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.
Comprehensive Health Screen WGS Bundle
Privacy Forever Data Protection
We don`t sell or share your data with 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).
Our Tests Vs Our Competitors
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 Whole Genome Sequencing |  |  |  |  |  |
| Amount of Genome Tested | ~100% | Less than 0.1% | Less than 0.1% | Less than 0.1% | ~100% | Less than 0.1% |
| Genome Quality | 30x (Clinical Grade) | not whole genome | not whole genome | not whole genome | 30x (Clinical Grade) | not whole genome |
| Rating | ||||||
| HIPAA compliance |  |  | | | | |
| Free DNA Data Download | | | | | | |
| Obtains Data on Entire Genome | | | | | | |
| Wide Assortment of DNA Analysis Apps & Reports | | | | | | |
| 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) |