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Welcome
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Services
- Cervical Screening London
- HSL Advanced Diagnostics
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HSL Biochemistry
- About HSL Biochemistry
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- Specialties
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Tests
- 17-Hydroxyprogesterone (17-OHP)
- Angiotensin converting enzyme (ACE)
- Adrenocorticotropic hormone (ACTH)
- Active B12
- Alpha Feto Protein (AFP)
- Albumin
- Alkaline Phosphatase (ALP)
- Alkaline Phosphatase Isoenzymes
- Alpha 1 Antitrypsin
- Alpha-1 Antitrypsin Phenotyping
- Alanine aminotransferase (ALT)
- Amikacin
- Ammonia
- Amylase
- Androstenedione
- Antimullerian Hormone (AMH)
- Anti-Thyroglobulin Antibodies
- Apolipoprotein A1
- Apolipoprotein B
- Aspartate aminotransferase (AST)
- B2-Microglobulin
- Human chorionic gonadotropin (HCG)
- Bicarbonate
- Bile Acids
- CA 125
- CA 15-3
- CA 19-9
- Calcitonin
- Calcium
- Carbamazepine
- CEA
- Caeruloplasmin
- Chloride
- Cholesterol
- Chromium
- Chromogranin A
- Urine Citrate
- CK-MB
- Cobalt
- Complement C3
- Complement C4
- Conjugated Bilirubin (Direct Bilirubin)
- Copper
- Albumin-adjusted Calcium (calculated)
- Cortisol
- Creatine Kinase (Ck)
- Creatine Kinase Isoenzymes
- Creatinine clearance (Calculated)
- C-Reactive protein (CRP)
- Cryoglobulins
- CSF Glucose
- CSF Lactate
- CSF Protein
- CSF Xanthochromia
- Ciclosporin A
- Dehydroepiandrosterone sulphate (DHEAS)
- Digoxin
- Direct low-density lipoprotein (Direct LDL)
- Enhanced Liver Fibrosis (ELF) Testing
- Erythropeitin (EPO)
- Estimated GFR (eGFR) (calculated)
- Oestradiol
- Ethanol
- Faecal Calprotectin
- Ferritin
- Floating Beta
- Folate
- Free beta human chorionic gonadotropin (free bHCG)
- Fructosamine
- Follicle Stimulating Hormone (FSH)
- Free triiodothyronine (FT3)
- Free thyroxine (FT4)
- Gentamicin
- Gamma glutamyltransferase (GGT)
- Glucose
- Growth Hormone
- Haemoglobin A1c
- Haptoglobin
- HDL
- High Senstitivity C-Reactive protein (hsCRP)
- High Sensitivity Troponin I
- High Sensitivity Troponin T
- Homocysteine
- Immunoglobulin A (IgA)
- Immunoglobulin E (IgE)
- Immunoglobulin G (IgG)
- Immunoglobulin G Subclasses (IgG1-4)
- Immunoglobulin M (IgM)
- Insulin
- Insulin-like growth factor 1 (IGF-1)
- Iron
- Lactate
- Lactate dehydrogenase (LDH)
- LDL-Cholesterol (Calculated)
- Luteinising Hormone
- Lipase
- Lipoprotein electrophoresis
- Lipoprotein (a)
- Lithium
- Macroprolactin
- Magnesium
- Methotrexate
- Non-high density lipoprotein (non-HDL calculated)
- n-Terminal pro b-type natriuretic peptide (NTproBNP)
- Osmolality
- Oxalate
- Urine Oxalate
- Pregnancy associated plasma protein-A (PAPPA)
- Primary Hyperoxaluria metabolites
- Primary Hyperoxaluria metabolites (glycolate, glycerate, dihydroxyglutarate)
- Phenytoin
- Phosphate
- Metanephrines (normetanephrine, metanephrine, 3-methoxytyramine)
- Potassium
- Procalcitonin
- Progesterone
- Prolactin
- Protein Electrophoresis
- Paracetamol (Acetaminophen)
- Parathyroid Hormone (PTH)
- Salicylate
- Selenium
- Serum amyloid A (SAA)
- Serum Free Light Chains
- Serum Immunofixation
- Sex Hormone Binding Globulin (SHBG)
- Sirolimus
- Sodium
- Tacrolimus
- Testosterone
- Theophylline
- Thyroglobulin
- Total Bilirubin
- Total Glycated Haemoglobin (Boronate Affinity)
- Total Iron Binding Capacity (TIBC) (Calculated)
- Total Protein
- Prostate Specific Antigen (PSA)
- Transferrin
- Transferrin Saturation (Calculated)
- Triglyceride
- Thyroid Stimulating Hormone (TSH)
- Unsaturated iron binding capacity (UIBC)
- Urate
- Urea
- Urine 5-hydroxyindoleacetic acid (5HIAA)
- Urine Albumin:Creatinine Ratio (Calculated)
- Urine Albumin
- Urine Amphetamine Screen
- Urine Amylase
- Urine Barbiturate Screen
- Urine Benzodiazepine Screen
- Urine Bence Jones Protein (BJP)
- Urine Calcium
- Urine Cannabinoids Screen
- Urine Cocaine Screen
- Urine Copper
- Urine Cotinine
- Urine Creatinine
- Urine Cystine and homocystine screen
- Urine Ethanol
- Urine Glucose
- Urine Magnesium
- Urine metadrenaline (normetanephrine, metanephrine, 3-methoxytyramine)
- Urine Methadone Screen
- Urine Opiate Screen
- Urine Phosphate
- Urine porphobilinogen screen (PBG)
- Urine Potassium
- Urine Protein
- Urine Protein Electrophoresis
- Urine Protein:creatinine Ratio (Calculated)
- Urine Reducing Substances Screen
- Urine Sodium
- Urine Steroid Profile
- Urine Total Porphyrins
- Urine Urea
- Urine Zinc
- Valproate
- Vancomycin
- Vitamin B12
- 25-Hydroxyvitamin D
- Zinc
- Calculus Analysis
- Creatinine
- Urine Urate
- Helicobacter pylori antigen
- HSL Blood Transfusion
- HSL Cellular Pathology
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HSL Manual Haematology (Immunophenotyping and Immune Monitoring)
- Staff/key personnel
-
Tests
- Bone Marrow Aspirate (BMA)
- Cerebral Spinal Fluid Morphology (CSF), Pleural Fluid morphology and Ascites Fluid morphology
- Acute Leukaemia Screen + MRD
- Chronic Leukaemia Screen + MRD
- Myeloperoxidase Stain
- Esterase Stain
- Iron Stain (BMA)
- Haemosiderin
- Myeloma Flow
- PNH
- CD20/CD21
- CD57
- NBT
- Common Variable Immunodeficiency (CVID) (B-Cells)
- T-Cell Immunodeficiency (TCID) (T-Cells)
- T Cell Proliferation
-
HSL Genetics
- Staff/Key personnel
- Specimens
- Request procedures
- Specialties
-
Tests
- 1p36 Deletion Syndrome – karyotype + FISH
- 21-Hydroxylase Deficiency (Congenital Adrenal Hyperplasia)
- 22q11 & 10p14 deletion (Di George Syndrome) – BOBs (5 days) + karyotype (15 days)
- 22q11 & 10p14 deletion (Di George Syndrome) – BOBs only
- Achromatopsia NGS Panel – full gene sequencing
- Aicardi-Goutiares Syndrome NGS Panel – full gene sequencing
- Alagille Syndrome NGS Panel – full sequencing JAG1 + NOTCH2 genes
- ALL Genome profile
- Alpha Fetoprotein on Amniotic fluid
- Alpha Thalassaemia – multiplex PCR and HBA MLPA for large deletions
- Alpha Thalassaemia – multiplex PCR for common large deletions
- Alpha-1 Antitrypsin Genotype – PI*M, PI*S, PI*Z
- Alport Syndrome NGS Panel – full sequencing with deletions and duplications
- AML Genome profile
- AML/ALL Molecular MRD – NPM1, PML-RARA, CBFB-MYH11, RUNX1-RUNX1T1, ETV6-RUNX1
- AmnioBOBs only – rapid aneuploidy diagnosis for all chromosomes + common microdeletion syndromes
- Amniocentesis culture (karyotype) only
- Amniocentesis – rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (10-15 days)
- Amniocentesis – rapid PCR diagnosis for common aneuploidies (2 days) + culture (10-15 days)
- AmnioPCR only – rapid common aneuploidy diagnosis by QF-PCR
- Amylotrophic Lateral Sclerosis (Motor Neurone Disease) NGS Panel – full gene sequencing
- Androgen Insensitivity – AR gene sequencing
- Aneurysm/Connective Tissue Disorders/Ehlers-Danlos Syndrome NGS Panel – full gene sequencing + deletions/duplications
- Angelman Syndrome (Primary Screen) – methylation PCR
- Angelman/Rett Syndromes NGS Panel – full gene sequencing
- Aniridia, Isolated – PAX6 gene sequencing + deletions/duplications
- Anophthalmia/Microphthalmia/Coloboma NGS Panel – full gene sequencing
- Thrombophilia due to antithrombin III deficiency
- Aortopathy/Marfan Syndrome and Thoracic Aortic and Dissection NGS Panel – full gene sequencing
- Apert Syndrome – common FGFR2 variants
- Apolipoprotein E genotype – E2, E3, E4
- Array CGH (Comparative Genomic Hybridisation)
- Ashkenazi Breast Cancer Screen – common variants
- Ashkenazi Jewish Carrier Screen
- Ataxia NGS Panel – full gene sequencing
- Autoinflammation/Periodic Fever NGS Panel – full gene sequencing
- Azoospermia – karyotype + cystic fibrosis screen + polyT(5T) + Y deletions
- B cell clonality assay (IgH and IgK)
- Bardet-Biedl Syndrome NGS Panel – full gene sequencing
- Batten Disease (Neuronal Ceroid Lipofuscinosis) NGS Panel – full gene sequencing
- BCR-ABL diagnostic assay
- BCR/ABL Quantitative – fusion gene sizes p190 + p210
- Becker/Duchenne Muscular Dystrophy – deletions/duplications
- Beckwith-Wiedemann Syndrome – methylation studies on 11p15 imprinting domains KvDMR + H19
- Behcet’s Disease – HLA Tissue Typing B*51
- Beta Thalassaemia – beta-globin gene sequencing
- Beta Thalassaemia – beta-globin gene sequencing, ARMS PCT, RE-PCR, Gap-PCR, HBB MLPA
- Inherited bleeding and platelet disorders (R90)
- Blood PCR for Chromosome 13, 18, 21 and sex chromosomes
- Breast Cancer Ashkenazi Screen – common variants
- Breast Cancer NGS Panel – full gene sequencing
- Breast Cancer – BRCA1 + BRCA2 only gene sequencing + deletions/duplications
- Brugada Syndromea/Long-QT NGS Panel – full gene sequencing
- C-KIT D816V variant by PCR for Mastocytosis
- CADASIL – NOTCH3 gene sequencing
- CAKUT (Congenital Anomalies of Kidney & Urinary Tract) NGS Panel – full gene sequencing
- Cancer, Comprehensive NGS Panel – full gene sequencing + deletions/duplications
- Cardio-Facio-Cutaneous/Noonan/LEOPARD/Costello Syndromes NGS Panel – full gene sequencing
- Cardiomyopathy, Dilated NGS Panel – full gene sequencing + deletions/duplications
- Cardiomyopathy, Hypertrophic NGS Panel – full gene sequencing + deletions/duplications
- Cardiovascular, Comprehensive NGS Panel – full gene sequencing + deletions/duplications
- Carrier Screen (Ashkenazi Jewish)
- Carrier Screen (Ashkenazi Jewish) – Partnered Report
- Carrier Screen (Pan-Ethnic)
- Carrier Screen (Pan-Ethnic) – Partnered Report
- Charcot-Marie-Tooth Syndrome NGS Panel – full gene sequencing
- Charcot-Marie-Tooth Type 1A – PMP22 duplications
- CHARGE Syndrome – CHD7 gene sequencing
- Cholestasis, Intrahepatic NGS Panel – full gene sequencing
- Chromosome Analysis (Amniocentesis) – culture only
- Chromosome Analysis (Amniocentesis)– rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (10-15 days)
- Chromosome Analysis (Amniocentesis)– rapid PCR diagnosis for common aneuploidies (2 days) + culture (10-15 days)
- Chromosome Analysis (Blood)
- Chromosome Analysis (Chorionic Villus) – culture only
- Chromosome Analysis (Chorionic Villus) – rapid PCR diagnosis for common aneuploidies (2 days) + culture (10-15 days)
- Chromosome Analysis (Chorionic Villus)– rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (10-15 days)
- Chromosome Analysis (Product of Conception) – BOBs rapid aneuploidy diagnosis for all chromosomes (5 days) + culture (25 days)
- Chromosome Analysis (Products of Conception)
- Chromosome Analysis (Solid Tissue)
- Chromosome banding karyotype
- Chromosome Y Deletion – AZFa, AZFb, AZFc + SRY
- CLL Genome profile
- CLL Prognostification FISH screen
- Coeliac Disease – HLA DQ2/DQ8 genotyping
- Colorectal Cancer NGS Panel – full gene sequencing + deletions/duplications
- Comparative Genomic Hybridisation (Array CGH)
- Comprehensive Neuropathy NGS Panel – full gene sequencing
- Congenital Absence of Vas Deferens – karyotype + cystic fibrosis screen + polyT(5T) + Y deletions
- Connective Tissue Disorders/Ehlers-Danlos Syndrome/Aneurysm NGS Panel – full gene sequencing + deletions/duplications
- Cornelia de Lange Syndrome NGS Panel – full gene sequencing
- Costello/Noonan/LEOPARD/Cardio-Facio-Cutaneous Syndromes NGS Panel – full gene sequencing
- Craniosynostosis NGS Panel
- Cri du Chat Syndrome – BOBs (5 days) + karyotype (15 days)
- Cri du Chat Syndrome – BOBs only
- CVS PCR for common aneuploidies (2 days)+ culture (10-15 days)
- CVSBOBs only – rapid aneuploidy diagnosis for all chromosomes + common microdeletion syndromes
- CVSBOBs – rapid BOBs aneuploidy diagnosis for all chromosomes (3-5 days) + culture (10-15 days)
- Cystic Fibrosis (139 common variants) – reflex to Poly T when CFS required
- Deafness NGS Panel – full gene sequencing
- Diabetes Panel – Obesity NGS
- DiGeorge Syndrome (22q11 & 10p14 deletion) – BOBs (5 days) + karyotype (15 days)
- DiGeorge Syndrome (22q11 & 10p14) – BOBs only
- Dihydropyrimidine Dehydrogenase deficiency screening (Fluoropyrimidine Toxicity)
- Dilated Cardiomyopathy NGS Panel – full gene sequencing + deletions/duplications
- DNA Extraction & Storage – 3 years (longer upon request)
- DNA Identity Profile – 15 STR markers
- Duchenne Muscular Dystrophy – deletions/duplications only
- Duchenne Muscular Dystrophy – full sequencing DMD1 gene
- DVT/Pre-travel Screen
- Ehlers-Danlos Syndrome/Aneurysm/Connective Tissue Disorders NGS Panel – full gene sequencing + deletions/duplications
- Endometrial Cancer NGS Panel – full gene sequencing + deletions/duplications
- Epidermolysis Bullosa NGS Panel – full sequencing
- Epilepsy, Adolescent/Adult Onset Panel – sequencing + deletions/duplications
- Epilepsy, Comprehensive NGS Panel – full sequencing + deletions/duplications
- Fabry Disease, X-linked – GLA gene sequencing
- Facioscapulohumeral Muscular Dystropy (FSHD) – D4Z4 repeat deletion
- Factor II Prothrombin – G20210A variant
- Factor V Leiden – G1691A variant
- Factor VIII (F8) Severe Haemophilia A – common 1/22 intron inversion
- Familial Adenomatous Polyposis (FAP) – full gene sequencing + deletions/duplications
- Familial Exudative Vitreoretinopathy (FEVR) NGS Panel– full gene sequencing
- Familial Hypercholesterolaemia NGS Panel
- Familial Hypocalciuric Hypercalcaemia (FHH) Panel – full sequencing CASR + AP2S1 + GNA11 genes
- Familial Medullary Thyroid Carcinoma – hotspot sequencing RET gene
- Fatty Acid Oxidation Disorders NGS Panel – full gene sequencing
- FLT3-ITD and FLT3-TKD screening assay
- Fragile X Syndrome screen – FMR1 repeat analysis PCR
- Friedreich Ataxia – frataxin gene repeat analysis
- Gaucher disease – full gene sequencing
- Genetic Reproductive Profile (Male)
- Gilbert Syndrome – common UGT1A1 repeat variation
- Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency – full G6PD gene sequencing
- Glycogen storage disease type 2 (Pompe) mutation analysis
- Haemochromatosis – HFE common variants C282Y + H63D
- Haemoglobin variants (alpha and beta globin gene variants) including sickle cell – ARMS PCR, RE-PCR, alpha and beta gene sequencing
- Haemophilia A (Severe) – Factor VIII (F8) common 1/22 intron inversion
- Haemophilia A CVS Variant Analysis (Known Genotype) – F8 Intron 22 Inversion, F8 Intron 1 Inversion, Sequence analysis of known variants for F8 gene
- Haemophilia B CVS Variant Analysis (Known Genotype) – Sequence analysis of known variants for F9
- Hearing Loss NGS Panel – full gene sequencing
- Hereditary Cancer NGS Panel, Comprehensive – full gene sequencing + deletions/duplications
- Hereditary Colon Cancer (Lynch Syndrome) NGS Panel – full gene sequencing + deletions/duplications
- Hereditary Neuropathy with Liability to Pressure Palsy – PMP22 deletion analysis
- Hereditary Spastic Paraplegia NGS Panel – full gene sequencing + deletions/duplications
- HFE gene (Haemochromatosis) – common variants C282Y + H63D
- Hirschprung Disease NGS Panel – full gene sequencing with deletions and duplications
- HLA Tissue Typing A
- HLA Tissue Typing A+B
- HLA Tissue Typing A+B+C (Class I)
- HLA Tissue Typing A/B/C/DRB1/3/4/5/DQB1 (Class I & II)
- HLA Tissue Typing A/B/DRB1/3/4/5
- HLA Tissue Typing A/B/DRB1/3/4/5/DQB1
- HLA Tissue Typing B
- HLA Tissue Typing B*27 only
- HLA Tissue Typing B*51 (Behcet’s Disease)
- HLA Tissue Typing B*57:01 high resolution
- HLA Tissue Typing C
- HLA Tissue Typing Coeliac Disease – DQ2/DQ8
- HLA Tissue Typing DRB1/3/4/5
- HLA Tissue Typing DRB1/3/4/5/DQB1 (Class II)
- HLA Tissue Typing Narcolepsy – DQB1*06:02
- HPFH and δβthalassaemia – Gap PCR, HBB MLPA, beta and gamma globin gene sequencing
- Huntington Disease – HD gene repeat analysis PCR
- Hyperinsulinism NGS Panel – full gene sequencing
- Hyperparathyroidism – CASR sequencing
- Identity Profile (DNA) – 15 STR markers
- IDH1/2 screening assay
- IgVH mutation analysis for CLL
- Intellectual Disability NGS Panel – full gene sequencing + deletions/duplications
- Iron Overload Profile
- Joubert/Meckel-Gruber Syndrome NGS Panel – full gene sequencing
- Kallmann Syndrome NGS Panel – full gene sequencing
- Kennedy Disease (Spinal Bulbar Muscular Atrophy) – AR repeat expansion
- Kidney/Urinary Tract Cancer NGS Panel – full gene sequencing + deletions/duplications
- Krabbe Disease – GALC sequencing + 502T/del common deletion
- Lactose Intolerance Gene
- Langer-Giedion Syndrome – BOBs (5 days) + karyotype (15 days)
- Langer-Giedion Syndrome – BOBs only
- Leber’s Congenital Amaurosis NGS Panel – full gene sequencing
- Leber’s Hereditary Optic Neuropathy – m.3460G>A + m.11778G>A + m.14484T>C common variants
- Leigh and Leigh Like Syndrome NGS Panel – full gene sequencing + deletions/duplications
- LEOPARD/Noonan/Cardio-Facio-Cutaneous/Costello Syndromes NGS Panel – full gene sequencing
- Leukaemia (Rapid Acute) DNA and RNA NGS Panel
- Leukaemia Fusion Gene Screening Assay (Q30)
- Leukaemia/Lymphoma RNA Sequencing (Fusion Gene and SNV/Indel) Panel
- Li-Fraumeni Syndrome (p53-related cancer predisposition) – TP53 sequencing + MLPA
- Limb-Girdle Muscular Dystrophy (LGMD) NGS Panel – full gene sequencing
- Lissencephaly NGS Panel – full gene sequencing
- Loeys-Dietz Syndrome/Marfan Syndrome/Aortic Aneurysm and Dissection NGS Panel – full gene sequencing
- Long-QT Syndrome / Brugada Syndrome – full gene sequencing
- Lowe (Oculocerebrorenal) Syndrome – OCRL sequencing
- Lung Disorders NGS Panel – full gene sequencing
- Lynch Syndrome (HNPCC) NGS Panel – full gene sequencing + deletions/duplications
- Lysosomal Storage Disorders NGS Panel – full gene sequencing
- Male Genetic Reproductive Profile
- Marfan Syndrome and Thoracic Aortic Aneurysm and Dissection NGS Panel – full gene sequencing
- Marfan Syndrome – FBN1 sequencing + deletions/duplications
- Maturity-Onset Diabetes of the Young (MODY) NGS Panel – full gene sequencing
- MDP Genome profile
- MDS Genome profile
- Meckel-Gruber/Joubert Syndrome NGS Panel – full sequencing across 38 genes
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency – ACADM sequencing
- Melanoma Comprehensive Cancer NGS Panel – full gene sequencing + deletions/duplications
- Microdeletion (common) Syndromes – BOBs only
- Microphthalmia/Anophthalmia /Coloboma NGS Panel – full gene sequencing
- Miller-Dieker Syndrome – BOBs (5 days) + karyotype (15 days)
- Miller-Dieker Syndrome – BOBs only
- Mitochondrial genome sequencing
- Mitochondrial genome – full mitochondrial DNA sequencing + deletions
- Molecular Karyotyping
- Motor Neurone Disease (Amylotrophic Lateral Sclerosis) NGS Panel – full gene sequencing
- MTHFR – common C677T + A1298C variants
- Mucopolysaccharidosis NGS Panel – full gene sequencing
- Multiple Endocrine Neoplasia Type 1 – full MEN1 sequencing
- Multiple Endocrine Neoplasia Type 2 – RET gene hotspot sequencing
- Myeloid Gene Panel
- Myeloma FISH high risk markers screen
- Myeloma Genome profile
- Myeloproliferative Neoplasm NGS Screening Panel
- Myotonic Dystrophy Type 1 – DMPK repeat PCR
- Myotonic Dystrophy Type 2 (PROMM) – ZNF9 repeat PCR
- Narcolepsy (HLA DQB1*06:02)
- Nephrotic Syndrome, Steroid-Resistant NGS Panel – full gene sequencing
- Nervous System/Brain Cancer NGS Panel – full gene sequencing + deletions/duplications
- Neurofibromatosis Type 1 – NF1 + SPRED1 sequencing + deletions/duplications
- Neurofibromatosis Type 2 (Bilateral Acoustic) – NF2 sequencing + deletions/duplications
- Neuronal Ceroid Lipofuscinosis (Batten Disease) NGS Panel – full gene sequencing
- Next-generation sequencing
- Non-Invasive Prenatal Testing – common aneuploidy screening from maternal blood
- Noonan Syndrome Prenatal Screening – PTPN11 exons 3 & 8 only
- Noonan/LEOPARD/Cardio-Facio-Cutaneous/Costello Syndromes NGS Panel – full gene sequencing
- Nystagmus, X-linked Infantile – FRMD7 gene sequencing
- Oculopharyngeal Muscular Dystrophy – PABPN1 repeat analysis
- Optic Atrophy NGS Panel – full sequencing OPA1 + OPA3 genes
- Osteogenesis Imperfecta NGS Panel – full gene sequencing
- Ovarian Cancer NGS Panel – full gene sequencing + deletions/duplications
- p53-related cancer predisposition (Li-Fraumeni Syndrome) – TP53 sequencing + MLPA
- Pancreatic Cancer NGS Panel – full gene sequencing + deletions/duplications
- Paraganglioma/Pheochromocytoma NGS Panel – full gene sequencing + deletions/duplications
- Paternity Testing (postnatal and prenatal) – sample required from each person being tested (3 people)
- Pelizaeus-Merzbacher Disease – PLP1 sequencing + deletions/duplications
- Pendred Syndrome – SLC26A4 gene sequencing
- Periodic Fever/Autoinflammation NGS Panel – full gene sequencing
- Peutz-Jegher Syndrome – STK11 sequencing + deletions/duplications
- Phelan-McDermid Syndrome – karyotype + FISH
- Pheochromocytoma/Paraganglioma NGS Panel – full gene sequencing + deletions/duplications
- Pigmentation/Oculocutaneous Albinism/Hermansky-Pudlak Syndrome NGS Panel – full gene sequencing
- POLG-Related Disorders – full POLG sequencing + copy number variant
- Polycystic Kidney/NGS Panel – full gene sequencing
- Pontocerebellar Hypoplasia NGS Panel – full gene sequencing
- Postnatal array CGH
- Prader-Willi Syndrome (Primary Screen) – methylation PCR
- Pre-Travel Screen (DVT)
- Prenatal array CGH
- Prenatal Diagnosis (BOBs + Culture)
- Primary Ciliary Dyskinesia (PCD) NGS Panel – full gene sequencing
- Primary Hyperoxaluria Panel – full gene sequencing + CNV
- Product of Conception BOBs only – rapid aneuploidy diagnosis for all chromosomes
- Product of Conception – rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (25 days)
- Prostate Cancer NGS Panel – full gene sequencing + deletions/duplications
- Thrombophilia due to protein C deficiency
- PTEN-related disorders (including Bannayan-Riley-Ruvalcaba, Cowden & Proteus Syndromes) – sequencing + deletions/duplications
- QF-PCR rapid common aneuploidy screen
- Recurrent Miscarriage Profile (female)
- Renal Cysts and Diabetes (RCAD) – HNF-1β sequencing + deletions/duplications
- Renal/Urinary Tract Cancer NGS Panel – full gene sequencing + deletions/duplications
- Retinal Detachment NGS Panel – full sequencing across 25 genes
- Retinal Disorders NGS Panel – full gene sequencing
- Retinoblastoma – RB1 sequencing + deletions/duplications
- Rett Syndrome (MECP2 gene only) – full sequencing + deletions/duplications
- Rett/Angelman Syndromes NGS Panel – full gene sequencing
- Short Stature – SHOX variant screening + deletions/duplications
- Short-Chain Acyl-CoA Dehydrogenase Deficiency – ACADS sequencing
- Silver-Russell Syndrome – methylation studies on 11p15 imprinting domains KvDMR + H19
- Single FISH test as per request
- Skeletal Dysplasia NGS Panel – full gene sequencing
- Smith-Lemli-Opitz Syndrome – DHCR7 sequencing
- Smith-Magenis Syndrome – BOBs (5 days) + karyotype (15 days)
- Smith-Magenis Syndrome – BoBs only
- Sotos Syndrome (Cerebral Gigantism)– NSD1 sequencing + deletions/duplications
- Spastic Paraplegia NGS Panel – full gene sequencing + deletions/duplications + mitochondrial DNA
- Spinal Bulbar Muscular Atrophy (Kennedy Disease) – AR repeat analysis
- Spinal Muscular Atrophy – SMN1 deletions/duplications
- Spinocerebellar Ataxia NGS Panel – full gene sequencing
- Spinocerebellar Ataxia – multiplex SCA1+2+3+6+7+17 common repeat expansions
- SRY (Sex-determining Region Y)
- Systemic mastocystosis – C-Kit common variants (KIT D816V)
- T cell clonality assay (TCR beta and TCR gamma)
- Tay Sachs Screen – common variants
- Thrombophilia with a likely monogenic cause (R97)
- Thrombotic Risk Profile
- Thyroid Cancer NGS Panel – full gene sequencing + deletions/duplications
- Torsion Dystonia (DYT1) – TOR1A common variant c.904-906delGAG
- Treacher-Collins Syndrome NGS Panel – full sequencing POLR1C + POLR1D + TCOF1
- Tuberous Sclerosis – full TSC1 + TSC2 gene sequencing
- Urinary Tract/Renal Cancer NGS Panel – full gene sequencing + deletions/duplications
- Usher Syndrome NGS Panel – full gene sequencing
- Very Long-Chain Acyl-CoA Dehydrogenase Deficiency – ACADVL sequencing
- Von Hippel-Lindau Syndrome – VHL sequencing + deletions/duplications
- Wolf-Hirschhorn Syndrome – BOBs (5 days) + karyotype (15 days)
- Wolf-Hirschhorn Syndrome – BOBs only
- Xmn and gamma gene – gamma globin gene sequencing, RE PCR
- Y chromosome microdeletions – AZFa + AZFb + AZFc + SRY
- Zellweger Syndrome/Peroxisomal Disorders NGS Panel – full gene sequencing
- Ziwig Endotest®
- Zygosity testing – comparative DNA profile
- Chromosome Analysis (Stem Cells) - Rapid BOBs aneuploidy DNA analysis for all chromosomes (5 days)
- Cytochrome P450 2C19 (CYP2C19) genotyping
-
Tests by area
- Bleeding and platelet disorders
- Cardiac disorders
- Deafness
- Dermatology
- DNA identity, relationships and storage
- Endocrine disorders
- Endomentrial disorders
- Haematological disorders
- Gastrointestinal disorders
- Hepatic disorders
- Immunology
- Muscular / Neurological disorders
- Non-invasive Prenatal screening
- Oncology
- Opthalmology
- Paediatric disorders
- Pharmacogenomics
- Prenatal diagnosis
- Renal disorders
- Reproductive health
- Respiratory disorders
- Rheumatology
- Thrombosis
- Stem cells
- Oncogenomics (haematological cytogenetics) tests
-
HSL Haematology
- Staff/Key personnel
-
Tests
- Anaemia Profile
- Antenatal Profile
- APTT/KCCT
- Atypical Antibody Screen (handwritten tube label)
- Blood Film Examination
- Blood Group
- Carboxyhaemoglobin
- Coagulation Profile 1
- Coagulation Profile 2
- D-Dimers (Fibrinogen Degradation Products)
- DVT/Pre-travel Screen
- ESR
- Fibrinogen
- Full Blood Count
- Haematology Profile
- Haemoglobin
- Immune Function Evaluation (Total)
- INR
- Lymphocyte Subsets (CD3/CD4/CD8)
- Malarial Parasites
- Mean Cell Volume (MCV)
- Microfilaria Blood Film
- Natural Killer Profile 2
- PAI1 4G/5G Polymorphism
- Paul Bunnell (Monospot)
- Pre-Travel Screen (DVT)
- Prothrombin Time
- Prothrombin Time + Dose
- Reticulocyte Count
- Thrombin Time
- Vitamin K (With PIVKA II)
- Total Glycated Haemoglobin (Boronate Affinity)
-
Special haemostasis tests
- Activated Protein C Resistance
- ADAMTS – 13 Activity Assay
- Anticoagulation monitoring
- Antithrombin Ill
- Factor II Assay
- Factor II Prothrombin Gene FX2
- Factor V Assay
- Factor V Leiden
- Factor VII Assay
- Factor VIII Assay
- Factor VIII Inhibiting Antibody
- Factor IX Assay
- Factor IX Inhibiting Antibody
- Factor X Assay
- Factor XI Assay
- Factor XII Assay
- Factor XIII Assay
- Hughes Syndrome
- Lupus Anticoagulant and Anticardiolipin Abs
- Lupus Anticoagulant only
- Miscarriage/Thrombotic Risk Profile
- Plasma Viscosity
- Platelet Aggregation Studies
- Platelet function assay (PFA-100 assay)
- Protein C
- Protein S Free Ag
- Taipan Snake Venom Time
- Thrombotic Risk Profile
- Von Willebrand Profile
- Von Willebrands Multimers
- HSL Manual Haematology (Red Cells)
-
HSL Immunology
- Staff/Key personnel
- Specialties
-
Tests
- Acetylcholine Receptor Antibodies
- AChR Cluster
- Actin Antibodies
- ADA (Adenosine deaminase) (Nucleotide Metabolism)
- Adrenal Cortex Antibodies
- Adulimimab Antibodies
- Alpha 3 Ganglionic Antibodies
- Anti-mitochondrial Antibodies (M2)
- AMPA 1 and 2 Antibodies
- ANCA (Anti-Neutrophil Cytoplasmic Antibodies)
- Anti-Nuclear Antibodies
- AP50 (Alternative Pathway)
- Apoptosis Assay
- Aquaporin 4 Antibodies (Neuromyelitis Optica)
- Aspergillus Fumigatus Precipitins
- Autoantibody Profile I
- Autoantibody Profile II
- Avian Precipitins (11 Species)
- B2 Microglobulin
- Basal Ganglia Antibodies
- Beta 2 Glycoprotein 1 Antibodies
- BPO (M2-3E) Antibodies
- BRAF-V600E
- Bruton's Tyrosine Kinase (BTK)
- Bruton's Tyrosine Kinase (BTK) Gene
- C1 Esterase Inhibitor (Functional)
- C1 Esterase gene
- C1 Esterase Inhibitor (Antigenic)
- C1 Inhibitor Antibodies
- C1q Binding Immune Complex
- C2
- C2 Gene
- C3 Complement
- C3 Nephritic Factor
- C3-C4 Complement
- C3d
- C4 Complement
- C7 Gene
- C8 Gene
- Candida Stimulation
- Cardiolipin Antibodies (IgG IgM)
- Cartilage Antibodies
- CASPR2 Antibodies
- CCP Antibodies (RF)
- CD40
- CD40 Ligand (CD154)
- CD40L Gene Mutation Analysis
- CENP A Antibodies
- CENP B Antibodies
- Centromere Autoantibodies
- CGD Proteins p22, gp47, 67, gp91
- CH100 (Classical pathway)
- Chlamydia Species Specific Antibodies Screen
- Coeliac/Gluten Profile 2
- Coeliac/Gluten Sensitivity Profile
- Colloid Antigen-2 Antibodies
- Common Gamma Chain
- Crithidia Antibodies (dsDNA Abs)
- Cytokine Defect Investigations
- DC Phenotype
- Dihydrohodamine-123-Respiratory-Burst Assay (DHR)
- DNA (Double Stranded) Antibodies
- DNA (Single Stranded) Antibodies
- Dock 8 Mutation Analysis
- Dock 8 Protein
- DVT/Pre-travel Screen
- EJ Antibodies
- Endomysial Antibodies (IgA)
- Extractable Nuclear Antibodies (nRNP, Sm, Ro, La, Jo-1, Scl-70, CENP-B)
- Factor B Level
- Factor H Antibodies
- Factor H Level
- Factor I Antibody
- Factor I Level
- Farmers Lung Precipitins
- FH3L
- Fibrillarin Antibodies
- FLT3 Ligand
- Functional C1 Esterase Inhibitor
- GABAR Antibodies
- Ganglionic Alpha 3 Acetylcholine Receptor Antibodies
- Ganglioside GM1, GD1B, GQ1B Antibodies
- Gastric Parietal Cell Autoantibodies
- GATA2 Sequencing
- Gliadin Antibodies (IgG) (deamidated)
- Glomerular Basement Membrane Antibodies
- Glutamic Acid Decarboxylase Antibodies (GAD 65)
- Gluten Allergy Profile
- Gluten Sensitivity Evaluation
- Gluten/Coeliac Profile 2
- Glycine Receptor Antibodies
- GMCSF Antibodies
- gp210 Antibodies
- Granule Release Assay
- Granulocyte Antibodies
- Granulocyte Immunology
- H. Pylori Antibodies (IgG)
- Haemophilus Influenzae Antibodies (HIB)
- Histamine
- Histamine (Urine)
- Histamine Releasing Urticaria Test
- Histone Antibodies
- HMG CoA Reductase Autoantibodies
- Human Anti-Mouse Antibodies
- IFN Gamma Antibodies
- IgA Antibodies
- IgG Subclasses (IgG1, IgG2, IgG3, IgG4)
- IL17 (Th17)
- IL2R Gene Mutation Analysis
- IL6/Interleukin 6
- IL7R alpha and JAK3 gene Mutation Analysis
- Immune Function Evaluation (Total)
- Immune-Complexes
- Immuno Solid Phase Allergen Chip (ISAC)
- Immunoglobulin E – Total
- Immunoglobulins (IgG, IgM, IgA)
- Infliximab Antibodies
- Infliximab Levels
- Inner Ear Antigen (Ottoblot)
- Insulin Antibodies IgG
- Interferon – Alpha
- Interferon – Gamma
- Interleukin 1 Beta
- Interleukin 10
- Interleukin 2
- Interleukin 4
- Interleukin 6
- Interleukin 8
- Intrinsic Factor Antibodies
- Islet Cell Antibodies
- ITK mutation analysis
- JAK 3
- Jo-1 Antibodies
- Ku Antibodies
- La Antibodies
- LC-1 Antibodies
- Legionella Antibodies
- Leukotriene E4
- LGI 1 Antibodies
- Liver Cytosol Antibodies
- Liver Kidney Microsomal (IIF)
- LKM-1 (immunoblot)
- Lupus Anticoagulant and Anticardiolipin Antibodies
- Lymphocyte Antibodies
- M2-3E (BPO) Antibodies
- Mast Cell Tryptase
- MBL (Mannose Binding Lectin)
- MDA5 Antibodies
- Meningococcal Antibodies (A, C, W, Y)
- Meningococcal Serum Bactericidal Titre
- MHC Class 1
- Mi-2a Antibodies
- Mi-2b Antibodies
- Mitochondrial Antibodies
- Mitochondrial Antibodies M2
- Mitochondrial mutation M.1555 analysis
- MOG [Myelin Oligodendrocyte Glycoprotein] Antibodies
- MUSK Antibodies
- Musk Cluster Antibodies
- Myasthenia Gravis Evaluation
- Myelin Associated Glycoprotein Antibodies (MAG)
- Myelin Basic Protein Antibodies
- Myeloperoxidase (MPO) Antibodies
- Myocardial Antibodies
- Myositis Immunoblot (Mi-2a, Mi-2b, TIF1g, MDA5, NXP2, SAE1, Ku, PM-Scl100, PM-Scl75, Jo-1, SRP, PL-7, PL-12, EJ, OJ, Ro-52)
- NBT Test (Nitro Blue Tetrazolium)
- Neuronal Antibodies (Hu, Ri, Yo, Cv2, Ma2)
- Neutrophil Antibodies
- Neutrophil Phenotypic Analysis (CD11a and CD18)
- NK Killing
- NMDA Receptor Antibodies
- NOR90 Antibodies
- nRNP Antibodies
- Nucleotide Metabolism (ADA and PNP)
- NXP2 Antibodies
- OJ Antibodies
- Ovarian Autoantibodies
- Pancreatic Islet Cell Antibodies
- Parathyroid Antibodies
- PDGRF Antibodies
- Pemphigus-Pemphigoid Autoantibodies
- Perforin
- Phagocytosis Assay
- Phosphatidylserine Antibodies
- Phospholipase A2 Receptor
- Pituitary Antibodies
- PL-12 Antibodies
- PL-7 Antibodies
- Platelet Antibodies
- PML Antibodies
- PM-Scl100 Antibodies
- PM-Scl75 Antibodies
- Pneumococcal Antibodies – Serotype Specific
- Pneumococcal Antibody (PCP)
- PNP (Nucleotide Metabolism)
- PRF1 (perforin) gene and MUNC 13-4 mutation analysis
- Proliferation Assay
- Proteinase 3 Antibodies
- Purkinje Cell Antibodies (Hu and Yo)
- Quantiferon Gold
- Retinal Antibodies
- Rheumatoid Factor
- Rheumatology Profile 1 (Screen)
- Rheumatology Profile 2 (Connective Tissue)
- Rheumatology Profile 3 (Rheumatoid/Basic)
- Rheumatology Profile 4 (Systemic Lupus)
- Rheumatology Profile 5 (Mono Arthritis)
- Rheumatology Profile 6 (Rheumatoid Plus)
- Rheumatology Profile 7 (Sjogrens Syndrome)
- RNA Polymerase Antibodies
- Ro Antibodies
- Ro-52 Antibodies
- RP11 Antibodies
- RP155 Antibodies
- SAE1 Antibodies
- Salivary Gland Antibodies
- SAP
- Scl-70 Antibodies
- Scleroderma Immunoblot (Scl-70, CENP A, CENP B, RP11, RP155, Fibrillarin, NOR90, Th/To, PM-Scl100, PM-Scl75, Ku, PDGFR, Ro-52)
- Serotype Specific Pneumococcal Antibodies
- Signal Recognition Particle (SRP) Antibodies
- Signal Transducer and Activator of Transcription 3 Gene (STAT3)
- Skin (Pemphigus/Pemphigoid) Autoantibodies
- SLA (Soluble Liver Antigen) Antibodies
- SLA/LP Antibodies
- Sm Antibodies
- Smooth Muscle Antibodies
- Soluble IL2 receptor (CD25)
- Sp100 Antibodies
- Specific IgE to Allergen
- Sperm Antibodies (Serum)
- Staphylolysin Titre Antibodies (SGOT)
- STAT4 Tyrosine Phosphorylation
- STAT5 Tyrosine Phosphorylation
- Steroid Cell Antibodies
- Streptolysin Titre Antibodies/ASOT
- Striated/Skeletal Muscle Antibodies
- Sulfatide Antibodies
- Synthetase Antibodies (PL7, PL12, EJ, OJ)
- T Cell Receptor Excision Circlet Analysis (TRECS)
- T Cell Spectratyping
- TB Quantiferon®-TB Gold
- Testicular Autoantibodies
- Tetanus Toxoid Antibody
- TGN (TGN Antibodies)
- Th/To Antibodies
- Thyroglobulin Antibodies
- Thyroid Antibodies (incl. Thyroglobulin + Thyroid Peroxidase Antibodies)
- Thyroid Peroxidase Antibodies/Anti TPO
- Tissue Battery (AMA Anti mitochondrial antibody, SMA smooth muscle antibody, LKM1 liver kidney microsomal 1, GPCA Gastric parietal cell antibody)
- Tissue Transglutaminase IgA (Coeliac)
- Tissue Transglutaminase IgG
- TNFRSF6 (FAS) gene mutation analysis
- Total IgE
- Total Immune Function Evaluation
- Total Immunoglobulin E
- Transmembrane Activator and CAML interactor (TACI)
- TSH-Receptor Antibodies
- U3-RNP Antibodies (Fibrillarin)
- Urticaria Test (Histamine Releasing)
- V Beta Repertoire
- Vascular Endothelial Growth Factor
- VDRL (RPR)
- Voltage Gated Calcium Channel Antibodies
- Voltage Gated Potassium Channel Antibodies
- WAS Protein
- XIAP
- Zinc Transporter 8
- Factor XII Gene
- IA2 Antibodies
- TIF1γ Antibodies
- HSL Microbiology
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HSL Parasitology
- About HSL Parasitology
- Staff/Key personnel
- Specimens
- Request procedures
- Reporting times
- Results
- Advisory service
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Tests for parasitic diseases and specimen requirements
- Amoebiasis (Entamoeba histolytica)
- Babesiosis
- Cryptosporidium spp
- Cyclosporiasis
- Cystoisosporiasis
- Cysticercosis and Taeniasis
- Ectoparasites
- Enterobiasis
- Fascioliasis
- Filariasis
- Free-living Amoebae
- Giardiasis
- Hydatid disease (Echinococcosis)
- Human Helminthiasis (worm identification)
- Intestinal Protozoa
- Leishmaniasis
- Microsporidiosis
- Malaria
- Schistosomiasis
- Strongyloidiasis
- Toxocariasis
- Toxoplasmosis
- Trichinosis
- Trypanosomiasis
- Visceral Larva Migrans
- HSL Rapid Response Laboratories
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HSL Special Coagulation
- Staff/Key personnel
- Preparing patients
- Specimens
-
Tests
- Activated Partial Thromboplastin Time (APTT)
- Activated Protein C Ratio with Factor V Deficient Plasma
- Antithrombin Activity
- Antithrombin Antigen
- Apixaban Level
- APTT 50 / 50 Mix
- APTT Inhibitor Screen
- APTT Ratio for UFH Monitoring
- Argatroban Level – Direct Thrombin Inhibitors
- Chromogenic Factor IX
- Chromogenic Factor VIII (Biophen)
- Chromogenic Factor VIII (Coamatic – Bovine Factors)
- Chromogenic Nijmegen FVIII Bethesda
- Clauss Fibrinogen
- Dabigatran Level – Direct Thrombin Inhibitors
- Dalteparin
- Danaparoid Level
- Edoxaban Level
- Emicizumab Level
- Enoxaparin Level
- Factor II – Extrinsic One Stage PT Assays
- Factor IX Antigen (ELISA)
- Factor IX Inhibitor
- Factor IX using SynthaFax APTT Reagent
- Factor IX – Intrinsic One Stage APTT Assays
- Factor V Leiden G1691A and Prothrombin (FII) G20210A gene mutations
- Factor V – Extrinsic One Stage PT Assays
- Factor VII – Extrinsic One Stage PT Assays
- Factor VIII Inhibitor
- Factor VIII – Intrinsic One Stage APTT Assays
- Factor X – Extrinsic One Stage PT Assays
- Factor XI Antigen (ELISA)
- Factor XI Inhibitor
- Factor XI – Intrinsic One Stage APTT Assays
- Factor XII – Intrinsic One Stage APTT Assays
- Factor XIII Activity
- Factor XIII Antigen (ELISA)
- Fibrinogen Antigen
- Fondaparinux Level
- FVII Antigen
- High Molecular Weight Kinninogen HMWK (Fitzgerald Trait)
- Low Molecular Weight Heparin (Anti-Xa)
- Lupus Screen – Dilute Russell Viper Test and Confirmation
- Lupus Screen – Silica Clot Time and Confirmation
- PFA-200 (Collagen/ADP Closure Time (seconds))
- PFA-200 (Collagen/Epinephrine Closure Time (seconds))
- Plasmin Inhibitor Activity
- Plasminogen Activator Inhibitor-1 Antigen (PAI-1 Ag) (ELISA)
- Plasminogen Activity
- Platelet Aggregate Size Surface Coverage (IMPACT-R)
- Platelet Aggregation (Light Transmission Aggregometry)
- Platelet Factor 4 IgG Heparin Induced Thrombocytopenia Screen HIT
- Platelet Lummiaggregometry
- Platelet Nucleotides
- Porcine FVIII Inhibitor
- PreKallikrein (Fletcher Trait)
- Protein C Activity
- Protein C Antigen (ELISA)
- Protein S Activity
- Protein S Free
- Protein S Total (ELISA)
- Prothrombin F 1+2
- Prothrombin Time (PT) / INR
- Reptilase time
- Rivaroxaban Level
- ROTEM
- Thrombin Generation Assay
- Thrombin Time
- Thrombin-Antithrombin Complexes
- Tinzaparin Level
- Tissue Plasminogen Activator (t-PA) Antigen
- Unfractionated Heparin (Anti-Xa)
- VWF Activity Latex
- VWF Antigen (ELISA)
- VWF Antigen Latex
- VWF Collagen Binding (ELISA)
- VWF Inhibitor Screen
- VWF Multimer
- VWF Ristocetin co-factor
- VWFVIII Binding
- ADAMTS 13 IgG Activity
- ADAMTS 13 Inhibitor
- Glycoprotein Ib (RFH users only)
- Glycoprotein IIb/IIIa (RFH users only)
- PIVKA
- Vitamin K1
- Warfarin Level
- Factors affecting test performance
- Sample rejection/acceptance criteria
- Requesting additional tests
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HSL Virology
- Staff/Key personnel
- Specimens
- Request procedures
- Specialities
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Tests
- 16s bacterial sequencing
- 18s fungal sequencing
- Adenovirus by PCR
- Adenovirus DNA Quantitation by PCR
- Alphavirus Investigations
- Arbovirus Antibodies/Abs
- BK Polyoma Virus by PCR (quantitative)
- Bone marrow screen donor antibody screen
- Chagas Disease Serology (S American Trypanosomiasis) T Cruzi
- Chikungunya Virus Abs
- CMV DNA by PCR (Guthrie/Dried blood spots)
- CMV DNA by PCR (other)
- CMV DNA by PCR (Urine)
- CMV DNA Quantitation (by PCR)
- CMV Resistance
- Coronavirus – COVID-19 IgG Antibody (SARS-CoV-2)
- Coronavirus – COVID-19 PCR (SARS-CoV-2)
- CSF Screen by PCR (CMV, EBV, HSV, VZV, Enterovirus, Parechovirus)
- Cytomegalovirus (CMV-DNA) Amnio
- Cytomegalovirus (IgG/IgM) Antibodies
- Cytomegalovirus IgG Avidity
- Dengue Fever PCR
- EBV DNA quantitative PCR
- Epstein-Barr Virus (EBV) Antibodies VCA IgG/IgM and EBNA IgG
- Hantavirus Serology/PCR
- Hepatitis (Acute) Screen
- Hepatitis A (IgM)
- Hepatitis A Immunity (Total)
- Hepatitis A RNA by PCR
- Hepatitis B (PCR) Genotype
- Hepatitis B Core Antibody – IgM
- Hepatitis B Core Antibody – Total
- Hepatitis B DNA (Viral load)
- Hepatitis B Immunity
- Hepatitis B Profile
- Hepatitis B Resistant Mutation
- Hepatitis B Surface Antibody
- Hepatitis B Surface Antigen
- Hepatitis B Surface Antigen Quantitification
- Hepatitis B ‘e’ Antigen and Antibody
- Hepatitis C Antibodies
- Hepatitis C Antigen (Early detection)
- Hepatitis C Genotype
- Hepatitis C NS3 Resistance
- Hepatitis C NS5a Resistance
- Hepatitis C NS5b Resistance
- Hepatitis C RNA (Viral Load)
- Hepatitis Delta RNA (Viral load)
- Hepatitis Delta total Antibody
- Hepatitis E IgG/IgM
- Hepatitis E RNA (Quantitative PCR)
- Herpes Simplex 1 and 2 IgG typing
- Herpes Simplex I/II Antibody Profile (IgG)
- Herpes Simplex I/II by PCR (Swab)
- HIV 1 Proviral DNA
- HIV Screening: HIV1& 2 Abs/p24 Ag (4th Gen)
- HIV-1 Avidity (RITA/STARHS)
- HIV-1 Genotypic Resistance (Integrase)
- HIV-1 Genotypic Resistance (RT & Protease)
- HIV-1 RNA Viral Load by PCR
- HIV-1 Tropism
- HIV-2 Drug Resistance
- HIV-2 Proviral DNA
- HIV-2 RNA (Quantitative or Qualitative) by PCR
- HTLV 1& 2 Abs. (Human T Lymphotropic Virus Type I-II)
- HTLV by PCR
- Human Herpes Virus 6 by quantitative PCR
- Human Herpes Virus 8 (HHV8) by qualitative/quantitative PCR
- Human Parvovirus B19 – Quantitative DNA PCR
- JC Polyoma Virus by PCR
- Measles Antibodies (IgG) Immunity
- Measles Antibodies (IgM)
- Measles PCR
- Measles, Mumps, Rubella (MMR)
- Mumps Antibodies (IgG)
- Mumps Antibodies (IgM)
- Mumps PCR
- Needle Stick Injury Profile
- Neurological Viral Screen
- Parvovirus Antibodies (IgM)
- Parvovirus IgG Antibodies
- Parvovirus Quantitative DNA by PCR
- Polio Virus 1, 2, 3 Antibodies
- Rabies Antibody
- Respiratory PCR
- Rubella Antibody (IgG)
- Rubella Antibody (IgM)
- Rubella Avidity
- Rubella PCR
- Torch Screen
- Transplant screen donor antibody screen
- Travel fever viral screen
- Varicella zoster Antibodies (IgG)
- Vesicular Rash by PCR
- Viral Eye by PCR (HSV/VZV/ADENO)
- West Nile Virus Abs
- West Nile Virus PCR
- Zika Abs IgM and IgG – Antibody detection from 15 days
- Zika RNA by PCR
- Varicella Zoster – DNA
- Gastro-Intestinal PCR (Adenovirus, Astrovirus, Rotavirus, Norovirus, Sapovirus.)
- Genital Ulcer PCR (HSV, Syphilis)
- HIV-1 PCR Qualitative
- Monkey Pox PCR
- Neurological Viral PCR
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Molecular microbiology (Sexual health) test library
- Chlamydia (PCR swab)
- Chlamydia (Thin Prep)
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- Chlamydia/Gonorrhoea (Thin Prep)
- Chlamydia/Gonorrhoea (Throat)
- Chlamydia/Gonorrhoea (Urine)
- Chlamydia/Gonorrhoea/Trichomonas by PCR
- Gonorrhoea (PCR swab)
- Gonorrhoea (Thin Prep)
- Gonorrhoea (Urine)
- Haemophilus ducreyi by PCR
- HPV (mRNA HR-HPV) (ThinPrep)
- Lymphogranuloma Venerium (LGV)
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- Mycoplasma genitalium by PCR
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News
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- Lights! Camera! Action!
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- Get It Right First Time
- Qualifications and Portfolios
- Interview with Nikos Panagiotou
- Spotlight on the heads of sample reception, The Halo Building and Manchester Site
- A New Variant
- Sonic Healthcare UK – proud to support the World Doctors Orchestra
- Focus on patient reception at 76 Wimpole St
- Introducing Michelle Joseph
- Spotlight on David Allen, HSL-Advanced Diagnostics
- Celebrating Excellence Award
- Focus on R&D
- How COVID has changed the way we train
- Spotlight – The Journey to Automation
- Thanks from the Health Minister
- Spotlight on Brian Madden
- Personal Covid Reflections – Tim Herriman, Group Laboratory Director and Tom Amies, HSL Chief Financial Officer share their experiences
- Cervical Screening made more convenient
- The next phase of the COVID-19: Causes for concern?
- Spotlight – Naina Chavda, COVID-19 Surge Operations Manager
- Providing pathology services at Barnet Hospital
- Halo Level 9 Surge Lab – now up and running
- Spotlight: Diane Benson, Operational Site Lead, Manchester
- Cervical Screening London – a first birthday and other developments
- New Year’s Honour for Dr Paul Grant
- Champions league
- Introducing Nick Read, Group Chief Financial Officer (CFO)
- Goodbye to Professor Chiodini
- Queen’s Jubilee Honours for Dr Lisa Levett
- Artificial intelligence within pathology
- Spotlight on TDL Trials
- Big department, Big changes...
- Supporting NHS England’s scheme to identify people with communicable diseases
- Collaborative working key to success of haemophilia gene therapy trial...
- Spotlight on TDL POCT Ops
- Transforming Blood Transfusion
- Building for the future at Northwick Park
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- Introducing Sonic Training Academy
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- Recognition for Scientific Excellence during the COVID-19 Pandemic
- Congratulations to our GIRFT winners!
- Health Minister visits laboratory
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- Back to school: Encouraging the next generation of scientists
- From tragedy to diagnosis: a genetic search for answers
- Spotlight on HSL Operations Manager, Oneal Joseph
- A rapid transfer
- The rise and rise of self-collect pathology services
- A visit from the Governor of the Bank of England
- Art of Pathology
- Biomedical Science Day – as you’ve never seen it!
- Congratulations go to: Get It Right First Time Winners
- Evolving technologies: How Sonic Healthcare UK is keeping pace
- An IBMS Congress to remember for Sonic Healthcare UK
- Spotlight on Sarah Watters
- Focus on Thrombotic Thrombocytopenic Purpura (TTP)
- A new level of learning at the Sonic Training Academy
- Sharing the Learning
- Celebrating Excellence in Continuous Improvement
- Spotlight on Donna Wiles, Laboratory Manager at the Cleveland Clinic London
- The Sonic Training Academy’s First Open Day
- Celebrating success: Colleagues honoured at IBMS AGM
- A New Lab for the Whittington Hospital
- Welcome to Our New HSL Consultant Specialty Leads
- Simulation Training – Putting Theory into Practice
- A New Radiology Ordering System for GPs
- Congratulations to Graham Hogan
- Welcome to Stephen Symonds
- Supporting Self-sampling Screening
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