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METHOD AND SYSTEM FOR SEQUENCE ALIGNMENT AND VARIANT CALLING

机译:序列对齐和变量计算的方法和系统

摘要

A method to align a next generation sequencing read to a reference sequence includes: (a) receiving a sequencing read; (b) performing a first alignment of the sequencing read to a reference sequence so as to identify a target sequence within the reference sequence whereto the sequencing read maps; (c) selecting a first and a second anchor sequence; (d) attaching the first anchor sequence to the upstream region of the sequencing read and the second anchor sequence to the downstream region of the sequencing read so as to generate an extended sequencing read; (e) attaching the first anchor sequence to the upstream region of the target sequence and the second anchor sequence to the downstream region of the target sequence, so as to generate an extended target sequence; (f) performing a second alignment of the extended sequencing read to the extended target sequence, so that the second alignment is more correctly mapped to the target sequence than the first alignment; (g) identifying a position where one or more bases between the extended sequencing read and the extended target sequence are different based on the second alignment resu and (h) calling a variant based on the identification in step (g).
机译:将下一代测序读段与参考序列比对的方法包括:(a)接收测序读段; (b)对测序读段与参考序列进行第一次比对,以鉴定该参考读段内的目标序列,所述测序读段对应于所述靶序列; (c)选择第一和第二锚序列; (d)将第一锚定序列连接至测序读段的上游区域,并且将第二锚定序列连接至测序读段的下游区域,以产生延伸的测序读段; (e)将第一锚定序列附着于靶序列的上游区域,并将第二锚定序列附着于靶序列的下游区域,以产生延伸的靶序列; (f)对延伸的测序进行第二次比对,将其与延伸的靶序列进行比对,从而使第二比对比第一比对更正确地定位于靶序列; (g)基于第二比对结果,确定延伸测序读段和延伸靶序列之间的一个或多个碱基不同的位置; (h)基于步骤(g)中的标识来调用变体。

著录项

  • 公开/公告号WO2019129239A1

    专利类型

  • 公开/公告日2019-07-04

    原文格式PDF

  • 申请/专利权人 ACT GENOMICS CO. LTD.;

    申请/专利号WO2018CN125053

  • 发明设计人 WU KO-WEN;LI KUN-LIN;

    申请日2018-12-28

  • 分类号C12Q1/68;

  • 国家 WO

  • 入库时间 2022-08-21 11:54:04

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