ScopeCambridge University Hospitals NHS Foundation Trust
24 capabilities
Verified Oct 2026
One of 2,018 in United Kingdom
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Details
Cambridge Genomics Laboratory, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Hills Road
Cambridge CB2 0QQ , United Kingdom
Cambridge CB2 0QQ , United Kingdom
Accreditation
Active
UKAS
8840
nhs.net
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Accreditation Details
Accreditation Body
UKAS
Number
8840
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 (24)
| Standard Reference | Description | Category |
|---|---|---|
| G-Banding/Karyotyping | G-banding/Karyotyping: | Culturing and processing of human | Histopathology / Cytology |
| Detection of SNVs and small indels | Detection of SNVs and small indels | Molecular Diagnostics / PCR |
| Detection of chromosomal rearrangements or aberrations arising from: (e.g) | Detection of chromosomal rearrangements or aberrations arising from: (e.g.) | Molecular Diagnostics / PCR |
| Detection of fusion genes | Detection of fusion genes | Molecular Diagnostics / PCR |
| Detection of gene fusions | Detection of gene fusions | Molecular Diagnostics / PCR |
| Detection of pathogenic and likely pathogenic DNA copy number variants and copy number neutral loss of heterozygosity (in diagnostic samples) | Detection of pathogenic and likely pathogenic DNA copy number variants and copy number neutral loss of heterozygosity (in diagnostic samples) | Molecular Diagnostics / PCR |
| Detection of whole exon deletions/duplications and specific methylation abnormalities | Detection of whole exon deletions/duplications and specific methylation abnormalities | Molecular Diagnostics / PCR |
| Determination of methylation status | Determination of methylation status | Molecular Diagnostics / PCR |
| Genomic analysis for the purpose of clinical diagnosis of rare and inherited disease and cancer | Genomic analysis for the purpose of clinical diagnosis of rare and inherited disease and cancer | Molecular Diagnostics / PCR |
| Next Generation Sequencing | Next generation sequencing | Molecular Diagnostics / PCR |
| Next Generation Sequencing for Small Variants | Next Generation Sequencing for Small Variants | Molecular Diagnostics / PCR |
| Quantification of RNA transcripts | Quantification of RNA transcripts | Molecular Diagnostics / PCR |
| See CU-UK-DTA-5 | See CU-UK-DTA-5 | Molecular Diagnostics / PCR |
| CU-UK-DTA-8 | CU-UK-DTA-8 | Other |
| CU-UK-DTA-9 | CU-UK-DTA-9 | Other |
| Confirmation of genomic rearrangements - using locus specific probes: Deletion | Confirmation of genomic rearrangements - using locus specific probes: Deletion | Other |
| Copy Number/Amplification | Copy Number/Amplification | Other |
| DNA Quantification for QC purposes | DNA Quantification for QC purposes | Other |
| Detection and analysis of genomic rearrangements and imbalances | Detection and analysis of genomic rearrangements and imbalances | Other |
| Developmental Disorders | Developmental disorders | Other |
| Haematological/Oncology disorders (Preparative Pre-examination steps listed first) Cytogenetic examinations | Haematological/Oncology disorders (Preparative Pre-examination steps listed first) Cytogenetic examinations | Other |
| Reproductive Medicine Disorders | Reproductive medicine disorders | Other |
| See CU-UK-DTA-2 | See CU-UK-DTA-2 | Other |
| See CU-UK-DTA-8 | See CU-UK-DTA-8 | Other |
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