JP2010004884A5 - - Google Patents

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Publication number
JP2010004884A5
JP2010004884A5 JP2009151195A JP2009151195A JP2010004884A5 JP 2010004884 A5 JP2010004884 A5 JP 2010004884A5 JP 2009151195 A JP2009151195 A JP 2009151195A JP 2009151195 A JP2009151195 A JP 2009151195A JP 2010004884 A5 JP2010004884 A5 JP 2010004884A5
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JP
Japan
Prior art keywords
reagent
dna
nucleic acid
abasic
polyamine
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JP2009151195A
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English (en)
Japanese (ja)
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JP2010004884A (ja
JP5596308B2 (ja
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Publication of JP2010004884A5 publication Critical patent/JP2010004884A5/ja
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JP2009151195A 2008-06-26 2009-06-25 核酸増幅技術におけるキャリーオーバー汚染の防止のための改良方法 Active JP5596308B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US7611108P 2008-06-26 2008-06-26
US61/076,111 2008-06-26

Publications (3)

Publication Number Publication Date
JP2010004884A JP2010004884A (ja) 2010-01-14
JP2010004884A5 true JP2010004884A5 (enExample) 2012-03-08
JP5596308B2 JP5596308B2 (ja) 2014-09-24

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JP2009151195A Active JP5596308B2 (ja) 2008-06-26 2009-06-25 核酸増幅技術におけるキャリーオーバー汚染の防止のための改良方法

Country Status (6)

Country Link
US (1) US8669061B2 (enExample)
EP (1) EP2138590B1 (enExample)
JP (1) JP5596308B2 (enExample)
CN (1) CN101613730B (enExample)
CA (1) CA2670300C (enExample)
ES (1) ES2386023T3 (enExample)

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Publication number Priority date Publication date Assignee Title
US8669061B2 (en) 2008-06-26 2014-03-11 Roche Molecular Systems, Inc. Method for the prevention of carryover contamination in nucleic acid amplification technologies
US20150024398A1 (en) * 2011-08-05 2015-01-22 Ibis Biosciences, Inc. Analysis of genetic biomarkers for forensic analysis and fingerprinting
ES2449665B2 (es) * 2012-09-19 2014-07-17 Servizo Galego De Saúde-Conselleria De Sanidade, Xunta De Galicia Procedimiento para el diagnóstico clínico de una enfermedad infecciosa basada en el empleo de la PCR cuantitativa, oligonucleótidos marcados de 8 a 9 nucleótidos de longitud y la UNG del Bacalao del Atlántico (Gadus morhua).
EP3071711A1 (en) * 2013-11-18 2016-09-28 Rubicon Genomics Degradable adaptors for background reduction
US10036061B2 (en) * 2013-12-20 2018-07-31 Roche Molecular Systems, Inc. Oligonucleotide inhibitor of DNA polymerases
AU2015270774B2 (en) * 2014-06-05 2021-10-14 Qiagen Gmbh Optimization of DNA amplification reactions
EP3690060B1 (en) * 2014-10-08 2021-12-08 Cornell University Method for identification and relative quantification of nucleic acid sequence expression, splice variant, translocation, copy number, or methylation changes using combined nuclease, ligation, and polymerase reactions with carryover prevention
CN104389026A (zh) * 2014-10-30 2015-03-04 北京诺禾致源生物信息科技有限公司 单细胞转录组测序文库的构建方法及其应用
JP6623324B2 (ja) * 2015-09-07 2019-12-25 株式会社ファスマック 等温増幅反応産物の多項目同時検出方法
EP3485038B1 (en) 2016-07-12 2020-12-23 H. Hoffnabb-La Roche Ag Primer extension target enrichment
ES2875318T3 (es) 2016-07-18 2021-11-10 Hoffmann La Roche Procedimiento para generar colecciones de ADN circular monocatenario para secuenciación de molécula única
JP2021506314A (ja) 2017-12-21 2021-02-22 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 単一方向デュアルプローブプライマー伸長による標的濃縮
EP3966335A4 (en) * 2019-05-07 2023-06-28 Suzhou Qi Biodesign biotechnology Company Limited Improved gene editing system
EP4031679A1 (en) 2019-09-20 2022-07-27 F. Hoffmann-La Roche AG Immune repertoire profiling by primer extension target enrichment
CN115698337A (zh) 2020-06-08 2023-02-03 豪夫迈·罗氏有限公司 用于检测基因组中的结构重排的方法和组合物
CN113186037B (zh) * 2021-04-23 2022-12-13 山东博弘基因科技有限公司 一种核酸清除剂
US20250002900A1 (en) * 2021-10-15 2025-01-02 Qiagen Sciences, Llc Methods for Producing DNA Libraries and Uses Thereof
CN114214395A (zh) * 2021-12-31 2022-03-22 上海星耀医学科技发展有限公司 一种提高基因检测准确性的核酸扩增方法与试剂盒
EP4555101A1 (en) 2022-07-14 2025-05-21 F. Hoffmann-La Roche AG Variant allele enrichment by unidirectional dual probe primer extension
CN116773291B (zh) * 2023-03-31 2024-04-19 艾普拜生物科技(苏州)有限公司 一种石蜡切片dna预处理试剂及方法
WO2024222446A1 (zh) * 2023-04-23 2024-10-31 南京诺唯赞生物科技股份有限公司 一种去除非目标核酸模板的方法

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ATE176002T1 (de) * 1990-07-24 1999-02-15 Hoffmann La Roche Verringerung von nicht spezifischer amplifikation während einer (in vitro) nukleinsäure amplifikation unter verwendung von modifizierten nukleinsäure basen
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