It All Starts With Your Sequence
Whole genome sequencing is the only genetic test you’ll ever need, because it obtains data on all your genes and chromosomes end-to-end. Once you’re sequenced, you’ll be able to obtain insights from the data throughout the rest of your life.
Ready to Get Sequenced?
Start with our Health Screen WGS Super Bundle, or explore a range of tailored bundles designed to provide insights across key health areas. Discover the bundle that’s right for you!
Already Have DNA Data?
If you’ve taken a DNA test elsewhere, upload your raw DNA data for free to get started.
LIMITED TIME EARLY BLACK FRIDAY SUPER SALE
Health Screen WGS Super Bundle
$1199
$299
+ Free Shipping
Privacy Forever Data Protection
We don’t sell your data to anyone
Bundle Includes
- Easy-To-Use DNA Collection Kit
- 30x Whole Genome Sequencing
- Unlimited Access To Your Genetic Data
- Privacy Forever Protection Of Your Data
- 1 Month Premium Genome Plan
- Advanced AnalysisAdvanced Genetic Analysis & Insights
Full Access To All Data
Full Access To All Raw Data & Analyzed Data
Accepted Payment Methods
Obtains data on around 3 billion positions within your genome (100% of your genome). Also includes the ability to download your raw genome data files for no additional fee. This includes FASTQ, BAM and VCFs covering all genetic variations: Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (INDELs), Structural Variations (SVs), Copy Number Variations (CNVs) and Mitochondrial Heteroplasmy (MITO).
Ready to Get Sequenced?
Start with our Health Screen WGS Super Bundle, or explore a range of tailored bundles designed to provide insights across key health areas. Discover the bundle that’s right for you!
Our Tests Vs Our Competitors
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Whole Genome Sequencing |
Health | ||||||
Genetic Counseling Available |
DNA Guidance for Life | ||||||
GenomeLock DNA Security | ||||||
One Genome Technology | ||||||
Real-Time Health Updates | ||||||
Real-Time Data Updates |
Single Nucleotide Variants (SNPs or SNVs) | ||||||
Insertions & Deletions (INDELs, DIPs or DIVs) | ||||||
Copy Number Variants (CNVs) | ||||||
Structural Variants (SVs) | ||||||
Mitochondrial Heteroplasmy | ||||||
Reference Genome Alignment | (most up-to-date) | (from 2009) | (from 2009) | (from 2009) | (from 2009) | (from 2009) |
Already received your kit?
Get started by activating your kit and start tracking your DNA analysis, the first step on your personalized journey.
Already have data from a DNA test?
If you’ve taken a DNA test elsewhere, such as a genetic genealogy website, upload your raw DNA data for free to get started.