The last DNA test you will ever need
Arrives before Christmas at 30% off
Founded in 2015 with the mission of providing truly private genome sequencing, we have proudly sequenced thousands of genomes and kept zero customer data. Today we guarantee the same level of privacy as well as the highest quality bioinformatics and genome analysis on the market.
Process
1.Order
After ordering online, you will receive your sample kit within 5 business days.
2. Sample
Follow the easy instructions to give your sample, then ship it to us in the prepaid packaging.
3. Receive
After 8 weeks you will receive your genome data and report.
What You Get
All Your Genome Data
We deliver all your raw and processed genome files including FASTQ, BAM, VCF, and annotated VCF. We also deliver the code we used to process your genome.
Access to Genome Explorer
With your purchase, you will have free access to Guardiome's Genome Explorer App coming in late 2024. In the app you can run premade analyses or search any variant, gene, or region in your genome.
Your Genome Report
An in-depth report of impactful variants you carry and their predicted consequences.
Genomics Done Right
All-American
From the time we receive your sample to the time we send you your genome data and report, our entire service takes place on American soil.
FDA-Benchmarked
We are the only consumer genomics company that benchmarks our bioinformatics pipelines against US FDA standards, giving you complete confidence in the genome files you receive from us.
Completely Private
We do not keep your genome data because profiting from your data is not part of our business model. About 60 days after sending you your genome data on a secure hard drive, we delete it.
Based on Quality Research
Our genome analysis is based studies which are manually reviewed by our experienced scientists and bioinformaticians.
Physician Friendly
Our reports are designed to be readable by you and by your doctor. Your report will contain the important details your doctor will want to know before taking the next steps.
For Life
Whether you ordered yesterday or years ago, your inquiry as a customer will be met with a response from our bioinformatics team within 24 hours.
Our Service Will…
Inform Your Choices
Your genome contains information that could help you live a healthier and happier life. Our bioinformaticians check your entire genome for impactful variants and deliver you an easy-to-understand report which will inform you of the following and more.
Save You Time
Many people who get a genetic test will get another one, and then another. This is because most genetic testing services are incomplete. So whether you ordering through your doctor or in the direct-to-consumer market, the amount of time you will spend researching, monitoring, and interpreting these incomplete tests can add up to more than 40 hours. By comparison, our customers usually spend about 5 hours from ordering to complete interpretation.
Give You the Power
We are the only genomics company who delivers all your genome files on a secure hard drive to your doorstep. Having your raw genome data (FASTQ) allows you to have it reanalyzed later by whoever you choose. Having your annotated variant call file (VCF) allows you the look at your variants with third-party software or Guardiome’s Genome Explorer App. You can do all of this with the peace of mind as you are the only person who can access your genome data.
Continue to Help
In late 2024, Guardiome’s Genome Explorer App will be released to customers. In the app, you can run premade analyses or search your genome for any variant, gene, or region. When you read about a gene in the news, you can search for it in the app to check for impactful variants you have in that gene. Being able to search your genome freely like this will make addressing health, wellness, and lifestyle concerns easier and faster. Your genome sequence will be at your fingertips.
Guardiome vs Others
Statistics
>90%
Of people are expected to be the carrier of at least one genetic disease.
~80%
Of rare diseases have a genetic basis.
>95%
Of people carry a pharmacogenomic variant that would influence medication-related outcomes.
~15%
Of children’s hospital admissions have a genetic basis.