送到帧移动和响应消息,以便它们可以灵活地应用于使用各种语言的程序。
    • 6. 发明授权
    • Vector-based method for visualizing secondary structure of RNA molecules
    • 用于可视化RNA分子二级结构的基于矢量的方法
    • US06651010B1
    • 2003-11-18
    • US09210305
    • 1998-12-11
    • Kyungsook HanDohyung KimHong-Jin Kim
    • Kyungsook HanDohyung KimHong-Jin Kim
    • G06F1900
    • G06F19/26G06F19/16
    • There is disclosed a method for visualizing secondary structures of RNA molecules, by which nearly overlap-free polygonal displays of RNA secondary structures are produced with minimal distortion to structural elements, with minimal search for positioning them, and with minimal user intervention. While vector and vector space are used to determine the direction and space of a structural element, two heuristics are adopted for the task of searching for the space and direction of structural elements. With the aid of the two heuristics, loops are positioned in decreasing order of their sizes and a helix is positioned, depending on the position of its adjacent loop which has been positioned. In consideration of both a potentially open and wide vector space and an allowed vector space, a structural element is positioned.
    • 公开了一种用于可视化RNA分子的二级结构的方法,通过该方法,以最小的搜索定位它们并且以最小的用户干预,以最小的变形结构元素产生RNA二级结构的几乎无重叠的多边形显示。 虽然使用向量和向量空间来确定结构元素的方向和空间,但是为了搜索结构元素的空间和方向,采用了两种启发式方法。 借助于这两种启发式方式,环路按其尺寸的降序排列,根据已定位的相邻环的位置,定位螺旋线。 考虑到潜在开放和宽的向量空间和允许的向量空间,定位了结构元件。