A  |  B  |  C  |  D  |  E  |  F  |  G  |  H  |  I  |  J  |  K  |  L  |  M  |  N  |  O  |  P  |  Q  |  R  |  S  |  T  |  U  |  V  |  W  |  X  |  Y  |  Z

Tests: P

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

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
Pan-Ethnic/Jewish Carrier Screening
Pancreatic Cancer NGS Panel – full sequencing across 22 genes + deletions/duplications
Pancreatic Peptide
Pancreatitis (Hereditary) – PRSS1 hotspot sequencing + deletions/duplications + SPINK1 N34S common mutation
Paraganglioma/Pheochromocytoma NGS Panel – full sequencing across 11 genes + deletions/duplications
Paragomius Serology
Parathyroid Antibodies
Parathyroid Hormone (Whole)
Parathyroid Related Peptide
Parvovirus Antibodies (IgM)
Parvovirus DNA by PCR
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 sequencing across 36 genes
Pertussis (Whooping Cough) Antibodies
PEth (Phosphatidylethanol)
Pethidine – Urine
Peutz-Jegher Syndrome – STK11 sequencing + deletions/duplications
Phelan-McDermid Syndrome – karyotype + FISH
Phencyclidine (PCP)
Phenytoin (Epanutin)
Pheochromocytoma/Paraganglioma NGS Panel – full sequencing across 11 genes + deletions/duplications
Phosphate (24 hour Urine)
Phospholipid Antibodies
Pigmentation/Oculocutaneous Albinism/ Hermansky-Pudlak Syndrome NGS Panel – full sequencing across 30 genes
Pituitary Antibodies
Pituitary Function Profile
PLAC Test (Lp-PLA2)
Plasminogen Activator Inhibitor – 1
Platelet Aggregation Studies
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 + copy number variant
Polio Virus 1, 2, 3 Antibodies
Polycystic Kidney/NGS Panel – full sequencing across 7 genes
Polycystic Ovary Syndrome Profile
Polycystic Ovary Syndrome SHORT
Pontocerebellar Hypoplasia NGS Panel – full sequencing across 9 genes
Porphyrin (Blood)
Porphyrins (Faeces)
Porphyrins Full Screen (Total: Urine, Stool, Blood)
Porphyrins Screen (Urine)
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)
Prenatal Diagnosis for haemoglobinopathies
Pre-Travel Screen (DVT)
Primary Ciliary Dyskinesia (PCD) NGS Panel – full sequencing of 38 genes
Primary Hyperoxaluria Panel – full sequencing across 3 genes + CNV
Primidone (Mysoline)
Procollagen 1 Peptide N-Terminal (NTX)
Procollagen III Peptide
Products of Conception – rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (25 days)
Products of Conception (BOBs + Culture)
Products of Conception BOBs only – rapid aneuploidy diagnosis for all chromosomes
Prolactin (Macro)
Prostate Cancer NGS Panel – full sequencing across 12 genes + deletions/duplications
Prostate Profile (Total & Free PSA)
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
Pseudoachondroplasia (Multiple Epiphyseal Dysplasia) – COMP hotspot sequencing
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)