Explore molecular and genetic testing services for oncology, prenatal screening, inherited conditions, and clinical research. Each test page explains the method, sample requirements, and intended use.
Next-Generation Sequencing (NGS)
High-throughput sequencing for broad genetic analysis across targeted panels and clinical applications.
View test detailsFluorescence In Situ Hybridization (FISH)
Targeted detection of chromosomal and genetic abnormalities using fluorescent probes.
View test detailsPolymerase Chain Reaction (PCR)
Focused molecular analysis for detecting selected variants, markers, and infectious targets.
View test detailsMaternal Serum Screening
Pregnancy screening that estimates the chance of selected chromosomal conditions and neural tube defects.
View test detailsNon-Invasive Prenatal Testing (NIPT)
Cell-free DNA screening for selected chromosomal conditions using a maternal blood sample.
View test detailsBRCA1 and BRCA2 Testing
Genetic analysis of BRCA1 and BRCA2 for hereditary breast and ovarian cancer risk assessment.
View test detailsBCR-ABL1 Testing
Molecular testing used in the evaluation and monitoring of BCR-ABL1–positive haematological conditions.
View test detailsSolid Tumour Testing
Molecular profiling services designed to support evidence-based oncology care.
View test detailsWhole Exome Sequencing (WES)
Sequencing focused on protein-coding regions for selected inherited conditions and complex diagnostic questions.
View test detailsWhole Genome Sequencing (WGS)
Genome-wide sequencing for comprehensive analysis in selected clinical and research applications.
View test detailsResearch and Development
Collaborative molecular and cytogenetic project support for academic and clinical research teams.
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