What if you couldtalk to your genome?
Talk to your genome™. Whole-genome sequencing, plus an AI agent that answers any question about your DNA. You own the data, and every answer.
Results in 3–4 weeks with Talk to Your Genome or Deep Research, 6–8 weeks with Standard.
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Ask your genome anything.
Take a swab. We sequence your whole genome, then you explore your DNA through questions in plain English.
01
Order your kit
Ships to your door in the US.
02
Take a DNA swab
Mail it back in the prepaid box.
03
We sequence it
Whole-genome sequencing in a CLIA-certified lab.
04
Talk to your genome
Ask the AI Agent anything about your DNA.
You ask
“Why does coffee keep me up at night?”
Your genome
You carry a slow-metabolizer variant in CYP1A2, so caffeine stays in your system longer than average.
Based on 2 variants in your genome
You ask
“Am I a carrier for anything?”
Your genome
You carry one copy of a variant in HFE linked to iron absorption. Carriers usually have no symptoms.
Based on 1 variant in your genome
You ask
“Where did my lactose tolerance come from?”
Your genome
You have the LCT variant common in Northern European ancestry that keeps lactase active into adulthood.
Based on 3 variants in your genome
Example answers for illustration. Research use only, not a medical diagnosis.
Order your genome.
Get your genome sequenced, annotated, and delivered to you. Analysis Agent available for private data exploration.
Genome Explorer
Standard
30x WGS
$399
Your genome, sequenced and analyzed in 6–8 weeks
Your complete 30x genome as raw data, ready to download and explore.
- +High-depth whole genome sequencing (30x)
- +Data only: raw files (FASTQ, VCF)
- +5 genetic trait reports
- +Free storage for 90 days after delivery
- ×No analysis tools or long-term hosting
AI Agent available for self-driven data exploration, starting at $8.25/month
Order nowCitizen Scientist
Talk to Your Genome
30X WGS + Analysis
$599
Your genome, sequenced and analyzed in 3–4 weeks
Standard data plus the tools to keep using it: AI Agent access and Genomelink reports, included for your first year.
- +High-depth whole genome sequencing (30x)
- +Raw files (FASTQ, VCF)
- +AI Agent access, first year included
- +Up to 500 genetic trait reports via Genomelink, first year included
- +Indefinite data hosting
AI Agent and Genomelink reports included for your first year
Order nowGenomic Pioneer
Deep Research
100x WGS
$1,199
Your genome, sequenced and analyzed in 3–4 weeks
Your complete 100x genome as raw data, built for rare-variant discovery and research questions.
- +Ultra-deep whole genome sequencing (100x)
- +Data only: raw files (FASTQ, VCF)
- +5 genetic trait reports
- +Rare & structural variant discovery
- +Track non-inherited mutations
- +Free storage for 90 days after delivery
- ×No analysis tools or long-term hosting
AI Agent available for self-driven data exploration, starting at $8.25/month
Order nowAll samples are sequenced in a CLIA-certified laboratory, but results are for research use only.
Already have your genome sequenced?
Ask anything with Superbio.
If you've already had your genome sequenced, bring your FASTQ, BAM or VCF file to Superbio, where you can re-process with a variety of computational techniques, or ask conversational questions and get answers grounded in real evidence.
Who we are.
Supergene.ai is a new offering from Superbio.ai, an AI software startup created by serial entrepreneur and Stanford professor Ronjon Nag, with a team of industry veterans from Alphabet and Apple, to democratize advanced scientific research. Superbio's latest product is an AI genomics explorer called Locus, which we noticed many people were using to analyze their own genomes. This motivated us to offer personal sequencing services, helping more people access their own data before deciding whether to analyze it with Superbio.
Our team comes from
FAQs before we start.
How is this different from 23andMe?
23andMe genotypes a small, pre-selected set of around 600,000 positions in your DNA. We sequence your entire genome (all 3 billion base pairs!) at 30x depth, so we capture the novel and rare variants that consumer chips simply can't see. And instead of a fixed set of pre-written reports, you get your complete raw data (FASTQ, VCF), owned entirely by you, plus an AI Agent you can ask anything, again and again, as the science evolves.
How is my data kept private?
Your genome and reports are delivered via Superbio, in an encrypted, private cloud storage bucket accessible from the browser. We recommend you keep it here, because the files are too big for many laptops. From here, our AI Agent can access the processed data and answer your questions. Throughout this process, your data is anonymized, and personal identifiers are never exposed.
Is deeper sequencing worth it for me?
30x is the standard depth for disease risk analysis, and what most people should buy. 100x is for rare and structural variant discovery, best for discovering rare and structural variants.
Do I own my data?
Yes. You can download your FASTQ and VCF files at any time, and delete everything from our servers in one click. Deletion is permanent, so download your files first.
How long do you host my data?
Standard and Deep Research are data-only plans. They include 90 days of hosting from delivery, so you have time to download your files. After that, the data is deleted from our servers. With Talk to Your Genome or an active AI Agent subscription, your genome stays hosted indefinitely. If you cancel, we keep it for 3 more months before deleting it. Your physical sample is kept only if you add sample storage.
Is this a medical diagnosis?
No. All samples are sequenced in a CLIA-certified laboratory, but results are for research use only.
All samples are sequenced in a CLIA-certified laboratory, but results are for research use only.