Beyond a fixed marker set
Genotyping arrays check selected positions. Whole-genome sequencing creates a broader dataset you can return to as interpretation advances.
Rebody packaging concept. Your collection kit may look different.
At-home cheek-swab collectionExplore your results with AI CoachMore context for your genetic insights.
Whole Genome Sequencing Test Kit, 30×
$499One-time sequencing test
Higher-depth whole-genome sequencing with an annotated .genome bundle and downloadable genomic files.
- At-home cheek-swab collection kit
- Typical files in 2–3 weeks after lab receipt
- gVCF and FASTQ files available on request
Order your kit
Start your order with Rebody. Secure checkout by Genome Computer.
Before you collect your sample
Follow the preparation and collection instructions supplied with your cheek-swab kit, then return the sample as directed.
30× average sequencing depth Collect with a cheek swab Explore your genetic insights
The value of depth
More reads. A richer starting point.
Whole-genome sequencing reads across your genome. At 30× average depth, repeated reads support more confident variant calls than low-pass sequencing.
Files you can take with you
Get an annotated .genome bundle, with gVCF and raw FASTQ files available from Genome Computer on request.
Context for better questions
Explore available insights on nutrition, caffeine response, fitness and medication response. Bring meaningful findings into a conversation with your coach or clinician.
Collection-kit conceptFrom cheek swab to genomic data
Collect at home. Explore for years.
Order your sequencing kit
Start your order with Rebody and verify your email, then continue to secure checkout. Your connected order returns to Rebody for tracking.
Swab and return
Collect your cheek sample and send it back using the instructions supplied with your kit.
Receive your genome
Genome Computer sequences and annotates your sample. Its published turnaround is typically 2–3 weeks after the lab receives it.
Bring your questions to Rebody
Connect eligible results or upload your existing DNA files. Explore what is available with the AI Coach.
Also in Rebody
Go deeper with your AI Coach.
A report is a starting point. Connect your available genetic insights to Rebody and ask what they mean in the context of your bloodwork, goals and health history.
The coach can read ready insight panels, explain their findings, and surface the evidence behind them. You can follow up on a finding without starting over.
Open your AI CoachGenome Computer integration is in limited rollout. Connected panels require provider access and an active Genome Computer subscription.
Questions to bring to your coach
What do my genetic insights say about caffeine response?
How do my nutrition findings relate to the bloodwork I uploaded?
Which findings should I bring to my clinician?
Answers use the findings available in your record. Examples shown are questions, not individual results.
DNA + bloodwork
Inherited context. Measurable change.
Your genome helps explain inherited variation. Bloodwork measures markers at a particular point in time. Together, they give you more to discuss than either report alone.
Explore testosterone blood testingBring your existing lab results
What does 30× mean?
30× describes average sequencing depth: each position is read about 30 times on average. Coverage varies across the genome. Greater depth improves the confidence of variant calls compared with low-pass sequencing.
How do I collect my sample?
Use the cheek swab supplied in your kit. Follow the enclosed preparation, collection and return instructions. You collect the sample at home; a blood draw is not needed.
What files do I receive?
Genome Computer provides an annotated .genome bundle. Its current offer also includes gVCF and FASTQ files on request. These are different formats: FASTQ contains raw sequencing reads, while gVCF records variants and confidently sequenced regions.
How does the Rebody AI Coach use my genome?
With your permission, the coach can read available, ready genetic insight panels from your connected Genome Computer account. It can discuss them alongside your available bloodwork, health goals and treatment record, with the evidence and sources supplied by the provider. This connection is in limited rollout. Panel access depends on provider capability and an active Genome Computer subscription; buying a kit alone does not unlock all coach features. You can also upload existing raw DNA files from the DNA page in your account.
Where do I pay, and what is included in the price?
Start with Rebody’s guided order form. Genome Computer hosts payment, shipping and sequencing; your connected order and results return to Rebody. The advertised sequencing price is $499; review the final total and terms in hosted checkout. Access is currently limited to enabled accounts. Genome insight subscriptions are separate from the sequencing purchase.
Can I order another kit if I already have results?
Yes. Your connected genome stays available in Rebody, and each additional sequencing purchase is linked as a separate order so you can follow its progress.
Is this a diagnostic test?
This product provides genomic data for exploration and does not diagnose a condition or prescribe treatment. Review findings that could affect medical decisions with a qualified clinician or genetic counselor. The AI Coach does not replace that review.
Whole-genome sequencing · 30×
Order through your Rebody account.
Start with your test, verify your email, and continue to secure checkout. Your order and results stay connected to Rebody.
Already sequenced? Connect or upload your DNA
One-time sequencing test$499
Order your kit Review the final price and purchase terms in Genome Computer’s hosted checkout.