PL2805280T3 - Procesy diagnostyczne będące czynnikiem warunków doświadczalnych - Google Patents
Procesy diagnostyczne będące czynnikiem warunków doświadczalnychInfo
- Publication number
- PL2805280T3 PL2805280T3 PL13707938.0T PL13707938T PL2805280T3 PL 2805280 T3 PL2805280 T3 PL 2805280T3 PL 13707938 T PL13707938 T PL 13707938T PL 2805280 T3 PL2805280 T3 PL 2805280T3
- Authority
- PL
- Poland
- Prior art keywords
- experimental conditions
- diagnostic processes
- factor experimental
- factor
- diagnostic
- Prior art date
Links
- 238000002405 diagnostic procedure Methods 0.000 title 1
Classifications
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/20—Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/10—Ploidy or copy number detection
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
- G16B30/10—Sequence alignment; Homology search
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
- G16B30/20—Sequence assembly
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B40/00—ICT specially adapted for biostatistics; ICT specially adapted for bioinformatics-related machine learning or data mining, e.g. knowledge discovery or pattern finding
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Biophysics (AREA)
- Biotechnology (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Evolutionary Biology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Medical Informatics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Theoretical Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Pathology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261589202P | 2012-01-20 | 2012-01-20 | |
| US201261663477P | 2012-06-22 | 2012-06-22 | |
| US201261709899P | 2012-10-04 | 2012-10-04 | |
| PCT/US2012/059123 WO2013052913A2 (en) | 2011-10-06 | 2012-10-05 | Methods and processes for non-invasive assessment of genetic variations |
| PCT/US2013/022290 WO2013109981A1 (en) | 2012-01-20 | 2013-01-18 | Diagnostic processes that factor experimental conditions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2805280T3 true PL2805280T3 (pl) | 2022-11-21 |
Family
ID=48799714
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL13707938.0T PL2805280T3 (pl) | 2012-01-20 | 2013-01-18 | Procesy diagnostyczne będące czynnikiem warunków doświadczalnych |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US11697849B2 (pl) |
| EP (2) | EP2805280B1 (pl) |
| JP (2) | JP6431769B2 (pl) |
| AU (1) | AU2013209499B2 (pl) |
| CA (1) | CA2861856C (pl) |
| ES (1) | ES2929923T3 (pl) |
| HU (1) | HUE059847T2 (pl) |
| LT (1) | LT2805280T (pl) |
| PL (1) | PL2805280T3 (pl) |
| WO (1) | WO2013109981A1 (pl) |
Families Citing this family (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12152275B2 (en) | 2010-05-18 | 2024-11-26 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| US20140235474A1 (en) | 2011-06-24 | 2014-08-21 | Sequenom, Inc. | Methods and processes for non invasive assessment of a genetic variation |
| US10424394B2 (en) | 2011-10-06 | 2019-09-24 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US9984198B2 (en) | 2011-10-06 | 2018-05-29 | Sequenom, Inc. | Reducing sequence read count error in assessment of complex genetic variations |
| US9367663B2 (en) | 2011-10-06 | 2016-06-14 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10196681B2 (en) | 2011-10-06 | 2019-02-05 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP2764458B1 (en) | 2011-10-06 | 2021-04-07 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| PL2805280T3 (pl) | 2012-01-20 | 2022-11-21 | Sequenom, Inc. | Procesy diagnostyczne będące czynnikiem warunków doświadczalnych |
| US20230279494A1 (en) * | 2012-01-20 | 2023-09-07 | Sequenom, Inc. | Methods for non-invasive assessment of fetal genetic variations that factor experimental conditions |
| US9605313B2 (en) | 2012-03-02 | 2017-03-28 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US9920361B2 (en) | 2012-05-21 | 2018-03-20 | Sequenom, Inc. | Methods and compositions for analyzing nucleic acid |
| US10504613B2 (en) | 2012-12-20 | 2019-12-10 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10497461B2 (en) * | 2012-06-22 | 2019-12-03 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US20140100126A1 (en) * | 2012-08-17 | 2014-04-10 | Natera, Inc. | Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data |
| 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 |
| US10844424B2 (en) | 2013-02-20 | 2020-11-24 | Bionano Genomics, Inc. | Reduction of bias in genomic coverage measurements |
| CN105229168B (zh) | 2013-02-20 | 2020-07-17 | 生物纳米基因有限公司 | 纳米流体中分子的表征 |
| US11060145B2 (en) | 2013-03-13 | 2021-07-13 | Sequenom, Inc. | Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus |
| HUE061261T2 (hu) | 2013-04-03 | 2023-05-28 | Sequenom Inc | Eljárások és folyamatok genetikai variánsok nem invazív értékelésére |
| IL309903A (en) | 2013-05-24 | 2024-03-01 | Sequenom Inc | Methods and processes for non-invasive assessment of genetic variations |
| AU2014284180B2 (en) | 2013-06-21 | 2020-03-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US20150073894A1 (en) * | 2013-09-06 | 2015-03-12 | Metamarkets Group Inc. | Suspect Anomaly Detection and Presentation within Context |
| PL3053071T3 (pl) * | 2013-10-04 | 2024-03-18 | Sequenom, Inc. | Metody i procesy nieinwazyjnej oceny zmienności genetycznych |
| CN105874082B (zh) * | 2013-10-07 | 2020-06-02 | 塞昆纳姆股份有限公司 | 用于非侵入性评估染色体改变的方法和过程 |
| CN105830077B (zh) * | 2013-10-21 | 2019-07-09 | 维里纳塔健康公司 | 用于在确定拷贝数变异中改善检测的灵敏度的方法 |
| GB2520765A (en) * | 2013-12-02 | 2015-06-03 | Vanadis Diagnostics Ab | Multiplex detection of nucleic acids |
| US10417258B2 (en) | 2013-12-19 | 2019-09-17 | Exposit Labs, Inc. | Interactive multi-dimensional nested table supporting scalable real-time querying of large data volumes |
| CN106164295B (zh) | 2014-02-25 | 2020-08-11 | 生物纳米基因公司 | 减小基因组覆盖测量中的偏差 |
| EP3736344A1 (en) | 2014-03-13 | 2020-11-11 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US12001667B2 (en) | 2014-03-26 | 2024-06-04 | Unanimous A. I., Inc. | Real-time collaborative slider-swarm with deadbands for amplified collective intelligence |
| US12099936B2 (en) | 2014-03-26 | 2024-09-24 | Unanimous A. I., Inc. | Systems and methods for curating an optimized population of networked forecasting participants from a baseline population |
| US11151460B2 (en) * | 2014-03-26 | 2021-10-19 | Unanimous A. I., Inc. | Adaptive population optimization for amplifying the intelligence of crowds and swarms |
| US11269502B2 (en) | 2014-03-26 | 2022-03-08 | Unanimous A. I., Inc. | Interactive behavioral polling and machine learning for amplification of group intelligence |
| CA2945962C (en) | 2014-04-21 | 2023-08-29 | Natera, Inc. | Detecting mutations and ploidy in chromosomal segments |
| US12492429B2 (en) | 2014-04-21 | 2025-12-09 | Natera, Inc. | Detecting mutations and ploidy in chromosomal segments |
| EP3149202A1 (en) * | 2014-05-26 | 2017-04-05 | Ebios Futura S.r.l. | Method of prenatal diagnosis |
| CA3191504A1 (en) * | 2014-05-30 | 2015-12-03 | Sequenom, Inc. | Chromosome representation determinations |
| BR112016027848A2 (pt) | 2014-05-30 | 2017-08-22 | Verinata Health Inc | Método para avaliação de número de cópias de uma sequência de interesse, meio legível por máquina não transitória, e, sistema para avaliação de número de cópias de uma sequência de interesse |
| US20180173845A1 (en) * | 2014-06-05 | 2018-06-21 | Natera, Inc. | Systems and Methods for Detection of Aneuploidy |
| SG11201702066UA (en) * | 2014-07-21 | 2017-04-27 | Illumina Inc | Polynucleotide enrichment using crispr-cas systems |
| US20160026759A1 (en) * | 2014-07-22 | 2016-01-28 | Yourgene Bioscience | Detecting Chromosomal Aneuploidy |
| US11783911B2 (en) | 2014-07-30 | 2023-10-10 | Sequenom, Inc | Methods and processes for non-invasive assessment of genetic variations |
| JP2016042836A (ja) * | 2014-08-25 | 2016-04-04 | 富士フイルム株式会社 | 検査通知出力装置、検査通知出力方法、検査通知出力プログラム、及び遺伝子染色体検査システム |
| US10892035B2 (en) | 2014-10-10 | 2021-01-12 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| MA40939A (fr) | 2014-12-12 | 2017-10-18 | Verinata Health Inc | Utilisation de la taille de fragments d'adn acellulaire pour déterminer les variations du nombre de copies |
| EP3235010A4 (en) | 2014-12-18 | 2018-08-29 | Agilome, Inc. | Chemically-sensitive field effect transistor |
| US10020300B2 (en) | 2014-12-18 | 2018-07-10 | Agilome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
| US10006910B2 (en) | 2014-12-18 | 2018-06-26 | Agilome, Inc. | Chemically-sensitive field effect transistors, systems, and methods for manufacturing and using the same |
| US9859394B2 (en) | 2014-12-18 | 2018-01-02 | Agilome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
| US9857328B2 (en) | 2014-12-18 | 2018-01-02 | Agilome, Inc. | Chemically-sensitive field effect transistors, systems and methods for manufacturing and using the same |
| US9618474B2 (en) | 2014-12-18 | 2017-04-11 | Edico Genome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
| EP4450636A3 (en) | 2015-05-18 | 2025-01-01 | Karius, Inc. | Compositions and methods for enriching populations of nucleic acids |
| EP3118324A1 (en) * | 2015-07-13 | 2017-01-18 | Cartagenia N.V. | Method for analyzing copy number variation in the detection of cancer |
| BE1023266B1 (nl) * | 2015-07-13 | 2017-01-17 | Cartagenia N.V. | Systeem en methodologie voor de analyse van genomische gegevens die zijn verkregen van een onderwerp |
| BE1023267B1 (nl) * | 2015-07-13 | 2017-01-17 | Cartagenia N.V. | Werkwijze voor het analyseren van kopienummervariatie bij de detectie van kanker |
| AU2016310501B2 (en) | 2015-08-25 | 2019-11-07 | Nantomics, Llc | Systems and methods for genetic analysis of metastases |
| US10153894B2 (en) | 2015-11-05 | 2018-12-11 | Microsoft Technology Licensing, Llc | Homomorphic encryption with optimized encoding |
| US10075289B2 (en) | 2015-11-05 | 2018-09-11 | Microsoft Technology Licensing, Llc | Homomorphic encryption with optimized parameter selection |
| US9900147B2 (en) | 2015-12-18 | 2018-02-20 | Microsoft Technology Licensing, Llc | Homomorphic encryption with optimized homomorphic operations |
| US10095831B2 (en) | 2016-02-03 | 2018-10-09 | Verinata Health, Inc. | Using cell-free DNA fragment size to determine copy number variations |
| AU2017237199B2 (en) | 2016-03-25 | 2020-11-05 | Karius, Inc. | Synthetic nucleic acid spike-ins |
| CN109074429B (zh) * | 2016-04-20 | 2022-03-29 | 华为技术有限公司 | 基因组变异检测方法、装置及终端 |
| WO2017201081A1 (en) | 2016-05-16 | 2017-11-23 | Agilome, Inc. | Graphene fet devices, systems, and methods of using the same for sequencing nucleic acids |
| GB201609221D0 (en) | 2016-05-25 | 2016-07-06 | Oxford Nanopore Tech Ltd | Method |
| US20170342477A1 (en) | 2016-05-27 | 2017-11-30 | Sequenom, Inc. | Methods for Detecting Genetic Variations |
| US10296709B2 (en) | 2016-06-10 | 2019-05-21 | Microsoft Technology Licensing, Llc | Privacy-preserving genomic prediction |
| CA3030894A1 (en) | 2016-07-27 | 2018-02-01 | Sequenom, Inc. | Methods for non-invasive assessment of genomic instability |
| EP3491560A1 (en) | 2016-07-27 | 2019-06-05 | Sequenom, Inc. | Genetic copy number alteration classifications |
| WO2018064486A1 (en) | 2016-09-29 | 2018-04-05 | Counsyl, Inc. | Noninvasive prenatal screening using dynamic iterative depth optimization |
| WO2018136888A1 (en) | 2017-01-20 | 2018-07-26 | Sequenom, Inc. | Methods for non-invasive assessment of genetic alterations |
| US11929143B2 (en) | 2017-01-20 | 2024-03-12 | Sequenom, Inc | Methods for non-invasive assessment of copy number alterations |
| CA3194557A1 (en) | 2017-01-20 | 2018-07-26 | Sequenom, Inc. | Sequencing adapter manufacture and use |
| WO2018140521A1 (en) | 2017-01-24 | 2018-08-02 | Sequenom, Inc. | Methods and processes for assessment of genetic variations |
| CN106778069B (zh) * | 2017-02-17 | 2020-02-14 | 广州精科医学检验所有限公司 | 确定胎儿染色体中微缺失微重复的方法及设备 |
| IL317916A (en) | 2017-03-17 | 2025-02-01 | Sequenom Inc | Methods and processes for assessing genetic mosaicism |
| US11342047B2 (en) | 2017-04-21 | 2022-05-24 | Illumina, Inc. | Using cell-free DNA fragment size to detect tumor-associated variant |
| US11869630B2 (en) | 2017-07-18 | 2024-01-09 | Congenica Ltd. | Screening system and method for determining a presence and an assessment score of cell-free DNA fragments |
| GB2564847A (en) * | 2017-07-18 | 2019-01-30 | Congenica Ltd | Knowledgebase for non-invasive prenatal genetic screening and diagnosis |
| EP3781714B1 (en) | 2018-04-14 | 2026-01-07 | Natera, Inc. | Methods for cancer detection and monitoring by means of personalized detection of circulating tumor dna |
| US12234509B2 (en) | 2018-07-03 | 2025-02-25 | Natera, Inc. | Methods for detection of donor-derived cell-free DNA |
| WO2020104394A1 (en) | 2018-11-19 | 2020-05-28 | Sistemas Genómicos, S.L. | Method and computer program product for analysis of fetal dna by massive sequencing |
| FI4428234T3 (fi) | 2018-11-21 | 2026-03-10 | Karius Inc | Suoran kirjastonmuodostuksen menetelmiä, -järjestelmiä ja -koostumuksia |
| US11746385B2 (en) * | 2019-05-21 | 2023-09-05 | Lexent Bio, Inc. | Methods of detecting tumor progression via analysis of cell-free nucleic acids |
| EP4052259A1 (en) | 2019-10-31 | 2022-09-07 | Sequenom, Inc. | Application of mosaicism ratio in multifetal gestations and personalized risk assessment |
| US11475981B2 (en) | 2020-02-18 | 2022-10-18 | Tempus Labs, Inc. | Methods and systems for dynamic variant thresholding in a liquid biopsy assay |
| US11211144B2 (en) | 2020-02-18 | 2021-12-28 | Tempus Labs, Inc. | Methods and systems for refining copy number variation in a liquid biopsy assay |
| US11211147B2 (en) | 2020-02-18 | 2021-12-28 | Tempus Labs, Inc. | Estimation of circulating tumor fraction using off-target reads of targeted-panel sequencing |
| CN111753529B (zh) * | 2020-06-03 | 2021-07-27 | 杭州云嘉云计算有限公司 | 一种基于拼音相同或相似的中文文本纠错方法 |
| JP7719606B2 (ja) * | 2021-01-15 | 2025-08-06 | シスメックス株式会社 | 核酸分析方法および核酸分析装置 |
| US12190294B2 (en) | 2023-03-04 | 2025-01-07 | Unanimous A. I., Inc. | Methods and systems for hyperchat and hypervideo conversations across networked human populations with collective intelligence amplification |
| US11949638B1 (en) | 2023-03-04 | 2024-04-02 | Unanimous A. I., Inc. | Methods and systems for hyperchat conversations among large networked populations with collective intelligence amplification |
Family Cites Families (159)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US4683195A (en) | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
| US5720928A (en) | 1988-09-15 | 1998-02-24 | New York University | Image processing and analysis of individual nucleic acid molecules |
| US5075212A (en) | 1989-03-27 | 1991-12-24 | University Of Patents, Inc. | Methods of detecting picornaviruses in biological fluids and tissues |
| US5143854A (en) | 1989-06-07 | 1992-09-01 | Affymax Technologies N.V. | Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof |
| US5641628A (en) | 1989-11-13 | 1997-06-24 | Children's Medical Center Corporation | Non-invasive method for isolation and detection of fetal DNA |
| JP3068180B2 (ja) | 1990-01-12 | 2000-07-24 | アブジェニックス インコーポレイテッド | 異種抗体の生成 |
| US5091652A (en) | 1990-01-12 | 1992-02-25 | The Regents Of The University Of California | Laser excited confocal microscope fluorescence scanner and method |
| US5432054A (en) | 1994-01-31 | 1995-07-11 | Applied Imaging | Method for separating rare cells from a population of cells |
| EP0699687B1 (en) | 1994-08-31 | 2004-01-28 | Mitsubishi Pharma Corporation | Process for purifying recombinant human serum albumin |
| US5846719A (en) | 1994-10-13 | 1998-12-08 | Lynx Therapeutics, Inc. | Oligonucleotide tags for sorting and identification |
| ATE199571T1 (de) | 1994-12-23 | 2001-03-15 | Imperial College | Automatisches sequenzierungs verfahren |
| US5795782A (en) | 1995-03-17 | 1998-08-18 | President & Fellows Of Harvard College | Characterization of individual polymer molecules based on monomer-interface interactions |
| US5670325A (en) | 1996-08-14 | 1997-09-23 | Exact Laboratories, Inc. | Method for the detection of clonal populations of transformed cells in a genomically heterogeneous cellular sample |
| RU2251572C2 (ru) | 1996-04-25 | 2005-05-10 | Дженикон Сайенсиз Корпорейшн, Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния | Анализ аналитов с использованием частиц в качестве метки |
| US5786146A (en) | 1996-06-03 | 1998-07-28 | The Johns Hopkins University School Of Medicine | Method of detection of methylated nucleic acid using agents which modify unmethylated cytosine and distinguishing modified methylated and non-methylated nucleic acids |
| US5928870A (en) | 1997-06-16 | 1999-07-27 | Exact Laboratories, Inc. | Methods for the detection of loss of heterozygosity |
| US6300077B1 (en) | 1996-08-14 | 2001-10-09 | Exact Sciences Corporation | Methods for the detection of nucleic acids |
| US6100029A (en) | 1996-08-14 | 2000-08-08 | Exact Laboratories, Inc. | Methods for the detection of chromosomal aberrations |
| US6403311B1 (en) | 1997-02-12 | 2002-06-11 | Us Genomics | Methods of analyzing polymers using ordered label strategies |
| GB9704444D0 (en) | 1997-03-04 | 1997-04-23 | Isis Innovation | Non-invasive prenatal diagnosis |
| US6566101B1 (en) | 1997-06-16 | 2003-05-20 | Anthony P. Shuber | Primer extension methods for detecting nucleic acids |
| US6570001B1 (en) | 1997-06-20 | 2003-05-27 | Institut Pasteur | Polynucleotides and their use for detecting resistance to streptogramin A or to streptogramin B and related compounds |
| JP2002521064A (ja) | 1998-07-30 | 2002-07-16 | ソレックサ リミテッド | アレイ生体分子およびシークエンシングにおけるその使用 |
| US6263286B1 (en) | 1998-08-13 | 2001-07-17 | U.S. Genomics, Inc. | Methods of analyzing polymers using a spatial network of fluorophores and fluorescence resonance energy transfer |
| US6818395B1 (en) | 1999-06-28 | 2004-11-16 | California Institute Of Technology | Methods and apparatus for analyzing polynucleotide sequences |
| US20050287592A1 (en) | 2000-08-29 | 2005-12-29 | Yeda Research And Development Co. Ltd. | Template-dependent nucleic acid polymerization using oligonucleotide triphosphates building blocks |
| AU7537200A (en) | 1999-09-29 | 2001-04-30 | Solexa Ltd. | Polynucleotide sequencing |
| US6946273B1 (en) | 1999-10-29 | 2005-09-20 | Stratagene California | Compositions and methods utilizing DNA polymerases |
| US20010049102A1 (en) | 2000-02-24 | 2001-12-06 | Huang Xiaohua C. | Methods for determining single nucleotide variations |
| US6664056B2 (en) | 2000-10-17 | 2003-12-16 | The Chinese University Of Hong Kong | Non-invasive prenatal monitoring |
| WO2002042496A2 (en) | 2000-11-27 | 2002-05-30 | The Regents Of The University Of California | Methods and devices for characterizing duplex nucleic acid molecules |
| DE10112515B4 (de) | 2001-03-09 | 2004-02-12 | Epigenomics Ag | Verfahren zum Nachweis von Cytosin-Methylierungsmustern mit hoher Sensitivität |
| CA2440754A1 (en) | 2001-03-12 | 2002-09-19 | Stephen Quake | Methods and apparatus for analyzing polynucleotide sequences by asynchronous base extension |
| AU2002318386A1 (en) | 2001-06-21 | 2003-01-08 | Agilent Technologies, Inc. | Methods for characterization of nucleic acid molecules |
| 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 |
| US20030157489A1 (en) | 2002-01-11 | 2003-08-21 | Michael Wall | Recursive categorical sequence assembly |
| US6977162B2 (en) | 2002-03-01 | 2005-12-20 | Ravgen, Inc. | Rapid analysis of variations in a genome |
| US7285394B2 (en) | 2002-03-15 | 2007-10-23 | Epigenomics Ag | Discovery and diagnostic methods using 5-methylcytosine DNA glycosylase |
| US20040110208A1 (en) | 2002-03-26 | 2004-06-10 | Selena Chan | Methods and device for DNA sequencing using surface enhanced Raman scattering (SERS) |
| US7744816B2 (en) | 2002-05-01 | 2010-06-29 | Intel Corporation | Methods and device for biomolecule characterization |
| US20050019784A1 (en) | 2002-05-20 | 2005-01-27 | Xing Su | Method and apparatus for nucleic acid sequencing and identification |
| US7005264B2 (en) | 2002-05-20 | 2006-02-28 | Intel Corporation | Method and apparatus for nucleic acid sequencing and identification |
| US6952651B2 (en) | 2002-06-17 | 2005-10-04 | Intel Corporation | Methods and apparatus for nucleic acid sequencing by signal stretching and data integration |
| US8034567B2 (en) | 2002-09-06 | 2011-10-11 | Trustees Of Boston University | Quantification of gene expression |
| EP1613723B1 (en) | 2002-11-27 | 2013-05-15 | Sequenom, Inc. | Fragmentation-based methods for sequence variation detection and discovery |
| JP5183063B2 (ja) | 2003-07-05 | 2013-04-17 | ザ ジョンズ ホプキンス ユニバーシティ | 遺伝的変異の検出および列挙のための方法ならびに組成物 |
| WO2005017025A2 (en) | 2003-08-15 | 2005-02-24 | The President And Fellows Of Harvard College | Study of polymer molecules and conformations with a nanopore |
| WO2005023091A2 (en) | 2003-09-05 | 2005-03-17 | The Trustees Of Boston University | Method for non-invasive prenatal diagnosis |
| ATE435301T1 (de) | 2003-10-16 | 2009-07-15 | Sequenom Inc | Nicht invasiver nachweis fötaler genetischer merkmale |
| US20050095599A1 (en) | 2003-10-30 | 2005-05-05 | Pittaro Richard J. | Detection and identification of biopolymers using fluorescence quenching |
| US7169560B2 (en) | 2003-11-12 | 2007-01-30 | Helicos Biosciences Corporation | Short cycle methods for sequencing polynucleotides |
| US20050147980A1 (en) | 2003-12-30 | 2005-07-07 | Intel Corporation | Nucleic acid sequencing by Raman monitoring of uptake of nucleotides during molecular replication |
| US20060046258A1 (en) | 2004-02-27 | 2006-03-02 | Lapidus Stanley N | Applications of single molecule sequencing |
| US20100216153A1 (en) * | 2004-02-27 | 2010-08-26 | Helicos Biosciences Corporation | Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities |
| US20100216151A1 (en) | 2004-02-27 | 2010-08-26 | Helicos Biosciences Corporation | Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities |
| US7279337B2 (en) | 2004-03-10 | 2007-10-09 | Agilent Technologies, Inc. | Method and apparatus for sequencing polymers through tunneling conductance variation detection |
| US7238485B2 (en) | 2004-03-23 | 2007-07-03 | President And Fellows Of Harvard College | Methods and apparatus for characterizing polynucleotides |
| CN102925549A (zh) | 2004-08-13 | 2013-02-13 | 哈佛学院院长等 | 超高处理量光学-纳米孔dna读出平台 |
| DE602005016712D1 (de) | 2004-11-29 | 2009-10-29 | Univ Regensburg Klinikum | Rter dna |
| EP1859050B1 (en) | 2005-03-18 | 2012-10-24 | The Chinese University Of Hong Kong | A method for the detection of chromosomal aneuploidies |
| US7960105B2 (en) | 2005-11-29 | 2011-06-14 | National Institutes Of Health | Method of DNA analysis using micro/nanochannel |
| EP3002338B1 (en) | 2006-02-02 | 2019-05-08 | The Board of Trustees of The Leland Stanford Junior University | Non-invasive fetal genetic screening by digital analysis |
| WO2007100911A2 (en) | 2006-02-28 | 2007-09-07 | University Of Louisville Research Foundation | Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms |
| TW200741192A (en) | 2006-03-10 | 2007-11-01 | Koninkl Philips Electronics Nv | Methods and systems for identification of DNA patterns through spectral analysis |
| US7282337B1 (en) | 2006-04-14 | 2007-10-16 | Helicos Biosciences Corporation | Methods for increasing accuracy of nucleic acid sequencing |
| US20090075252A1 (en) | 2006-04-14 | 2009-03-19 | Helicos Biosciences Corporation | Methods for increasing accuracy of nucleic acid sequencing |
| EP2602321B1 (en) | 2006-05-31 | 2017-08-23 | Sequenom, Inc. | Methods and compositions for the extraction and amplification of nucleic acid from a sample |
| US8137912B2 (en) | 2006-06-14 | 2012-03-20 | The General Hospital Corporation | Methods for the diagnosis of fetal abnormalities |
| EP2029779A4 (en) | 2006-06-14 | 2010-01-20 | Living Microsystems Inc | HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS |
| CN101501251A (zh) | 2006-06-16 | 2009-08-05 | 塞昆纳姆股份有限公司 | 扩增、检测和定量样品中核酸的方法和组合物 |
| US20080081330A1 (en) | 2006-09-28 | 2008-04-03 | Helicos Biosciences Corporation | Method and devices for analyzing small RNA molecules |
| US8262900B2 (en) | 2006-12-14 | 2012-09-11 | Life Technologies Corporation | Methods and apparatus for measuring analytes using large scale FET arrays |
| EP1944273A1 (en) | 2007-01-15 | 2008-07-16 | Rockwool International A/S | Process and apparatus for making mineral fibers |
| US8003319B2 (en) | 2007-02-02 | 2011-08-23 | International Business Machines Corporation | Systems and methods for controlling position of charged polymer inside nanopore |
| CA2964611C (en) | 2007-03-28 | 2021-06-01 | Bionano Genomics, Inc. | Methods of macromolecular analysis using nanochannel arrays |
| JP5646987B2 (ja) | 2007-04-04 | 2014-12-24 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | ナノポアを使用するための組成物、デバイス、システム、及び方法 |
| GB0713143D0 (en) | 2007-07-06 | 2007-08-15 | Ucl Business Plc | Nucleic acid detection method |
| US9218449B2 (en) | 2007-07-23 | 2015-12-22 | The Chinese University Of Hong Kong | Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis |
| KR20220146689A (ko) | 2007-07-23 | 2022-11-01 | 더 차이니즈 유니버시티 오브 홍콩 | 핵산 서열 불균형의 결정 |
| US12180549B2 (en) | 2007-07-23 | 2024-12-31 | The Chinese University Of Hong Kong | Diagnosing fetal chromosomal aneuploidy using genomic sequencing |
| EP2195452B1 (en) | 2007-08-29 | 2012-03-14 | 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 |
| KR20100089060A (ko) | 2007-10-04 | 2010-08-11 | 할싸이언 몰레큘러 | 전자 현미경으로 핵산 중합체를 시퀀싱하는 방법 |
| US7767400B2 (en) | 2008-02-03 | 2010-08-03 | Helicos Biosciences Corporation | Paired-end reads in sequencing by synthesis |
| AU2009223671B2 (en) | 2008-03-11 | 2014-11-27 | Sequenom, Inc. | Nucleic acid-based tests for prenatal gender determination |
| WO2009120808A2 (en) | 2008-03-26 | 2009-10-01 | Sequenom, Inc. | Restriction endonuclease enhanced polymorphic sequence detection |
| CA2729159C (en) | 2008-06-30 | 2020-01-14 | Bionanomatrix, Inc. | Methods and devices for single-molecule whole genome analysis |
| JP2011527191A (ja) | 2008-07-07 | 2011-10-27 | オックスフォード ナノポア テクノロジーズ リミテッド | 塩基検出細孔 |
| EP2682460B1 (en) | 2008-07-07 | 2017-04-26 | Oxford Nanopore Technologies Limited | Enzyme-pore constructs |
| CN102216456A (zh) | 2008-09-16 | 2011-10-12 | 塞昆纳姆股份有限公司 | 基于甲基化富集母体样品中胎儿核酸的非侵入性产前诊断用方法和组合物 |
| 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 |
| ES2620012T3 (es) | 2008-09-20 | 2017-06-27 | The Board Of Trustees Of The Leland Stanford Junior University | Diagnóstico no invasivo de la aneuploidia fetal por secuenciación |
| WO2010053587A2 (en) | 2008-11-07 | 2010-05-14 | Mlc Dx Incorporated | Methods of monitoring conditions by sequence analysis |
| US20110301042A1 (en) | 2008-11-11 | 2011-12-08 | Helicos Biosciences Corporation | Methods of sample encoding for multiplex analysis of samples by single molecule sequencing |
| US9181578B2 (en) | 2008-11-18 | 2015-11-10 | Bionano Genomics, Inc. | Polynucleotide mapping and sequencing |
| WO2010065470A2 (en) | 2008-12-01 | 2010-06-10 | Consumer Genetics, Inc. | Compositions and methods for detecting background male dna during fetal sex determination |
| US9051602B2 (en) | 2008-12-22 | 2015-06-09 | Celula, Inc. | Methods and genotyping panels for detecting alleles, genomes, and transcriptomes |
| US8455260B2 (en) | 2009-03-27 | 2013-06-04 | Massachusetts Institute Of Technology | Tagged-fragment map assembly |
| EP2414545B1 (en) | 2009-04-03 | 2017-01-11 | Sequenom, Inc. | Nucleic acid preparation compositions and methods |
| US8246799B2 (en) | 2009-05-28 | 2012-08-21 | Nabsys, Inc. | Devices and methods for analyzing biomolecules and probes bound thereto |
| US20100330557A1 (en) | 2009-06-30 | 2010-12-30 | Zohar Yakhini | Genomic coordinate system |
| US9725315B2 (en) | 2009-09-28 | 2017-08-08 | Bionano Genomics, Inc. | Nanochannel arrays and near-field illumination devices for polymer analysis and related methods |
| AU2010310638A1 (en) | 2009-10-21 | 2012-05-03 | Bionano Genomics, Inc. | Methods and related devices for single molecule whole genome analysis |
| PL2496717T3 (pl) | 2009-11-05 | 2017-11-30 | The Chinese University Of Hong Kong | Analiza genomowa płodu z matczynej próbki biologicznej |
| EP2516680B1 (en) | 2009-12-22 | 2016-04-06 | Sequenom, Inc. | Processes and kits for identifying aneuploidy |
| US10388403B2 (en) | 2010-01-19 | 2019-08-20 | Verinata Health, Inc. | Analyzing copy number variation in the detection of cancer |
| US20120270739A1 (en) | 2010-01-19 | 2012-10-25 | Verinata Health, Inc. | Method for sample analysis of aneuploidies in maternal samples |
| US10662474B2 (en) | 2010-01-19 | 2020-05-26 | Verinata Health, Inc. | Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing |
| WO2011091063A1 (en) | 2010-01-19 | 2011-07-28 | Verinata Health, Inc. | Partition defined detection methods |
| US9323888B2 (en) | 2010-01-19 | 2016-04-26 | Verinata Health, Inc. | Detecting and classifying copy number variation |
| ES2704701T3 (es) | 2010-01-19 | 2019-03-19 | Verinata Health Inc | Nuevo protocolo de preparación de bibliotecas de secuenciación |
| WO2011090556A1 (en) | 2010-01-19 | 2011-07-28 | Verinata Health, Inc. | Methods for determining fraction of fetal nucleic acid in maternal samples |
| US20110312503A1 (en) | 2010-01-23 | 2011-12-22 | Artemis Health, Inc. | Methods of fetal abnormality detection |
| EP2569453B1 (en) | 2010-05-14 | 2015-12-16 | Fluidigm Corporation | Nucleic acid isolation methods |
| CA3037126C (en) | 2010-05-18 | 2023-09-12 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| US20120046877A1 (en) | 2010-07-06 | 2012-02-23 | Life Technologies Corporation | Systems and methods to detect copy number variation |
| EP2596127A2 (en) | 2010-07-23 | 2013-05-29 | Esoterix Genetic Laboratories, LLC | Identification of differentially represented fetal or maternal genomic regions and uses thereof |
| US8700338B2 (en) * | 2011-01-25 | 2014-04-15 | Ariosa Diagnosis, Inc. | Risk calculation for evaluation of fetal aneuploidy |
| BR112013016193B1 (pt) | 2010-12-22 | 2019-10-22 | Natera, Inc. | método ex vivo para determinar se um suposto pai é o pai biológico de um feto que está em gestação em uma gestante e relatório |
| WO2012088348A2 (en) | 2010-12-23 | 2012-06-28 | Sequenom, Inc. | Fetal genetic variation detection |
| US20120190020A1 (en) | 2011-01-25 | 2012-07-26 | Aria Diagnostics, Inc. | Detection of genetic abnormalities |
| BR112013020220B1 (pt) | 2011-02-09 | 2020-03-17 | Natera, Inc. | Método para determinar o estado de ploidia de um cromossomo em um feto em gestação |
| US20120219950A1 (en) * | 2011-02-28 | 2012-08-30 | Arnold Oliphant | Assay systems for detection of aneuploidy and sex determination |
| GB2484764B (en) | 2011-04-14 | 2012-09-05 | Verinata Health Inc | Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies |
| WO2012162884A1 (zh) | 2011-05-31 | 2012-12-06 | 北京贝瑞和康生物技术有限公司 | 检测胚胎或肿瘤染色体拷贝数的试剂盒、装置和方法 |
| US20140235474A1 (en) * | 2011-06-24 | 2014-08-21 | Sequenom, Inc. | Methods and processes for non invasive assessment of a genetic variation |
| SG191757A1 (en) | 2011-06-29 | 2013-08-30 | Bgi Health Service Co Ltd | Noninvasive detection of fetal genetic abnormality |
| WO2013019361A1 (en) | 2011-07-07 | 2013-02-07 | Life Technologies Corporation | Sequencing methods |
| US9367663B2 (en) | 2011-10-06 | 2016-06-14 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP2764459B1 (en) | 2011-10-06 | 2021-06-30 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10424394B2 (en) | 2011-10-06 | 2019-09-24 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US9984198B2 (en) | 2011-10-06 | 2018-05-29 | Sequenom, Inc. | Reducing sequence read count error in assessment of complex genetic variations |
| EP2764458B1 (en) | 2011-10-06 | 2021-04-07 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10196681B2 (en) | 2011-10-06 | 2019-02-05 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US8688388B2 (en) | 2011-10-11 | 2014-04-01 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| ES2624686T3 (es) | 2011-10-11 | 2017-07-17 | Sequenom, Inc. | Métodos y procesos para la evaluación no invasiva de variaciones genéticas |
| WO2013086352A1 (en) * | 2011-12-07 | 2013-06-13 | Chronix Biomedical | Prostate cancer associated circulating nucleic acid biomarkers |
| PL2805280T3 (pl) * | 2012-01-20 | 2022-11-21 | Sequenom, Inc. | Procesy diagnostyczne będące czynnikiem warunków doświadczalnych |
| US9892230B2 (en) | 2012-03-08 | 2018-02-13 | The Chinese University Of Hong Kong | Size-based analysis of fetal or tumor DNA fraction in plasma |
| CA2874195C (en) | 2012-05-21 | 2020-08-25 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10504613B2 (en) | 2012-12-20 | 2019-12-10 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10497461B2 (en) | 2012-06-22 | 2019-12-03 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| GB2533006B (en) | 2012-09-04 | 2017-06-07 | Guardant Health Inc | Systems and methods to detect copy number variation |
| US20140065621A1 (en) | 2012-09-04 | 2014-03-06 | Natera, Inc. | Methods for increasing fetal fraction in maternal blood |
| US10482994B2 (en) | 2012-10-04 | 2019-11-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| WO2014055790A2 (en) | 2012-10-04 | 2014-04-10 | 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 |
| HUE061261T2 (hu) | 2013-04-03 | 2023-05-28 | Sequenom Inc | Eljárások és folyamatok genetikai variánsok nem invazív értékelésére |
| IL309903A (en) | 2013-05-24 | 2024-03-01 | Sequenom Inc | Methods and processes for non-invasive assessment of genetic variations |
| AU2014284180B2 (en) | 2013-06-21 | 2020-03-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US20150004601A1 (en) | 2013-06-28 | 2015-01-01 | Ariosa Diagnostics, Inc. | Massively parallel sequencing of random dna fragments for determination of fetal fraction |
| WO2015026967A1 (en) | 2013-08-20 | 2015-02-26 | Natera, Inc. | Methods of using low fetal fraction detection |
| US10174375B2 (en) | 2013-09-20 | 2019-01-08 | The Chinese University Of Hong Kong | Sequencing analysis of circulating DNA to detect and monitor autoimmune diseases |
| PL3053071T3 (pl) | 2013-10-04 | 2024-03-18 | Sequenom, Inc. | Metody i procesy nieinwazyjnej oceny zmienności genetycznych |
| CN105874082B (zh) | 2013-10-07 | 2020-06-02 | 塞昆纳姆股份有限公司 | 用于非侵入性评估染色体改变的方法和过程 |
| CA3191504A1 (en) | 2014-05-30 | 2015-12-03 | Sequenom, Inc. | Chromosome representation determinations |
| US11783911B2 (en) | 2014-07-30 | 2023-10-10 | Sequenom, Inc | Methods and processes for non-invasive assessment of genetic variations |
| US20180327844A1 (en) | 2015-11-16 | 2018-11-15 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
-
2013
- 2013-01-18 PL PL13707938.0T patent/PL2805280T3/pl unknown
- 2013-01-18 JP JP2014553484A patent/JP6431769B2/ja active Active
- 2013-01-18 EP EP13707938.0A patent/EP2805280B1/en active Active
- 2013-01-18 AU AU2013209499A patent/AU2013209499B2/en active Active
- 2013-01-18 ES ES13707938T patent/ES2929923T3/es active Active
- 2013-01-18 HU HUE13707938A patent/HUE059847T2/hu unknown
- 2013-01-18 EP EP22197208.6A patent/EP4148739A1/en active Pending
- 2013-01-18 CA CA2861856A patent/CA2861856C/en active Active
- 2013-01-18 LT LTEPPCT/US2013/022290T patent/LT2805280T/lt unknown
- 2013-01-18 WO PCT/US2013/022290 patent/WO2013109981A1/en not_active Ceased
- 2013-01-30 US US13/754,817 patent/US11697849B2/en active Active
-
2017
- 2017-02-28 JP JP2017037416A patent/JP2017099406A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP4148739A1 (en) | 2023-03-15 |
| CA2861856C (en) | 2020-06-02 |
| JP2015513392A (ja) | 2015-05-14 |
| US11697849B2 (en) | 2023-07-11 |
| CA2861856A1 (en) | 2013-07-25 |
| AU2013209499A1 (en) | 2014-08-14 |
| AU2013209499B2 (en) | 2018-05-10 |
| HK1202672A1 (en) | 2015-10-02 |
| ES2929923T3 (es) | 2022-12-02 |
| WO2013109981A1 (en) | 2013-07-25 |
| HUE059847T2 (hu) | 2023-01-28 |
| EP2805280B1 (en) | 2022-10-05 |
| JP6431769B2 (ja) | 2018-11-28 |
| US20130150253A1 (en) | 2013-06-13 |
| LT2805280T (lt) | 2022-12-27 |
| JP2017099406A (ja) | 2017-06-08 |
| EP2805280A1 (en) | 2014-11-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HUE059847T2 (hu) | Kísérleti körülményeket fakturáló diagnosztikai folyamatok | |
| IL254716B (en) | Zinc-lysine conjugate | |
| DK3327112T3 (en) | Agse-deficient stamme | |
| DK2830816T3 (en) | Hidtil ukendt coatingkoncept | |
| EP2934531A4 (en) | COMBINATION | |
| EP2935220A4 (en) | PERI-carbinol | |
| EP2874517A4 (en) | SEAT LIFTING ARRANGEMENT | |
| HUP1200607A2 (en) | Diagnostic method | |
| GB201211792D0 (en) | Photocatalysts | |
| EP2905847A4 (en) | TOGETHER | |
| EP2911673A4 (en) | COMBINATION | |
| EP2920142A4 (en) | MÉTHANOFULLERRÈNES | |
| GB201218341D0 (en) | Diagnostic method | |
| EP2925728A4 (en) | COMBINATION | |
| PL2631512T3 (pl) | Pierścień uszczelniający | |
| GB201304493D0 (en) | Not published | |
| EP2908815A4 (en) | COMBINATION | |
| EP2908816A4 (en) | ASSOCIATION | |
| GB201203966D0 (en) | Secure exam | |
| GB201216178D0 (en) | Combination | |
| AU345893S (en) | Treehouse | |
| GB201203045D0 (en) | Chrismar | |
| GB201202980D0 (en) | Stop-love | |
| GB201202979D0 (en) | Ecotunnel | |
| GB201202916D0 (en) | E-Space |