JP2022548504A5 - - Google Patents

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Publication number
JP2022548504A5
JP2022548504A5 JP2022512862A JP2022512862A JP2022548504A5 JP 2022548504 A5 JP2022548504 A5 JP 2022548504A5 JP 2022512862 A JP2022512862 A JP 2022512862A JP 2022512862 A JP2022512862 A JP 2022512862A JP 2022548504 A5 JP2022548504 A5 JP 2022548504A5
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JP
Japan
Prior art keywords
dna
sequencing
adapter
read
stranded
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2022512862A
Other languages
English (en)
Japanese (ja)
Other versions
JP2022548504A (ja
Filing date
Publication date
Priority claimed from EP19198542.3A external-priority patent/EP3795685A1/en
Application filed filed Critical
Publication of JP2022548504A publication Critical patent/JP2022548504A/ja
Publication of JP2022548504A5 publication Critical patent/JP2022548504A5/ja
Pending legal-status Critical Current

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JP2022512862A 2019-09-20 2020-09-21 低頻度バリアントの検出およびレポートを容易にするためのdnaライブラリー生成方法 Pending JP2022548504A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP19198542.3A EP3795685A1 (en) 2019-09-20 2019-09-20 Methods for dna library generation to facilitate the detection and reporting of low frequency variants
EP19198542.3 2019-09-20
PCT/EP2020/076246 WO2021053208A1 (en) 2019-09-20 2020-09-21 Methods for dna library generation to facilitate the detection and reporting of low frequency variants

Publications (2)

Publication Number Publication Date
JP2022548504A JP2022548504A (ja) 2022-11-21
JP2022548504A5 true JP2022548504A5 (https=) 2023-09-08

Family

ID=67998258

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022512862A Pending JP2022548504A (ja) 2019-09-20 2020-09-21 低頻度バリアントの検出およびレポートを容易にするためのdnaライブラリー生成方法

Country Status (8)

Country Link
US (1) US20220364080A1 (https=)
EP (3) EP3795685A1 (https=)
JP (1) JP2022548504A (https=)
KR (1) KR20220064959A (https=)
AU (1) AU2020349622A1 (https=)
BR (1) BR112022004821A2 (https=)
CA (1) CA3149056A1 (https=)
WO (1) WO2021053208A1 (https=)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT202200027138A1 (it) 2022-12-29 2024-06-29 Centro Di Riferimento Oncologico Metodo per la correzione di errori nel sequenziamento di acidi nucleici
CN117437978A (zh) * 2023-12-12 2024-01-23 北京旌准医疗科技有限公司 一种二代测序数据的低频基因突变分析方法、装置及其应用
US20260049302A1 (en) 2024-08-14 2026-02-19 Sophia Genetics S.A. Systems and methods for assaying various regions of a genome at different resolutions

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10844428B2 (en) * 2015-04-28 2020-11-24 Illumina, Inc. Error suppression in sequenced DNA fragments using redundant reads with unique molecular indices (UMIS)
EP3475863B1 (en) 2016-06-22 2023-12-06 Sophia Genetics S.A. Methods for processing next-generation sequencing genomic data
WO2018144159A1 (en) * 2017-01-31 2018-08-09 Counsyl, Inc. Capture probes using positive and negative strands for duplex sequencing
ES2898644T3 (es) * 2017-06-27 2022-03-08 Hoffmann La Roche Adaptadores de ácido nucleico modulares
WO2019084245A1 (en) * 2017-10-27 2019-05-02 Myriad Women's Health, Inc. METHODS AND COMPOSITIONS FOR PREPARING NUCLEIC ACID LIBRARIES
GB201804642D0 (en) * 2018-03-22 2018-05-09 Inivata Ltd Methods of labelling nucleic acids
WO2019204702A1 (en) * 2018-04-20 2019-10-24 Board Of Regents, The University Of Texas System Error-correcting dna barcodes
WO2020043803A1 (en) * 2018-08-28 2020-03-05 Sophia Genetics S.A. Methods for asymmetric dna library generation and optionally integrated duplex sequencing

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