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Tests: P

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

See discontinued tests to find out which tests are no longer available.

Please use the search box below to filter this list

Test name
P2Y12 Receptor Platelet Function Analysis (Clopidogrel Resistance)
p53-related cancer predisposition (Li-Fraumeni Syndrome) – TP53 sequencing + MLPA
PAI1 4G/5G Polymorphism
Pancreatic Cancer NGS Panel – full gene sequencing + deletions/duplications
Pancreatic Peptide
Paraganglioma/Pheochromocytoma NGS Panel – full gene sequencing + deletions/duplications
Paragomius Serology
Parathyroid Antibodies
Parathyroid Hormone (Whole)
Parathyroid Related Peptide
Parvovirus Antibodies (IgM)
Parvovirus IgG Antibodies
Parvovirus IgG/IgM Abs
Paternity Testing (postnatal and prenatal) – sample required from each person being tested (3 people)
Paul Bunnell (Monospot)
Peach Components
Peanut Components
Pelizaeus-Merzbacher Disease – PLP1 sequencing + deletions/duplications
Pemphigus/Pemphigoid Autoantibodies
Pendred Syndrome – SLC26A4 gene sequencing
Periodic Fever/Autoinflammation NGS Panel – full gene sequencing
Pertussis (Whooping Cough) Antibodies
PEth (Phosphatidylethanol)
Peutz-Jegher Syndrome – STK11 sequencing + deletions/duplications
Phelan-McDermid Syndrome – karyotype + FISH
Phencyclidine (PCP)
Phenytoin (Epanutin)
Pheochromocytoma/Paraganglioma NGS Panel – full gene sequencing + deletions/duplications
Phosphate (24 hour Urine)
Pituitary Antibodies
Pituitary Function Profile
PLAC Test (Lp-PLA2)
Plasminogen Activator Inhibitor – 1
Platelet Aggregation Studies
Platelet Function Test Screen – PFA-100/200
Pleural Fluid for Culture
Pneumococcal Antibodies – Serotype Specific
Pneumococcal Antibody Screen
Pneumococcal Antigen
Pneumocystis Jiroveci (PCP) Examination
Pneumonia (Atypical) Screen
POLG-Related Disorders – full POLG sequencing + deletions and duplications
Polycystic Kidney/NGS Panel – full gene sequencing
Polycystic Ovary Syndrome Profile
Polycystic Ovary Syndrome SHORT
Pontocerebellar Hypoplasia NGS Panel – full gene sequencing
Porphyrin (Blood)
Porphyrin (Stool)
Porphyrin (Urine)
Porphyrins Full Screen (Total: Urine, Stool, Blood)
Postnatal array CGH
Post-Travel Screen 1 (Prior to 6 weeks)
Post-Travel Screen 2 (Prior to 6 weeks)
PR-10 Proteins
Prader-Willi Syndrome (Primary Screen) – methylation PCR
Pregnancy (Serum) [Quantitative]
Pregnancy Test (Urine)
Pregnanetriol (Urine)
Prenatal array CGH
Prenatal Diagnosis (BOBs + Culture)
Pre-Travel Screen (DVT)
Primary Ciliary Dyskinesia (PCD) NGS Panel – full gene sequencing
Primary Hyperoxaluria Panel – full gene sequencing + CNV
Primidone (Mysoline)
Procollagen 1 Peptide N-Terminal (NTX)
Procollagen III Peptide
Products of Conception – rapid BOBs aneuploidy diagnosis for all chromosomes (10 days) + culture (25 days)
Products of Conception (BOBs + Culture)
Products of Conception BOBs only – rapid aneuploidy diagnosis for all chromosomes
Progesterone (Self-collect)
Prolactin (Macro)
Prolactin (Self-collect)
Prostate Cancer NGS Panel – full sequencing + deletions/duplications
Prostate Profile (Total & Free PSA)
Prostate Specific Antigen (Total) (Self-collect)
Prostate Specific Antigen (Total)*
Prostatic Acid Phosphatase
Protein (Urine)
Protein 14.3.3 (Creutzfeldt–Jakob Disease)
Protein C
Protein C Deficiency – PROC Gene Variant Analysis (Known Genotype)
Protein C Deficiency – PROC Gene Variant Analysis (Unknown Genotype)
Protein Electrophoresis incl. immunoglobin
Protein S Activity
Protein S Free Ag
Protein Total (Blood)
Protein/Creatinine Ratio (Urine)
Proteinase 3 Ab
Prothrombin Time
Prothrombin Time + Dose
PTEN-related disorders (including Bannayan-Riley-Ruvalcaba, Cowden & Proteus Syndromes) – sequencing + deletions/duplications
Purkinje Cell Antibody (Hu and Yo)
Pyruvate Kinase (M2-PK)
Pyruvate Kinase (M2-PK)