BR0010739A - Processo de análise da predisposição genética de um paciente a pelo menos uma doença e amplificação de uma sequência e de duas sequências - Google Patents
Processo de análise da predisposição genética de um paciente a pelo menos uma doença e amplificação de uma sequência e de duas sequênciasInfo
- Publication number
- BR0010739A BR0010739A BR0010739-5A BR0010739A BR0010739A BR 0010739 A BR0010739 A BR 0010739A BR 0010739 A BR0010739 A BR 0010739A BR 0010739 A BR0010739 A BR 0010739A
- Authority
- BR
- Brazil
- Prior art keywords
- disease
- patient
- polymorphic region
- resolution
- amplification
- Prior art date
Links
Classifications
-
- 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
- C12Q1/6881—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for tissue or cell typing, e.g. human leukocyte antigen [HLA] probes
-
- 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
-
- 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
- C12Q2600/16—Primer sets for multiplex assays
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Immunology (AREA)
- Analytical Chemistry (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Cell Biology (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
"PROCESSO DE ANáLISE DA PREDISPOSIçãO GENéTICA DE UM PACIENTE A PELO MENOS UMA DOENçA E AMPLIFICAçãO DE UMA SEQuêNCIA E DE DUAS SEQuêNCIAS". A presente invenção refere-se a um processo de análise da predisposição genética de um paciente a pelo menos uma doença. Ela consiste igualmente em uma amplificação adaptada a um tal processo. O processo consiste em colocar uma amostra líquida que contém pelo menos um tipo de amplicons, proveniente da amplificação de, pelo menos, uma região polimórfica de interesse em relação com a ou as doenças pesquisadas, em presença de sondas escolhidas da seguinte forma: pelo menos uma sonda específica de tipagem, dita com baixa resolução, capaz de se hibridizar na região polimórfica de interesse de, pelo menos, uma sonda específica de sub-tipagem, dita com alta resolução, a ou as sondas com alta resolução que permitem discriminar o ou os alelos associados com a susceptibilidade genética e/ou o ou os alelos associados à resistência a dita ou as ditas doenças, de acordo com sua hibridização ou sua não hibridização. A invenção encontrou uma aplicação preferencial no domínio dos diagnósticos.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9906599A FR2793808B1 (fr) | 1999-05-20 | 1999-05-20 | Procede d'analyse de la predisposition genetique d'un patient a au moins une maladie |
FR9915314A FR2793809B1 (fr) | 1999-05-20 | 1999-12-06 | Procede d'analyse de la predisposition genetique d'un patient a au moins une maladie et amplification adaptee a un tel procede |
PCT/FR2000/001385 WO2000071750A1 (fr) | 1999-05-20 | 2000-05-19 | Procede d'analyse de la predisposition genetique d'un patient a au moins une maladie et amplification adaptee a un tel procede |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0010739A true BR0010739A (pt) | 2002-02-19 |
Family
ID=26234969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0010739-5A BR0010739A (pt) | 1999-05-20 | 2000-05-19 | Processo de análise da predisposição genética de um paciente a pelo menos uma doença e amplificação de uma sequência e de duas sequências |
Country Status (12)
Country | Link |
---|---|
US (1) | US7060438B1 (pt) |
EP (1) | EP1179091B2 (pt) |
JP (1) | JP2003500067A (pt) |
CN (1) | CN1351672A (pt) |
AT (1) | ATE279535T1 (pt) |
AU (1) | AU772175B2 (pt) |
BR (1) | BR0010739A (pt) |
CA (1) | CA2374440A1 (pt) |
DE (1) | DE60014887T3 (pt) |
ES (1) | ES2230109T5 (pt) |
FR (1) | FR2793809B1 (pt) |
WO (1) | WO2000071750A1 (pt) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2829580B1 (fr) | 2001-09-07 | 2004-02-13 | Bio Merieux | Procede de lecture, de detection ou de quantification, hybrides ou complexes utilises dans ce procede et biopuce mettant en oeuvre ledit procede |
AU2003298655A1 (en) | 2002-11-15 | 2004-06-15 | Bioarray Solutions, Ltd. | Analysis, secure access to, and transmission of array images |
EP1536021A1 (en) * | 2003-11-27 | 2005-06-01 | Consortium National de Recherche en Genomique (CNRG) | Method for HLA typing |
US7848889B2 (en) * | 2004-08-02 | 2010-12-07 | Bioarray Solutions, Ltd. | Automated analysis of multiplexed probe-target interaction patterns: pattern matching and allele identification |
FR2881437B1 (fr) | 2005-01-31 | 2010-11-19 | Biomerieux Sa | Procede pour le diagnostic/pronostic d'un syndrome septique |
FR2906537A1 (fr) | 2006-09-28 | 2008-04-04 | Biomerieux Sa | Procede de diagnostic in vitro du cancer broncho-pulmonaire par detection des transcrits majoritaires alternatifs du gene klk8 codant la kallicreine 8 et son utilisation pour le pronostic de survie |
BR112012027535B1 (pt) * | 2010-04-27 | 2020-01-28 | Fundacio Hospital Univ Vall Dhebron Institut De Recerca | método in vitro para a detecção da susceptibilidade em desenvolver efeitos colaterais adversos relacionados com bioimplantes, uso de um kit e uso de antígenos como marcadores |
JP5916718B2 (ja) | 2010-06-04 | 2016-05-11 | ビオメリューBiomerieux | 結腸直腸癌の予後判定のための方法及びキット |
US9110079B2 (en) | 2010-09-29 | 2015-08-18 | Biomerieux | Method and kit for establishing an in vitro prognosis on a patient exhibiting SIRS |
WO2012129758A1 (en) | 2011-03-25 | 2012-10-04 | Biomerieux | Method and kit for determining in vitro probability for individual to suffer from colorectal cancer |
US10072300B2 (en) | 2013-05-21 | 2018-09-11 | Biomerieux | Kit for the prognosis of colorectal cancer |
EP3620984B1 (en) | 2018-09-06 | 2024-04-10 | Accenture Global Solutions Limited | Digital quality control using computer visioning with deep learning |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5567809A (en) * | 1986-03-13 | 1996-10-22 | Hoffmann-La Roche Inc. | Methods and reagents for HLA DRbeta DNA typing |
US5702885A (en) * | 1990-06-27 | 1997-12-30 | The Blood Center Research Foundation, Inc. | Method for HLA typing |
NL9002259A (nl) * | 1990-10-17 | 1992-05-18 | Eurodiagnostics B V | Werkwijze voor het bepalen van een genotype door het vergelijken van de nucleotidensequentie van leden van een genfamilie, alsmede kit voor het opsporen van genetische variaties. |
GB9024005D0 (en) | 1990-11-05 | 1990-12-19 | British Bio Technology | Process for amplifying nucleic acid |
FR2679252B1 (fr) * | 1991-07-17 | 1993-12-10 | Bio Merieux | Systeme de sondes permettant d'effectuer le typage hla dr, et procede de typage utilisant lesdites sondes. |
US5976789A (en) * | 1991-07-17 | 1999-11-02 | Bio Merieux | System of probes enabling HLA-DR typing to be performed, and typing method using said probes |
JPH0690757A (ja) * | 1991-08-23 | 1994-04-05 | Kitasato Inst:The | Hla−drタイピング用塩基配列群とそれを用いた hla−drタイピング法 |
JPH08308596A (ja) * | 1995-03-10 | 1996-11-26 | Wakunaga Pharmaceut Co Ltd | Hlaの検出 |
US5939542A (en) | 1995-03-10 | 1999-08-17 | Wakunaga Seiyaku Kabushiki Kaisha | Detection of HLA-DR |
US6994958B2 (en) * | 1995-11-29 | 2006-02-07 | Anthony Nolan Bone Marrow Trust | Methods for separating and/or identifying DNA molecules |
FR2749308B1 (fr) * | 1996-06-03 | 1998-07-24 | Bio Merieux | Sondes nucleotidiques et procede pour determiner le typage hla dqb1 |
US6287764B1 (en) * | 1997-02-11 | 2001-09-11 | William H. Hildebrand | Class I sequence based typing of HLA-A, -B, and -C alleles by direct DNA sequencing |
EP0887423A1 (en) * | 1997-06-26 | 1998-12-30 | Biotest Ag | A method for determining the Histocompatibility locus antigen class II |
EP1003917A1 (en) * | 1997-08-11 | 2000-05-31 | Visible Genetics Inc. | Method and kit for hla class i typing dna |
US5910413A (en) * | 1997-10-10 | 1999-06-08 | Visible Genetics, Inc. | Method and kit for amplification, sequencing and typing of classical HLA class I genes |
-
1999
- 1999-12-06 FR FR9915314A patent/FR2793809B1/fr not_active Expired - Fee Related
-
2000
- 2000-05-19 AU AU47660/00A patent/AU772175B2/en not_active Ceased
- 2000-05-19 US US09/979,088 patent/US7060438B1/en not_active Expired - Fee Related
- 2000-05-19 AT AT00929650T patent/ATE279535T1/de not_active IP Right Cessation
- 2000-05-19 BR BR0010739-5A patent/BR0010739A/pt not_active Application Discontinuation
- 2000-05-19 CN CN00807807A patent/CN1351672A/zh active Pending
- 2000-05-19 DE DE60014887T patent/DE60014887T3/de not_active Expired - Lifetime
- 2000-05-19 EP EP00929650A patent/EP1179091B2/fr not_active Expired - Lifetime
- 2000-05-19 ES ES00929650T patent/ES2230109T5/es not_active Expired - Lifetime
- 2000-05-19 WO PCT/FR2000/001385 patent/WO2000071750A1/fr active IP Right Grant
- 2000-05-19 JP JP2000620127A patent/JP2003500067A/ja not_active Ceased
- 2000-05-19 CA CA002374440A patent/CA2374440A1/fr not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP1179091B2 (fr) | 2009-02-25 |
DE60014887T2 (de) | 2005-10-13 |
EP1179091B1 (fr) | 2004-10-13 |
FR2793809B1 (fr) | 2006-07-28 |
FR2793809A1 (fr) | 2000-11-24 |
AU772175B2 (en) | 2004-04-08 |
ES2230109T3 (es) | 2005-05-01 |
CN1351672A (zh) | 2002-05-29 |
CA2374440A1 (fr) | 2000-11-30 |
WO2000071750A1 (fr) | 2000-11-30 |
JP2003500067A (ja) | 2003-01-07 |
EP1179091A1 (fr) | 2002-02-13 |
US7060438B1 (en) | 2006-06-13 |
ES2230109T5 (es) | 2009-06-05 |
ATE279535T1 (de) | 2004-10-15 |
DE60014887D1 (de) | 2004-11-18 |
DE60014887T3 (de) | 2009-09-24 |
AU4766000A (en) | 2000-12-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA10 | Dismissal: dismissal - article 33 of industrial property law | ||
B11Y | Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette] |