GENETIC DIAGNOSTIC EXPERTISE
Genetic insights to support personalised care
When a clinical question involves inherited risk, complex diagnosis, treatment response or reproductive planning, you need clear, clinically relevant genetic information.
Our genetics teams support you with testing, counselling and expert interpretation across routine and complex cases. By integrating genetic insights with pathology, radiology and laboratory data, we help provide a more complete clinical picture and support confident decision-making.
Genetics at a glance
Genetic services and expertise
Our genetics portfolio supports inherited risk assessment, diagnosis, treatment decisions, reproductive health and follow-up across a broad range of clinical questions.
Genetic testing to support the investigation of inherited conditions and family risk, including clinically appropriate follow-up for relatives.
Testing to support hereditary cancer risk assessment, tumour-related genetic questions and selected therapy-relevant pathways.
Analysis of selected genetic variants that may influence medication response, supporting treatment considerations where clinically relevant.
Genetic diagnostics for reproductive health, carrier screening, prenatal diagnostics and chromosomal questions.
Genomic testing to support complex, multisystemic or unexplained clinical presentations, including selected metabolic, cardiovascular and inherited vision-related questions.
Analysis of chromosomal abnormalities, genomic imbalances and structural variants in prenatal, postnatal, oncology and reproductive contexts.
Selected molecular monitoring solutions, including ctDNA-based approaches, can support follow-up and treatment-response assessment where clinically appropriate.
Signatera™ for molecular residual disease monitoring
Signatera™ is a personalised, tumour-informed ctDNA test designed to support molecular residual disease monitoring in selected solid tumours.
By tracking tumour-specific DNA signals in the blood over time, it can provide additional molecular information for recurrence risk assessment, treatment-response monitoring and follow-up discussions where clinically appropriate.
Liquid biopsy for blood-based tumour profiling
NGS-based ctDNA liquid biopsy analyses tumour-derived DNA fragments circulating in the blood to identify clinically relevant genomic alterations.
It can support molecular profiling in selected advanced solid tumours, particularly when tissue is insufficient or not feasible, and may provide additional information for treatment planning, response monitoring or disease evolution.
BladderCare™ for bladder cancer follow-up
BladderCare™ is a urine-based genomic test that can support the monitoring of non-muscle invasive bladder cancer.
It provides molecular information that may help physicians assess recurrence risk and support follow-up decisions alongside cystoscopy, cytology and clinical evaluation.
Pharmacogenetics for medication response questions
Pharmacogenetic testing analyses selected genetic variants that may influence how a patient responds to certain medications.
The results can support physicians when considering treatment choice, dosage or follow-up, particularly when drug response, metabolism or tolerability are clinically relevant.
WHY UNILABS
Why choose Unilabs for genetic diagnostics?
Unilabs supports healthcare professionals with genetic testing, specialist interpretation and counselling support across routine and complex clinical questions.
Specialist genetic support: Geneticists, molecular specialists and counselling teams support test selection, interpretation and patient-related questions.
Clinically relevant methods: NGS, Sanger sequencing, genotyping and cytogenetic methods are selected according to the clinical question.
Integrated diagnostic perspective: Genetic insights can be connected with laboratory, pathology and radiology when broader clinical context is needed.
GENETIC COUNSELLING & INTERPRETATION
Support for genetic results and patient communication
Genetic results can influence diagnosis, treatment decisions and family risk. When needed, our genetics experts and genetic counsellors support test selection, result interpretation and communication with patients and relatives.
Meet our Experts
(en) Our medical specialists, scientists and diagnostic experts support healthcare professionals across multiple disciplines. They can help with test selection, interpretation and complex diagnostic questions.