JP2019530098A5 - - Google Patents

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Publication number
JP2019530098A5
JP2019530098A5 JP2019516412A JP2019516412A JP2019530098A5 JP 2019530098 A5 JP2019530098 A5 JP 2019530098A5 JP 2019516412 A JP2019516412 A JP 2019516412A JP 2019516412 A JP2019516412 A JP 2019516412A JP 2019530098 A5 JP2019530098 A5 JP 2019530098A5
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JP
Japan
Prior art keywords
service provider
genomic
job
clinical
user interface
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Ceased
Application number
JP2019516412A
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English (en)
Japanese (ja)
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JP2019530098A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/EP2017/074886 external-priority patent/WO2018060485A1/en
Publication of JP2019530098A publication Critical patent/JP2019530098A/ja
Publication of JP2019530098A5 publication Critical patent/JP2019530098A5/ja
Ceased legal-status Critical Current

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JP2019516412A 2016-09-29 2017-09-29 協調的な変異選択及び治療合致レポートのための方法及び装置 Ceased JP2019530098A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662401319P 2016-09-29 2016-09-29
US62/401,319 2016-09-29
PCT/EP2017/074886 WO2018060485A1 (en) 2016-09-29 2017-09-29 A method and apparatus for collaborative variant selection and therapy matching reporting

Publications (2)

Publication Number Publication Date
JP2019530098A JP2019530098A (ja) 2019-10-17
JP2019530098A5 true JP2019530098A5 (enExample) 2020-11-05

Family

ID=59974459

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2019516412A Ceased JP2019530098A (ja) 2016-09-29 2017-09-29 協調的な変異選択及び治療合致レポートのための方法及び装置

Country Status (5)

Country Link
US (2) US20190362807A1 (enExample)
EP (1) EP3520007A1 (enExample)
JP (1) JP2019530098A (enExample)
CN (1) CN109791795A (enExample)
WO (2) WO2018060365A1 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180166170A1 (en) * 2016-12-12 2018-06-14 Konstantinos Theofilatos Generalized computational framework and system for integrative prediction of biomarkers
JP6953586B2 (ja) 2019-06-19 2021-10-27 シスメックス株式会社 患者検体の核酸配列の解析方法、解析結果の提示方法、提示装置、提示プログラム、及び患者検体の核酸配列の解析システム
EP3792923A1 (en) * 2019-09-16 2021-03-17 Siemens Healthcare GmbH Method and device for exchanging information regarding the clinical implications of genomic variations
US11593188B2 (en) * 2020-06-29 2023-02-28 Vmware, Inc. Method and apparatus for providing asynchronicity to microservice application programming interfaces
CN113223612B (zh) * 2021-04-30 2024-08-02 阿里巴巴达摩院(杭州)科技有限公司 基因组的特征提取方法
WO2022251587A1 (en) * 2021-05-28 2022-12-01 ObjectiveGI, Inc. System and method for identifying candidates for clinical trials

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ518022A (en) * 1999-08-27 2004-01-30 Iris Biotechnologies Inc Analysis and diagnosis by intelligent processing of remotely generated genetic hybridization profiles
JP2005309836A (ja) * 2004-04-22 2005-11-04 Link Genomics Kk がん診断支援システム
JPWO2007055244A1 (ja) * 2005-11-08 2009-04-30 国立大学法人名古屋大学 遺伝子変異検出用アレイ及び検出方法
US8140270B2 (en) * 2007-03-22 2012-03-20 National Center For Genome Resources Methods and systems for medical sequencing analysis
JP6420543B2 (ja) * 2011-01-19 2018-11-07 コーニンクレッカ フィリップス エヌ ヴェＫｏｎｉｎｋｌｉｊｋｅ Ｐｈｉｌｉｐｓ Ｎ．Ｖ． ゲノムデータ処理方法
CN104094266A (zh) * 2011-11-07 2014-10-08 独创系统公司 用于识别原因性基因组变体的方法和系统
US9635088B2 (en) * 2012-11-26 2017-04-25 Accenture Global Services Limited Method and system for managing user state for applications deployed on platform as a service (PaaS) clouds
US9418203B2 (en) * 2013-03-15 2016-08-16 Cypher Genomics, Inc. Systems and methods for genomic variant annotation
US10129078B2 (en) * 2014-10-30 2018-11-13 Equinix, Inc. Orchestration engine for real-time configuration and management of interconnections within a cloud-based services exchange
WO2016100638A1 (en) * 2014-12-17 2016-06-23 Foundation Medicine, Inc. Computer-implemented system and method for identifying similar patients
WO2016103036A1 (en) * 2014-12-24 2016-06-30 Oncompass Gmbh System and method for adaptive medical decision support

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