公开(公告)号：US20070219824A1

公开(公告)日：2007-09-20

申请号：US11384231

申请日：2006-03-17

申请人： Jean Rawlings ,  Jonathan Arthur ,  David Anderson

发明人： Jean Rawlings ,  Jonathan Arthur ,  David Anderson

IPC分类号： G06Q10/00 ,  G06Q40/00

CPC分类号： G06F19/328 ,  G06F19/3481 ,  G06Q10/10 ,  G06Q40/08 ,  G06Q50/22 ,  G16H50/70

摘要： In a system and method for identifying aberrations in treatment pattern for a medical condition, a group of healthcare claim data to be analyzed is identified, wherein the group of healthcare claim data to be analyzed includes claim data representing treatment of the medical condition. Actual treatment pattern data is generated that represents the claim data in the group of healthcare claim data to be analyzed. Defined treatment pattern data for the medical condition is retrieved and compared to the actual treatment pattern data to identify one or more discrepancies therebetween, and corresponding comparison data representing the results of the comparison is generated. The actual treatment pattern data may represent a patient's treatment for the medical condition, and the defined treatment pattern data may represent treatment of a group of other patients for the medical condition. Alternatively, the actual treatment pattern data may represent treatment of multiple patients for the medical condition by a healthcare provider, and the defined treatment pattern data may represent an established procedure for treatment of the medical condition. The system and method may also generate the defined treatment pattern data by identifying and compiling claim data relating to treatment of the medical condition from a database of historical claim data.

摘要翻译： 在用于识别用于医疗状况的治疗模式中的畸变的系统和方法中，识别要分析的一组医疗保健要求数据，其中所述待分析的医疗保健要求数据组包括表示医疗状况的治疗的索赔数据。 生成实际治疗模式数据，其表示要分析的医疗保健索赔数据组中的索赔数据。 检索用于医疗条件的定义的治疗模式数据，并将其与实际治疗模式数据进行比较，以识别其间的一个或多个差异，并生成表示比较结果的相应比较数据。 实际治疗模式数据可以表示患者对于医疗状况的治疗，并且所定义的治疗模式数据可以表示治疗一组其他患者的医疗状况。 或者，实际治疗模式数据可以表示由医疗保健提供者处理多个患者的医疗状况，并且所定义的治疗模式数据可以表示用于治疗医疗状况的既定程序。 系统和方法还可以通过从历史声明数据的数据库中识别和编辑与治疗医疗状况有关的声明数据来生成定义的治疗模式数据。

公开(公告)号：US20100062424A1

公开(公告)日：2010-03-11

申请号：US11992710

申请日：2006-09-28

申请人： Jim Manos ,  Jonathan Arthur ,  Colin Harbour ,  Barbara Rose

发明人： Jim Manos ,  Jonathan Arthur ,  Colin Harbour ,  Barbara Rose

IPC分类号： C12Q1/68

CPC分类号： C12Q1/689 ,  C12Q1/04 ,  C12Q2600/158 ,  G01N2333/21

摘要： Disclosed herein are methods for determining whether an opportunistic bacterium is infectious.

摘要翻译： 本文公开了用于确定机会性细菌是否是感染性的方法。

公开(公告)号：US20100043261A1

公开(公告)日：2010-02-25

申请号：US12302958

申请日：2007-05-30

申请人： Jonathan Arthur ,  Liam McGrath

发明人： Jonathan Arthur ,  Liam McGrath

IPC分类号： G09F19/00 ,  G09F15/00

CPC分类号： G09F1/06 ,  G09F1/065 ,  G09F15/0025 ,  G09F15/0062

摘要： A self-expanding display unit (1) comprising at least one display sheet (3, 5) of a substantially rigid and foldable material having a display face (7,9), a biasing means for bending the display face of the display sheet into a substantially convex shape, and bracing means (2) acting against the biasing means to limit the amount by which the display sheet (3, 5) bends. The display sheet comprises a plurality of panels, delimited from adjacent panels by crease lines. The bracing means (2) comprises a single, substantially rigid and foldable bracing sheet (2) having a plurality of bracing panels (50), each of which is delimited from an adjacent bracing panel by a fold line (52). The fold lines (52) and the crease lines are coincident with each other. Such a device is stable in operation and is efficient to use and manufacture.

摘要翻译： 一种自扩展显示单元（1），包括至少一个具有显示面（7,9）的基本刚性和可折叠材料的显示片（3,5），用于将显示片的显示面弯曲成的偏置装置 基本上是凸起的形状，以及支撑装置（2），其作用在偏压装置上，以限制显示片（3,5）弯曲的量。 显示片包括多个面板，通过折痕线从相邻面板界定。 支撑装置（2）包括具有多个支撑面板（50）的单个基本刚性且可折叠的支撑片（2），每个支撑面板（50）通过折叠线（52）与相邻的支撑面板界定。 折线（52）和折痕线彼此重合。 这种装置在运行中是稳定的并且是有效的使用和制造。

公开(公告)号：US08458939B2

公开(公告)日：2013-06-11

申请号：US12302958

申请日：2007-05-30

申请人： Jonathan Arthur ,  Liam McGrath

发明人： Jonathan Arthur ,  Liam McGrath

IPC分类号： G09F15/00

CPC分类号： G09F1/06 ,  G09F1/065 ,  G09F15/0025 ,  G09F15/0062

摘要： A self-expanding display unit (1) comprising at least one display sheet (3, 5) of a substantially rigid and foldable material having a display face (7,9), a biasing means for bending the display face of the display sheet into a substantially convex shape, and bracing means (2) acting against the biasing means to limit the amount by which the display sheet (3, 5) bends. The display sheet comprises a plurality of panels, delimited from adjacent panels by crease lines. The bracing means (2) comprises a single, substantially rigid and foldable bracing sheet (2) having a plurality of bracing panels (50), each of which is delimited from an adjacent bracing panel by a fold line (52). The fold lines (52) and the crease lines are coincident with each other. Such a device is stable in operation and is efficient to use and manufacture.

摘要翻译： 一种自扩张显示单元（1），包括至少一个具有显示面（7,9）的基本刚性和可折叠材料的显示片（3,5），用于将所述显示片的显示面弯曲成的偏置装置 基本上是凸起的形状，以及支撑装置（2），其作用在偏压装置上，以限制显示片（3,5）弯曲的量。 显示片包括多个面板，通过折痕线从相邻面板界定。 支撑装置（2）包括具有多个支撑面板（50）的单个基本刚性且可折叠的支撑片（2），每个支撑面板（50）通过折叠线（52）与相邻的支撑面板界定。 折线（52）和折痕线彼此重合。 这种装置在运行中是稳定的并且是有效的使用和制造。

公开(公告)号：US20060210972A1

公开(公告)日：2006-09-21

申请号：US10507257

申请日：2003-03-13

申请人： Jonathan Arthur ,  Marc Wilkins ,  Mathew Traini

发明人： Jonathan Arthur ,  Marc Wilkins ,  Mathew Traini

IPC分类号： C12Q1/68 ,  G06F19/00

CPC分类号： C07K14/35 ,  C07K5/1008 ,  C07K14/47 ,  G16B20/00 ,  G16B30/00

摘要： A method of identifying one or more proteins in an unannotated DNA sequence is disclosed. The method involves dividing the DNA sequence into a plurality of sequence fragments of substantially the same length (about 300 to 5000 base pairs, most typically 1000 to 1050 base pairs. A six frame translation is then performed on each of the DNA sequence fragments to obtain six translated amino acid sequence fragments for each DNA sequence fragment. Each of the translated sequence fragments is subjected to theoretical digestion to obtain a plurality of cleaved peptide sequences. Next experimental empirical data for peptide fragments from a protein digested in the same manner as the theoretical digestion is compared with the theoretical data generated in step for each of the translated sequence fragments to identify one or more translated sequence fragments which include a substantial number of peptides present in the digested protein. The sequence fragment which has the greatest number of theoretical peptide masses correlating to the empirical data indicates the likely location of the protein of interest in the DNA sequence. To avoid problem where the sequence is divided at the site of a protein, the DNA sequence is duplicated and the original and duplicate are split in such a manner that the sequence fragments from the original overlap the cuts in the original genome sequence.

摘要翻译： 公开了鉴定未记录DNA序列中的一种或多种蛋白质的方法。 该方法包括将DNA序列划分成大致相同长度的多个序列片段（约300至5000个碱基对，最典型地为1000至1050个碱基对），然后对每个DNA序列片段进行六帧翻译以获得 每个DNA序列片段的6个翻译的氨基酸序列片段，将每个翻译的序列片段进行理论消化以获得多个切割的肽序列。来自与理论相同方式消化的蛋白质的肽片段的下一个实验经验数据 将消化与每个翻译的序列片段的步骤中产生的理论数据进行比较，以鉴定包含存在于消化蛋白质中的大量肽的一个或多个翻译的序列片段，具有最大数目的理论肽质量的序列片段 与经验数据相关表明可能的位置 DNA序列中的目的蛋白质。 为了避免序列在蛋白质位点分裂的问题，DNA序列被重复，原始和重复的分裂方式使原始序列的序列与原始基因组序列中的切割重叠。