Oxford University Hospitals NHS Foundation Trust

30 capabilities Verified Oct 2026 One of 2,018 in United Kingdom
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Oxford Medical Genetics Laboratories, Churchill Hospital, Old Road, Headington
Headington OX3 7LE , United Kingdom

Accreditation

Active UKAS 8694
+44 (0) 1865-226001
ouh.nhs.uk Prefer to enquire through us? Send an enquiry
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Accreditation Details

Accreditation Body

UKAS

Number

8694

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

Oxford University Hospitals NHS Foundation Trust Headington Oxford University Hospitals NHS Foundation Trust Headington Oxford University Hospitals NHS Foundation Trust Headington Oxford University Hospitals NHS Foundation Trust Headington Oxford University Hospitals NHS Foundation Trust Headington Oxford University Hospitals NHS Foundation Trust Headington Oxford University Hospitals NHS Foundation Trust Oxford

Test Capabilities (30)
Standard Reference Description Category
MEASUREMENT Measurement Electrical
Copy Number [Definitive list:GEN DOC 926] Copy Number [Definitive list:GEN DOC 926] Molecular Diagnostics / PCR
Deletions Deletions 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 nucleic acid sequence variants - SNVs and small indels [Definitive list:GEN DOC 926] measurement Detection of nucleic acid sequence variants - SNVs and small indels [Definitive list:GEN DOC 926] measurement Molecular Diagnostics / PCR
Detection of whole or partial gene deletions, duplications probe specific SNVs and indels and methylation status [Definitive list: DOC 926] measurement Detection of whole or partial gene deletions, duplications probe specific SNVs and indels and methylation status [Definitive list: DOC 926] measurement Molecular Diagnostics / PCR
Fusions Fusions Molecular Diagnostics / PCR
Genomic analysis for the purpose of clinical diagnosis of rare disease and cancer Genomic analysis for the purpose of clinical diagnosis of rare disease and cancer Molecular Diagnostics / PCR
Lymphoma B Clonality (IgH rearrangements) Lymphoma B Clonality (IgH rearrangements) Molecular Diagnostics / PCR
Lymphoma T Clonality (TCR re-arrangements) Lymphoma T Clonality (TCR re-arrangements) Molecular Diagnostics / PCR
SNVs and indels [Definitive list: DOC 926] SNVs and indels [Definitive list: DOC 926] Molecular Diagnostics / PCR
SNVs, indels [Definitive list: GEN DOC 926] SNVs, indels [Definitive list: GEN DOC 926] Molecular Diagnostics / PCR
SNVs, indels and CNVs [Definitive list:GEN DOC 926] measurement SNVs, indels and CNVs [Definitive list:GEN DOC 926] measurement Molecular Diagnostics / PCR
Screening of large targeted single or multigene panels for nucleic acid sequence variants; SNVs, indels [Definitive list: DOC 926] measurement Screening of large targeted single or multigene panels for nucleic acid sequence variants; SNVs, indels [Definitive list: DOC 926] measurement Molecular Diagnostics / PCR
Screening of large targeted single or multigene panels for nucleic acid sequence variants; SNVs, indels and CNVs [Definitive list:GEN DOC 926] Screening of large targeted single or multigene panels for nucleic acid sequence variants; SNVs, indels and CNVs [Definitive list:GEN DOC 926] Molecular Diagnostics / PCR
Targeted analysis of the genome for copy number alterations, balanced chromosome rearrangements, mosaicism and formation of gene fusions Targeted analysis of the genome for copy number alterations, balanced chromosome rearrangements, mosaicism and formation of gene fusions Molecular Diagnostics / PCR
Targeted detection and quantification of known germline and somatic variants; SNVs, CNVs [Definitive list: DOC 926] Targeted detection and quantification of known germline and somatic variants; SNVs, CNVs [Definitive list: DOC 926] Molecular Diagnostics / PCR
Using locus specific probes for: Translocations and/or inversion Using locus specific probes for: Translocations and/or inversion Molecular Diagnostics / PCR
(Preparative Pre-examination steps for FISH) (Preparative Pre-examination steps for FISH) Other
926] 926] Other
DOC 926] DOC 926] Other
Detection of expansions including triplet repeats, microsatellite marker analysis, detection of specific Detection of expansions including triplet repeats, microsatellite marker analysis, detection of specific Other
Detection of specific SNVs and indels (including confirmatory testing) [Definitive list as per GEN Detection of specific SNVs and indels (including confirmatory testing) [Definitive list as per GEN Other
Developmental Disorders Developmental disorders Other
Haematological/Oncology disorders (Preparative Pre- examination steps listed first) [Definitive list:DOC 926] Haematological/Oncology disorders (Preparative Pre- examination steps listed first) [Definitive list:DOC 926] Other
Presence/absence of DNA regions (including confirmatory testing) [Definitive list: GEN DOC Presence/absence of DNA regions (including confirmatory testing) [Definitive list: GEN DOC Other
Reproductive Medicine Disorders Reproductive medicine disorders Other
SNVs and indels (including confirmatory testing) [Definitive list :DOC 926] measurement SNVs and indels (including confirmatory testing) [Definitive list :DOC 926] measurement Other
Screening of large targeted single or multigene panels for nucleic acid sequence variants Screening of large targeted single or multigene panels for nucleic acid sequence variants; Other
[Definitive list: DOC 926] measurement [Definitive list: DOC 926] measurement Other

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