NHS Greater Glasgow and Clyde

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Details

Laboratory Genetics, West of Scotland Genetic Services, Level 2B, Laboratory Medicine, Queen Elizabeth University Hospital, Govan Road
Glasgow G51 4TF , United Kingdom

Accreditation

Active UKAS 8290
+44 (0) 141 354 9313
ggc.scot.nhs.uk Prefer to enquire through us? Send an enquiry
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Accreditation Details

Accreditation Body

UKAS

Number

8290

Status

Active

Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official UKAS records.

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Other locations

NHS Greater Glasgow and Clyde 21 Shelley Road NHS Greater Glasgow and Clyde Glasgow NHS Greater Glasgow and Clyde Glasgow NHS Greater Glasgow and Clyde Paisley NHS Greater Glasgow and Clyde 10-16 Alexandra Parade NHS Greater Glasgow and Clyde Glasgow NHS Greater Glasgow and Clyde Glasgow NHS Greater Glasgow and Clyde Glasgow

Test Capabilities (94)
Standard Reference Description Category
RET RET Hematology
Sarcoma Sarcoma Histopathology / Cytology
Acute Myeloid Leukaemia (AML)/ Myelodysplastic Syndrome (MDS) Acute Myeloid Leukaemia (AML)/ Myelodysplastic Syndrome (MDS) Molecular Diagnostics / PCR
Angelman Syndrome Angelman Syndrome Molecular Diagnostics / PCR
Arthrogryposis (CE Subpanel) Arthrogryposis (CE Subpanel) Molecular Diagnostics / PCR
BRAF BRAF Molecular Diagnostics / PCR
Becker Muscular Dystrophy Becker Muscular Dystrophy Molecular Diagnostics / PCR
Beckwith-Weidemann Syndrome Beckwith-Weidemann Syndrome Molecular Diagnostics / PCR
Breast Cancer (hereditary) (NGS, 8 gene panel) Breast Cancer (hereditary) (NGS, 8 gene panel) Molecular Diagnostics / PCR
Breast and Ovarian cancer (hereditary) (NGS, 14 gene panel) Breast and Ovarian cancer (hereditary) (NGS, 14 gene panel) Molecular Diagnostics / PCR
Breast, ovarian and colorectal cancer (hereditary) (NGS, 22 gene panel) Breast, ovarian and colorectal cancer (hereditary) (NGS, 22 gene panel) Molecular Diagnostics / PCR
CADASIL CADASIL Molecular Diagnostics / PCR
CHARGE Syndrome CHARGE Syndrome Molecular Diagnostics / PCR
Chondrodysplasia Punctata (CE subpanel) Chondrodysplasia Punctata (CE subpanel) Molecular Diagnostics / PCR
Cowden Syndrome Cowden Syndrome Molecular Diagnostics / PCR
Cytogenetic and Molecular Genetic examination activities for the purpose of genetic investigations Cytogenetic and Molecular Genetic examination activities for the purpose of genetic investigations Molecular Diagnostics / PCR
Cytogenetic and Molecular Genetic investigations for the detection of germline mutations and genomic imbalance related to the following: Aneuploidy testing for common trisomies (T13, T18, T21, X and Y) Cytogenetic and Molecular Genetic investigations for the detection of germline mutations and genomic imbalance related to the following: Aneuploidy testing for common trisomies (T13, T18, T21, X and Y) Molecular Diagnostics / PCR
Cytogenetic and Molecular Genetic investigations for the detection of somatic mutations and genomic imbalance related to the following: Acute Lymphoblastic Leukaemia (ALL), including: â–ª Minimal residual disease (MRD) Paediatric ALL (including. SNP microarray) Cytogenetic and Molecular Genetic investigations for the detection of somatic mutations and genomic imbalance related to the following: Acute Lymphoblastic Leukaemia (ALL), including: â–ª Minimal residual disease (MRD) Paediatric ALL (including. SNP microarray) Molecular Diagnostics / PCR
DICER1 syndrome (CE) DICER1 syndrome (CE) Molecular Diagnostics / PCR
DiGeorge Syndrome DiGeorge Syndrome Molecular Diagnostics / PCR
Dihydropyrimidine Dehydrogenase (DPYD) Dihydropyrimidine Dehydrogenase (DPYD) Molecular Diagnostics / PCR
Dilated Cardiomyopathy Dilated Cardiomyopathy Molecular Diagnostics / PCR
Disorders of Sexual Development (NGS, 56 gene panel) Disorders of Sexual Development (NGS, 56 gene panel) Molecular Diagnostics / PCR
Duchenne Muscular Dystrophy Duchenne Muscular Dystrophy Molecular Diagnostics / PCR
Epilepsy (NGS, 104 gene panel) Epilepsy (NGS, 104 gene panel) Molecular Diagnostics / PCR
Episodic ataxia type 1 & type 2 (KCNA1 and CACNA1A) Episodic ataxia type 1 & type 2 (KCNA1 and CACNA1A) Molecular Diagnostics / PCR
FMR1-related disorders FMR1-related disorders Molecular Diagnostics / PCR
FOXL2 variant analysis FOXL2 variant analysis Molecular Diagnostics / PCR
Familial Hemiplegic Migraine (FHM) (NGS, 5 gene panel) Familial Hemiplegic Migraine (FHM) (NGS, 5 gene panel) Molecular Diagnostics / PCR
Fibrodysplasia Ossificans Fibrodysplasia ossificans Molecular Diagnostics / PCR
Fragile X syndrome Fragile X syndrome Molecular Diagnostics / PCR
Fragile X syndrome, including Fragile X syndrome, including Molecular Diagnostics / PCR
HRAS HRAS Molecular Diagnostics / PCR
KRAS KRAS Molecular Diagnostics / PCR
MLH1 promoter methylation analysis MLH1 promoter methylation analysis Molecular Diagnostics / PCR
NRAS NRAS Molecular Diagnostics / PCR
Neurodegeneration with Brain Iron accumulation (CE subpanel) Neurodegeneration with Brain Iron accumulation (CE subpanel) Molecular Diagnostics / PCR
POLE POLE Molecular Diagnostics / PCR
Rhabdomyolysis (CE Subpanel) Rhabdomyolysis (CE Subpanel) Molecular Diagnostics / PCR
SMA/dHMN (CE Subpanel) SMA/dHMN (CE Subpanel) Molecular Diagnostics / PCR
Somatic NGS, 2 gene panel (BRCA1, BRCA2) Somatic NGS, 2 gene panel (BRCA1, BRCA2) Molecular Diagnostics / PCR
TP53 TP53 Molecular Diagnostics / PCR
Y deletions Y deletions Molecular Diagnostics / PCR
Adult granulosa cell tumours Adult granulosa cell tumours Other
Brain and CNS Cancer (including Glioma) including; 1p36/1q25 and 19q13/19p13 IDH1/IDH2 and BRAF MGMT promoter methylation in Glioma Brain and CNS Cancer (including Glioma) including; 1p36/1q25 and 19q13/19p13 IDH1/IDH2 and BRAF MGMT promoter methylation in Glioma Other
Breast Cancer (acquired) Breast Cancer (acquired) Other
Chimerism Analysis Chimerism analysis Other
Chromosome investigation for inherited and congenital abnormalities Chromosome investigation for inherited and congenital abnormalities Other
Colorectal Cancer (acquired) including Colorectal Cancer (acquired) including; Other
Developmental delay, including Developmental delay, including; Other
Endometrial tumour (2 gene panel) Endometrial tumour (2 gene panel) Other
FXTAS FXTAS Other
Fertility investigations, including Fertility investigations, including; Other
Gorlin Syndrome (CE subpanel) Gorlin Syndrome (CE subpanel) Other
Haematological Malignancy, not otherwise specified Haematological Malignancy, not otherwise specified Other
Hereditary Ataxia (CE subpanel) Hereditary Ataxia (CE subpanel) Other
Hereditary Haemochromatosis (HFE related) Hereditary Haemochromatosis (HFE related) Other
Hereditary Spastic Paraplegia (CE subpanel) Hereditary Spastic Paraplegia (CE subpanel) Other
Lesch Nyhan Syndrome Lesch Nyhan Syndrome Other
Li-Fraumeni Syndrome Li-Fraumeni Syndrome Other
Limb Girdle Muscular Dystrophy 1B laminopathy Limb Girdle Muscular Dystrophy 1B laminopathy Other
Limb Girdle Muscular Dystrophy type 2I and 2R Limb Girdle Muscular Dystrophy type 2I and 2R Other
Lung Cancer, Non-Small Cell (acquired); â–ª ALK1 â–ª ROS1 â–ª EGFR â–ª BRAF KRAS Lung Cancer, Non-Small Cell (acquired); â–ª ALK1 â–ª ROS1 â–ª EGFR â–ª BRAF KRAS Other
Lymphoproliferative Neoplasms (LPN), including: â–ª Chronic Lymphocytic Leukaemia (CLL) â–ª Lymphoma â–ª Myeloma Waldenstr Ó§ ms macroglobulinaemia Lymphoproliferative Neoplasms (LPN), including: â–ª Chronic Lymphocytic Leukaemia (CLL) â–ª Lymphoma â–ª Myeloma Waldenstr Ó§ ms macroglobulinaemia Other
Malignant Melanoma (hereditary) (NGS, 5 gene panel) Malignant Melanoma (hereditary) (NGS, 5 gene panel) Other
Malignant Melanoma â–ª BRAF â–ª KIT PDGFRA Malignant Melanoma â–ª BRAF â–ª KIT PDGFRA Other
Microdeletion/Microduplication syndromes Microdeletion/Microduplication syndromes Other
Myeloproliferative Disorders (MPD), including; â–ª Chronic Myeloid Leukaemia (CML) â–ª Polycythaemia Vera â–ª Essential Thrombocythaemia Myelofibrosis Myeloproliferative Disorders (MPD), including; â–ª Chronic Myeloid Leukaemia (CML) â–ª Polycythaemia Vera â–ª Essential Thrombocythaemia Myelofibrosis Other
Myotonic Dystrophy (type 1) Myotonic Dystrophy (type 1) Other
Osteochondromas Osteochondromas Other
Osteopetrosis Osteopetrosis Other
Ovarian Cancer (hereditary) (NGS, 8 gene panel) Ovarian Cancer (hereditary) (NGS, 8 gene panel) Other
POF POF Other
Pancreatic Cancer (hereditary) 9 gene panel Pancreatic Cancer (hereditary) 9 gene panel Other
Phenylketonuria Phenylketonuria Other
Prader Willi Syndrome Prader Willi Syndrome Other
Pregnancy loss Pregnancy loss Other
Prenatal Diagnosis Prenatal Diagnosis Other
Progressiva Progressiva Other
Prostate cancer Prostate cancer; Other
Respiratory Disease (CE subpanel) Respiratory Disease (CE subpanel) Other
Rett and Rett-like Syndrome Rett and Rett-like Syndrome Other
Rhabdoid tumour Rhabdoid tumour Other
SHOX related SHOX related Other
Sex determination Sex determination Other
Short Stature, including: Turner syndrome Short Stature, including: • Turner syndrome SHOX related Other
Sickle Cell Anaemia Sickle Cell Anaemia Other
Silver Russell Syndrome Silver Russell Syndrome Other
Solid Tumours, not otherwise specified Solid Tumours, not otherwise specified Other
TERT TERT Other
Thiopurine methyltransferase (TPMT) Thiopurine methyltransferase (TPMT) Other
Thyroid tumour (6 gene panel) Thyroid tumour (6 gene panel) Other
Uveal Melanoma (acquired) Uveal Melanoma (acquired) Other
X-inactivation Studies X-inactivation Studies Other

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