METHOD OF ANALYZING GENOME BY GENOME ANALYZING DEVICE
    11.
    发明申请
    METHOD OF ANALYZING GENOME BY GENOME ANALYZING DEVICE 审中-公开
    通过基因分析装置分析基因组的方法

    公开(公告)号:US20150199476A1

    公开(公告)日:2015-07-16

    申请号:US14597052

    申请日:2015-01-14

    CPC classification number: G16B30/00 G16B20/00

    Abstract: Provided is a method for analyzing a genome by a genome analyzing device. The method of analyzing a genome of the present invention includes: reading sequencing data of the genome from a storage device; selecting a position to be analyzed among positions corresponding to the sequencing data; and determining a base type at the selected position by using base types and quality values of bases corresponding to the selected position among the sequencing data.

    Abstract translation: 提供了一种通过基因组分析装置分析基因组的方法。 分析本发明的基因组的方法包括:从存储装置读取基因组的测序数据; 在与排序数据相对应的位置中选择要分析的位置; 以及通过使用与所述排序数据中的所选择的位置相对应的碱基的碱基类型和质量值来确定所选位置处的碱基类型。

    IMAGE PROCESSING DEVICE AND CALCIFICATION ANALYSIS SYSTEM INCLUDING THE SAME

    公开(公告)号:US20210174498A1

    公开(公告)日:2021-06-10

    申请号:US16950573

    申请日:2020-11-17

    Abstract: The image processing device includes a voxel extractor, a learner, and a predictor. The voxel extractor extracts a target voxel and neighboring voxels adjacent to the target voxel from a 3D image. The learner generates vectors corresponding to the target voxel and the neighboring voxels, respectively, generates vector weights corresponding to each of the vectors, based on the vectors and a parameter group, and adjusts the parameter group, based on an analysis result of the target voxel generated by applying the vector weights to the vectors. The predictor generates vectors corresponding to the target voxel and the neighboring voxels, respectively, generates correlation weights among the vectors by applying a parameter group to the vectors, generates vector weights corresponding to each of the vectors by applying the correlation weights to the vectors, and generates an analysis result of the target voxel by applying the vector weights to the vectors.

    DEVICE AND METHOD OF PROCESSING MULTI-DIMENSIONAL TIME SERIES MEDICAL DATA

    公开(公告)号:US20190180882A1

    公开(公告)日:2019-06-13

    申请号:US16031162

    申请日:2018-07-10

    Abstract: Provided are a device and method for processing multi-dimensional time series medical data. The device for processing multi-dimensional time series medical data according to an embodiment of the present invention includes a network interface, a preprocessing unit, a data analysis unit, and a processor. The network interface may receive time series medical data including first visit data corresponding to the first time and second visit data corresponding to the second time before the first time. The preprocessing unit preprocesses the time series medical data to generate the modeling data. The preprocessing unit is configured to preprocess the first visit data based on a difference between the first time and the second time. The data analysis unit may generate a time series analysis model for predicting future visit data from the modeling data.

    APPARATUS AND METHOD FOR PROVIDING CUSTOMIZED PERSONAL HEALTH SERVICE
    17.
    发明申请
    APPARATUS AND METHOD FOR PROVIDING CUSTOMIZED PERSONAL HEALTH SERVICE 审中-公开
    提供定制个人健康服务的设备和方法

    公开(公告)号:US20160147960A1

    公开(公告)日:2016-05-26

    申请号:US14949727

    申请日:2015-11-23

    CPC classification number: G16H50/20 G16H10/60 G16H50/70

    Abstract: Disclosed herein are an apparatus and method for providing a customized personal health service based on personal health information. The apparatus includes a health information input unit for receiving individual health information, a similar case search unit for calculating weights of the health information for respective features and calculating similarities based on the weights, thus searching for similar cases, a health pattern analysis and future health prediction unit for analyzing patterns of found similar cases and predicting a health pattern of the corresponding individual, a healthcare planning unit for designing individual customized healthcare plans based on the predicted health pattern for the corresponding individual, and a healthcare knowledge base including a knowledge map required for calculation of the weights of the health information for respective features and a knowledge map required for the analysis and prediction of patterns.

    Abstract translation: 本文公开了一种用于基于个人健康信息提供定制的个人健康服务的装置和方法。 该装置包括用于接收个人健康信息的健康信息输入单元,用于计算各特征的健康信息的权重并基于权重计算相似度的类似病例搜索单元,从而搜索类似情况,健康模式分析和未来健康 用于分析发现的类似病例的模式和预测相应个体的健康模式的预测单元,用于基于相应个体的预测健康模式设计个体定制医疗保健计划的医疗保健计划单元以及包括所需知识图的保健知识库 用于计算各个特征的健康信息的权重以及分析和预测模式所需的知识图。

    APPARATUS AND METHOD FOR COUNTING ALLELES
    18.
    发明申请
    APPARATUS AND METHOD FOR COUNTING ALLELES 审中-公开
    装置和计算方法

    公开(公告)号:US20160147937A1

    公开(公告)日:2016-05-26

    申请号:US14937342

    申请日:2015-11-10

    CPC classification number: G16B30/00

    Abstract: An apparatus and method for counting alleles are disclosed herein. The apparatus for counting alleles includes a file input unit and a counting unit. The file input unit receives one or more files including human genome data. The counting unit reads the files on a predetermined window size basis by means of parallel reading using multi-threading based on the position information of the files, performs allele counting, and merges the results of the counting.

    Abstract translation: 本文公开了一种计数等位基因的装置和方法。 用于计数等位基因的装置包括文件输入单元和计数单元。 文件输入单元接收包括人类基因组数据的一个或多个文件。 计数单元借助于基于文件的位置信息的多线程的并行读取以预定的窗口尺寸读取文件,执行等位基因计数,并且合并计数结果。

    METHOD AND APPARATUS FOR DETECTING TRANSLOCATION
    19.
    发明申请
    METHOD AND APPARATUS FOR DETECTING TRANSLOCATION 审中-公开
    用于检测交换的方法和装置

    公开(公告)号:US20160145680A1

    公开(公告)日:2016-05-26

    申请号:US14949813

    申请日:2015-11-23

    CPC classification number: C12Q1/6827 C12Q1/6816 G16B20/00 G16B30/00

    Abstract: Disclosed are a method and an apparatus for detecting a translocation. The apparatus acquires BAM for a first pair of chromosomes and a second pair of chromosomes. Also, the apparatus detects a translocation generated in at least one chromosome by selecting at least one translocation case corresponding to the translocation information produced on the basis of BAM from among multiple translocation cases in which a translocation may be generated in at least one of the first and the second chromosomes.

    Abstract translation: 公开了用于检测易位的方法和装置。 该装置获取第一对染色体和第二对染色体的BAM。 此外,该装置通过从多个易位位置案例中选择至少一个与基于BAM产生的易位信息相对应的易位信息来检测在至少一个染色体中产生的易位,其中可能在第一个 和第二条染色体。

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