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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.

Top view of the packing for a whole genome sequencing kit

Whole Genome Sequencing Bundle

Privacy Forever Data Protection

We don`t sell or share your data with anyone.

HSA/FSA

INCLUDES

Privacy Forever protection of all of your data

Wellness and Longevity View

Genome Explorer v3

1 Month Premium Genome Plan

Full Access To All Raw Genome Data & Analyzed Data

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    30x genome sequencing depth
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    100% of your genome
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    3 billion genetic variants
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    All 30,000 genes sequenced
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    All chromosomes fully sequenced incl. the mitochondrial & Y chromosomes
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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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Whole Genome Sequencing

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Overview
Amount of Genome Tested~100%Less than 0.1%Less than 0.1%Less than 0.1%~100%Less than 0.1%
Genome Quality30x (Clinical Grade)not whole genomenot whole genomenot whole genome30x (Clinical Grade)not whole genome
Rating
HIPAA complianceYesNoNoNoNoNo
Free DNA Data DownloadYesYesYesYesNoYes
Obtains Data on Entire GenomeYesNoNoNoYesNo
Wide Assortment of DNA Analysis Apps & ReportsYesNoNoNoNoNo
HealthYesFewFewFewYesNo
Genetic Counseling AvailableYesNoNoNoNoNo
DNA Guidance for LifeYesNoNoNoNoNo
GenomeLock DNA SecurityYesNoNoNoNoNo
One Genome TechnologyYesNoNoNoNoNo
Real-Time Health UpdatesYesNoNoNoNoNo
Real-Time Data UpdatesYesNoNoNoNoNo
Single Nucleotide Variants (SNPs or SNVs)YesPartialPartialPartialYesPartial
Insertions & Deletions (INDELs, DIPs or DIVs)YesFewFewFewYesFew
Copy Number Variants (CNVs)YesNoNoNoYesNo
Structural Variants (SVs)YesNoNoNoYesNo
Mitochondrial HeteroplasmyYesNoNoNoNoNo
Reference Genome Alignment

hg38/GRCh38

(most up-to-date)

hg19/GRCh37

(from 2009)

hg19/GRCh37

(from 2009)

hg19/GRCh37

(from 2009)

hg19/GRCh37

(from 2009)

hg19/GRCh37

(from 2009)

23andMe is a registered trademark of 23andMe, Inc., AncestryDNA is a registered trademark of Ancestry Operations Inc. dba Ancestry, Family Tree DNA is a registered trademark of Gene By Gene, Ltd., MyHeritage is a registered trademark of MyHeritage Ltd., Dante Labs is a registered trademark of Dante Labs, Inc., Nebula Genomics is a registered trademark of Nebula Genomics, Inc., HomeDNA is a trademark of DNA Diagnostic Center, Inc., Living DNA is a registered trademark of Living DNA Ltd., Vitagene is a registered trademark of Vitagene, 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., Ancestry Operations Inc. dba Ancestry, Gene By Gene, Ltd., MyHeritage Ltd., Dante Labs, Inc., Nebula Genomics, Inc., DNA Diagnostic Center, Inc., Living DNA Ltd., or Vitagene, Inc.

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