Search for a diagnostic test
22 Result(s)
Caption
: Accreditation
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UNITED KINGDOM
Avon
BRISTOL
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
Technique(s)
: BS-Pyrosequencing, FISH

UNITED KINGDOM
Devon
PLYMOUTH
Molecular diagnosis of Oligodendrogliomas (1p & 19q LOH)
Plymouth Derriford Hospital
Purpose(s)
: Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Deletion / Duplication analysis
Technique(s)
: PCR based techniques

UNITED KINGDOM
Avon
BRISTOL
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
Technique(s)
: BS-Pyrosequencing, FISH

UNITED KINGDOM
Lanarkshire
GLASGOW
Molecular cytogenetic diagnosis of Oligodendrogliomas by FISH analysis (1p & 19q LOH)
Queen Elizabeth University Hospital
Purpose(s)
: Somatic genetics
Specialty(ies)
: Cytogenetics
Technique(s)
: FISH

UNITED KINGDOM
Greater London
LONDON
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
Technique(s)
: FISH

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
Technique(s)
: FISH

SPAIN
Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of glial tumor (gene panel)
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
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, FISH

CANADA
Ontario
MISSISSAUGA
Molecular Cytogenetic Solid Tumor Analysis (Paraffin Embedded Tissue ALK, MYC, ERBB2)
Trillium Health Partners- Credit Valley Site
Purpose(s)
: Somatic genetics
Specialty(ies)
: Cytogenetics
Objective(s)
: Detection of chromosome alterations large in size
Technique(s)
: FISH

GERMANY
Baden-Württemberg
TÜBINGEN
Molecular analysis of somatic mutation in tumour tissue for therapeutic decisions (Somatic Tumor Panel, 710 genes)
CeGaT GmbH
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

FRANCE
NORMANDIE
ROUEN
Diagnosis of rare genetic tumor (Phenotyping in oncogenetics) (Whole exome)
CHU de Rouen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Whole Exome Sequencing (WES)

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

ITALY
LOMBARDIA
MILANO
Molecular diagnosis of oligodendrogliomas (1p & 19q LOH)
ASST Santi Paolo e Carlo, Ospedale San Paolo - Università degli Studi di Milano
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

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
Technique(s)
: Sanger sequencing, MLPA based techniques, BS-Pyrosequencing

SPAIN
Baleares
PALMA DE MALLORCA
Diagnosis of hereditary cancer (panel)
Hospital Universitari Son Espases
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

SPAIN
Comunidad Valenciana
VALENCIA
Diagnosis of solid tumors (panel)
INCLIVA - Facultad de Medicina de la Universidad de Valencia
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis
Technique(s)
: NGS sequencing (except WES)

SPAIN
Castilla - León
SALAMANCA
Diagnosis of gliomas (IDH1, IDH2, MGMT genes; Chr. 1p, del(1p); Chr. 19q, del(19p))
BIOSALAB Molecular Biology Solutions
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics, Cytogenetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons, Methylation analysis, Detection of microdeletions/microduplications
Technique(s)
: Sanger sequencing, BS-Pyrosequencing, FISH

GERMANY
Nordrhein-Westfalen
BONN
Histopathological, molecular and cell biological analysis of tumor biopsies of the nervous system
Universitätsklinikum Bonn (AöR)
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: 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
Specialty(ies)
: Pathology

ITALY
TOSCANA
SIENA
Molecular diagnosis of tuomours of nervous system
Azienda Ospedaliera Universitaria Senese - Policlinico 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
Technique(s)
: MLPA based techniques, FISH

GERMANY
Niedersachsen
HANNOVER
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
Technique(s)
: Sanger sequencing

ITALY
LOMBARDIA
MILANO