JP2021513364A5 - - Google Patents

Info

Publication number
JP2021513364A5
JP2021513364A5 JP2020564824A JP2020564824A JP2021513364A5 JP 2021513364 A5 JP2021513364 A5 JP 2021513364A5 JP 2020564824 A JP2020564824 A JP 2020564824A JP 2020564824 A JP2020564824 A JP 2020564824A JP 2021513364 A5 JP2021513364 A5 JP 2021513364A5
Authority
JP
Japan
Prior art keywords
subject
computer
genotoxic
double
mutation
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.)
Granted
Application number
JP2020564824A
Other languages
English (en)
Japanese (ja)
Other versions
JP2021513364A (ja
JP7420388B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2019/017908 external-priority patent/WO2019160998A1/en
Publication of JP2021513364A publication Critical patent/JP2021513364A/ja
Publication of JP2021513364A5 publication Critical patent/JP2021513364A5/ja
Priority to JP2023222575A priority Critical patent/JP2024038208A/ja
Application granted granted Critical
Publication of JP7420388B2 publication Critical patent/JP7420388B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2020564824A 2018-02-13 2019-02-13 遺伝毒性を検出し、評価するための方法および試薬 Active JP7420388B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2023222575A JP2024038208A (ja) 2018-02-13 2023-12-28 遺伝毒性を検出し、評価するための方法および試薬

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201862630228P 2018-02-13 2018-02-13
US62/630,228 2018-02-13
US201862737097P 2018-09-26 2018-09-26
US62/737,097 2018-09-26
PCT/US2019/017908 WO2019160998A1 (en) 2018-02-13 2019-02-13 Methods and reagents for detecting and assessing genotoxicity

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2023222575A Division JP2024038208A (ja) 2018-02-13 2023-12-28 遺伝毒性を検出し、評価するための方法および試薬

Publications (3)

Publication Number Publication Date
JP2021513364A JP2021513364A (ja) 2021-05-27
JP2021513364A5 true JP2021513364A5 (https=) 2022-02-21
JP7420388B2 JP7420388B2 (ja) 2024-01-23

Family

ID=67619087

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2020564824A Active JP7420388B2 (ja) 2018-02-13 2019-02-13 遺伝毒性を検出し、評価するための方法および試薬
JP2023222575A Pending JP2024038208A (ja) 2018-02-13 2023-12-28 遺伝毒性を検出し、評価するための方法および試薬

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2023222575A Pending JP2024038208A (ja) 2018-02-13 2023-12-28 遺伝毒性を検出し、評価するための方法および試薬

Country Status (13)

Country Link
US (1) US20210355532A1 (https=)
EP (1) EP3752639A4 (https=)
JP (2) JP7420388B2 (https=)
KR (1) KR20200123159A (https=)
CN (1) CN111836905A (https=)
AU (2) AU2019221549C1 (https=)
BR (1) BR112020016516A2 (https=)
CA (1) CA3091022A1 (https=)
IL (1) IL276637A (https=)
MX (1) MX2020008472A (https=)
RU (1) RU2020130024A (https=)
SG (1) SG11202007648WA (https=)
WO (1) WO2019160998A1 (https=)

Families Citing this family (18)

* 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)
CA3006792A1 (en) 2015-12-08 2017-06-15 Twinstrand Biosciences, Inc. Improved adapters, methods, and compositions for duplex sequencing
SG11201906428SA (en) 2017-01-18 2019-08-27 Illumina Inc Methods and systems for generation and error-correction of unique molecular index sets with heterogeneous molecular lengths
AU2018261332B2 (en) 2017-05-01 2024-12-05 Illumina, Inc. Optimal index sequences for multiplex massively parallel sequencing
EP3622089B1 (en) 2017-05-08 2024-07-17 Illumina, Inc. Method for sequencing using universal short adapters for indexing of polynucleotide samples
US11447818B2 (en) 2017-09-15 2022-09-20 Illumina, Inc. Universal short adapters with variable length non-random unique molecular identifiers
AU2018366213B2 (en) 2017-11-08 2025-05-15 Twinstrand Biosciences, Inc. Reagents and adapters for nucleic acid sequencing and methods for making such reagents and adapters
BR112021000409A2 (pt) * 2018-07-12 2021-04-06 Twinstrand Biosciences, Inc. Métodos e reagentes para caracterizar edição genômica, expansão clonal e aplicações associadas
GB201911095D0 (en) * 2019-08-02 2019-09-18 Randox Laboratories Ltd Biological status classification
IL303423A (en) * 2020-12-07 2023-08-01 Hoffmann La Roche Techniques for generating predictive results related to oncology treatment lines using artificial intelligence
CN112614544B (zh) * 2020-12-28 2024-05-17 杭州瑞普基因科技有限公司 Kraken2软件输出结果的优化方法及鉴定样本中物种类型的方法
CN112553356A (zh) * 2020-12-31 2021-03-26 江苏意诺飞生物科技有限公司 一种高通量检测和判定幽门螺旋杆菌耐药性的方法
CN113554285B (zh) * 2021-07-05 2024-04-26 中国水产科学研究院黄海水产研究所 暴发水母种群波动对渔业资源风险影响的量化评估方法
NL2029132B1 (en) * 2021-09-06 2023-03-21 Prinses Maxima Centrum Voor Kinderoncologie B V Means and methods for assessing genotoxicity
CN115713968A (zh) * 2022-11-21 2023-02-24 苏州新格元生物科技有限公司 一种评估基因毒性的方法、装置、存储介质和设备
US12514461B2 (en) * 2023-08-23 2026-01-06 Wisconsin Alumni Research Foundation System and method for analyzing gene expression using diffusion weighted magnetic resonance imaging (MRI)
KR102698843B1 (ko) * 2024-01-23 2024-08-26 주식회사 이콜트리 유전독성 시험 자동화 시스템 및 방법
WO2025216210A1 (ja) * 2024-04-08 2025-10-16 株式会社ペルセウスプロテオミクス 識別用分子を用いた核酸分子の特定

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5510099A (en) * 1987-05-01 1996-04-23 Stratagene Mutagenesis testing using transgenic non-human animals carrying test DNA sequences
KR100300932B1 (ko) * 1992-07-06 2001-10-22 조이스 브린톤 리포터유전자에융합된세균의스트레스프로모터를이용하여독성을측정하는방법및진단키트
GB0905410D0 (en) * 2009-03-28 2009-05-13 Gentronix Ltd Genotoxicity testing
PT2828218T (pt) * 2012-03-20 2020-11-11 Univ Washington Through Its Center For Commercialization Métodos para baixar a taxa de erro da sequenciação paralela massiva de adn utilizando sequenciação duplex de consensus
AU2013267609C1 (en) * 2012-05-31 2019-01-03 Board Of Regents, The University Of Texas System Method for accurate sequencing of DNA
EP2706123A1 (en) * 2012-09-05 2014-03-12 Rijksinstituut Voor Volksgezondheid En Milieu In vitro method for determining genotoxic and non-genotoxic carcinogenicity of a compound.
ES2674928T3 (es) * 2012-11-05 2018-07-05 Gmdx Co Pty Ltd Métodos para determinar la causa de la mutagénesis somática
JP6262922B1 (ja) * 2017-02-16 2018-01-17 花王株式会社 物質の遺伝毒性の評価方法
BR112021000409A2 (pt) * 2018-07-12 2021-04-06 Twinstrand Biosciences, Inc. Métodos e reagentes para caracterizar edição genômica, expansão clonal e aplicações associadas

Similar Documents

Publication Publication Date Title
JP2021513364A5 (https=)
RU2020130024A (ru) Способы и реагенты для обнаружения и оценки генотоксичности
JP7637139B2 (ja) がん予測パイプラインにおけるrna発現コールを自動化するためのシステムおよび方法
KR102803386B1 (ko) 서열분석 기반 어세이의 유효성을 보장하기 위한 품질 관리 주형
JP7696975B2 (ja) 腫瘍遺伝子変異量の正規化
CN109767810B (zh) 高通量测序数据分析方法及装置
KR102638152B1 (ko) 서열 변이체 호출을 위한 검증 방법 및 시스템
JP2019531700A5 (https=)
CN110846411B (zh) 一种基于二代测序的单独肿瘤样本区分基因突变类型的方法
JP7514224B2 (ja) マイクロサテライト不安定性を評価するための方法およびシステム
US12043873B2 (en) Molecule counting of methylated cell-free DNA for treatment monitoring
CN112592976B (zh) 一种检测met基因扩增的方法及装置
JP6262203B2 (ja) Rna完全性の測定方法
JP2025529015A (ja) がん分類のためのフィーチャとしてのメチル化に基づく年齢予測
CN110475874A (zh) 脱靶序列在dna分析中的应用
KR20220082545A (ko) 전사체 분석을 이용한 인트론 유지 검출을 통해 퇴행성 뇌 질환을 진단하는 방법
JP7362901B2 (ja) 塩基のメチル化度の算出方法及びプログラム
CN119943142B (zh) 一种基于ctDNA的实体瘤MRD检测方法、检测系统和计算机可读取介质
HK40122673A (zh) 用於治疗监测的甲基化无细胞dna的分子计数
WO2026094720A1 (ja) 性質判定モデルの生成方法、性質判定モデル、性質判定方法、性質判定装置、プログラム及び記録媒体
WO2025221921A1 (en) Methods of improved somatic mutation detection
JP2025536913A (ja) Dna標本における組織同定のための成分混合モデル
BR112020013636B1 (pt) Método para analisar uma amostra materna obtida de uma gestante para facilitar determinação pré-natal da presença de um distúrbio genético, método para identificação de contaminação associada a pelo menos um entre preparação de biblioteca de sequenciamento e sequenciamento de alto rendimento, e método para caracterização associada a pelo menos um entre preparação de biblioteca de sequenciamento e sequenciamento
WO2022051618A1 (en) ASSESSMENT AND QUANTIFICATION OF IMPERFECT dsDNA BREAK REPAIR FOR CANCER DIAGNOSIS AND TREATMENT
Finkelstein et al. Microarray quality control and assessment