[go: up one dir, main page]

MX2019000037A - Metodos para perfilado de fragmentoma de acidos nucleicos libres de celula. - Google Patents

Metodos para perfilado de fragmentoma de acidos nucleicos libres de celula.

Info

Publication number
MX2019000037A
MX2019000037A MX2019000037A MX2019000037A MX2019000037A MX 2019000037 A MX2019000037 A MX 2019000037A MX 2019000037 A MX2019000037 A MX 2019000037A MX 2019000037 A MX2019000037 A MX 2019000037A MX 2019000037 A MX2019000037 A MX 2019000037A
Authority
MX
Mexico
Prior art keywords
cell
methods
dna
nucleic acids
free nucleic
Prior art date
Application number
MX2019000037A
Other languages
English (en)
Inventor
Abdueva Diana
Original Assignee
Guardant Health Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Guardant Health Inc filed Critical Guardant Health Inc
Publication of MX2019000037A publication Critical patent/MX2019000037A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B25/00ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
    • G16B25/10Gene or protein expression profiling; Expression-ratio estimation or normalisation
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B20/00ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
    • G16B20/10Ploidy or copy number detection
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B20/00ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
    • G16B20/20Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B30/00ICT specially adapted for sequence analysis involving nucleotides or amino acids
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B30/00ICT specially adapted for sequence analysis involving nucleotides or amino acids
    • G16B30/10Sequence alignment; Homology search
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B40/00ICT specially adapted for biostatistics; ICT specially adapted for bioinformatics-related machine learning or data mining, e.g. knowledge discovery or pattern finding
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/154Methylation markers
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B20/00ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medical Informatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Theoretical Computer Science (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Evolutionary Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Artificial Intelligence (AREA)
  • Software Systems (AREA)
  • Public Health (AREA)
  • Evolutionary Computation (AREA)
  • Epidemiology (AREA)
  • Databases & Information Systems (AREA)
  • Data Mining & Analysis (AREA)
  • Computer Vision & Pattern Recognition (AREA)
  • Bioethics (AREA)
  • Organic Chemistry (AREA)
  • Pathology (AREA)
  • Immunology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Oncology (AREA)
  • Microbiology (AREA)
  • Hospice & Palliative Care (AREA)
  • General Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La presente descripción contempla varios usos de ADN libre de célula. Los métodos proporcionados en la presente pueden usar información de secuencia de una manera global y de macroescala, con o sin información de variantes somáticas, para valorar un perfil de fragmentoma que puede ser representativo de un tejido de origen, enfermedad, progresión, etc. En un aspecto, en la presente se describe un método para determinar la presencia o ausencia de una anormalidad genética en fragmentos de ácido desoxirribonucleico (ADN) de ADN libre de célula obtenido de un sujeto, el método que comprende: (a) construir una distribución multiparamétrica de los fragmentos de ADN sobre una pluralidad de posiciones base en un genoma; y (b) sin tomar en cuenta una identidad base de cada posición base en un primer locus, usar la distribución multiparamétrica para determinar la presencia o ausencia de la anormalidad genética en el primer locus en el sujeto.
MX2019000037A 2016-07-06 2017-07-06 Metodos para perfilado de fragmentoma de acidos nucleicos libres de celula. MX2019000037A (es)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201662359151P 2016-07-06 2016-07-06
US201662420167P 2016-11-10 2016-11-10
US201662437172P 2016-12-21 2016-12-21
US201762489399P 2017-04-24 2017-04-24
PCT/US2017/040986 WO2018009723A1 (en) 2016-07-06 2017-07-06 Methods for fragmentome profiling of cell-free nucleic acids

Publications (1)

Publication Number Publication Date
MX2019000037A true MX2019000037A (es) 2019-07-10

Family

ID=60913158

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2019000037A MX2019000037A (es) 2016-07-06 2017-07-06 Metodos para perfilado de fragmentoma de acidos nucleicos libres de celula.

Country Status (11)

Country Link
EP (2) EP4322168A3 (es)
JP (3) JP7448310B2 (es)
KR (1) KR102610098B1 (es)
CN (1) CN109689891B (es)
AU (1) AU2017292854B2 (es)
BR (1) BR112019000296A2 (es)
CA (1) CA3030038A1 (es)
ES (1) ES2967443T3 (es)
MX (1) MX2019000037A (es)
SG (1) SG11201811556RA (es)
WO (1) WO2018009723A1 (es)

Families Citing this family (108)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11111543B2 (en) 2005-07-29 2021-09-07 Natera, Inc. System and method for cleaning noisy genetic data and determining chromosome copy number
US9424392B2 (en) 2005-11-26 2016-08-23 Natera, Inc. System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals
US11111544B2 (en) 2005-07-29 2021-09-07 Natera, Inc. System and method for cleaning noisy genetic data and determining chromosome copy number
US11408031B2 (en) 2010-05-18 2022-08-09 Natera, Inc. Methods for non-invasive prenatal paternity testing
US11322224B2 (en) 2010-05-18 2022-05-03 Natera, Inc. Methods for non-invasive prenatal ploidy calling
EP2854057B1 (en) 2010-05-18 2018-03-07 Natera, Inc. Methods for non-invasive pre-natal ploidy calling
US11332793B2 (en) 2010-05-18 2022-05-17 Natera, Inc. Methods for simultaneous amplification of target loci
US11326208B2 (en) 2010-05-18 2022-05-10 Natera, Inc. Methods for nested PCR amplification of cell-free DNA
US9677118B2 (en) 2014-04-21 2017-06-13 Natera, Inc. Methods for simultaneous amplification of target loci
US12221653B2 (en) 2010-05-18 2025-02-11 Natera, Inc. Methods for simultaneous amplification of target loci
US12152275B2 (en) 2010-05-18 2024-11-26 Natera, Inc. Methods for non-invasive prenatal ploidy calling
US20190010543A1 (en) 2010-05-18 2019-01-10 Natera, Inc. Methods for simultaneous amplification of target loci
US11339429B2 (en) 2010-05-18 2022-05-24 Natera, Inc. Methods for non-invasive prenatal ploidy calling
US11939634B2 (en) 2010-05-18 2024-03-26 Natera, Inc. Methods for simultaneous amplification of target loci
US10316362B2 (en) 2010-05-18 2019-06-11 Natera, Inc. Methods for simultaneous amplification of target loci
US11332785B2 (en) 2010-05-18 2022-05-17 Natera, Inc. Methods for non-invasive prenatal ploidy calling
EP2673729B1 (en) 2011-02-09 2018-10-17 Natera, Inc. Methods for non-invasive prenatal ploidy calling
EP3907297A1 (en) 2011-04-15 2021-11-10 The Johns Hopkins University Safe sequencing system
US20140100126A1 (en) 2012-08-17 2014-04-10 Natera, Inc. Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data
ES2886507T5 (es) 2012-10-29 2024-11-15 Univ Johns Hopkins Prueba de Papanicolaou para cánceres de ovario y de endometrio
JP6659575B2 (ja) 2014-04-21 2020-03-04 ナテラ, インコーポレイテッド 変異の検出および染色体分節の倍数性
US20180173845A1 (en) 2014-06-05 2018-06-21 Natera, Inc. Systems and Methods for Detection of Aneuploidy
US11479812B2 (en) 2015-05-11 2022-10-25 Natera, Inc. Methods and compositions for determining ploidy
ES2960201T3 (es) 2015-07-23 2024-03-01 Univ Hong Kong Chinese Análisis de los patrones de fragmentación del ADN acelular
WO2017027653A1 (en) 2015-08-11 2017-02-16 The Johns Hopkins University Assaying ovarian cyst fluid
CN109312400A (zh) 2016-03-25 2019-02-05 凯锐思公司 合成核酸掺入物
WO2017181202A2 (en) 2016-04-15 2017-10-19 Natera, Inc. Methods for lung cancer detection
US11485996B2 (en) 2016-10-04 2022-11-01 Natera, Inc. Methods for characterizing copy number variation using proximity-litigation sequencing
US10011870B2 (en) 2016-12-07 2018-07-03 Natera, Inc. Compositions and methods for identifying nucleic acid molecules
JP7300989B2 (ja) 2016-12-22 2023-06-30 ガーダント ヘルス, インコーポレイテッド 核酸分子を解析するための方法およびシステム
DK3574108T3 (da) 2017-01-25 2024-09-16 Univ Hong Kong Chinese Diagnostisk anvendelse ved brug af nukleinsyrefragment
WO2019016353A1 (en) * 2017-07-21 2019-01-24 F. Hoffmann-La Roche Ag CLASSIFICATION OF SOMATIC MUTATIONS FROM A HETEROGENEOUS SAMPLE
IL319255A (en) 2017-08-07 2025-04-01 Univ Johns Hopkins Methods and materials for cancer assessment and treatment
WO2019060716A1 (en) 2017-09-25 2019-03-28 Freenome Holdings, Inc. SAMPLE EXTRACTION METHODS AND SYSTEMS
CA3085933A1 (en) 2017-12-14 2019-06-20 Tai Diagnostics, Inc. Assessing graft suitability for transplantation
WO2019147663A1 (en) * 2018-01-24 2019-08-01 Freenome Holdings, Inc. Methods and systems for abnormality detection in the patterns of nucleic acids
EP3762513A1 (en) * 2018-03-08 2021-01-13 St. Johns University Circulating serum cell-free dna biomarkers and methods
EP3765633A4 (en) * 2018-03-13 2021-12-01 Grail, Inc. PROCESS AND SYSTEM FOR THE SELECTION, ADMINISTRATION AND ANALYSIS OF HIGH DIMENSIONAL DATA
WO2019178563A1 (en) * 2018-03-15 2019-09-19 The Board Of Trustees Of Leland Stanford Junior University Methods using nucleic acid signals for revealing biological attributes
CA3095056A1 (en) * 2018-04-13 2019-10-17 Freenome Holdings, Inc. Machine learning implementation for multi-analyte assay of biological samples
AU2019253112A1 (en) * 2018-04-13 2020-10-29 Grail, Llc Multi-assay prediction model for cancer detection
JP7573443B2 (ja) 2018-04-14 2024-10-25 ナテラ, インコーポレイテッド 循環腫瘍dnaの個別化された検出を用いる癌検出およびモニタリングの方法
CN112888459B (zh) 2018-06-01 2023-05-23 格里尔公司 卷积神经网络系统及数据分类方法
WO2020006369A1 (en) * 2018-06-29 2020-01-02 Guardant Health, Inc. Methods and systems for analysis of ctcf binding regions in cell-free dna
US12234509B2 (en) 2018-07-03 2025-02-25 Natera, Inc. Methods for detection of donor-derived cell-free DNA
US20200075124A1 (en) * 2018-09-04 2020-03-05 Guardant Health, Inc. Methods and systems for detecting allelic imbalance in cell-free nucleic acid samples
JP7654538B2 (ja) * 2018-10-08 2025-04-01 フリーノム ホールディングス,インク. 転写因子プロファイリング
GB201818159D0 (en) * 2018-11-07 2018-12-19 Cancer Research Tech Ltd Enhanced detection of target dna by fragment size analysis
WO2020106893A1 (en) 2018-11-21 2020-05-28 Karius, Inc. Direct-to-library methods, systems, and compositions
CN113227468A (zh) * 2018-11-21 2021-08-06 卡里乌斯公司 感染性疾病的检测和预测
US10468141B1 (en) * 2018-11-28 2019-11-05 Asia Genomics Pte. Ltd. Ancestry-specific genetic risk scores
US11581062B2 (en) 2018-12-10 2023-02-14 Grail, Llc Systems and methods for classifying patients with respect to multiple cancer classes
ES2968457T3 (es) * 2018-12-19 2024-05-09 Univ Hong Kong Chinese Características de los extremos del ADN extracelular circulante
EP3899049A1 (en) * 2018-12-21 2021-10-27 F. Hoffmann-La Roche AG Identification of global sequence features in whole genome sequence data from circulating nucelic acid
CA3122109A1 (en) * 2018-12-21 2020-06-25 Grail, Inc. Systems and methods for using fragment lengths as a predictor of cancer
WO2020150258A1 (en) * 2019-01-15 2020-07-23 Luminist, Inc. Methods and systems for detecting liver disease
EP3914731A1 (en) * 2019-01-24 2021-12-01 Illumina, Inc. Methods and systems for monitoring organ health and disease
CN113661249B (zh) 2019-01-31 2025-07-01 夸登特健康公司 用于分离无细胞dna的组合物和方法
EP3924503A4 (en) 2019-02-12 2023-03-08 Tempus Labs, Inc. DETECTION OF LOSS OF HETEROZYGOTIA OF HUMAN LEUCOCYTE ANTIGEN
US11475978B2 (en) 2019-02-12 2022-10-18 Tempus Labs, Inc. Detection of human leukocyte antigen loss of heterozygosity
WO2020176659A1 (en) * 2019-02-27 2020-09-03 Guardant Health, Inc. Methods and systems for determining the cellular origin of cell-free dna
WO2020214547A1 (en) * 2019-04-15 2020-10-22 Natera, Inc. Improved liquid biopsy using size selection
EP4425506A3 (en) 2019-05-22 2024-12-04 Grail, Inc. Systems and methods for determining whether a subject has a cancer condition using transfer learning
US11939636B2 (en) 2019-05-31 2024-03-26 Guardant Health, Inc. Methods and systems for improving patient monitoring after surgery
WO2020247263A1 (en) 2019-06-06 2020-12-10 Natera, Inc. Methods for detecting immune cell dna and monitoring immune system
WO2021007462A1 (en) * 2019-07-09 2021-01-14 The Translational Genomics Research Institute METHODS OF DETECTING DISEASE AND TREATMENT RESPONSE IN cfDNA
WO2021041968A1 (en) * 2019-08-28 2021-03-04 Grail, Inc. Systems and methods for predicting and monitoring treatment response from cell-free nucleic acids
CN110706749B (zh) * 2019-09-10 2022-06-10 至本医疗科技(上海)有限公司 一种基于组织器官分化层次关系的癌症类型预测系统和方法
US11891653B2 (en) 2019-09-30 2024-02-06 Guardant Health, Inc. Compositions and methods for analyzing cell-free DNA in methylation partitioning assays
EP4041888A4 (en) * 2019-10-11 2023-11-01 Guardant Health, Inc. Use of cell free bacterial nucleic acids for detection of cancer
CN114746560A (zh) 2019-11-26 2022-07-12 夸登特健康公司 改进甲基化多核苷酸结合的方法、组合物和系统
CA3163405A1 (en) * 2019-11-29 2021-06-03 GC Genome Corporation Artificial intelligence-based chromosomal abnormality detection method
CN115151657A (zh) * 2019-12-20 2022-10-04 安可济控股有限公司 用于疾病检测的方法和系统
US20230042332A1 (en) * 2019-12-24 2023-02-09 Vib Vzw Disease Detection in Liquid Biopsies
EP4143338A1 (en) 2020-04-30 2023-03-08 Guardant Health, Inc. Methods for sequence determination using partitioned nucleic acids
EP4154255A4 (en) * 2020-05-22 2024-07-17 Aqtual, Inc. METHODS FOR CHARACTERIZING CELL-FREE NUCLEIC ACID FRAGMENTS
WO2023282916A1 (en) 2021-07-09 2023-01-12 Guardant Health, Inc. Methods of detecting genomic rearrangements using cell free nucleic acids
EP4407042A3 (en) 2020-07-10 2024-09-18 Guardant Health, Inc. Methods of detecting genomic rearrangements using cell free nucleic acids
EP4585697A2 (en) 2020-07-30 2025-07-16 Guardant Health, Inc. Methods for isolating cell-free dna
EP4205126A1 (en) 2020-08-25 2023-07-05 Guardant Health, Inc. Methods and systems for predicting an origin of a variant
EP4214329A4 (en) * 2020-09-17 2024-12-04 The Regents of the University of Colorado, a body corporate Signatures in cell-free dna to detect disease, track treatment response, and inform treatment decisions
US20220154285A1 (en) 2020-09-30 2022-05-19 Guardant Health, Inc. Analysis of methylated dna comprising methylation-sensitive or methylation-dependent restrictions
EP4232599A1 (en) 2020-10-23 2023-08-30 Guardant Health, Inc. Compositions and methods for analyzing dna using partitioning and base conversion
EP4251765A1 (en) 2020-11-30 2023-10-04 Guardant Health, Inc. Compositions and methods for enriching methylated polynucleotides
CN114634982A (zh) * 2020-12-15 2022-06-17 广州市基准医疗有限责任公司 一种检测多核苷酸变异的方法
EP4015650A1 (en) * 2020-12-18 2022-06-22 Nipd Genetics Biotech Limited Methods for classifying a sample into clinically relevant categories
WO2022140629A1 (en) 2020-12-23 2022-06-30 Guardant Health, Inc. Methods and systems for analyzing methylated polynucleotides
WO2022174109A1 (en) 2021-02-12 2022-08-18 Guardant Health, Inc. Methods and compositions for detecting nucleic acid variants
WO2022204730A1 (en) 2021-03-25 2022-09-29 Guardant Health, Inc. Methods and compositions for quantifying immune cell dna
EP4347884A1 (en) * 2021-05-24 2024-04-10 University of Essex Enterprises Limited Method and system for identifying genomic regions with condition sensitive occupancy/positioning of nucleosomes and/or chromatin
KR20220160805A (ko) * 2021-05-28 2022-12-06 한국과학기술원 조직 특이적 조절지역의 무세포 dna 분포를 이용한 인공지능 기반 암 조기진단 방법
CN113838533B (zh) * 2021-08-17 2024-03-12 福建和瑞基因科技有限公司 一种癌症检测模型及其构建方法和试剂盒
CA3236814A1 (en) * 2021-11-17 2023-05-25 Maximilian Diehn Systems and methods for gene expression and tissue of origin inference from cell-free dna
WO2023197004A1 (en) 2022-04-07 2023-10-12 Guardant Health, Inc. Detecting the presence of a tumor based on methylation status of cell-free nucleic acid molecules
EP4532762A1 (en) * 2022-06-02 2025-04-09 The Board Of Trustees Of The Leland Stanford Junior University Single molecule sequencing and methylation profiling of cell-free dna
WO2024006908A1 (en) 2022-06-30 2024-01-04 Guardant Health, Inc. Enrichment of aberrantly methylated dna
US20240043935A1 (en) * 2022-07-29 2024-02-08 Centre For Novostics Limited Epigenetics analysis of cell-free dna
WO2024073508A2 (en) 2022-09-27 2024-04-04 Guardant Health, Inc. Methods and compositions for quantifying immune cell dna
CN115295074B (zh) * 2022-10-08 2022-12-16 南京世和基因生物技术股份有限公司 基因标志物在恶性肺结节筛查中的应用、筛查模型的构建方法和检测装置
WO2024138180A2 (en) 2022-12-22 2024-06-27 Guardant Health, Inc. Integrated targeted and whole genome somatic and dna methylation sequencing workflows
WO2024137880A2 (en) 2022-12-22 2024-06-27 Guardant Health, Inc. Methods involving methylation preserving amplification with error correction
WO2024233502A1 (en) 2023-05-05 2024-11-14 Guardant Health, Inc. Cell-free dna blood-based test for cancer screening
WO2025019370A1 (en) * 2023-07-14 2025-01-23 Natera, Inc. Methods for assaying circulating tumor dna
WO2025029475A1 (en) 2023-07-28 2025-02-06 Guardant Health, Inc. Methods to enrich nucleotide variants by negative selection
WO2025038399A1 (en) 2023-08-11 2025-02-20 Guardant Health, Inc. Methylated enrichment methods for single-molecule genetic and epigenetic sequencing
CN117230165A (zh) * 2023-09-01 2023-12-15 深圳湾实验室 一种无创产前检测胎儿染色体拷贝数异常的优化方法
WO2025064706A1 (en) 2023-09-19 2025-03-27 Guardant Health, Inc. Detecting the presence of a tumor based on methylation status of cell-free nucleic acid molecules
WO2025076452A1 (en) 2023-10-06 2025-04-10 Guardant Health, Inc. Detecting tumor-related information based on methylation status of cell-free nucleic acid molecules

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
CA2741117A1 (en) * 2008-10-30 2010-05-06 Centre De Recherche Public De La Sante Biomarkers for heart failure
CN101901345B (zh) * 2009-05-27 2013-02-27 复旦大学 一种差异蛋白质组学的分类方法
US11322224B2 (en) * 2010-05-18 2022-05-03 Natera, Inc. Methods for non-invasive prenatal ploidy calling
EP2426217A1 (en) * 2010-09-03 2012-03-07 Centre National de la Recherche Scientifique (CNRS) Analytical methods for cell free nucleic acids and applications
WO2013015793A1 (en) * 2011-07-26 2013-01-31 Verinata Health, Inc. Method for determining the presence or absence of different aneuploidies in a sample
WO2013052913A2 (en) * 2011-10-06 2013-04-11 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US9367663B2 (en) * 2011-10-06 2016-06-14 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
BR112014020211A2 (pt) * 2012-02-16 2017-07-04 Oxford Nanopore Tech Ltd métodos para analisar uma série ordenada por tempo de medições de um polímero, para estimar a presença, ausência ou quantidade de um polímero alvo, e para determinar uma alteração em um polímero, programa de computador, e, dispositivos de análise e de diagnóstico
CN107435070A (zh) * 2012-04-12 2017-12-05 维里纳塔健康公司 拷贝数变异的检测和分类
US10497461B2 (en) * 2012-06-22 2019-12-03 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
WO2014149134A2 (en) * 2013-03-15 2014-09-25 Guardant Health Inc. Systems and methods to detect rare mutations and copy number variation
US20160040229A1 (en) * 2013-08-16 2016-02-11 Guardant Health, Inc. Systems and methods to detect rare mutations and copy number variation
WO2014039556A1 (en) 2012-09-04 2014-03-13 Guardant Health, Inc. Systems and methods to detect rare mutations and copy number variation
US20130309666A1 (en) * 2013-01-25 2013-11-21 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
AU2014281635B2 (en) * 2013-06-17 2020-05-28 Verinata Health, Inc. Method for determining copy number variations in sex chromosomes
US9499870B2 (en) * 2013-09-27 2016-11-22 Natera, Inc. Cell free DNA diagnostic testing standards
CN111534580B (zh) 2013-12-28 2024-06-04 夸登特健康公司 用于检测遗传变异的方法和系统
KR102566176B1 (ko) * 2014-05-30 2023-08-10 베리나타 헬스, 인코포레이티드 태아 아-염색체 홀배수체 및 복제수 변이 탐지
JP2017522908A (ja) * 2014-07-25 2017-08-17 ユニヴァーシティ オブ ワシントン セルフリーdnaを生じる組織及び/又は細胞タイプを決定する方法、並びにそれを用いて疾患又は異常を識別する方法
EP3502273B1 (en) * 2014-12-12 2020-07-08 Verinata Health, Inc. Cell-free dna fragment

Also Published As

Publication number Publication date
AU2017292854A1 (en) 2019-01-24
KR20190026837A (ko) 2019-03-13
EP3481966A1 (en) 2019-05-15
CN109689891A (zh) 2019-04-26
ES2967443T3 (es) 2024-04-30
EP3481966B1 (en) 2023-11-08
EP4322168A3 (en) 2024-05-15
JP7448310B2 (ja) 2024-03-12
WO2018009723A1 (en) 2018-01-11
JP2019531700A (ja) 2019-11-07
EP3481966A4 (en) 2019-08-07
SG11201811556RA (en) 2019-01-30
KR102610098B1 (ko) 2023-12-04
JP2022025101A (ja) 2022-02-09
AU2017292854B2 (en) 2023-08-17
EP4322168A2 (en) 2024-02-14
BR112019000296A2 (pt) 2019-04-16
CN109689891B (zh) 2024-06-18
CA3030038A1 (en) 2018-01-11
JP2024119898A (ja) 2024-09-03

Similar Documents

Publication Publication Date Title
MX2019000037A (es) Metodos para perfilado de fragmentoma de acidos nucleicos libres de celula.
EP4269577A3 (en) Nucleobase editors and uses thereof
MX2023014124A (es) Identificacion, fabricacion y uso de neoantigeno.
FI3604532T3 (fi) Uusia crispr-entsyymejä ja järjestelmiä
MX2016016713A (es) Procesos y sistemas para el montaje de secuencias de acido nucleico.
AU2017257225A1 (en) Allele editing and applications thereof
WO2019108555A8 (en) Models for targeted sequencing
MX2015017110A (es) Integracion dirigida.
HK1258869A1 (zh) 寡核酸變體文庫及其合成
EP4428863A3 (en) Methods and compositions for determining ploidy
CA2983023A1 (en) Methods for screening bacteria, archaea, algae, and yeast using crispr nucleic acids
BR112015012375A2 (pt) modificação e regulação de genoma à base de crispr
MX2022009242A (es) Producto en desarrollo de analisis de secuenciacion de alineacion y variante.
SG10201809564YA (en) Composition for cleaving a target dna comprising a guide rna specific for the target dna and cas protein-encoding nucleic acid or cas protein, and use thereof
EP3699280A3 (en) Novel cas9 systems and methods of use
EA201992795A1 (ru) Способ получения эукариотических клеток с отредактированной днк и набор, используемый в этом способе
WO2014145820A3 (en) Multiple tagging of long dna fragments
MX2018001617A (es) Composiciones de crispr-cas9 diseñados y metodos de uso.
EP4375373A3 (en) Cas variants for gene editing
NZ728437A (en) Methods for increasing cas9-mediated engineering efficiency
HK1246180A1 (zh) 使用自然殺傷細胞治療血液病症、實體瘤或感染性疾病的方法
WO2018170614A8 (zh) 基因组大片段直接克隆和dna多分子组装新技术
WO2014116729A3 (en) Haplotying of hla loci with ultra-deep shotgun sequencing
HRP20211419T1 (hr) Predviđanje epitopa t-stanica korisnih za cijepljenje
EP3845640A3 (en) Modified tranposases for improved insertion sequence bias and increased dna input tolerence