From raw data to clear insights

Vogelview takes your genetic or medical data and translates it into a structured, easy-to-read report — backed by curated research, not AI guesses.

Upload your DNA file or lab results

Drag and drop a raw DNA file from 23andMe, AncestryDNA, Nebula Genomics, or any VCF-compatible provider. Or upload a medical lab report — blood tests, metabolic panels, urine analysis, and more. We support PDF, CSV, TXT, and VCF formats.

Our system interprets your data

Your file is parsed, normalized, and matched against our curated knowledge base of peer-reviewed genomic and clinical research. Each variant or biomarker is scored against evidence-based rules — no large language model guesswork, no hallucinations.

Read plain-English insights

Your personal report arrives in minutes. Every finding is presented in three parts: the exact scientific finding, what it means in plain English, and why it matters in everyday life. Evidence levels are clearly labeled so you always know how much weight to give each insight.

No genetics knowledge required

If you can read a report, you can understand your results.

No genetics background requiredResults in under 5 minutesEvidence levels on every findingSecure — your data stays yours