Atlas Baseline
Whole-genome sequencing, delivered as data you can keep. One sample, your whole genome, in open standard formats.
Sequence once. Return to the data when new questions arise.
From genomic foundation to specialized clinical panels.
Whole genome sequencing and longitudinal epigenetic monitoring. Variant re-annotation is in preparation, pharmacogenomic context is available as an add-on. Sequenced today. Ready for the questions that come next.
Whole-genome sequencing, delivered as data you can keep. One sample, your whole genome, in open standard formats.
Longitudinal epigenetic age tracking. Two samples per year, structured methylation reports.
Re-annotate any existing VCF against the latest clinical knowledge.
Targeted genetic risk panels. Built on the same scientific framework as established clinical genetics.
Bundle: cardiovascular, hypercholesterolemia, thrombosis, and metabolic modules.
The full preventive panel: 12 modules in one report (the hereditary cancer gene set, nine single-disease modules, ACMG Core and pharmacogenetics).
21-gene pharmacogenetic panel per CPIC and DPWG guidelines -- informs prescribing and dosing across pain medication, anticoagulants, cardiovascular drugs, antidepressants, chemotherapy and immunosuppressants.
56-gene cardiovascular panel: cardiomyopathies, arrhythmias, aortopathies.
28-gene thrombosis and coagulation panel for inherited bleeding and clotting disorders.
8-gene panel for hemochromatosis and Wilson disease and related storage disorders.
4-gene panel for familial hypercholesterolemia (LDLR, APOB, PCSK9, LDLRAP1).
5-gene panel for systemic storage diseases that can show in the eye.
2-gene panel for malignant hyperthermia susceptibility (RYR1, CACNA1S).
8-gene panel for monogenic diabetes (MODY) and other inherited diabetes forms.
27-gene panel for adult-onset inherited metabolic disorders.
Polygenic read on hair-loss risk across 389 published risk loci -- the visible question, with the underlying androgen-signaling, metabolic, and cardiovascular biology surfaced alongside.
2-gene panel for autosomal dominant polycystic kidney disease.
Family planning panels and predictive panels for major neurodegenerative conditions. Genetic counseling is strongly recommended for predictive panels.
Couples carrier screening for autosomal-recessive and X-linked conditions.
Single-individual carrier screening for autosomal-recessive and X-linked conditions.
Fertility-focused genetic panel for couples investigating subfertility.
Predictive panel for early-onset Alzheimer and frontotemporal dementia genes.
Predictive panel for hereditary Parkinson disease genes including LRRK2 and GBA.
Book a 30-min Genetic Counseling consultation for €140. A specialist in human genetics helps you scope the right test for your situation.