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Tests: C

Test codes, sample requirements and turnaround times for our most requested tests.

Please use the search box below to filter this list

Test name
C Peptide
C Reactive Protein
C Reactive Protein (High Sensitivity)
C1 Esterase Inhibitor
C1 Esterase: Function & Total
C1q Binding Immune Complex
C3 Complement
C3/C4 Complement
C4 Complement
CA 125
CA 15-3
CA 19-9
CA 50
CA 72-4
CADASIL – NOTCH3 gene sequencing
Cadmium (Blood)
Cadmium (Urine)
CAKUT (Congenital Anomalies of Kidney & Urinary Tract) NGS Panel – full sequencing across 38 genes
Calcitonin
Calcium
Calcium (24 hour Urine)
Calcium/Creatinine Ratio
Calprotectin
Calprotectin/Elastase Profile
Calreticulin – CALR exon 9 mutation screen
Campylobacter Jejuni Antibodies
Cancer, Comprehensive NGS Panel – full sequencing across 123 genes + deletions/duplications
Candida Antibodies
Candida Antigen
Cannabinoids (Urine) Screen
Carbamazepine (Tegretol)
Carbapenemase producing organism screen
Carbohydrate Deficient Glycoprotein
Carbohydrate Deficient Transferrin (CDT)
Carbohydrate Metabolism Deficiency NGS Panel – full sequencing across 47 genes + deletions/duplications + mitochondrial DNA
Carboxyhaemoglobin
Carcino Embryonic Antigen
Cardiac Enzymes (not chest pain)
Cardio-Facio-Cutaneous/Noonan/LEOPARD/Costello Syndromes NGS Panel – full sequencing across 20 genes
Cardiolipin Antibodies (IgG+IgM)
Cardiomyopathy, Arrhythmogenic Right Ventricular NGS Panel – sequencing across 34 genes + deletions/duplications
Cardiomyopathy, Comprehensive NGS Panel – full sequencing across 111 genes + deletions/duplications
Cardiomyopathy, Dilated NGS Panel – full sequencing across 78 genes + deletions/duplications
Cardiomyopathy, Hypertrophic NGS Panel – full sequencing across 86 genes + deletions/duplications
Cardiovascular Risk Profile 1
Cardiovascular Risk Profile 2
Carnitine – Free &Total
Carotenes
Carrier Screen (Pan-ethnic or Jewish)
Cartilage Antibodies
Cashew Components
Cat Components
Cat Scratch Fever (Bartonella IgG+IgM)
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) NGS Panel – full sequencing across 9 genes + deletions/duplications
Catecholamines (Plasma)
Catecholamines (Urine)
CCP Antibodies (RF)
CD16
CD19 B Cells
CD20
CD25
CD3/CD4/CD8
CD56
CD57
Celery Components
Centromere Autoantibodies
Cerebellar Hypoplasia NGS Panel – full sequencing across 8 genes
Ceruloplasmin
Cervical Cytology
CH50 (Classical pathway)
Chagas Disease Serology (S.American Trypanosomiasis) T. Cruzi
Charcot-Marie-Tooth Syndrome NGS Panel – full sequencing across 59 genes
Charcot-Marie-Tooth Type 1A – PMP22 duplications
CHARGE Syndrome – CHD7 gene sequencing
Chediak-Higashi Syndrome – LYST gene sequencing
Chest Pain Profile
Chikungunya Virus Abs
Chlamydia (PCR swab)
Chlamydia (Thin Prep)
Chlamydia (Urine)
Chlamydia Species Specific (MIF) Ab Screen
Chlamydia/Gonorrhoea (PCR Swab)
Chlamydia/Gonorrhoea (Rectal)
Chlamydia/Gonorrhoea (Thin Prep)
Chlamydia/Gonorrhoea (Throat)
Chlamydia/Gonorrhoea (Urine)
Chlamydia/Gonorrhoea/Trichomonas by PCR
Chloride
Cholestasis, Intrahepatic NGS Panel – full sequencing across 15 genes
Cholesterol
Cholesterol (Familial Hypercholesterolaemia)
Cholinesterase (Blood)
Cholinesterase (Serum/Pseudo)
Chromium (Blood)
Chromium (Urine)
Chromogranin A
Chromogranin A & B
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) – rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (10-15 days)
Chromosome Analysis (Chorionic Villus) – rapid PCR diagnosis for common aneuploidies (2 days) + culture (10-15 days)
Chromosome Analysis (Chorionic Villus)– culture only
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 Analysis (Stem Cells)
Chromosome Y Deletion – AZFa, AZFb, AZFc + SRY
Chronic Fatigue Syndrome Profile
Citrate (Blood)
Citrate (Urine)
CK (MB Fraction)
CK Isoenzymes
C-KIT (Common mutation KIT D816V Gene)
Clobazam
Clomipramine (Anafranil)
Clonazepam
Clostridium Difficile Toxin by PCR
CMV DNA (by PCR)
CMV DNA by PCR (Semen)
CMV DNA by PCR (Urine)
CMV Resistance
Coagulation Profile 1
Coagulation Profile 2
Cobalt (Blood)
Cobalt (Serum)
Cobalt (Urine)
Cocaine (Urine) Screen
Coccidioidomycosis Antibodies
Cockayne Syndrome NGS Panel – full sequencing ERCC6 + ERCC8
Coeliac Disease – HLA DQ2/DQ8 Genotype
Coeliac/Gluten Profile 2
Coeliac/Gluten Sensitivity Profile
Coenzyme Q10
Cold Agglutinin
Collagen (Type I, II, IV) Antibodies
Collagen Type 1 Cross-Linked N-Telopeptide – NTX
Colloid Antigen-2 Antibodies
Colorectal Cancer NGS Panel – full sequencing across 18 genes + deletions/duplications
Comparative Genomic Hybridisation (Array CGH)
Complement C1q
Complement C2
Complement C5
Complement C6
Complement C7
Complement C8
Complement C9
Complement Factor H
Complex PSA (Prostate Specific Ag)
Congenital Absence of Vas Deferens – karyotype + cystic fibrosis screen + polyT(5T) + Y deletions
Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) – 8 mutations + deletions/duplications
Congenital Central Hypoventilation Syndrome (CCHS) – PHOX2B polyalanine repeat analysis
Congenital Central Hypoventilation Syndrome (CCHS)– full sequencing PHO X2B gene
Congenital Disorders of Glycosylation NGS Panel – full sequencing across 45 genes + deletions/duplications + mitochondrial DNA
Congenital Muscular Dystrophy NGS Panel – full sequencing across 27 genes
Connective Tissue Disorders/Ehlers-Danlos Syndrome/Aneurysm NGS Panel – full sequencing across 46 genes + deletions/duplications
Connexin-26 Associated Deafness – full sequencing GJB2 gene (+ GJB6 common deletion)
Coombs (Direct Antiglobulin Test)
Copper (Serum)
Copper (Urine)
Cornelia de Lange Syndrome NGS Panel – full sequencing across 8 genes
Coronavirus – COVID-19 IgG Antibody (SARS-CoV-2)  NEW
Coronavirus – COVID-19 PCR (SARS-CoV-2)  NEW
Cortisol
Cortisol (Urine)
Cortisol Binding Globulin
Costello/Noonan/LEOPARD/Cardio-Facio-Cutaneous Syndromes NGS Panel – full sequencing across 20 genes
Cotinine (Saliva)
COVID-19 RNA  NEW
Cow’s Milk Components
Coxsackie Antibodies (IgM)
Craniosynostosis and related disorders NGS Panel
Creatine Kinase (CK, CPK)
Creatinine
Creatinine (Urine)
Creatinine Clearance
Cri du Chat Syndrome – BOBs (5 days) + karyotype (15 days)
Cri du Chat Syndrome – BOBs only
Crosslaps (Serum DPD)
Cryoglobulins
Cryptococcal Antigen
Cryptosporidium
Cryptosporidium Antigen Detection
CSF for Microscopy and Culture
CSF Screen by PCR
CT/GC/Trichomonas/Mgen NEW
Culture (Any site)
CVS PCR for common aneuploidies (2 days) + culture (10-15 days)
CVSBOBs – rapid BOBs aneuploidy diagnosis for all chromosomes (3-5 days) + culture (10-15 days)
CVSBOBs only – rapid aneuploidy diagnosis for all chromosomes + common microdeletion syndromes
Cyclic Amp (Urine)
Cyclosporin (Monoclonal)
Cyfra 21-1
CYP450 2D6 Genotyping
Cystatin C
Cystic Fibrosis – 139 common mutations
Cystic Fibrosis Poly T (5T, 7T, 9T)
Cysticercosis (Taenia Solium) Serology
Cystine – Quantitative (Beta-CTX)
Cytomegalovirus (CMV-DNA) Amnio
Cytomegalovirus (IgG/IgM) Antibodies
Cytomegalovirus (PCR) Urine
Cytomegalovirus Avidity
Cytomegalovirus DNA (PCR)
Cytomegalovirus IgM