DK3649257T3 - Berigelse af målrettede genomiske regioner til multiplekset parallel analyse - Google Patents

Berigelse af målrettede genomiske regioner til multiplekset parallel analyse Download PDF

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Publication number
DK3649257T3
DK3649257T3 DK18745508.4T DK18745508T DK3649257T3 DK 3649257 T3 DK3649257 T3 DK 3649257T3 DK 18745508 T DK18745508 T DK 18745508T DK 3649257 T3 DK3649257 T3 DK 3649257T3
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Prior art keywords
enrichment
genomic regions
parallel analysis
targeted genomic
multiplex parallel
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DK18745508.4T
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English (en)
Inventor
George Koumbaris
Marios Ioannides
Elena KYPRI
Acilleas Achilleos
Petros MINA
Kyriakos Tsangaras
Philippos Patsalis
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Nipd Genetics Public Company Ltd
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    • C12Q1/6806Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay
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    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
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    • 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
    • G06COMPUTING OR CALCULATING; COUNTING
    • G06FELECTRIC DIGITAL DATA PROCESSING
    • G06F17/00Digital computing or data processing equipment or methods, specially adapted for specific functions
    • G06F17/10Complex mathematical operations
    • G06F17/18Complex mathematical operations for evaluating statistical data, e.g. average values, frequency distributions, probability functions, regression analysis
    • 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
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/185Modifications characterised by incorporating bases where the precise position of the bases in the nucleic acid string is important
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
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    • C12Q2525/204Modifications characterised by specific length of the oligonucleotides
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    • C12Q2535/00Reactions characterised by the assay type for determining the identity of a nucleotide base or a sequence of oligonucleotides
    • C12Q2535/122Massive parallel sequencing
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    • C12Q2537/00Reactions characterised by the reaction format or use of a specific feature
    • C12Q2537/10Reactions characterised by the reaction format or use of a specific feature the purpose or use of
    • C12Q2537/159Reduction of complexity, e.g. amplification of subsets, removing duplicated genomic regions
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    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers

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DK18745508.4T 2017-07-07 2018-07-06 Berigelse af målrettede genomiske regioner til multiplekset parallel analyse DK3649257T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762529667P 2017-07-07 2017-07-07
PCT/EP2018/068402 WO2019008148A1 (en) 2017-07-07 2018-07-06 ENRICHMENT OF TARGETED GENOMIC REGIONS FOR MULTIPLEXED PARALLEL ANALYSIS

Publications (1)

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DK3649257T3 true DK3649257T3 (da) 2022-07-04

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DK18745508.4T DK3649257T3 (da) 2017-07-07 2018-07-06 Berigelse af målrettede genomiske regioner til multiplekset parallel analyse

Country Status (11)

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US (1) US12270069B2 (da)
EP (1) EP3649257B1 (da)
AU (1) AU2018296568B2 (da)
CA (1) CA3068198A1 (da)
CY (1) CY1125226T1 (da)
DK (1) DK3649257T3 (da)
ES (1) ES2920280T3 (da)
PL (1) PL3649257T3 (da)
PT (1) PT3649257T (da)
WO (1) WO2019008148A1 (da)
ZA (1) ZA201908614B (da)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2920280T3 (es) 2017-07-07 2022-08-02 Nipd Genetics Public Company Ltd Enriquecimiento de regiones genómicas blanco para análisis paralelo multiplexado
ES2925394T3 (es) 2017-07-07 2022-10-17 Nipd Genetics Public Company Ltd Análisis paralelo multiplexado con enriquecimiento de blancos para la evaluación del riesgo de portar alteraciones genéticas
PT3649258T (pt) 2017-07-07 2022-05-25 Nipd Genetics Public Company Ltd Análise paralela multiplexada enriquecida com alvo para avaliação de amostras de adn fetal
WO2019008172A1 (en) 2017-07-07 2019-01-10 Nipd Genetics Public Company Limited ENRICHED MULTIPLEXED PARALLEL ANALYSIS IN TARGET FOR TUMOR BIOMARKER EVALUATION
CN113621692B (zh) * 2021-10-12 2022-02-22 北京求臻医疗器械有限公司 人类fgfr1基因拷贝数变异核酸标准物质及其制备方法、及试剂盒

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3591068A1 (en) 2006-02-02 2020-01-08 The Board of Trustees of the Leland Stanford Junior University Non-invasive fetal genetic screening by digital analysis
US20080194414A1 (en) * 2006-04-24 2008-08-14 Albert Thomas J Enrichment and sequence analysis of genomic regions
WO2008027548A2 (en) * 2006-09-01 2008-03-06 Dana-Farber Cancer Institute, Inc. Microarray-based global chromatin structure mapping
CA3069082C (en) 2008-09-20 2022-03-22 The Board Of Trustees Of The Leland Stanford Junior University Noninvasive diagnosis of fetal aneuploidy by sequencing
US20110039304A1 (en) * 2009-08-12 2011-02-17 President And Fellows Of Harvard College Methods to Generate Oligonucleotide Pools and Enrich Target Nucleic Acid Sequences
CA2780827A1 (en) * 2009-12-31 2011-07-07 Ventana Medical Systems, Inc. Methods for producing uniquely specific nucleic acid probes
EP2370599B1 (en) 2010-01-19 2015-01-21 Verinata Health, Inc Method for determining copy number variations
US20120270739A1 (en) 2010-01-19 2012-10-25 Verinata Health, Inc. Method for sample analysis of aneuploidies in maternal samples
US20130123120A1 (en) * 2010-05-18 2013-05-16 Natera, Inc. Highly Multiplex PCR Methods and Compositions
EP3187597B1 (en) 2011-02-09 2020-06-03 Natera, Inc. Methods for non-invasive prenatal ploidy calling
US20150203907A1 (en) * 2014-01-17 2015-07-23 Florida State University Research Foundation Genome capture and sequencing to determine genome-wide copy number variation
GB201414451D0 (en) * 2014-08-14 2014-10-01 Oxford Gene Technology Operations Ltd Hybridisation column for nucleic acid enrichment
WO2016040446A1 (en) 2014-09-10 2016-03-17 Good Start Genetics, Inc. Methods for selectively suppressing non-target sequences
EP3666902B1 (en) 2015-05-22 2024-07-03 Medicover Public Co Ltd Multiplexed parallel analysis of targeted genomic regions for non-invasive prenatal testing
PT3649258T (pt) 2017-07-07 2022-05-25 Nipd Genetics Public Company Ltd Análise paralela multiplexada enriquecida com alvo para avaliação de amostras de adn fetal
ES2920280T3 (es) 2017-07-07 2022-08-02 Nipd Genetics Public Company Ltd Enriquecimiento de regiones genómicas blanco para análisis paralelo multiplexado

Also Published As

Publication number Publication date
US20200157602A1 (en) 2020-05-21
AU2018296568A1 (en) 2020-01-16
AU2018296568B2 (en) 2024-11-14
ZA201908614B (en) 2022-07-27
US12270069B2 (en) 2025-04-08
PT3649257T (pt) 2022-05-19
CA3068198A1 (en) 2019-01-10
EP3649257B1 (en) 2022-03-30
WO2019008148A9 (en) 2019-05-16
EP3649257A1 (en) 2020-05-13
WO2019008148A1 (en) 2019-01-10
ES2920280T3 (es) 2022-08-02
CY1125226T1 (el) 2024-09-20
PL3649257T3 (pl) 2022-07-18

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