Genetics
Your genome, read carefully and explained plainly.
Sequencing is the easy part. Our value lies in curation, interpretation and the counselling conversation that turns variants into decisions.
Programmes
From single gene to whole genome.
Whole Genome & Exome
Deep sequencing with clinical-grade variant curation against ACMG guidelines.
- 30x whole genome
- Clinical exome
- Reanalysis at 12 months
- Secondary findings on request
Rare Disease Diagnostics
Ending diagnostic odysseys with trio sequencing and phenotype-driven analysis.
- Trio and family studies
- Mitochondrial panels
- Neuromuscular panels
- Paediatric syndromes
Carrier & Reproductive
Expanded carrier screening for couples planning a family, with joint counselling.
- 500+ gene carrier screen
- Pre-implantation support
- Non-invasive prenatal testing
- Fertility genomics
Genetic Counselling
Certified counsellors guide every stage, before and after the result.
- Pre-test consultation
- Result interpretation
- Family cascade planning
- Multilingual sessions
Process
How a genomic case moves through our lab.
- 01
Counselling
Goals, family history and consent, discussed without rush.
- 02
Sequencing
Illumina NovaSeq platforms with strict quality thresholds.
- 03
Curation
Variant classification by a multidisciplinary board.
- 04
Report
A plain-language report and a follow-up consultation.
Ready when you are.
Same-week appointments across London, Bucharest and Munich, with results delivered securely to your private portal.