CN114026646A - 用于评估肿瘤分数的系统和方法 - Google Patents

用于评估肿瘤分数的系统和方法 Download PDF

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CN114026646A
CN114026646A CN202080037877.1A CN202080037877A CN114026646A CN 114026646 A CN114026646 A CN 114026646A CN 202080037877 A CN202080037877 A CN 202080037877A CN 114026646 A CN114026646 A CN 114026646A
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tumor
sample
allele
coverage
locus
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伯纳德·芬德勒
杰森·D·休斯
史蒂文·罗尔斯
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Foundation Medical Co
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    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B40/00ICT specially adapted for biostatistics; ICT specially adapted for bioinformatics-related machine learning or data mining, e.g. knowledge discovery or pattern finding
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    • 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
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B20/00ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
    • G16B20/10Ploidy or copy number detection
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B20/00ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
    • G16B20/20Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/20ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
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    • 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
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/112Disease subtyping, staging or classification
    • CCHEMISTRY; METALLURGY
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    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers

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  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
CN202080037877.1A 2019-05-20 2020-05-20 用于评估肿瘤分数的系统和方法 Pending CN114026646A (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962850474P 2019-05-20 2019-05-20
US62/850,474 2019-05-20
PCT/US2020/033821 WO2020236941A1 (en) 2019-05-20 2020-05-20 Systems and methods for evaluating tumor fraction

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CN114026646A true CN114026646A (zh) 2022-02-08

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US (2) US20220243279A1 (https=)
EP (1) EP3973530A4 (https=)
JP (1) JP7702360B2 (https=)
KR (1) KR20220011140A (https=)
CN (1) CN114026646A (https=)
AU (2) AU2020279752A1 (https=)
BR (1) BR112021022879A2 (https=)
CA (1) CA3140066A1 (https=)
IL (1) IL288182A (https=)
SG (1) SG11202111947PA (https=)
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Cited By (2)

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Publication number Priority date Publication date Assignee Title
CN114530200A (zh) * 2022-03-18 2022-05-24 北京阅微基因技术股份有限公司 基于计算snp熵值的混合样本鉴定方法
CN121305088A (zh) * 2025-12-09 2026-01-09 中国人民解放军空军军医大学 迁移学习驱动的颅内肿瘤影像数据全自动分割方法

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ES3022582T3 (en) 2013-05-10 2025-05-28 Found Medicine Inc Analysis of genetic variants
JP2023552391A (ja) * 2020-12-03 2023-12-15 ファウンデーション・メディシン・インコーポレイテッド 治療を選択し、予想される治療転帰を判定するための木ベースのモデル
EP4266315A4 (en) * 2020-12-16 2024-11-20 Seedna Inc. METHOD FOR CALCULATING THE RELIABILITY VALUE OF A POLYMORPHISM LOCUS SIGNAL
CN113025716A (zh) * 2021-03-02 2021-06-25 北京大学第一医院 一种用于人肿瘤分级的基因组合及其用途
WO2022271159A1 (en) * 2021-06-22 2022-12-29 Foundation Medicine, Inc. Systems and methods for evaluating tumor fraction
EP4374376A4 (en) * 2021-07-23 2025-05-28 Foundation Medicine, Inc. METHODS FOR DETERMINING VARIANT FREQUENCY AND MONITORING DISEASE PROGRESSION
JP2024538725A (ja) * 2021-10-08 2024-10-23 ファウンデーション・メディシン・インコーポレイテッド コピー数変化呼び出しに対する汚染を検出及び除去するための方法及びシステム
EP4430614A4 (en) * 2021-11-12 2025-12-17 Found Medicine Inc Circulating tumor DNA fraction and uses thereof
WO2023096658A1 (en) * 2021-11-23 2023-06-01 Foundation Medicine, Inc. Methods and systems for reporting clinically-actionable potential germline pathogenic variant sequences
US20250037823A1 (en) 2021-12-08 2025-01-30 Foundation Medicine, Inc. Methods and systems for highlighting clinical information in diagnostic reports
CN119585730A (zh) * 2022-07-15 2025-03-07 基金会医学公司 用于确定患者样品中循环肿瘤dna分数的方法和系统
WO2024081859A2 (en) * 2022-10-14 2024-04-18 Foundation Medicine, Inc. Methods and systems for performing genomic variant calls based on identified off-target sequence reads
WO2024112967A1 (en) * 2022-11-27 2024-05-30 The University Of Chicago Methods for treating cancer with immunotherapy
EP4631049A4 (en) * 2022-12-09 2026-02-18 Found Medicine Inc METHODS AND SYSTEMS FOR DETERMINING THE CLONALITY OF SOMATIC SHORT VARIANTS
CN121219428A (zh) * 2023-05-15 2025-12-26 基金会医学公司 用于评定液体活检样品中循环肿瘤dna分数的方法和系统
WO2024238750A2 (en) * 2023-05-17 2024-11-21 Foundation Medicine, Inc. Clonal hematopoiesis burden as a biomarker for immune checkpoint inhibitor response
WO2025054202A1 (en) 2023-09-05 2025-03-13 Sana Biotechnology, Inc. Method of screening a sample comprising a transgene with a unique barcode
WO2025151838A1 (en) 2024-01-12 2025-07-17 Sana Biotechnology, Inc. Safety switches to control in vitro and in vivo proliferation of cell therapy products

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WO2014014497A1 (en) * 2012-07-20 2014-01-23 Verinata Health, Inc. Detecting and classifying copy number variation in a cancer genome
CN104662168A (zh) * 2012-06-21 2015-05-27 香港中文大学 用于癌症检测的血浆dna突变分析
WO2015164432A1 (en) * 2014-04-21 2015-10-29 Natera, Inc. Detecting mutations and ploidy in chromosomal segments
CN109196359A (zh) * 2016-02-29 2019-01-11 基础医疗股份有限公司 用于评估肿瘤突变负荷的方法和系统

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US20110301854A1 (en) * 2010-06-08 2011-12-08 Curry Bo U Method of Determining Allele-Specific Copy Number of a SNP
CA2945962C (en) * 2014-04-21 2023-08-29 Natera, Inc. Detecting mutations and ploidy in chromosomal segments
HUE058263T2 (hu) * 2015-02-10 2022-07-28 Univ Hong Kong Chinese Mutációk detektálása rákszûrési és magzatelemzési célból
BR112018005940A2 (pt) * 2015-09-25 2018-12-11 Contextual Genomics Inc métodos de garantia da qualidade molecular para uso em sequenciamento
CA3067419A1 (en) * 2017-06-20 2018-12-27 Illumina, Inc. Methods and systems for decomposition and quantification of dna mixtures from multiple contributors of known or unknown genotypes
JP7760242B2 (ja) * 2017-07-21 2025-10-27 ジェネンテック, インコーポレイテッド がんの治療法及び診断法

Patent Citations (4)

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CN104662168A (zh) * 2012-06-21 2015-05-27 香港中文大学 用于癌症检测的血浆dna突变分析
WO2014014497A1 (en) * 2012-07-20 2014-01-23 Verinata Health, Inc. Detecting and classifying copy number variation in a cancer genome
WO2015164432A1 (en) * 2014-04-21 2015-10-29 Natera, Inc. Detecting mutations and ploidy in chromosomal segments
CN109196359A (zh) * 2016-02-29 2019-01-11 基础医疗股份有限公司 用于评估肿瘤突变负荷的方法和系统

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114530200A (zh) * 2022-03-18 2022-05-24 北京阅微基因技术股份有限公司 基于计算snp熵值的混合样本鉴定方法
CN121305088A (zh) * 2025-12-09 2026-01-09 中国人民解放军空军军医大学 迁移学习驱动的颅内肿瘤影像数据全自动分割方法
CN121305088B (zh) * 2025-12-09 2026-03-17 中国人民解放军空军军医大学 迁移学习驱动的颅内肿瘤影像数据全自动分割方法

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JP7702360B2 (ja) 2025-07-03
EP3973530A1 (en) 2022-03-30
IL288182A (en) 2022-01-01
KR20220011140A (ko) 2022-01-27
US20220243279A1 (en) 2022-08-04
BR112021022879A2 (pt) 2022-03-22
AU2025271452A1 (en) 2026-01-29
WO2020236941A1 (en) 2020-11-26
AU2020279752A1 (en) 2022-01-06
JP2022533137A (ja) 2022-07-21
CA3140066A1 (en) 2020-11-26
SG11202111947PA (en) 2021-12-30
US20250259709A1 (en) 2025-08-14
EP3973530A4 (en) 2023-08-02

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