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Caption : Accreditation =Accreditation
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GERMANY

Sachsen
WEIßWASSER

Accreditation
Molecular diagnosis of glioblastoma (EGFR and PPARG genes)
Praxis Dr. Mato Nagel
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular diagnosis of Oligodendrogliomas (MG MT methylation, tumour marlers 1p & 19q)
Southmead Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Methylation analysis, Detection of microdeletions/microduplications
Technical procedure(s) : BS-Pyrosequencing, FISH

UNITED KINGDOM

Devon
PLYMOUTH

Accreditation
Molecular diagnosis of Oligodendrogliomas (1p & 19q LOH)
Plymouth Derriford Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Accreditation
Molecular cytogenetic diagnosis of glioblastoma by FISH (7p12 amplification)
BioAnalytica-GenoType SA
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular haemato-oncology diagnosis of Glioma (1p & 19q LOH)
Southmead Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Methylation analysis, Detection of microdeletions/microduplications
Technical procedure(s) : BS-Pyrosequencing, FISH

UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation
Molecular cytogenetic diagnosis of Oligodendrogliomas by FISH analysis (1p & 19q LOH)
Southern General Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of glioblastoma (EGFR gene)
Diagenom GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Baden-Württemberg
FREIBURG

Accreditation
Molecular diagnosis of glioblastoma (EGFR gene)
Praxis für Humangenetik Freiburg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular and molecular cytogenetic diagnosis of glioma (FISH: 1p/19q deletions, MGMT gene promoter methylation status and IDH1 gene mutations)
King's College Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Methylation analysis, Deletion / Duplication analysis
Technical procedure(s) : FISH

ESTONIA

Tartu
TARTU

Accreditation
Mocular diagnosis of disorders linked to BRAF mutations by RT-PCR
Asper Biotech Ltd.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

Ontario
MISSISSAUGA

Accreditation
Methylation Analysis of MGMT for Therapeutic Option/Prognosis in Glioblastoma
Trillium Health Partners- Credit Valley Site
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Methylation analysis

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of glial tumor (IDH1, EGFR genes)
Reference Laboratory Genetics
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Sequence analysis: entire coding region, Detection of microdeletions/microduplications
Technical procedure(s) : Sanger sequencing, FISH

GERMANY

Niedersachsen
HANNOVER

Accreditation
Molecular diagnosis of glioblastoma (EGFR gene)
amedes genetics im MVZ wagnerstibbe
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation
Molecular diagnosis of pilocytic astrocytoma (KIAA1549 gene)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Bayern
WÜRZBURG

Accreditation
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universität Würzburg - Biozentrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : NGS sequencing (except WES)

GERMANY

Baden-Württemberg
ULM

Accreditation
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : NGS sequencing (except WES)

GERMANY

Schleswig-Holstein
KIEL

Accreditation
Molecular cytogenetic diagnosis of glioblastoma (1p36-Deletion, 19q13-Deletion)
Praxis Dr. Lana Harder
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of microdeletions/microduplications
Technical procedure(s) : FISH

UNITED KINGDOM

Devon
EXETER

Accreditation
Molecular diagnosis of Non small-cell lung cancer response to Gefitinib/Erlotinib (EGFR TKD analysis: EGFR exons 18-21 by pyrosequencing/gene fragment analysis)
Royal Devon and Exeter Hospital - Wonford site
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of glioblastoma (EGFR gene)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Glioma (MGMT methylation analysis)
Toronto General Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Methylation analysis

CANADA

Ontario
TORONTO

Accreditation
Molecular Cytogenetic Diagnosis of Low Grade Astrocytoma (FISH BRAF)
The Hospital for Sick Children
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH

FRANCE

NORD-PAS-DE-CALAIS
LILLE

Accreditation
Diagnosis of intellectual disability (Panel)
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : NGS sequencing (except WES)

ITALY

VENETO
COSTOZZA DI LONGARE

Molecular diagnosis of diseases associated to TP53 (TP53 gene)
B.I.R.D. Foundation
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
MILANO

Molecular diagnosis of glioblastoma (MGMT gene promoter hypermethylation)
Azienda Ospedaliera "San Paolo" - Università degli Studi di Milano
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Methylation analysis

ITALY

LOMBARDIA
MILANO

Molecular diagnosis of oligodendrogliomas (1p & 19q LOH)
Azienda Ospedaliera "San Paolo" - Università degli Studi di Milano
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

País Vasco
SAN SEBASTIÁN

Molecular diagnosis of glioblastoma (TP53 gene / array-CGH)
Policlínica Gipuzkoa
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technical procedure(s) : Array based techniques

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Molecular cytogenetic diagnosis of Anaplastic oligodendroglioma (1p36/19q13: by FISH)
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Molecular cytogenetic diagnosis of Pilocytic astrocytoma (KIAA1549 and BRAF: by FISH)
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

GERMANY

Niedersachsen
OSNABRÜCK

Molecular diagnosis of TP53 gene associated diseases (sequencing)
Praxis Dres. Gencik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

SPAIN

Asturias
OVIEDO

Diagnosis of glial tumors (IDH1, IDH2, MGMT genes )
IMOMA - Instituto de Medicina Oncológica y Molecular de Asturias
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Methylation analysis, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques, BS-Pyrosequencing

AUSTRIA

TIROL
INNSBRUCK

Molecular cytogenetic diagnosis of oligodendroglioma (1p/19q LOH)
Medizinische Universität Innsbruck
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH

GERMANY

Sachsen
DRESDEN

Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : NGS sequencing (except WES)

IRELAND

County Dublin
DUBLIN

Glioblastoma testing on solid tumour samples (by 1p19q Array, MGMT methylation, BRAF Fusion, IDH1&2 methylation)
Beaumont Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Methylation analysis, Detection of microdeletions/microduplications
Technical procedure(s) : PCR based techniques, Array based techniques, BS-Pyrosequencing

GERMANY

Nordrhein-Westfalen
BONN

Histopathological, molecular and cell biological analysis of tumor biopsies of the nervous system
Universitätsklinikum Bonn
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Pathology

GERMANY

Nordrhein-Westfalen
DÜSSELDORF

Histopathological, molecular and cell biological analysis of tumor biopsies of the nervous system
Universitätsklinikum Düsseldorf
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Pathology

ITALY

TOSCANA
SIENA

Molecular diagnosis of tuomours of nervous system
Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

TURKEY

TURKEY
ESKISEHIR

Molecular diagnosis of Oligodendroglioma-1 by MLPA and FISH analysis
Eskisehir Osmangazi University Medical Faculty
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technical procedure(s) : MLPA based techniques, FISH

GERMANY

Niedersachsen
HANNOVER

Molecular diagnosis of glioma (FISH: 1p/19q deletions, MGMT gene: promoter methylation status, IDH1 gene: sequencing, BRAF gene: V600E)
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Baden-Württemberg
ULM

Molecular diagnosis of NADP-dependent isocitrate dehydrogenase in brain tumor and secondary glioblastom (IDH1 gene)
Klinik für Kinder- und Jugendmedizin des Universitätsklinikums Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

AUSTRIA

WIEN
WIEN

Molecular diagnosis of glial tumors (IDH1 and IDH2 genes)
Allgemeines Krankenhaus der Stadt Wien
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

UNITED KINGDOM

Surrey
SURREY

Molecular diagnosis of Glioblastoma (EGFR gene)
Institute of Cancer Research ICR
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

TUNISIA

TUNISIA
SOUSSE

Molecular diagnosis of glioblastoma (MGMT gene: MS-MLPA)
CHU Farhat Hached
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Uniparental disomy study
Technical procedure(s) : MLPA based techniques