JP2018500876A5 - - Google Patents

Download PDF

Info

Publication number
JP2018500876A5
JP2018500876A5 JP2017518990A JP2017518990A JP2018500876A5 JP 2018500876 A5 JP2018500876 A5 JP 2018500876A5 JP 2017518990 A JP2017518990 A JP 2017518990A JP 2017518990 A JP2017518990 A JP 2017518990A JP 2018500876 A5 JP2018500876 A5 JP 2018500876A5
Authority
JP
Japan
Prior art keywords
item
nucleotide sequence
genomic region
length
items
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
JP2017518990A
Other languages
English (en)
Japanese (ja)
Other versions
JP6971845B2 (ja
JP2018500876A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2015/054903 external-priority patent/WO2016057901A1/en
Publication of JP2018500876A publication Critical patent/JP2018500876A/ja
Publication of JP2018500876A5 publication Critical patent/JP2018500876A5/ja
Priority to JP2020187745A priority Critical patent/JP7773301B2/ja
Application granted granted Critical
Publication of JP6971845B2 publication Critical patent/JP6971845B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017518990A 2014-10-10 2015-10-09 遺伝子の変動の非侵襲的評価のための方法および処理 Active JP6971845B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2020187745A JP7773301B2 (ja) 2014-10-10 2020-11-11 遺伝子の変動の非侵襲的評価のための方法および処理

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462062748P 2014-10-10 2014-10-10
US62/062,748 2014-10-10
PCT/US2015/054903 WO2016057901A1 (en) 2014-10-10 2015-10-09 Methods and processes for non-invasive assessment of genetic variations

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2020187745A Division JP7773301B2 (ja) 2014-10-10 2020-11-11 遺伝子の変動の非侵襲的評価のための方法および処理

Publications (3)

Publication Number Publication Date
JP2018500876A JP2018500876A (ja) 2018-01-18
JP2018500876A5 true JP2018500876A5 (https=) 2018-09-27
JP6971845B2 JP6971845B2 (ja) 2021-11-24

Family

ID=54352504

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2017518990A Active JP6971845B2 (ja) 2014-10-10 2015-10-09 遺伝子の変動の非侵襲的評価のための方法および処理
JP2020187745A Active JP7773301B2 (ja) 2014-10-10 2020-11-11 遺伝子の変動の非侵襲的評価のための方法および処理
JP2022191456A Pending JP2023022220A (ja) 2014-10-10 2022-11-30 遺伝子の変動の非侵襲的評価のための方法および処理

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2020187745A Active JP7773301B2 (ja) 2014-10-10 2020-11-11 遺伝子の変動の非侵襲的評価のための方法および処理
JP2022191456A Pending JP2023022220A (ja) 2014-10-10 2022-11-30 遺伝子の変動の非侵襲的評価のための方法および処理

Country Status (6)

Country Link
US (3) US10892035B2 (https=)
EP (2) EP3730629A1 (https=)
JP (3) JP6971845B2 (https=)
AU (3) AU2015330734B2 (https=)
CA (1) CA2964158A1 (https=)
WO (1) WO2016057901A1 (https=)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HK1206055A1 (en) 2012-03-02 2015-12-31 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
CN105190656B (zh) 2013-01-17 2018-01-16 佩索纳里斯公司 用于遗传分析的方法和系统
US11365447B2 (en) 2014-03-13 2022-06-21 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US10125399B2 (en) 2014-10-30 2018-11-13 Personalis, Inc. Methods for using mosaicism in nucleic acids sampled distal to their origin
US11299783B2 (en) 2016-05-27 2022-04-12 Personalis, Inc. Methods and systems for genetic analysis
EP3464626B1 (en) 2016-05-27 2022-04-06 Sequenom, Inc. Methods for detecting genetic variations
CA3030894A1 (en) 2016-07-27 2018-02-01 Sequenom, Inc. Methods for non-invasive assessment of genomic instability
US11200963B2 (en) 2016-07-27 2021-12-14 Sequenom, Inc. Genetic copy number alteration classifications
US11929143B2 (en) 2017-01-20 2024-03-12 Sequenom, Inc Methods for non-invasive assessment of copy number alterations
US11352662B2 (en) 2017-01-20 2022-06-07 Sequenom, Inc. Sequence adapter manufacture and use
CA3198931A1 (en) 2017-01-20 2018-07-26 Sequenom, Inc. Methods for non-invasive assessment of genetic alterations
US11694768B2 (en) 2017-01-24 2023-07-04 Sequenom, Inc. Methods and processes for assessment of genetic variations
JP7370862B2 (ja) 2017-03-17 2023-10-30 セクエノム, インコーポレイテッド 遺伝子モザイク症のための方法およびプロセス
EP3655954A1 (en) 2017-07-18 2020-05-27 Congenica Ltd. Screening system and method
GB2564847A (en) * 2017-07-18 2019-01-30 Congenica Ltd Knowledgebase for non-invasive prenatal genetic screening and diagnosis
PL3658689T3 (pl) * 2017-07-26 2021-10-18 Trisomytest, S.R.O. Sposób nieinwazyjnego wykrywania prenatalnego aneuploidii chromosomów płodu z krwi matki w oparciu o sieć bayesowską
SK862017A3 (sk) * 2017-08-24 2020-05-04 Grendar Marian Doc Mgr Phd Spôsob použitia fetálnej frakcie a chromozómovej reprezentácie pri určovaní aneuploidného stavu v neinvazívnom prenatálnom testovaní
WO2019226992A1 (en) * 2018-05-24 2019-11-28 The Trustees Of Columbia University In The City Of New York Bacterial capture sequencing platform and methods of designing, constructing and using
KR102287096B1 (ko) * 2019-01-04 2021-08-09 테라젠지놈케어 주식회사 모체 시료 중 태아 분획을 결정하는 방법
CA3128973A1 (en) 2019-03-04 2020-09-10 Bhaskar Bhattacharyya Data compression and communication using machine learning
US20200303033A1 (en) * 2019-03-18 2020-09-24 Nantomics, Llc System and method for data curation
CN112823391B (zh) * 2019-06-03 2024-07-05 Illumina公司 基于检测限的质量控制度量
US11403641B2 (en) * 2019-06-28 2022-08-02 Paypal, Inc. Transactional probability analysis on radial time representation
EP4004559A4 (en) * 2019-07-31 2023-10-04 SomaLogic Operating Co., Inc. METHOD, APPARATUS AND COMPUTER READABLE MEDIUM FOR ADAPTIVE NORMALIZATION OF ANALYTE LEVELS
US20240395357A1 (en) 2019-10-31 2024-11-28 Sequenom, Inc. Application of mosaicism ratio in multifetal gestations and personalized risk assessment
EP4055610A4 (en) 2019-11-05 2023-11-29 Personalis, Inc. ESTIMATION OF TUMOR PURITY FROM SINGLE SAMPLES
EP4168569A4 (en) * 2020-06-18 2024-08-07 Personalis, Inc. Machine-learning techniques for predicting surface-presenting peptides
WO2022035670A1 (en) * 2020-08-09 2022-02-17 Myriad Women's Health, Inc. Bayesian sex caller
CN116134526A (zh) * 2020-08-15 2023-05-16 生命技术公司 具有合成等位基因阶梯库的dna分析仪
KR102795708B1 (ko) * 2020-11-27 2025-04-16 주식회사 지씨지놈 인공지능 기반 암 진단 및 암 종 예측방법
US11688507B2 (en) * 2020-12-29 2023-06-27 Kpn Innovations, Llc. Systems and methods for generating a metabolic dysfunction nourishment program
CN113158950B (zh) * 2021-04-30 2022-04-05 天津深析智能科技发展有限公司 一种重叠染色体自动分割方法
EP4413580A4 (en) 2021-10-05 2025-08-13 Personalis Inc PERSONALIZED TESTS FOR PERSONALIZED CANCER MONITORING
CN116149049B (zh) * 2023-02-28 2025-07-11 河北工业大学 一种利用非对称脉冲调控超连续谱中光畸形波的方法

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6927028B2 (en) 2001-08-31 2005-08-09 Chinese University Of Hong Kong Non-invasive methods for detecting non-host DNA in a host using epigenetic differences between the host and non-host DNA
CN1703521B (zh) 2002-09-06 2011-11-16 波士顿大学信托人 基因表达的定量
CA2507189C (en) 2002-11-27 2018-06-12 Sequenom, Inc. Fragmentation-based methods and systems for sequence variation detection and discovery
EP1641809B2 (en) 2003-07-05 2018-10-03 The Johns Hopkins University Method and compositions for detection and enumeration of genetic variations
US20100216153A1 (en) * 2004-02-27 2010-08-26 Helicos Biosciences Corporation Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities
EP1817430B1 (en) 2004-11-29 2009-09-16 Klinikum der Universität Regensburg Means and methods for detecting methylated dna
EP3260556B1 (en) 2006-05-31 2019-07-31 Sequenom, Inc. Methods for the extraction of nucleic acid from a sample
AU2007260750A1 (en) 2006-06-16 2007-12-21 Sequenom, Inc. Methods and compositions for the amplification, detection and quantification of nucleic acid from a sample
WO2009032781A2 (en) 2007-08-29 2009-03-12 Sequenom, Inc. Methods and compositions for universal size-specific polymerase chain reaction
WO2009032779A2 (en) 2007-08-29 2009-03-12 Sequenom, Inc. Methods and compositions for the size-specific seperation of nucleic acid from a sample
WO2009120808A2 (en) 2008-03-26 2009-10-01 Sequenom, Inc. Restriction endonuclease enhanced polymorphic sequence detection
EP3770255A1 (en) 2008-09-16 2021-01-27 Sequenom, Inc. Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses
US8476013B2 (en) 2008-09-16 2013-07-02 Sequenom, Inc. Processes and compositions for methylation-based acid enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses
EP3514244B1 (en) 2009-04-03 2021-07-07 Sequenom, Inc. Nucleic acid preparation methods
ES2534758T3 (es) 2010-01-19 2015-04-28 Verinata Health, Inc. Métodos de secuenciación en diagnósticos prenatales
EP2526415B1 (en) * 2010-01-19 2017-05-03 Verinata Health, Inc Partition defined detection methods
WO2011143659A2 (en) 2010-05-14 2011-11-17 Fluidigm Corporation Nucleic acid isolation methods
US9139874B2 (en) 2011-07-07 2015-09-22 Life Technologies Corporation Bi-directional sequencing compositions and methods
CA2850785C (en) 2011-10-06 2022-12-13 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
EP3243908B1 (en) 2011-10-11 2019-01-02 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
WO2013109981A1 (en) * 2012-01-20 2013-07-25 Sequenom, Inc. Diagnostic processes that factor experimental conditions
DK3663409T3 (da) 2012-05-21 2021-12-13 Sequenom Inc Fremgangsmåder og processer til ikke-invasiv bedømmelse af genetiske variationer
US10497461B2 (en) 2012-06-22 2019-12-03 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US10482994B2 (en) 2012-10-04 2019-11-19 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US20130309666A1 (en) 2013-01-25 2013-11-21 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
PL2981921T3 (pl) * 2013-04-03 2023-05-08 Sequenom, Inc. Metody i procesy nieinwazyjnej oceny zmienności genetycznych
EP4604127A3 (en) 2013-05-24 2025-12-03 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
HUE042654T2 (hu) * 2013-06-21 2019-07-29 Sequenom Inc Eljárás genetikai variációk nem-invazív megállapítására
IL304949B2 (en) 2013-10-04 2025-09-01 Sequenom Inc Methods and processes for non-invasive assessment of genetic variations
KR102429186B1 (ko) * 2013-10-21 2022-08-03 베리나타 헬스, 인코포레이티드 사본수 변동을 결정함에 있어서 검출의 감수성을 향상시키기 위한 방법
WO2016019042A1 (en) * 2014-07-30 2016-02-04 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations

Similar Documents

Publication Publication Date Title
JP2018500876A5 (https=)
Dunning et al. Statistical issues in the analysis of Illumina data
US20220223233A1 (en) Display of estimated parental contribution to ancestry
EP4300500B1 (en) Cell-free dna end characteristics
US11961589B2 (en) Models for targeted sequencing
AU2016355983B2 (en) Methods for detecting copy-number variations in next-generation sequencing
CN109949861B (zh) 肿瘤突变负荷检测方法、装置和存储介质
IL320112A (en) Methods and processes for non-invasive assessment of genetic variations
IL319365A (en) Methods and processes for assessing genetic variations
EP3518974A1 (en) Noninvasive prenatal screening using dynamic iterative depth optimization
CN110010197A (zh) 基于血液循环肿瘤dna的单核苷酸变异检测方法、装置和存储介质
JP2016526879A5 (https=)
JP2019522285A5 (https=)
CN109887546B (zh) 基于二代测序的单基因或多基因拷贝数检测系统及方法
US20240387000A1 (en) Base Coverage Normalization and Use Thereof in Detecting Copy Number Variation
JP2014520509A5 (https=)
US20190287646A1 (en) Identifying copy number aberrations
JP2017537380A5 (https=)
JPWO2015015585A1 (ja) 遺伝子変異分析装置、遺伝子変異分析システム及び遺伝子変異分析方法
KR102441856B1 (ko) 중요도 샘플링을 활용한 다중변이 연관연구 방법
CN117025795A (zh) 与清远麻鸡产蛋持续性相关的snp位点及其应用
US20140188397A1 (en) Methods of acquiring genome size and error
US20190139627A1 (en) System for Increasing the Accuracy of Non Invasive Prenatal Diagnostics and Liquid Biopsy by Observed Loci Bias Correction at Single Base Resolution
CN114944195A (zh) 一种拷贝数变异检测前的数据矫正方法
US11127485B2 (en) Techniques for fine grained correction of count bias in massively parallel DNA sequencing