The Newcastle upon Tyne Hospitals NHS Foundation Trust
61 capabilities
Verified Oct 2026
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Northern Genetics Service, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Institute of Genetic Medicine, Central Parkway, Newcastle upon Tyne
Newcastle upon Tyne NE1 3BZ , United Kingdom
Newcastle upon Tyne NE1 3BZ , United Kingdom
Accreditation
Active
UKAS
9028
nhs.net
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Accreditation Details
Accreditation Body
UKAS
Number
9028
Status
ActiveAccreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official UKAS records.
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Test Capabilities (61)
| Standard Reference | Description | Category |
|---|---|---|
| MEASUREMENT | Measurement | Electrical |
| G-Banding/Karyotyping | G-banding/Karyotyping: | Culturing and processing of human | Histopathology / Cytology |
| Immunohistochemistry analysis and interpretation of data to progress a diagnosis Antibodies listed below: -Dystroglycan -Sarcoglycan -Spectrin Caveolin 3 Collagen VI Desmin Fast myosin -Sarcoglycan Laminin 2 chain Laminin 5 chain MHC Class 1 Myosin heavy chain (neonatal) Myotilin nNOS p62 Slow myosin STIM1 Utrophin Valosin-containing protein measurement | Immunohistochemistry analysis and interpretation of data to progress a diagnosis Antibodies listed below: -Dystroglycan -Sarcoglycan -Spectrin Caveolin 3 Collagen VI Desmin Fast myosin -Sarcoglycan Laminin 2 chain Laminin 5 chain MHC Class 1 Myosin heavy chain (neonatal) Myotilin nNOS p62 Slow myosin STIM1 Utrophin Valosin-containing protein measurement | Histopathology / Cytology |
| Tumours | Tumours | Histopathology / Cytology |
| ALK-activating variants in neuroblastoma, HFE variants c.845G>A p.(Cys282Tyr) & c.187C>G p.(His63Asp) FLT3-TKD MYD88 | ALK-activating variants in neuroblastoma, HFE variants c.845G>A p.(Cys282Tyr) & c.187C>G p.(His63Asp) FLT3-TKD MYD88 | Molecular Diagnostics / PCR |
| Angelman/Prader Willi syndrome by bisulphite conversion | Angelman/Prader Willi syndrome by bisulphite conversion | Molecular Diagnostics / PCR |
| BCR-ABL monitoring in chronic myeloid leukaemia measurement | BCR-ABL monitoring in chronic myeloid leukaemia measurement | Molecular Diagnostics / PCR |
| BRAF | BRAF | Molecular Diagnostics / PCR |
| Classification of Microsatellite | Classification of Microsatellite | Molecular Diagnostics / PCR |
| Confirmatory and cascade testing | Confirmatory and cascade testing | Molecular Diagnostics / PCR |
| Confirmatory testing of fusion events by RT-PCR-analytic capacity as per GENE36 measurement | Confirmatory testing of fusion events by RT-PCR-analytic capacity as per GENE36 measurement | Molecular Diagnostics / PCR |
| Cystic Fibrosis (including neonatal screening) | Cystic Fibrosis (including neonatal screening) | Molecular Diagnostics / PCR |
| DPYD Mutation Detection for the following targets: DPYD c.1905+1G>A DPYD*2A rs3918290 DPYD c.2846A>T p.(Asp949Val) rs67376798 DPYD c.1679T>G p.(Ile560Ser) DYPD*13 rs55886062 DPYD c.1236G>A p.(Glu412Glu) HapB3 rs56038477 DPYD c.1129-5923C>G HapB3 rs75017182 measurement | DPYD Mutation Detection for the following targets: DPYD c.1905+1G>A DPYD*2A rs3918290 DPYD c.2846A>T p.(Asp949Val) rs67376798 DPYD c.1679T>G p.(Ile560Ser) DYPD*13 rs55886062 DPYD c.1236G>A p.(Glu412Glu) HapB3 rs56038477 DPYD c.1129-5923C>G HapB3 rs75017182 measurement | Molecular Diagnostics / PCR |
| Detection of SNVs and small indels and fusions associated with myeloid neoplasms -analytic capacity as per GENE119 | Detection of SNVs and small indels and fusions associated with myeloid neoplasms -analytic capacity as per GENE119 | Molecular Diagnostics / PCR |
| Detection of SNVs, small indels and CNVs associated with Familial | Detection of SNVs, small indels and CNVs associated with Familial | Molecular Diagnostics / PCR |
| Detection of insertions, deletions, substitutions, and other polymorphisms in NRAS | Detection of insertions, deletions, substitutions, and other polymorphisms in NRAS | Molecular Diagnostics / PCR |
| Detection of known or unknown sequence changes - analytic capacity as per SOPS measurement | Detection of known or unknown sequence changes - analytic capacity as per SOPS measurement | Molecular Diagnostics / PCR |
| Detection of nucleic acid sequence variants – SNVs, small indels and breakpoints | Detection of nucleic acid sequence variants – SNVs, small indels and breakpoints | Molecular Diagnostics / PCR |
| Determination of copy number changes | Determination of copy number changes | Molecular Diagnostics / PCR |
| EGFR | EGFR | Molecular Diagnostics / PCR |
| FLT3/NPM1 in AML | FLT3/NPM1 in AML | Molecular Diagnostics / PCR |
| FLUIDS | GENE35 | FLUIDS | GENE35 | Molecular Diagnostics / PCR |
| Genomics analysis for the purpose of clinical diagnosis of rare disease, inherited and acquired cancer | Genomics analysis for the purpose of clinical diagnosis of rare disease, inherited and acquired cancer | Molecular Diagnostics / PCR |
| Genomics analysis for the purpose of clinical diagnosis of rare disease, inherited and acquired cancer measurement | Genomics analysis for the purpose of clinical diagnosis of rare disease, inherited and acquired cancer measurement | Molecular Diagnostics / PCR |
| Genomics analysis for the purpose of clinical diagnosis or rare disease and cancer | Genomics analysis for the purpose of clinical diagnosis or rare disease and cancer | Molecular Diagnostics / PCR |
| Instability (MSI) status (stable/unstable) and genotyping of BRAF & NRAS/KRAS | Instability (MSI) status (stable/unstable) and genotyping of BRAF & NRAS/KRAS | Molecular Diagnostics / PCR |
| JAK2 V617F | JAK2 V617F | Molecular Diagnostics / PCR |
| KRAS | KRAS | Molecular Diagnostics / PCR |
| MGMT methylation status determined by bisulphite conversion measurement | MGMT methylation status determined by bisulphite conversion measurement | Molecular Diagnostics / PCR |
| Microsatellite instability by | Microsatellite instability by | Molecular Diagnostics / PCR |
| PCR and analysis of microsatellite markers | PCR and analysis of microsatellite markers | Molecular Diagnostics / PCR |
| TPMT | TPMT | Molecular Diagnostics / PCR |
| Tri/tetra nucleotide repeat fragment detection and interpretation (including PCR and TP-PCR) | Tri/tetra nucleotide repeat fragment detection and interpretation (including PCR and TP-PCR) | Molecular Diagnostics / PCR |
| X-inactivation | X-inactivation | Molecular Diagnostics / PCR |
| Analytic capacity as per SOP | Analytic capacity as per SOP | Other |
| Antibodies listed below: -Dystroglycan -Sarcoglycan measurement | Antibodies listed below: -Dystroglycan -Sarcoglycan measurement | Other |
| Break-apart probes | Break-apart probes | Other |
| By detection of microscopic chromosomal imbalance (gains and losses) expressed as changes to copy number measurement | By detection of microscopic chromosomal imbalance (gains and losses) expressed as changes to copy number measurement | Other |
| Copy Number/Amplification | Copy Number/Amplification | Other |
| Deletion | Deletion | Other |
| Detection of chromosomal aberrations in the diagnosis of Haematological malignancy, bone marrow failure syndromes | Detection of chromosomal aberrations in the diagnosis of Haematological malignancy, bone marrow failure syndromes | Other |
| Detection of chromosomal rearrangements or aberrations arising from (e.g) | Detection of chromosomal rearrangements or aberrations arising from (e.g) | Other |
| Determination of copy number – deletions and duplications- analytic capacity as per | Determination of copy number – deletions and duplications- analytic capacity as per | Other |
| Fusion products | Fusion products | Other |
| GENE51 | GENE51 | Other |
| Genetic examination for the purposes of clinical diagnosis | Genetic examination for the purposes of clinical diagnosis | Other |
| Haemato-Oncology and Solid | Haemato-Oncology and Solid | Other |
| Hypercholesterolemia and inherited cancers -analytic capacity as per GENE174 | Hypercholesterolemia and inherited cancers -analytic capacity as per GENE174 | Other |
| Identity / zygosity testing | Identity / zygosity testing | Other |
| Immunoblotting analysis and interpretation of data to progress a diagnosis | Immunoblotting analysis and interpretation of data to progress a diagnosis | Other |
| Insertion | Insertion | Other |
| Loss of pregnancy | Loss of pregnancy | Other |
| Monitoring stem-cell transplants | Monitoring stem-cell transplants | Other |
| Muscle Immunoanalysis | Muscle Immunoanalysis | Other |
| NUDT15 | NUDT15 | Other |
| Neoplastic Genetics including | Neoplastic Genetics including | Other |
| Non-haematological malignancies | Non-haematological malignancies | Other |
| Postnatal Disorders | Postnatal Disorders | Other |
| Prenatal Diagnosis | Prenatal Diagnosis | Other |
| Preparative pre-examination steps listed first measurement | Preparative pre-examination steps listed first measurement | Other |
| Validation of splicing variants and fusion events measurement | Validation of splicing variants and fusion events measurement | Other |
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