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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-KIT D816V mutation by PCR for Mastocytosis
C Peptide
C Reactive Protein
C Reactive Protein (Self-collect)
C Reactive Protein (High Sensitivity)
C Reactive Protein (High Sensitivity) (Self-collect)
C1 Esterase Inhibitor
C1 Esterase: Function & Total
C1q Binding Immune Complex
C3 Complement
C3/C4 Complement
C4 Complement
CA 15-3
CA 19-9
CA 50
CA 72-4
CA 125
CA 125 (Self-collect)
CADASIL – NOTCH3 gene sequencing
Cadmium (Blood)
Cadmium (Urine)
CAKUT (Congenital Anomalies of Kidney & Urinary Tract) NGS Panel – full gene sequencing
Calcitonin
Calcium
Calcium (Self-collect)
Calcium (24 hour Urine)
Calcium + Vitamin D (Self-collect)
Calcium/Creatinine Ratio
Calprotectin
Calprotectin, Faecal (Self-collect)
Calprotectin/Elastase Profile
Calreticulin – CALR exon 9 mutation screen
Campylobacter Jejuni Antibodies
Cancer, Comprehensive NGS Panel – full gene sequencing + deletions/duplications
Candida (Culture)
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 gene sequencing + deletions/duplications + mitochondrial DNA
Carboxyhaemoglobin
Carcino Embryonic Antigen
Cardiac Enzymes (not chest pain)
Cardio-Facio-Cutaneous/Noonan/LEOPARD/Costello Syndromes NGS Panel – full gene sequencing
Cardiolipin Antibodies (IgG+IgM)
Cardiomyopathy, Arrhythmogenic Right Ventricular NGS Panel – sequencing + deletions/duplications
Cardiomyopathy, Comprehensive NGS Panel – full gene sequencing + deletions/duplications
Cardiomyopathy, Dilated NGS Panel – full gene sequencing + deletions/duplications
Cardiomyopathy, Hypertrophic NGS Panel – full gene sequencing + deletions/duplications
Cardiovascular Risk Profile 1
Cardiovascular Risk Profile 2
Carotenes
Carrier Screen (Ashkenazi Jewish)
Carrier Screen (Ashkenazi Jewish) – Partnered Report
Carrier Screen (Pan-Ethnic)
Carrier Screen (Pan-Ethnic) – Partnered Report
Cartilage Antibodies
Cashew Components
Cat Components
Cat Scratch Fever (Bartonella IgG+IgM)
Catecholamines (Plasma)
Catecholamines (Urine)
CCP Antibodies (RF)
CD3/CD4/CD8
CD16
CD19 B Cells
CD20
CD25
CD56
CD57
Celery Components
Centromere Autoantibodies
Ceruloplasmin
Cervical Cytology
CH50 (Classical pathway)
Chagas Disease Serology (S.American Trypanosomiasis) T. Cruzi
Charcot-Marie-Tooth Syndrome NGS Panel – full gene sequencing
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 – Rectal (Self-collect)
Chlamydia/Gonorrhoea (Thin Prep)
Chlamydia/Gonorrhoea – Throat
Chlamydia/Gonorrhoea – Throat (Self-collect)
Chlamydia/Gonorrhoea – Urine
Chlamydia/Gonorrhoea – Urine (Self-collect)
Chlamydia/Gonorrhoea – Vaginal (Self-collect)
Chlamydia/Gonorrhoea/Trichomonas by PCR
Chloride
Cholestasis, Intrahepatic NGS Panel – full gene sequencing
Cholesterol
Cholesterol (Familial Hypercholesterolaemia)
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 (Products of Conception)
Chromosome Analysis (Products of Conception) – BOBs rapid aneuploidy diagnosis for all chromosomes (10 days) + culture (25 days)
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
Clobazam
Clomipramine (Anafranil)
Clonazepam
Clostridium Difficile Toxin by PCR
Coagulation Profile 1
Coagulation Profile 2
Cobalt (Blood)
Cobalt (Serum)
Cobalt (Urine)
Cocaine (Urine) Screen
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 gene sequencing + 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 Muscular Dystrophy NGS Panel – full gene sequencing
Connective Tissue Disorders/Ehlers-Danlos Syndrome/Aneurysm NGS Panel – full gene sequencing + deletions/duplications
Connexin-26 Associated Deafness – full sequencing of GJB2 gene
Connexin-30 Associated Deafness – full sequence of the GJB6 gene
Coombs (Direct Antiglobulin Test)
Copper (Serum)
Copper (Urine)
Cornelia de Lange Syndrome NGS Panel – full gene sequencing
Cortisol
Cortisol (Self-collect)
Cortisol (Urine)
Cortisol Binding Globulin
Costello/Noonan/LEOPARD/Cardio-Facio-Cutaneous Syndromes NGS Panel – full gene sequencing
Cotinine (Serum)
Cotinine (Urine)
COVID-19 (SARS-CoV-2) Abbott IgG Antibody
COVID-19 (SARS-CoV-2) Abbott IgM Antibody
COVID-19 (SARS-CoV-2) Rapid RNA Sequencing
COVID-19 (SARS-CoV-2) RNA by PCR
COVID-19 (SARS-CoV-2) RNA by PCR (Self-collect)
COVID-19 (SARS-CoV-2) Roche Elecsys Anti-SARS-CoV-2 S (SPIKE)
COVID-19 (SARS-CoV-2) Roche Elecsys Anti-SARS-CoV-2 S (SPIKE) (Self-collect)
COVID-19 (SARS-CoV-2) Roche Elecsys Anti-SARS-CoV-2 Total Antibody
COVID-19 (SARS-CoV-2) Roche Elecsys Anti-SARS-CoV-2 Total Antibody (Self-collect)
COVID-19 (SARS-CoV-2) T-SPOT®.COVID
COVID-19/FLU/RSV Screen
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 Detection by PCR
CSF for Microscopy and Culture
CSF Screen by PCR
CT/GC/Trichomonas/Mgen (PCR Swab)
CT/GC/Trichomonas/Mgen (Urine)
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
Cyclosporin (Monoclonal)
Cyfra 21-1
Cystatin C
Cystic Fibrosis (139 common mutations) – reflex to Poly T when required
Cystine – Quantitative (Beta-CTX)
Cytomegalovirus (CMV-DNA) Amnio
Cytomegalovirus (IgG/IgM) Antibodies
Cytomegalovirus (PCR) Semen
Cytomegalovirus (PCR) Urine
Cytomegalovirus Avidity
Cytomegalovirus DNA (PCR)
Cytomegalovirus Resistance