MX2012005217A - Analisis genomico a base de tamaño. - Google Patents
Analisis genomico a base de tamaño.Info
- Publication number
- MX2012005217A MX2012005217A MX2012005217A MX2012005217A MX2012005217A MX 2012005217 A MX2012005217 A MX 2012005217A MX 2012005217 A MX2012005217 A MX 2012005217A MX 2012005217 A MX2012005217 A MX 2012005217A MX 2012005217 A MX2012005217 A MX 2012005217A
- Authority
- MX
- Mexico
- Prior art keywords
- size
- chromosome
- haplotype
- size distribution
- fetus
- Prior art date
Links
Classifications
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- 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
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- 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
- C12Q1/6809—Methods for determination or identification of nucleic acids involving differential detection
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- 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
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- 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
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- 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
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- 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
- C12Q2600/112—Disease subtyping, staging or classification
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- 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
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- 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
- C12Q2600/172—Haplotypes
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Physics & Mathematics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Bioinformatics & Computational Biology (AREA)
- Evolutionary Biology (AREA)
- Medical Informatics (AREA)
- Theoretical Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- Pathology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Abstract
Se proveen sistemas, métodos y aparatos para efectuar un diagnostico prenatal de un desequilibrio de secuencia. Un desplazamiento (por ejemplo, a una distribución de tamaño más pequeña) puede significar un desequilibrio en ciertas circunstancias. Por ejemplo, se puede usar una distribución de tamaño de fragmentos de ácidos nucleicos de un cromosoma en alto riesgo para determinar una aneuploidia cromosomal fetal. Se puede usar una clasificación de tamaño de diferentes cromosomas para determinar intervalos de una clasificación de un cromosoma en alto riesgo a partir de una clasificación esperada. También, una diferencia entre un valor de tamaño estadístico para un cromosoma puede ser comparada con un valor de tamaño estadístico de otro cromosoma para identificar un desplazamiento significativo de tamaño. Un genotipo y haplotipo del feto pueden también ser determinados usando una distribución de tamaño para determinar si se presenta un desequilibrio de secuencia en una muestra materna, en relación con un genotipo o haplotipo de la madre, proporcionando mediante esto un genotipo o haplotipo del feto.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25907609P | 2009-11-06 | 2009-11-06 | |
US36039910P | 2010-06-30 | 2010-06-30 | |
PCT/EP2010/066935 WO2011054936A1 (en) | 2009-11-06 | 2010-11-05 | Size-based genomic analysis |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2012005217A true MX2012005217A (es) | 2012-07-23 |
Family
ID=43530526
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2012005217A MX2012005217A (es) | 2009-11-06 | 2010-11-05 | Analisis genomico a base de tamaño. |
MX2015002302A MX357692B (es) | 2009-11-06 | 2010-11-05 | Analisis genomico a base de tamaño. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2015002302A MX357692B (es) | 2009-11-06 | 2010-11-05 | Analisis genomico a base de tamaño. |
Country Status (12)
Country | Link |
---|---|
US (4) | US8620593B2 (es) |
EP (3) | EP4212630A1 (es) |
JP (2) | JP5770737B2 (es) |
CN (2) | CN107312844B (es) |
AU (1) | AU2010317019B2 (es) |
BR (1) | BR112012010708A2 (es) |
CA (1) | CA2780016C (es) |
EA (1) | EA034241B1 (es) |
IL (1) | IL219545A (es) |
MX (2) | MX2012005217A (es) |
TW (1) | TWI445854B (es) |
WO (1) | WO2011054936A1 (es) |
Families Citing this family (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106676188A (zh) * | 2007-07-23 | 2017-05-17 | 香港中文大学 | 利用基因组测序诊断胎儿染色体非整倍性 |
US8709726B2 (en) | 2008-03-11 | 2014-04-29 | Sequenom, Inc. | Nucleic acid-based tests for prenatal gender determination |
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 |
US8962247B2 (en) | 2008-09-16 | 2015-02-24 | Sequenom, Inc. | Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non invasive prenatal diagnoses |
PL3241914T3 (pl) | 2009-11-05 | 2019-08-30 | The Chinese University Of Hong Kong | Analiza genomowa płodu z matczynej próbki biologicznej |
MX2012005217A (es) * | 2009-11-06 | 2012-07-23 | Univ Hong Kong Chinese | Analisis genomico a base de tamaño. |
WO2011087760A2 (en) | 2009-12-22 | 2011-07-21 | Sequenom, Inc. | Processes and kits for identifying aneuploidy |
CN101921874B (zh) * | 2010-06-30 | 2013-09-11 | 深圳华大基因科技有限公司 | 基于Solexa测序法的检测人类乳头瘤病毒的方法 |
US8700338B2 (en) | 2011-01-25 | 2014-04-15 | Ariosa Diagnosis, Inc. | Risk calculation for evaluation of fetal aneuploidy |
US10533223B2 (en) | 2010-08-06 | 2020-01-14 | Ariosa Diagnostics, Inc. | Detection of target nucleic acids using hybridization |
US20130040375A1 (en) | 2011-08-08 | 2013-02-14 | Tandem Diagnotics, Inc. | Assay systems for genetic analysis |
US20130261003A1 (en) | 2010-08-06 | 2013-10-03 | Ariosa Diagnostics, In. | Ligation-based detection of genetic variants |
US10167508B2 (en) | 2010-08-06 | 2019-01-01 | Ariosa Diagnostics, Inc. | Detection of genetic abnormalities |
US11031095B2 (en) | 2010-08-06 | 2021-06-08 | Ariosa Diagnostics, Inc. | Assay systems for determination of fetal copy number variation |
US11203786B2 (en) | 2010-08-06 | 2021-12-21 | Ariosa Diagnostics, Inc. | Detection of target nucleic acids using hybridization |
US20140342940A1 (en) | 2011-01-25 | 2014-11-20 | Ariosa Diagnostics, Inc. | Detection of Target Nucleic Acids using Hybridization |
US20120034603A1 (en) | 2010-08-06 | 2012-02-09 | Tandem Diagnostics, Inc. | Ligation-based detection of genetic variants |
TWI532843B (zh) | 2010-11-30 | 2016-05-11 | 香港中文大學 | 與癌症有關之基因或分子變異之檢測 |
US9994897B2 (en) | 2013-03-08 | 2018-06-12 | Ariosa Diagnostics, Inc. | Non-invasive fetal sex determination |
US11270781B2 (en) | 2011-01-25 | 2022-03-08 | Ariosa Diagnostics, Inc. | Statistical analysis for non-invasive sex chromosome aneuploidy determination |
US8756020B2 (en) | 2011-01-25 | 2014-06-17 | Ariosa Diagnostics, Inc. | Enhanced risk probabilities using biomolecule estimations |
US10131947B2 (en) | 2011-01-25 | 2018-11-20 | Ariosa Diagnostics, Inc. | Noninvasive detection of fetal aneuploidy in egg donor pregnancies |
US8460872B2 (en) | 2011-04-29 | 2013-06-11 | Sequenom, Inc. | Quantification of a minority nucleic acid species |
US8712697B2 (en) | 2011-09-07 | 2014-04-29 | Ariosa Diagnostics, Inc. | Determination of copy number variations using binomial probability calculations |
US10424394B2 (en) | 2011-10-06 | 2019-09-24 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
EP2771483A1 (en) * | 2011-10-25 | 2014-09-03 | ONCOTYROL - Center for Personalized Cancer Medicine GmbH | Method for diagnosing a disease based on plasma-dna distribution |
WO2013131021A1 (en) | 2012-03-02 | 2013-09-06 | Sequenom Inc. | Methods and processes for non-invasive assessment of genetic variations |
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 |
WO2013138527A1 (en) | 2012-03-13 | 2013-09-19 | The Chinese University Of Hong Kong | Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis |
US9920361B2 (en) | 2012-05-21 | 2018-03-20 | Sequenom, Inc. | Methods and compositions for analyzing nucleic acid |
US10289800B2 (en) | 2012-05-21 | 2019-05-14 | Ariosa Diagnostics, Inc. | Processes for calculating phased fetal genomic sequences |
US10504613B2 (en) | 2012-12-20 | 2019-12-10 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
US11261494B2 (en) | 2012-06-21 | 2022-03-01 | The Chinese University Of Hong Kong | Method of measuring a fractional concentration of tumor DNA |
AU2013290102B2 (en) | 2012-07-13 | 2018-11-15 | Sequenom, Inc. | Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses |
JP2015522293A (ja) | 2012-07-19 | 2015-08-06 | アリオサ ダイアグノスティックス インコーポレイテッドAriosa Diagnostics,Inc. | 多重化連続ライゲーションに基づく遺伝子変異体の検出 |
GB201215449D0 (en) * | 2012-08-30 | 2012-10-17 | Zoragen Biotechnologies Llp | Method of detecting chromosonal abnormalities |
PT3354747T (pt) | 2012-09-20 | 2021-05-07 | Univ Hong Kong Chinese | Determinação não invasiva de metiloma de tumor a partir de plasma |
US10482994B2 (en) | 2012-10-04 | 2019-11-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
WO2014168711A1 (en) | 2013-03-13 | 2014-10-16 | Sequenom, Inc. | Primers for dna methylation analysis |
WO2014139477A1 (en) | 2013-03-15 | 2014-09-18 | The Chinese University Of Hong Kong | Determining fetal genomes for multiple fetus pregnancies |
CN112037860B (zh) * | 2013-06-13 | 2024-02-23 | 豪夫迈·罗氏有限公司 | 用于非入侵性性染色体非整倍性确定的统计分析 |
EP3011051B1 (en) * | 2013-06-21 | 2019-01-30 | Sequenom, Inc. | Method for non-invasive assessment of genetic variations |
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 |
WO2015138774A1 (en) | 2014-03-13 | 2015-09-17 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
CN106795558B (zh) | 2014-05-30 | 2020-07-10 | 维里纳塔健康公司 | 检测胎儿亚染色体非整倍性和拷贝数变异 |
SG11201610134PA (en) | 2014-06-06 | 2017-01-27 | Univ Cornell | Method for identification and enumeration of nucleic acid sequence, expression, copy, or dna methylation changes, using combined nuclease, ligase, polymerase, and sequencing reactions |
PT3543356T (pt) * | 2014-07-18 | 2021-10-04 | Univ Hong Kong Chinese | Análise dos padrões de metilação de tecidos em mistura de adn |
CN117402950A (zh) | 2014-07-25 | 2024-01-16 | 华盛顿大学 | 确定导致无细胞dna的产生的组织和/或细胞类型的方法以及使用其鉴定疾病或紊乱的方法 |
MX2017001405A (es) * | 2014-08-01 | 2017-05-17 | Ariosa Diagnostics Inc | Deteccion de acidos nucleicos diana mediante el uso de hibridacion. |
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 |
US10364467B2 (en) | 2015-01-13 | 2019-07-30 | The Chinese University Of Hong Kong | Using size and number aberrations in plasma DNA for detecting cancer |
US11242559B2 (en) | 2015-01-13 | 2022-02-08 | The Chinese University Of Hong Kong | Method of nuclear DNA and mitochondrial DNA analysis |
US10319463B2 (en) | 2015-01-23 | 2019-06-11 | The Chinese University Of Hong Kong | Combined size- and count-based analysis of maternal plasma for detection of fetal subchromosomal aberrations |
SG11201706529TA (en) | 2015-02-10 | 2017-09-28 | Univ Hong Kong Chinese | Detecting mutations for cancer screening and fetal analysis |
CN104789686B (zh) * | 2015-05-06 | 2018-09-07 | 浙江安诺优达生物科技有限公司 | 检测染色体非整倍性的试剂盒和装置 |
US11111538B2 (en) | 2015-05-22 | 2021-09-07 | Nipd Genetics Public Company Ltd | Multiplexed parallel analysis of targeted genomic regions for non-invasive prenatal testing |
CA2993588A1 (en) | 2015-07-20 | 2017-01-26 | The Chinese University Of Hong Kong | Methylation pattern analysis of haplotypes in tissues in dna mixture |
US10453556B2 (en) | 2015-07-23 | 2019-10-22 | The Chinese University Of Hong Kong | Analysis of fragmentation patterns of cell-free DNA |
MY188348A (en) | 2015-08-12 | 2021-12-02 | Univ Hong Kong Chinese | Single-molecule sequencing of plasma dna |
US10095831B2 (en) | 2016-02-03 | 2018-10-09 | Verinata Health, Inc. | Using cell-free DNA fragment size to determine copy number variations |
CA3020669A1 (en) * | 2016-04-11 | 2017-10-19 | Quantum Biosystems Inc. | Systems and methods for biological data management |
EP3518974A4 (en) | 2016-09-29 | 2020-05-27 | Myriad Women's Health, Inc. | NON-INVASIVE PRENATAL SCREENING USING DYNAMIC ITERATIVE DEEP OPTIMIZATION |
CN109890984B (zh) | 2016-10-19 | 2024-03-29 | 香港中文大学 | 通过母体血浆dna的甲基化和大小谱分析进行胎龄评估 |
EP3535415A4 (en) | 2016-10-24 | 2020-07-01 | The Chinese University of Hong Kong | TUMOR DETECTION METHODS AND SYSTEMS |
CN106591451B (zh) | 2016-12-14 | 2020-06-23 | 北京贝瑞和康生物技术有限公司 | 测定胎儿游离dna含量的方法及其用于实施该方法的装置 |
TWI803477B (zh) | 2017-01-25 | 2023-06-01 | 香港中文大學 | 使用核酸片段之診斷應用 |
CA3058551A1 (en) * | 2017-03-31 | 2018-10-04 | Premaitha Limited | Method of detecting a fetal chromosomal abnormality |
US11342047B2 (en) | 2017-04-21 | 2022-05-24 | Illumina, Inc. | Using cell-free DNA fragment size to detect tumor-associated variant |
IL272030B1 (en) | 2017-07-26 | 2024-11-01 | The Chinese Univ Of Hong Kong | Improving cancer screening using cell-free viral nucleic acids |
US11168356B2 (en) | 2017-11-02 | 2021-11-09 | The Chinese University Of Hong Kong | Using nucleic acid size range for noninvasive cancer detection |
CN108827887B (zh) * | 2018-03-19 | 2021-05-18 | 陕西学前师范学院 | 一种商陆基因组大小估计方法及基因组大小测量系统 |
CN112292458A (zh) | 2018-05-03 | 2021-01-29 | 香港中文大学 | 测量无细胞混合物特性的尺寸标记的优选末端和识别方向的分析 |
EP3947717A4 (en) | 2019-03-25 | 2022-12-28 | The Chinese University Of Hong Kong | DETERMINATION OF LINEAR AND ROUND SHAPES OF CIRCULATION NUCLEIC ACIDS |
EP4020484A4 (en) * | 2019-08-19 | 2023-08-30 | Green Cross Genome Corporation | METHOD FOR DETECTING A CHROMOSOME ABNORMALITY USING INFORMATION CONCERNING THE DISTANCE BETWEEN NUCLEIC ACID FRAGMENTS |
KR102662186B1 (ko) * | 2020-02-05 | 2024-05-07 | 더 차이니즈 유니버시티 오브 홍콩 | 임신 중 긴 세포유리 단편을 사용한 분자 분석 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0016742D0 (en) * | 2000-07-10 | 2000-08-30 | Simeg Limited | Diagnostic method |
US6664056B2 (en) * | 2000-10-17 | 2003-12-16 | The Chinese University Of Hong Kong | Non-invasive prenatal monitoring |
KR20030088464A (ko) * | 2001-03-23 | 2003-11-19 | 진셀 소시에테 아노님 | 2본쇄 dna 표적 서열을 3중 나선 상호작용에 의해 정제및 검출하는 방법 |
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 |
AU2004217872B2 (en) | 2003-03-05 | 2010-03-25 | Genetic Technologies Limited | Identification of fetal DNA and fetal cell markers in maternal plasma or serum |
AU2003901671A0 (en) * | 2003-04-02 | 2003-05-01 | The University Of Adelaide | Comparative genomic hybridization |
ATE435301T1 (de) | 2003-10-16 | 2009-07-15 | Sequenom Inc | Nicht invasiver nachweis fötaler genetischer merkmale |
JP5219516B2 (ja) * | 2005-03-18 | 2013-06-26 | ザ チャイニーズ ユニバーシティー オブ ホンコン | 染色体異数性の検出方法 |
US20070122823A1 (en) | 2005-09-01 | 2007-05-31 | Bianchi Diana W | Amniotic fluid cell-free fetal DNA fragment size pattern for prenatal diagnosis |
HUE030215T2 (en) | 2006-02-02 | 2017-04-28 | Univ Leland Stanford Junior | Non-invasive fetal genetic screening by digital analysis |
EP2351858B1 (en) | 2006-02-28 | 2014-12-31 | University of Louisville Research Foundation | Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms |
ES2391212T3 (es) * | 2006-12-07 | 2012-11-22 | Novartis Ag | Cribado genético prenatal no-invasivo |
US20100112590A1 (en) | 2007-07-23 | 2010-05-06 | The Chinese University Of Hong Kong | Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment |
CN106676188A (zh) | 2007-07-23 | 2017-05-17 | 香港中文大学 | 利用基因组测序诊断胎儿染色体非整倍性 |
US20090053719A1 (en) | 2007-08-03 | 2009-02-26 | The Chinese University Of Hong Kong | Analysis of nucleic acids by digital pcr |
WO2010053980A2 (en) | 2008-11-04 | 2010-05-14 | The Johns Hopkins University | Dna integrity assay (dia) for cancer diagnostics, using confocal fluorescence spectroscopy |
RU2011143425A (ru) | 2009-03-31 | 2013-05-10 | Оридис Биомаркерс Гмбх | Способ диагностики рака и мониторинга лечения рака |
WO2011053790A2 (en) | 2009-10-30 | 2011-05-05 | Fluidigm Corporation | Assay of closely linked targets in fetal diagnosis and coincidence detection assay for genetic analysis |
MX2012005217A (es) * | 2009-11-06 | 2012-07-23 | Univ Hong Kong Chinese | Analisis genomico a base de tamaño. |
US10662474B2 (en) | 2010-01-19 | 2020-05-26 | Verinata Health, Inc. | Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing |
GB2479080B (en) | 2010-01-19 | 2012-01-18 | Verinata Health Inc | Sequencing methods and compositions for prenatal diagnoses |
EP2536854B1 (en) | 2010-02-18 | 2017-07-19 | The Johns Hopkins University | Personalized tumor biomarkers |
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 |
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2010
- 2010-11-05 MX MX2012005217A patent/MX2012005217A/es active IP Right Grant
- 2010-11-05 EP EP23160186.5A patent/EP4212630A1/en active Pending
- 2010-11-05 EP EP18182983.9A patent/EP3406737B1/en active Active
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US8620593B2 (en) | 2013-12-31 |
BR112012010708A2 (pt) | 2016-03-29 |
IL219545A0 (en) | 2012-06-28 |
IL219545A (en) | 2015-02-26 |
JP5770737B2 (ja) | 2015-08-26 |
EA201200701A1 (ru) | 2012-12-28 |
JP2015165805A (ja) | 2015-09-24 |
EP3406737A1 (en) | 2018-11-28 |
EP2496713B1 (en) | 2018-07-18 |
JP6001721B2 (ja) | 2016-10-05 |
CN107312844B (zh) | 2021-01-22 |
TWI445854B (zh) | 2014-07-21 |
JP2013509870A (ja) | 2013-03-21 |
US20180237858A1 (en) | 2018-08-23 |
US20140080720A1 (en) | 2014-03-20 |
US11365448B2 (en) | 2022-06-21 |
US20220282332A1 (en) | 2022-09-08 |
WO2011054936A1 (en) | 2011-05-12 |
CN107312844A (zh) | 2017-11-03 |
EP4212630A1 (en) | 2023-07-19 |
CN102791881A (zh) | 2012-11-21 |
EP2496713A1 (en) | 2012-09-12 |
EA034241B1 (ru) | 2020-01-21 |
CA2780016A1 (en) | 2011-05-12 |
US9982300B2 (en) | 2018-05-29 |
TW201129736A (en) | 2011-09-01 |
AU2010317019A1 (en) | 2012-05-31 |
CN102791881B (zh) | 2017-08-08 |
CA2780016C (en) | 2017-09-19 |
US20110276277A1 (en) | 2011-11-10 |
AU2010317019B2 (en) | 2014-10-30 |
EP3406737B1 (en) | 2023-05-31 |
MX357692B (es) | 2018-07-19 |
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