Stop wondering. Start understanding.

You already know your body. Bystro helps you investigate it with the same research tools geneticists use, so you can finally understand what your DNA is actually saying.

All information uploaded to Bystro must be de-identified. Intended for research, educational, and informational purposes only.

Your genetic data has more to say.

Upload the raw genetic data you own and start asking questions from any device, anywhere.

Whole Genome VCF

Our primary format — clinical & research grade

23andMe

Raw data export supported

AncestryDNA

Raw data export supported

MyHeritage

Raw data export supported

Other Platforms

Most raw data formats accepted

Start with the data you have. We'll help you go deeper.

From DNA file to insight in minutes.

No pipelines. No programming. No PhD required.

01

Bring your data

Start with your 23andMe, AncestryDNA, MyHeritage, whole genome VCF, or data from any sequencing provider.

02

Bystro annotates

Your variants are cross-referenced across 200+ fields — population frequencies, clinical significance, pharmacogenomics, and more.

03

Ask in plain English

Ask anything about your health, training, medication response, or ancestry. No genetics background required.

04

Get cited answers

Every answer is grounded in your actual variants and cited to peer-reviewed sources. Nothing made up, nothing generic.

First, tell us what you’re curious about.

We’ll show you a tailored preview of what Bystro can find in your DNA. No account needed.

Q1 — What do you want to learn about? Pick any.

Your genome has answers.It's time to listen.

Upload the genetic data you already own and begin understanding yourself at a deeper level.

Research Use Only. For research, educational, and informational purposes. Not intended for medical diagnosis, treatment, or clinical use. Always consult qualified healthcare professionals.