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.
Rare Disease and Carrier 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) |