Atlas Baseline
Whole genome sequencing with AI-interpreted report. One sample, all of your DNA.
- 2–3 wks
- GenDG §9
Sequenced once. Interpreted across a lifetime.
From genomic foundation to specialized clinical panels. Sequenced in Berlin. Interpreted with clinical rigor.
Whole genome sequencing, longitudinal epigenetic monitoring, variant re-annotation, and pharmacogenomic context. The permanent reference layer for every future health decision.
Whole genome sequencing with AI-interpreted report. One sample, all of your DNA.
Longitudinal epigenetic age tracking. Two samples per year, AI-interpreted methylation reports.
Re-annotate any existing VCF against the latest clinical knowledge.
Targeted genetic risk panels with board-certified clinical interpretation. Built on the same scientific framework as established clinical genetics, with three-click ordering.
Curated bundle: hereditary cancer plus tumor-disease modules in one panel.
Bundle: cardiovascular, hypercholesterolemia, thrombosis, and metabolic modules.
The full preventive panel: every Atlas single module bundled together.
54-gene hereditary cancer panel covering breast, ovarian, colorectal, and rare syndromes.
81-gene ACMG SF v3.2 secondary-findings panel — every actionable medically-actionable gene.
21-gene pharmacogenetic panel per CPIC and DPWG guidelines -- informs prescribing and dosing across pain medication, anticoagulants, cardiovascular drugs, antidepressants, chemotherapy and immunosuppressants.
54-gene tumor-pathway module: somatic-pathway and tumor-predisposition genes.
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 hereditary eye conditions including retinal dystrophies.
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.
Trace-derived polygenic and epigenetic read on hair-loss risk -- 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. Our medical geneticist will help you scope the right test for your situation.