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DETECTION METHOD OF CROSS-CONTAMINATION BETWEEN SAMPLES IN NEXT-GENERATION SEQUENCING

机译:下一代测序中样品之间交叉污染的检测方法

摘要

To provide a technology for next-generation sequencing, in which a nucleic acid sample may be determined or identified, and cross-contamination etc. between samples may be quantitatively confirmed.SOLUTION: There is provided a method for preparing a library containing nucleic acid molecule fragments derived from a plurality of subjects, which is subjected to a nucleobase sequencing method where a plurality of sequencing reactions are performed in parallel. The method comprises: a step where each of nucleic molecules derived from respective of subjects is mixed with spike-in DNA specific to the subjects so as to prepare a library nucleic acid sample associated with each of the subjects; and a step where each of nucleic acid molecules or spike-in DNA prepared from nucleic acid molecules contained in the library nucleic acid sample associated with each of the subjects is provided with barcode sequence consisting of a nucleobase sequence specific to each sample so as to prepare a library derived from each subject. The spike-in DNA comprises an index sequence and an index search sequence consisting of a nucleobase sequence specific to each of the subjects.SELECTED DRAWING: Figure 1
机译:为了提供一种下一代测序技术,其中可以确定或鉴定核酸样品,并可以定量确认样品之间的交叉污染等。解决方案:提供了一种制备包含核酸分子的文库的方法衍生自多个受试者的片段,该片段经受核碱基测序方法,其中并行进行多个测序反应。该方法包括以下步骤:将源自各个受试者的每个核酸分子与对该受试者特异的刺入DNA混合,以制备与每个受试者相关的文库核酸样品;以及从由与每个受试者相关的文库核酸样品中包含的核酸分子制备的每个核酸分子或刺入DNA提供由每个样品特异的核碱基序列组成的条形码序列的步骤,以制备从每个主题派生的图书馆。刺突DNA包含一个索引序列和一个索引搜索序列,该序列由每个受试者特有的核碱基序列组成。

著录项

  • 公开/公告号JP2019131539A

    专利类型

  • 公开/公告日2019-08-08

    原文格式PDF

  • 申请/专利权人 KAZUSA DNA RESEARCH INSTITUTE;

    申请/专利号JP20190006291

  • 发明设计人 OBARA OSAMU;FUJIKI RYOJI;

    申请日2019-01-17

  • 分类号C40B40/06;C12Q1/6869;G01N33/53;C40B30/04;C12N15/09;

  • 国家 JP

  • 入库时间 2022-08-21 12:23:13

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