ScopeUHS
Official name: University Hospital Southampton NHS Foundation Trust (UHS)
23 capabilities
Verified Oct 2026
One of 2,018 in United Kingdom
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Details
Wessex Regional Genetics Laboratory, Salisbury District Hospital, Odstock Road
Salisbury SP2 8BJ , United Kingdom
Salisbury SP2 8BJ , United Kingdom
Accreditation
Active
UKAS
9005
uhs.nhs.uk
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Accreditation Details
Accreditation Body
UKAS
Number
9005
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 (23)
| Standard Reference | Description | Category |
|---|---|---|
| (1A) (ii) genotyping of specific mutations and genomic regions for both constitutional and acquired conditions[as per definitive list] (2A) | (1A) (ii) genotyping of specific mutations and genomic regions for both constitutional and acquired conditions[as per definitive list] (2A) | Molecular Diagnostics / PCR |
| D816V mutation | D816V mutation | Molecular Diagnostics / PCR |
| Detection of cryptic chromosome rearrangements in acute leukaemia | Detection of cryptic chromosome rearrangements in acute leukaemia | Molecular Diagnostics / PCR |
| Molecular Genetics | Molecular Genetics | Molecular Diagnostics / PCR |
| Molecular genetic examinations for the purpose of clinical diagnosis | Molecular genetic examinations for the purpose of clinical diagnosis | Molecular Diagnostics / PCR |
| Qualitative detection of the KIT | Qualitative detection of the KIT | Molecular Diagnostics / PCR |
| Screening for unknown somatic variants in myeloid disorders in multi-gene fixed panel Illumina | Screening for unknown somatic variants in myeloid disorders in multi-gene fixed panel Illumina | Molecular Diagnostics / PCR |
| TruSight Myeloid Panel (1B) | TruSight Myeloid Panel (1B) | Molecular Diagnostics / PCR |
| CD138 cell separation for Multiple | CD138 cell separation for Multiple | Other |
| Clinical Cytogenetics: Detection of aneuploidy, maternal cell contamination and confirmation of genetic sex | Clinical Cytogenetics: Detection of aneuploidy, maternal cell contamination and confirmation of genetic sex | Other |
| Confirmation of genomic rearrangements detected using alternative technologies [as per definitive list] | Confirmation of genomic rearrangements detected using alternative technologies [as per definitive list] | Other |
| Confirmation of genomic rearrangements detected using alternative technologies. Family follow-up studies | Confirmation of genomic rearrangements detected using alternative technologies. Family follow-up studies | Other |
| Cytogenetics examinations for the purpose of clinical diagnosis | Cytogenetics examinations for the purpose of clinical diagnosis | Other |
| Detection and analysis of genomic rearrangements and imbalances | Detection and analysis of genomic rearrangements and imbalances | Other |
| Detection of acquired chromosome rearrangements from patients with haemato-oncology disorders[as per definitive list] | Detection of acquired chromosome rearrangements from patients with haemato-oncology disorders[as per definitive list] | Other |
| Detection of chromosome abnormalities associated with: Reproductive disorders | Detection of chromosome abnormalities associated with: Reproductive disorders | Other |
| Detection of chromosome rearrangements in comparison with considered normal pattern (ISCN) | Detection of chromosome rearrangements in comparison with considered normal pattern (ISCN) | Other |
| Haemato-oncology disorders | Haemato-oncology disorders | Other |
| Myeloma | Myeloma | Other |
| Sex chromosome disorders | Sex chromosome disorders | Other |
| Sizing analysis haemato-oncology disorders (bone marrow and whole blood only) | Sizing analysis haemato-oncology disorders (bone marrow and whole blood only) | Other |
| [as per definitive list] | [as per definitive list] | Other |
| [as per definitive list] (2B) | [as per definitive list] (2B) | Other |
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