CN105555970A - 同时进行单体型分析和染色体非整倍性检测的方法和*** - Google Patents

同时进行单体型分析和染色体非整倍性检测的方法和*** Download PDF

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CN105555970A
CN105555970A CN201480050879.9A CN201480050879A CN105555970A CN 105555970 A CN105555970 A CN 105555970A CN 201480050879 A CN201480050879 A CN 201480050879A CN 105555970 A CN105555970 A CN 105555970A
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tested
sequencing
target gene
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CN105555970B (zh
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李剑
张现东
刘赛军
李尉
张彩芬
甄贺富
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Hainan Huada Gene Technology Co.,Ltd.
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BGI Shenzhen Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813Hybridisation assays
    • C12Q1/6827Hybridisation assays for detection of mutation or polymorphism

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Abstract

本发明提供了一种对样本同时进行目标基因单体型分析和染色体非整倍性检测的方法及其***,其中,所述方法包括步骤:基于样本基因组的至少一部分,构建目标区域测序文库,在构建区域测序文库的过程中,包括采用探针集进行筛选,探针集能够识别目标基因上下游的SNP和均匀分布于目标染色体的SNP;对目标区域测序文库进行测序,获得测序结果;将测序结果与参考序列比对,获得比对结果;基于比对结果,确定样本的SNP信息;基于样本的SNP信息,同时确定样本的目标基因单体型和染色体非整倍性信息。

Description

PCT国内申请,说明书已公开。

Claims (1)

  1. PCT国内申请,权利要求书已公开。
CN201480050879.9A 2013-09-30 2014-07-04 同时进行单体型分析和染色体非整倍性检测的方法和*** Active CN105555970B (zh)

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PCT/CN2013/084783 WO2015042980A1 (zh) 2013-09-30 2013-09-30 确定染色体预定区域中snp信息的方法、***和计算机可读介质
CNPCT/CN2013/084783 2013-09-30
PCT/CN2014/081672 WO2015043278A1 (zh) 2013-09-30 2014-07-04 同时进行单体型分析和染色体非整倍性检测的方法和***
CN201480050879.9A CN105555970B (zh) 2013-09-30 2014-07-04 同时进行单体型分析和染色体非整倍性检测的方法和***

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Cited By (4)

* Cited by examiner, † Cited by third party
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CN110628891A (zh) * 2018-06-25 2019-12-31 深圳华大智造科技有限公司 一种对胚胎进行基因异常筛查的方法
CN111276189A (zh) * 2020-02-26 2020-06-12 广州市金域转化医学研究院有限公司 基于ngs的染色体平衡易位检测分析***及应用
CN111373054A (zh) * 2018-05-31 2020-07-03 深圳华大临床检验中心 确定男性待测样本是否存在三倍体的方法、***和计算机可读介质
CN113436680A (zh) * 2020-05-22 2021-09-24 复旦大学附属妇产科医院 一种同时鉴别胚胎染色体结构异常和致病基因携带状态的方法

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CN105046105B (zh) * 2015-07-09 2018-02-02 天津诺禾医学检验所有限公司 染色体跨度的单体型图及其构建方法
WO2018053761A1 (zh) * 2016-09-22 2018-03-29 华为技术有限公司 一种数据处理方法、装置及计算节点
CN108220403B (zh) * 2017-12-26 2021-07-06 北京科迅生物技术有限公司 特定突变位点的检测方法、检测装置、存储介质及处理器
CA3143728A1 (en) * 2019-06-21 2020-12-24 Coopersurgical, Inc. System and method for determining genetic relationships between a sperm provider, oocyte provider, and the respective conceptus

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111373054A (zh) * 2018-05-31 2020-07-03 深圳华大临床检验中心 确定男性待测样本是否存在三倍体的方法、***和计算机可读介质
CN110628891A (zh) * 2018-06-25 2019-12-31 深圳华大智造科技有限公司 一种对胚胎进行基因异常筛查的方法
CN110628891B (zh) * 2018-06-25 2024-01-09 深圳华大智造科技股份有限公司 一种对胚胎进行基因异常筛查的方法
CN111276189A (zh) * 2020-02-26 2020-06-12 广州市金域转化医学研究院有限公司 基于ngs的染色体平衡易位检测分析***及应用
CN111276189B (zh) * 2020-02-26 2020-12-29 广州市金域转化医学研究院有限公司 基于ngs的染色体平衡易位检测分析***及应用
CN113436680A (zh) * 2020-05-22 2021-09-24 复旦大学附属妇产科医院 一种同时鉴别胚胎染色体结构异常和致病基因携带状态的方法
CN113436680B (zh) * 2020-05-22 2022-03-25 复旦大学附属妇产科医院 一种同时鉴别胚胎染色体结构异常和致病基因携带状态的方法

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WO2015042980A1 (zh) 2015-04-02
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CN106029899A (zh) 2016-10-12
CN105555970B (zh) 2020-06-05

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