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Ultrafast general searching device and method for whole genome sequencing

机译:用于全基因组测序的超快速通用搜索装置和方法

摘要

The present invention relates to a high-speed general-purpose search device for whole genome sequencing, mutations reference file is stored database; And sorting section for sorting the variation of the respective reference files on the basis of the reference transition interval mean value unit, the sorted reference period for extracting the maximum value of the variation interval maximum value extraction unit and the extracted maximum value and the interval is set to duplicate the conditions range search module that includes a search section which searches for duplicate reference variation interval has a duration that is overlapped with that of the query input by the user using the variation; characterized in that it comprises a The present invention relates to a high-speed general-purpose search method for whole genome sequencing, (a) aligning the respective reference variation based on the average value of the reference interval variation file; (B) extracting the largest section of the alignment with reference mutated interval maximum value; And (c) using the extracted maximum value and the set interval overlapping condition retrieving a reference interval and the variation with a period overlapping the transition query input by the user; characterized in that it comprises a According to the present invention, the search time for the whole genome sequence variation is obtained as a result of this analysis, and the effect is extremely reduced as compared with the conventional search method, which causes the whole genome sequence analysis and comparison to the variation obtained and comments The comment has the effect that an effective way. ;
机译:一种全基因组测序高速通用检索装置,突变参考文件存储数据库;并且,用于基于参考过渡间隔平均值单元对各个参考文件的变化进行分类的分类部分,用于提取变化间隔最大值提取单元的最大值以及所提取的最大值和间隔的分类参考周期为:设置为重复条件范围搜索模块,该条件范围搜索模块包括搜索部分,该搜索部分搜索重复的参考变化间隔的持续时间与用户使用该变化输入的查询的持续时间重叠;本发明涉及用于全基因组测序的高速通用搜索方法,(a)基于参考区间变异文件的平均值比对各自的参考变异; (B)提取具有参考突变间隔最大值的比对的最大部分;并且(c)使用提取的最大值和设置的间隔重叠条件,检索参考间隔和变化量,该间隔与用户输入的过渡查询重叠。根据本发明,其特征在于,它包括一个全基因组序列变异的搜索时间,作为该分析的结果,并且与引起整个基因组序列的常规搜索方法相比,其效果大大降低了。分析和比较获得的变体和评论评论是一种有效的方法。 ;

著录项

  • 公开/公告号KR101482010B1

    专利类型

  • 公开/公告日2015-01-14

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20130007329

  • 发明设计人 황규백;공석원;

    申请日2013-01-23

  • 分类号G06F19/10;G06F19/28;

  • 国家 KR

  • 入库时间 2022-08-21 14:58:50

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