JP7258871B2 - 遺伝子及びゲノムの検査並びに分析におけるバリアント解釈の、監査可能な継続的な最適化のための分子エビデンスプラットフォーム - Google Patents

遺伝子及びゲノムの検査並びに分析におけるバリアント解釈の、監査可能な継続的な最適化のための分子エビデンスプラットフォーム Download PDF

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JP7258871B2
JP7258871B2 JP2020522707A JP2020522707A JP7258871B2 JP 7258871 B2 JP7258871 B2 JP 7258871B2 JP 2020522707 A JP2020522707 A JP 2020522707A JP 2020522707 A JP2020522707 A JP 2020522707A JP 7258871 B2 JP7258871 B2 JP 7258871B2
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アレクサンドル コラヴィン,
カルロス エル. アラヤ,
ジェイソン エー. ロイター,
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JP2020522707A 2017-10-17 2018-10-17 遺伝子及びゲノムの検査並びに分析におけるバリアント解釈の、監査可能な継続的な最適化のための分子エビデンスプラットフォーム Active JP7258871B2 (ja)

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Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3701534B1 (en) 2017-10-17 2024-04-10 Invitae Corporation Molecular evidence platform for auditable, continuous optimization of variant interpretation in genetic and genomic testing and analysis
US10959277B2 (en) * 2019-04-01 2021-03-23 T-Mobile Usa, Inc. Mobile device network performance restoration and improvement
US10764062B2 (en) * 2019-06-03 2020-09-01 Alibaba Group Holding Limited Blockchain ledger compression
CN110602162B (zh) * 2019-08-06 2022-11-01 苏州龙信信息科技有限公司 终端取证方法、装置、设备和存储介质
CN110957006B (zh) * 2019-12-14 2023-08-11 杭州联川基因诊断技术有限公司 一种brca1/2基因变异的解读方法
CN112489812B (zh) * 2020-11-30 2021-07-06 北京华彬立成科技有限公司 药物开发分析方法、装置、电子设备和存储介质
US20230351337A1 (en) * 2022-04-29 2023-11-02 Bank Of America Corporation Generating and securing digital checks using distributed ledger and embedded chip methods
US12211039B2 (en) * 2022-09-20 2025-01-28 Veiovia Limited Externally validated proof of work for appending a block record to a blockchain with a data broker server
US11652650B1 (en) * 2022-09-20 2023-05-16 Veiovia Limited Externally validated proof of work for appending a block record to a blockchain with a commitment database server
US12216661B2 (en) 2022-09-20 2025-02-04 Veiovia Ltd. Externally validated proof of work for appending a block record to a blockchain with a mining node
WO2025115360A1 (ja) * 2023-11-30 2025-06-05 富士フイルム株式会社 木構造生成方法、情報処理装置、情報処理システム、及び木構造生成プログラム
CN119719955B (zh) * 2024-12-17 2025-09-05 四川大学华西医院 一种基于贝叶斯模型的证据优化方法、装置、计算机设备及存储介质

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000500647A (ja) 1995-10-24 2000-01-25 クレイジェン コーポレーション 配列決定を行なわないでサンプル中のdna配列を同定、分類または定量する方法及び装置
WO2016154584A1 (en) 2015-03-26 2016-09-29 Quest Diagnostics Investments Incorporated Alignment and variant sequencing analysis pipeline
US20160306923A1 (en) 2013-01-17 2016-10-20 Edico Genome, Inc. Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform
US20170270212A1 (en) 2016-03-21 2017-09-21 Human Longevity, Inc. Genomic, metabolomic, and microbiomic search engine

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6949692B2 (en) 1996-11-18 2005-09-27 Wisconsin Alumni Research Foundation Method for identifying mutants and molecules
US5780236A (en) 1996-11-18 1998-07-14 Wisconsin Alumni Research Foundation Method for identifying mutants and molecules
US7135286B2 (en) 2002-03-26 2006-11-14 Perlegen Sciences, Inc. Pharmaceutical and diagnostic business systems and methods
US20060223058A1 (en) * 2005-04-01 2006-10-05 Perlegen Sciences, Inc. In vitro association studies
US7702468B2 (en) 2006-05-03 2010-04-20 Population Diagnostics, Inc. Evaluating genetic disorders
EP2639319B1 (en) 2006-09-11 2015-07-08 Celera Corporation Genetic polymorphisms associated with Psoriasis, methods of detection and uses thereof
KR101325736B1 (ko) 2010-10-27 2013-11-08 삼성에스디에스 주식회사 바이오 마커 추출 장치 및 방법
EP2640857A4 (en) 2010-11-18 2014-04-30 Decode Genetics Ehf GENETIC RISK FACTORS OF SINUS NODE SYNDROME
WO2012155148A2 (en) 2011-05-12 2012-11-15 University Of Utah Research Foundation Predicting gene variant pathogenicity
US8718950B2 (en) * 2011-07-08 2014-05-06 The Medical College Of Wisconsin, Inc. Methods and apparatus for identification of disease associated mutations
US9773091B2 (en) * 2011-10-31 2017-09-26 The Scripps Research Institute Systems and methods for genomic annotation and distributed variant interpretation
US9779214B2 (en) 2012-01-06 2017-10-03 Molecular Health Gmbh Systems and methods for personalized de-risking based on patient genome data
US20140089009A1 (en) * 2012-09-27 2014-03-27 Wobblebase, Inc. Method for Personal Genome Data Management
CA2899859C (en) 2013-01-31 2022-08-16 Codexis, Inc. Methods, systems, and software for identifying biomolecules with interacting components
GB2525804B (en) * 2013-03-15 2020-08-05 Veracyte Inc Methods and compositions for classification of samples
WO2014149972A1 (en) * 2013-03-15 2014-09-25 The Scripps Research Institute Systems and methods for genomic annotation and distributed variant interpretation
US20160048633A1 (en) * 2013-03-15 2016-02-18 Cypher Genomics, Inc. Systems and methods for genomic variant annotation
EP3135103B1 (en) * 2013-06-14 2019-09-04 Keygene N.V. Directed strategies for improving phenotypic traits
US20150025861A1 (en) * 2013-07-17 2015-01-22 The Johns Hopkins University Genetic screening computing systems and methods
US10460830B2 (en) 2013-08-22 2019-10-29 Genomoncology, Llc Computer-based systems and methods for analyzing genomes based on discrete data structures corresponding to genetic variants therein
US20160314245A1 (en) 2014-06-17 2016-10-27 Genepeeks, Inc. Device, system and method for assessing risk of variant-specific gene dysfunction
JP2017527050A (ja) * 2014-06-30 2017-09-14 キアゲン レッドウッド シティ, インコーポレイテッドQiagen Redwood City, Inc. 配列に基づいた遺伝子検査の解釈および報告のための方法およびシステム
AU2015311866B2 (en) * 2014-09-03 2018-06-07 Nant Holdings Ip, Llc Synthetic genomic variant-based secure transaction devices, systems and methods
EP3286677A4 (en) 2015-04-22 2019-07-24 Genepeeks, Inc. DEVICE, SYSTEM AND METHOD FOR ASSESSING THE RISK OF VARIATION SPECIFIC GENDYS FUNCTION
US10185803B2 (en) * 2015-06-15 2019-01-22 Deep Genomics Incorporated Systems and methods for classifying, prioritizing and interpreting genetic variants and therapies using a deep neural network
EP3701534B1 (en) 2017-10-17 2024-04-10 Invitae Corporation Molecular evidence platform for auditable, continuous optimization of variant interpretation in genetic and genomic testing and analysis
US10978196B2 (en) * 2018-10-17 2021-04-13 Tempus Labs, Inc. Data-based mental disorder research and treatment systems and methods
US20200121715A1 (en) 2018-10-20 2020-04-23 MC Technology Holdings, LLC Composition comprising aqueous medium with reduced size water clusters to improve bioavailability of the aqueous medium and methods for making and using the compositions

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000500647A (ja) 1995-10-24 2000-01-25 クレイジェン コーポレーション 配列決定を行なわないでサンプル中のdna配列を同定、分類または定量する方法及び装置
US20160306923A1 (en) 2013-01-17 2016-10-20 Edico Genome, Inc. Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform
WO2016154584A1 (en) 2015-03-26 2016-09-29 Quest Diagnostics Investments Incorporated Alignment and variant sequencing analysis pipeline
US20170270212A1 (en) 2016-03-21 2017-09-21 Human Longevity, Inc. Genomic, metabolomic, and microbiomic search engine

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AU2018350975A1 (en) 2020-05-07
CN112074909B (zh) 2024-03-19
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IL274001A (en) 2020-05-31
US20240006021A1 (en) 2024-01-04
US12136472B2 (en) 2024-11-05
BR112020007449A2 (pt) 2020-10-20
AU2018350975B2 (en) 2023-11-23
CA3079389A1 (en) 2019-04-25
EP3701534A4 (en) 2021-08-04
US11798651B2 (en) 2023-10-24
US20200251179A1 (en) 2020-08-06
JP2020537795A (ja) 2020-12-24
EP3701534B1 (en) 2024-04-10
EP3701534C0 (en) 2024-04-10
US11462299B2 (en) 2022-10-04
EP3701534A1 (en) 2020-09-02
MX2020003709A (es) 2020-07-22
US20190189246A1 (en) 2019-06-20
WO2019079464A1 (en) 2019-04-25

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