Great Ormond Street Hospital for Children NHS Foundation Trust

31 capabilities Verified Oct 2026 One of 2,018 in United Kingdom
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Details

Rare & Inherited Disease Laboratory, NHS North Thames Genomic Laboratory, HubLevels 4-6, Barclay House, 37 Queen Square
37 Queen Square WC1N 3BH , United Kingdom

Accreditation

Active UKAS 7883
+44 (0) 207 762 6888
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Accreditation Details

Accreditation Body

UKAS

Number

7883

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

Great Ormond Street Hospital for Children NHS Foundation Trust London Great Ormond Street Hospital for Children NHS Foundation Trust London Great Ormond Street Hospital for Children NHS Foundation Trust London Great Ormond Street Hospital for Children NHS Foundation Trust Camelia Botnar Laboratories Great Ormond Street Hospital for Children NHS Foundation Trust London Great Ormond Street Hospital for Children NHS Foundation Trust Camelia Botnar Laboratories Great Ormond Street Hospital for Children NHS Foundation Trust Camelia Botnar Laboratories

Test Capabilities (31)
Standard Reference Description Category
DNA dosage analysis of mtDNA DNA dosage analysis of mtDNA Molecular Diagnostics / PCR
DNA profiling for detection of abnormal sequences associated with acquired cancer DNA profiling for detection of abnormal sequences associated with acquired cancer Molecular Diagnostics / PCR
Molecular Genetics examination procedures for the purposes of clinical diagnosis Molecular Genetics examination procedures for the purposes of clinical diagnosis Molecular Diagnostics / PCR
(NIPD) (NIPD) Other
(RHDO) (RHDO) Other
Acquired cytogenomic analysis Acquired cytogenomic analysis Other
Cell Free Fetal DNA (cffDNA) extraction from maternal plasma Cell Free Fetal DNA (cffDNA) extraction from maternal plasma Other
Chromosome analysis for Prenatal Diagnosis Chromosome analysis for Prenatal Diagnosis Other
Chromosome analysis for acquired cancers: - Haematological malignancies and solid tumours Chromosome analysis for acquired cancers: - Haematological malignancies and solid tumours Other
Chromosome analysis for; - Prenatal Diagnosis Chromosome analysis for; - Prenatal Diagnosis Other
Confirmation of Mosaicism from NGS Flexible scope limited to BioRad QX200 for Confirmation of Mosaicism from NGS Flexible scope limited to BioRad QX200 for Other
Cytogenetics examination procedures for the purposes of clinical diagnosis Cytogenetics examination procedures for the purposes of clinical diagnosis Other
Cytovision Karyotyping station and in house procedures Cytovision Karyotyping station and in house procedures Other
DNA and RNA profiling for detection of abnormal sequences associated with acquired cancer DNA and RNA profiling for detection of abnormal sequences associated with acquired cancer Other
DNA and RNA profiling for detection of abnormal sequences for common and rare inherited/predisposing genetic disease condition DNA and RNA profiling for detection of abnormal sequences for common and rare inherited/predisposing genetic disease condition Other
DNA and RNA profiling for detection of abnormal sequences for common and rare inherited/predisposing genetic disease condition by TWIST exomes DNA and RNA profiling for detection of abnormal sequences for common and rare inherited/predisposing genetic disease condition by TWIST exomes Other
DNA and RNA profiling for detection of repetitive sequences to exclude maternal cell contamination and identity testing DNA and RNA profiling for detection of repetitive sequences to exclude maternal cell contamination and identity testing Other
DNA profiling for detection of abnormal sequences by Multiplex ligation dependent Probe Analysis (MLPA) DNA profiling for detection of abnormal sequences by Multiplex ligation dependent Probe Analysis (MLPA) Other
DNA profiling for detection of abnormal sequences for common and rare inherited/predisposing genetic disease condition DNA profiling for detection of abnormal sequences for common and rare inherited/predisposing genetic disease condition Other
Developmental Disorders Developmental disorders Other
Extraction of DNA and RNA Extraction of DNA and RNA Other
Fragment analysis for repeat expansion disorders Fragment analysis for repeat expansion disorders Other
G-band analysis using Leica G-band analysis using Leica Other
Karyotyping (G-band) Chromosome analysis for acquired cancers: - Haematological malignancies Karyotyping (G-band) Chromosome analysis for acquired cancers: - Haematological malignancies Other
Mitochondrial whole genome sequencing Mitochondrial whole genome sequencing Other
Non-Invasive Prenatal examination procedures for the purposes of clinical diagnosis and antenatal screening Non-Invasive Prenatal examination procedures for the purposes of clinical diagnosis and antenatal screening Other
Non-invasive prenatal diagnosis Non-invasive prenatal diagnosis Other
Prenatal Diagnosis Prenatal Diagnosis Other
Relative Haplotype Dosage Analysis Relative Haplotype Dosage Analysis Other
Reproductive Medicine Disorders Reproductive medicine disorders Other
SNP genotyping SNP genotyping Other

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