Precision genomics for complex answers.
From hereditary risk and reproductive planning to oncology and rare disease — our genomics program blends validated technology with expert clinical interpretation.
End-to-end genetic & genomic testing
Molecular, cytogenetic and next-generation sequencing services delivered with clinical-grade quality.
Molecular Genetics
PCR, qPCR, Sanger sequencing and NGS-based panels for monogenic and polygenic disorders.
Cytogenetics
Karyotyping, FISH and chromosomal microarray for structural and numerical anomalies.
Oncogenomics
Solid tumor & hematologic malignancy panels, MRD monitoring and targeted therapy markers.
Reproductive Health
Carrier screening, NIPT, POC analysis and pre-implantation genetic testing support.
Hereditary Risk
BRCA, Lynch and comprehensive hereditary cancer & cardiac risk panels.
Rare Disease Dx
Whole exome and targeted panels with expert clinical interpretation.
A clinically-guided genomics workflow
Genetic Counselling
Pre-test consultation with certified counsellors to align testing with clinical goals.
Sample Accessioning
Blood, saliva, tissue or products of conception processed under strict chain-of-custody.
Assay & Sequencing
Validated NGS, Sanger and cytogenetic workflows on automated platforms.
Curated Reporting
ACMG-compliant variant classification with clinical actionability guidance.
Not sure which test is right?
Our team helps clinicians and families choose the right assay, interpret results, and plan next steps with confidence.