A single genetics screen for more than 10,000 rare diseases, syndromes, conditions and traits.
World's Most Comprehensive Rare Disease Screening
Screen for more than 10,000 Diseases
Whole Genome Sequencing
Our genome sequencing technology is fundamentally different from other DNA tests. We obtain 100% of your DNA data while other DNA test providers obtain data on less than 0.1%.
DNA tests like 23andMe and Ancestry are mainly for recreational purposes such as genealogy and superficial wellness insights. While our genome sequencing service can be used for genealogy, it’s designed for those seeking comprehensive, life-improving guidance about health and wellness.
How It Works
Start by ordering the world’s most comprehensive DNA test kit.
If you’ve taken a DNA test elsewhere, upload your raw DNA data for free to get started.
Whole Genome Sequencing
$389 $779
Privacy First Data Protection
We don’t sell or share your data with anyone.
Full Access To All Raw Genome Data & Analyzed Data:
100% of your genome
3 billion genetic variants
All 30,000 genes sequenced
All chromosomes fully sequenced including the mitochondrial & Y chromosomes
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).
DNA tests from 23andMe, AncestryDNA, and most other companies use older technology that produces data on a very small subset of the total genome.
Whole genome sequencing is an entirely different class of technology that tests every letter of your DNA, including all ~30,000 genes and all chromosomes end-to-end.
How do we get these numbers?
23andMe is a registered trademark of 23andMe, Inc. The use of the name and logo are for compatibility information only and does not imply approval or endorsement of Sequencing.com by 23andMe, Inc.
DNA tests from 23andMe, AncestryDNA, and most other companies use older technology that produces data on a very small subset of the total genome.
Whole genome sequencing is an entirely different class of technology that tests every letter of your DNA, including all ~30,000 genes and all chromosomes end-to-end.
How do we get these numbers?
23andMe is a registered trademark of 23andMe, Inc. The use of the name and logo are for compatibility information only and does not imply approval or endorsement of Sequencing.com by 23andMe, Inc.
DNA
RESOURCES
COMPANY
That's 5000x more information than most other traditional DNA Tests
That's 5000x more information than most other traditional DNA Tests
World's Most Comprehensive Rare Disease Screening
Screen for more than 10,000 Diseases
Whole Genome Sequencing
Our genome sequencing technology is fundamentally different from other DNA tests. We obtain 100% of your DNA data while other DNA test providers obtain data on less than 0.1%.
DNA tests like 23andMe and Ancestry are mainly for recreational purposes such as genealogy and superficial wellness insights. While our genome sequencing service can be used for genealogy, it’s designed for those seeking comprehensive, life-improving guidance about health and wellness.
How It Works
A single genetics screen for more than 10,000 rare diseases, syndromes, conditions and traits.
Start by ordering the world’s most comprehensive DNA test kit.
If you’ve taken a DNA test elsewhere, upload your raw DNA data for free to get started.
Whole Genome Sequencing
$389 $779
Privacy First Data Protection
We don’t sell or share your data with anyone.
Full Access To All Raw Genome Data & Analyzed Data:
100% of your genome
3 billion genetic variants
All 30,000 genes sequenced
All chromosomes fully sequenced incl. the mitochondrial & Y chromosomes
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).
DNA
RESOURCES
COMPANY