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                                                                  Laboratory officially designated for this diagnostic test =Laboratory officially designated for this diagnostic test            Accreditation =Accreditation ;

GERMANY

Sachsen
WEIßWASSER

Diagnosis of glioblastoma (EGFR and PPARG genes)
Praxis Dr. Mato Nagel
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
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
Service(s) : Methylation analysis, Detection of microdeletions/microduplications bs-pyrosequencing, fish

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Accreditation
UNITED KINGDOM

Devon
PLYMOUTH

Molecular diagnosis of Oligodendrogliomas (1p & 19q LOH)
Plymouth Derriford Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Deletion / Duplication analysis pcr based techniques

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Accreditation
UNITED KINGDOM

Avon
BRISTOL

Molecular haemato-oncology diagnosis of Glioma (1p & 19q LOH)
Southmead Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Service(s) : Methylation analysis, Detection of microdeletions/microduplications bs-pyrosequencing, fish

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Accreditation
GERMANY

Baden-Württemberg
ULM

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
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Diagnosis of glioblastoma (EGFR gene)
Diagenom GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
GERMANY

Bayern
MARTINSRIED/PLANEGG

Diagnosis of glioblastoma (EGFR gene)
MVZ Martinsried GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
GERMANY

Baden-Württemberg
FREIBURG

Diagnosis of glioblastoma (EGFR gene)
SYNLAB MVZ Freiburg GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Diagnosis of glial tumor (gene panel)
Reference Laboratory Genetics
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Service(s) : Sequence analysis: entire coding region, Detection of microdeletions/microduplications ngs sequencing (except wes), sanger sequencing, fish

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Accreditation
GERMANY

Niedersachsen
HANNOVER

Diagnosis of glioblastoma (EGFR gene)
amedes genetics im MVZ wagnerstibbe
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
GERMANY

Baden-Württemberg
TÜBINGEN

Diagnosis of pilocytic astrocytoma (KIAA1549 gene)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
FRANCE

GRAND-EST
STRASBOURG

Diagnosis of intellectual disability (Panel)
CHU de Strasbourg - Hôpital Civil
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Mutation scanning/screening and sequence analysis of selected exons ngs sequencing (except wes)

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Accreditation
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
Service(s) : Detection of chromosome alterations large in size fish

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Accreditation
GERMANY

Bayern
MÜNCHEN

Diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Medizinisch Genetisches Zentrum München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
GERMANY

Baden-Württemberg
ULM

Diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
GERMANY

Sachsen
DRESDEN

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
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
FRANCE

BRETAGNE
BREST

Diagnosis of intellectual disability (Panel)
CHU de Brest - Hôpital de la Cavale Blanche
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
BELGIUM

OOST-VLAANDEREN
GENT

Prognosis and therapeutic options in Glioblastoma (MGMT methylation specific PCR analysis)
Centrum Medische Genetica Gent - Universitair Ziekenhuis Gent
Purpose(s) : Somatic genetics
Specialty(ies) : Other

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Accreditation
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
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
FRANCE

CENTRE-VAL DE LOIRE
TOURS

Diagnosis of intellectual disability (Panel)
CHRU de Tours - Hôpital Bretonneau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
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
Service(s) : Sequence analysis: entire coding region whole exome sequencing (wes)

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Accreditation
BELGIUM

OOST-VLAANDEREN
GENT

Diagnosis of rare tumors (gene panel)
AZ Sint Lucas Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
BELGIUM

LIEGE
LIEGE

Diagnosis of glioblastoma (gene panel)
CHU de Liège - Domaine universitaire du Sart Tilman
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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Accreditation
BELGIUM

LIEGE
LIEGE

Diagnosis of glioblastoma (MGMT promoter methylation, by MS-PCR)
CHU de Liège - Domaine universitaire du Sart Tilman
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Other

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Accreditation
BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Diagnosis of brain tumors (gene panel)
Hôpital Universitaire de Bruxelles (H.U.B) - Site Hôpital Erasme
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Pathology
Service(s) : Mutation scanning/screening and sequence analysis of selected exons ngs sequencing (except wes)

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Accreditation
GERMANY

Schleswig-Holstein
KIEL

Diagnosis of glioblastoma (1p36-Deletion, 19q13-Deletion)
Praxis Dr. Lana Harder
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Service(s) : Detection of microdeletions/microduplications fish

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Accreditation
CANADA

Ontario
TORONTO

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

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Accreditation
ITALY

VENETO
COSTOZZA DI LONGARE

Diagnosis of diseases associated to TP53 (TP53 gene)
B.I.R.D. Foundation
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Targeted mutation analysis, Sequence analysis: entire coding region sanger sequencing

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ITALY

LOMBARDIA
MILANO

Molecular diagnosis of glioblastoma (MGMT gene promoter hypermethylation)
ASST Santi Paolo e Carlo, Ospedale San Paolo - Università degli Studi di Milano
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Methylation analysis

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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

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GERMANY

Niedersachsen
OSNABRÜCK

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

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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
Service(s) : Mutation scanning/screening and sequence analysis of selected exons, Methylation analysis, Deletion / Duplication analysis sanger sequencing, mlpa based techniques, bs-pyrosequencing

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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
Service(s) : Targeted mutation analysis, Methylation analysis, Detection of microdeletions/microduplications pcr based techniques, array based techniques, bs-pyrosequencing

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AUSTRIA

WIEN
WIEN

Molecular diagnosis of glial tumors (IDH1 gene)
Medizinische Universität Wien
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of rare neoplastic diseases (panel, qCancer Risk)
qGenomics
Purpose(s) : Risk assessment
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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SPAIN

La Rioja
LOGROÑO

Diagnosis of hereditary cancer (panel)
Hospital San Pedro
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis ngs sequencing (except wes)

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SPAIN

Galicia
A CORUÑA

Diagnosis of rare nervous system tumor (panel - 19 genes)
Health In Code. A Coruña
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Mutation scanning/screening and sequence analysis of selected exons ngs sequencing (except wes)

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SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of cancer (panel)
Fundación Instituto Valenciano de Oncología
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Mutation scanning/screening and sequence analysis of selected exons ngs sequencing (except wes)

More information

SPAIN

Asturias
OVIEDO

Diagnosis of rare tumor (panel)
IMOMA - Instituto de Medicina Oncológica y Molecular de Asturias
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis ngs sequencing (except wes)

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SPAIN

Baleares
PALMA DE MALLORCA

Diagnosis of hereditary cancer (panel)
Hospital Universitari Son Espases
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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SPAIN

Navarra
PAMPLONA

Diagnosis of solid tumors (panel)
CIMA - Centro de Investigación Médica Aplicada
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis ngs sequencing (except wes)

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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
Service(s) : Targeted mutation analysis ngs sequencing (except wes)

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SPAIN

Castilla - León
SALAMANCA

Diagnosis of gliomas (IDH1, IDH2, MGMT genes; 1p/19q co-deletion)
BIOSALAB Molecular Biology Solutions
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Service(s) : Targeted mutation analysis, Methylation analysis, Detection of chromosome alterations large in size sanger sequencing, bs-pyrosequencing, fish

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SPAIN

Comunidad Valenciana
PATERNA

Diagnosis of rare tumor (panel)
Seqplexing
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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AUSTRIA

STEIERMARK
GRAZ

Diagnosis of central nervous system tumors (Neuro NGS panel including IDH1/IDH2, MGMT promoter methylation, copy number variation including 1p19q, BRAF translocations)
Medizinische Universität Graz
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region ngs sequencing (except wes)

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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

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Laboratory officially designated for this diagnostic test
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

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Laboratory officially designated for this diagnostic test
GERMANY

Bayern
MÜNCHEN

Methylation Analysis of MGMT gene promoter region for Therapeutic Option/Prognosis in Glioblastoma
Zentrum für Neuropathologie und Prionforschung (ZNP)
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Methylation analysis bs-pyrosequencing

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ITALY

TOSCANA
SIENA

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

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AUSTRIA

WIEN
WIEN

Molecular diagnosis of glial tumors (IDH1 and IDH2 genes)
Universitätsklinikum - AKH Wien
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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AUSTRIA

TIROL
INNSBRUCK

Diagnosis of oligodendroglioma (1p/19q LOH)
Medizinische Universität Innsbruck
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Service(s) : Detection of chromosome alterations large in size fish

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ITALY

LOMBARDIA
MILANO

Diagnosis of glial tumors (MGMT, IDH1, IDH2 genes)
Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Other
Service(s) : Targeted mutation analysis, Methylation analysis pcr based techniques, bs-pyrosequencing

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