Whole Genome Sequencing = 100% of Your DNA
Our whole genome sequencing (WGS) service analyzes all of your DNA and provides the most comprehensive insight into your personal genetic profile.
While most DNA tests obtain less than 0.1% of your DNA, our WGS service obtains 100%. By having information about your entire genome, you can make decisions that are truly life-improving.
This Is Not A Traditional DNA Test – This Is Sequencing
DNA tests from 23andMe, AncestryDNA, and most other companies use older technology that produces data on a very small subset of your genome.
Whole genome sequencing is the world’s most advanced genetic testing technology that tests every letter of your DNA, including all ~30,000 genes and all chromosomes end-to-end.
|Gene||Condition||# of Genetic Variants Analyzed|
|BRCA 1/2||Breast, Ovarian, Other Cancers||23,975||3|
|KCNQ1||Preventable Sudden Death, SIDS||4,677||0|
|RYR1||Preventable Reaction to Anesthesia||3,839||0|
Our whole genome sequencing obtains information on your entire genome of more than 3 billion genetic variants.
100% of your DNA data is vital for evaluating your genetic risk for diseases and adverse reactions to medical treatments.
Receive personalized health guidance now and throughout your life, and learn about potential risk of diseases and conditions.
Sequence Once, Unlock a Lifetime of Scientific Discoveries
Whole genome sequencing is the only DNA test that obtains 100% of your genome. Once you have sequenced yourself, the data that's obtained will provide insights that help protect your health throughout your life.
Even if new genes are discovered in the future, you won't need to take another DNA test. We will simply reanalyze the data we’ve already obtained to provide you with insights about these new discoveries.
A Simple Cheek Swab is all it takes
The DNA collection process is incredibly simple. No appointments, no jabs, no spitting. Just a 2-minute painless mouth swab and our technology will do the rest.
Our collection kits make it easy to collect DNA from a person of any age, including newborns.
From $3 Billion To Less Than The Cost Of A Smartphone
Deciphering the human genome was not easy. Sequencing the first whole genome, which was completed in 2003, took 13 years and cost $3 billion dollars.
The information from the Human Genome Project has allowed us to better diagnose disease, detect certain diseases earlier, and make life-saving improvements in preventive medicine.
Thanks to rapid technological advancements over the last 20 years, the cost of whole genome sequencing is now within reach for virtually all people who want to have better control of their health and wellness.
Sequencing Is For Everyone Who Wants The Complete Picture
Anyone can use the information from our affordable sequencing service for their own personal edification. Health professionals also use it to help them gain more insight into their patients’ conditions in order to improve outcomes.
Become empowered to take action and make positive changes to your life when you receive health guidance that’s based on their DNA. Our service provides more information about your DNA than any other type of genetic testing.
Ready to Get Sequenced?
Start by ordering the most comprehensive DNA testing kit offered in the market.
Already Have DNA Data?
If you’ve taken a DNA test elsewhere, upload your raw DNA data for free to get started.Select Test Provider
Whole Genome Sequencing Bundle
Results in8-12 WeeksFrom Lab Receipt of Kit
Privacy Forever Data Protection
We don`t sell or share your data with anyone.
Wellness & Longevity Report
1 Month PLUS Genome Plan
Full Access To All Raw Genome Data & Analyzed Data
- 30x genome sequencing depth
- 100% of your genome
- 3 billion genetic variants
- All 30,000 genes sequenced
- All chromosomes fully sequenced incl. the mitochondrial & Y chromosomes
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).
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