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SYSTEM AND METHOD FOR SEQUENCE IDENTIFICATION IN REASSEMBLY VARIANT CALLING

机译:随机变量调用中序列识别的系统和方法

摘要

In one embodiment, a method for identifying candidate sequences for genotyping a genomic sample comprises obtaining a plurality of sequence reads mapping to a genomic region of interest. The plurality of sequence reads are assembled into a directed acyclic graph (DAG) comprising a plurality of branch sites representing variation present in the set of sequence reads, each branch site comprising two or more branches. A path through the DAG comprises a set of successive branches over two or more branch sites and represents a possible candidate sequence of the genomic sample. One or more paths through the DAG are ranked by calculating scores for one or more branch sites, wherein the calculated score comprises a number of sequence reads that span multiple branch sites in a given path. At least one path is selected as a candidate sequence based at least in part on its rank.
机译:在一个实施方案中,一种用于鉴定用于对基因组样品进行基因型分型的候选序列的方法包括获得映射到目标基因组区域的多个序列读数。多个序列读段被组装成有向无环图(DAG),其包括表示分支序列中存在的变化的多个分支位点,每个分支位点包括两个或更多个分支。通过DAG的路径包括两个或多个分支位点上的一组连续分支,代表了基因组样本的可能候选序列。通过计算一个或多个分支位点的得分对通过DAG的一条或多条路径进行排序,其中计算出的得分包括跨越给定路径中多个分支位点的多个序列读数。至少部分地基于其等级将至少一条路径选择为候选序列。

著录项

  • 公开/公告号US2019267110A1

    专利类型

  • 公开/公告日2019-08-29

    原文格式PDF

  • 申请/专利权人 SEVEN BRIDGES GENOMICS INC.;

    申请/专利号US201916276070

  • 发明设计人 IVAN JOHNSON;

    申请日2019-02-14

  • 分类号G16B20/20;G16B30/20;G16B30/10;C12Q1/68;

  • 国家 US

  • 入库时间 2022-08-21 12:07:03

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