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.
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Order your genome.
Get your genome sequenced, annotated, and delivered to you. Analysis Agent available for private data exploration.
Consumer grade
Basic
3x WGS and 40x WGS
$149
Your genome, sequenced and analyzed in 3-4 weeks
An accessible entry point for ancestry and basic analysis.
- +Low-pass whole genome sequencing (3x)
- +Closer look at key genes (40x whole exome sequencing)
- +Core ancestry, traits & carrier insights
- +Identify some pathogenic variants
- +Raw data download (gVCF, FASTQ)
- +Data delivered privately via AWS
AI Agent available for self-driven data exploration, starting at $8.25/month
Order nowClinical grade
Gold Standard
30x WGS
$399
Your genome, sequenced and analyzed in 3-4 weeks
The gold standard for lifelong genetic exploration and health optimization.
- +High-depth whole genome sequencing (30x)
- +50+ polygenic risk score report library unlocked
- +Understand your drug metabolism
- +Explore mitochondrial health
- +Upload blood panels & records for combined analysis
- +Raw data download (BAM, gVCF, FASTQ)
- +Data delivered privately via AWS
AI Agent available for self-driven data exploration, starting at $8.25/month
Order nowResearch grade
Deep Research
100x WGS
$999
Your genome, sequenced and analyzed in 4–6 weeks
Ultra-deep coverage for advanced exploration, rare-variant discovery, and research questions.
- +Research-grade whole genome sequencing (100x)
- +Everything in Gold Standard
- +Rare & structural variant discovery
- +Track non-inherited mutations
- +Data delivered privately via AWS
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.
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, BAM, 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?
3x is suitable for ancestry and basic insights. 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 patients with genetic conditions looking to pinpoint precise disease mechanisms.
Do I own my data?
Yes. You can download your FASTQ, BAM, and VCF files, and delete everything from our servers with just one click. The only copy of your data is delivered directly to you, so this action is final.
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.