How to use the directory
Search by clinical indication, specialty, specimen type or laboratory discipline. Each test entry should identify the clinical purpose, methodology, specimen requirements, stability, turnaround time, limitations and reporting approach.
Core test groups
Reproductive genetics
PGT-A, PGT-M, PGT-SR and related molecular work-up.
Prenatal genetics
NIPT/cell-free DNA screening and appropriate confirmatory pathways.
Oncology
Hereditary cancer testing, tumour genomic profiling, selected molecular biomarkers and liquid-biopsy applications.
Forensic genetics
Paternity and kinship testing.
Cytogenetics and molecular diagnostics
Chromosome, FISH, PCR/qPCR and sequencing-based investigations.
Histopathology and digital pathology
Tissue diagnosis, slide digitisation and consultation workflows.
Before you order
Before ordering
Confirm the clinical question, patient identifiers, informed consent requirements, relevant family history, previous molecular/pathology findings, specimen type and whether the result is intended for clinical, legal, research or immigration use.
Test-specific limitations
The ordering clinician should review the scope of the exact assay. A negative result excludes only reportable abnormalities within the validated analytical and interpretive limits of that test.
Clinical use note: This resource supports professional decision making but does not replace current specialty guidelines, multidisciplinary review, the validated scope of the exact laboratory assay, or patient-specific clinical judgement.
Ready to order a test?
Our team can help you choose the right investigation, specimen and pathway for your patient.