Two ways to decode your DNA
Personal health insights or two-parent family planning. Every report works with a supported DNA file you already have, including WGS.
How It Works
Upload data you already have. Get your report in minutes, not weeks.
Upload Your Data
Upload a provider raw-data file or a single-sample whole-genome VCF from any sequencing provider. No new kit required.
We Analyze
Our pipeline calculates risk scores from published GWAS, screens for disease variants, and predicts traits, typically within minutes.
Get Your Report
View your personalized report online or download it as a PDF. Results for individual reports are typically ready in about 20 minutes.
What Makes Us Different
Direct-to-consumer genetic health reports. No doctor visit and no mailing kit required.
Evidence-Based
Every score is built from a peer-reviewed GWAS by PhD computational biologists.
Fast Results
Health reports in ~20 minutes. No mailing kits or waiting weeks for lab results.
Use Existing Data
Every report supports WGS VCFs from any provider, plus 23andMe, AncestryDNA, MyHeritage, and tellmeGen.
Privacy First
Your data is encrypted and never sold. Delete your genetic data at any time from your profile.
Compatible With Your Data
Already have genetic data? Upload your file and get started immediately.
Consumer Genotyping Arrays
Whole Genome Sequencing
WGS from any provider
Upload a single-sample .vcf or .vcf.gz from Nebula, Dante Labs, Sequencing.com, Nucleus, or any other WGS provider. Use it with every health and family report.
WGS file requirements and report optionsAccepted formats: provider .txt/.csv files and single-sample whole-genome .vcf/.vcf.gz files.
About Genomisaur
Genomisaur was started by PhD computational biologists who work in human genetics. Every score in your report is built from a peer-reviewed GWAS, with the source publication and performance metrics linked from the score card.