The Fastest Sequencing Service
Confidential 30x whole genome sequencing with a 2-3 week turnaround.
Why Whole Genome Sequencing?
Detect genetic variants that increase your predisposition to preventable conditions and diseases.
How It Works
Compare The Numbers
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.
Compare The Numbers
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
Numbers That Outshine the Competition
Numbers That Outshine the Competition
What Our Customers Say
That's 5000x more information than most other traditional DNA tests
That's 5000x more information than most other traditional DNA tests
Support
DNA Education
Explore Reports
Our Difference
Why Whole Genome Sequencing?
How It Works
The Fastest Sequencing Service
Confidential 30x whole genome sequencing with a 2-3 week turnaround.
Our Difference
Products
Explore Reports
DNA Education
Support
What Our Customers Say
Featured In
Featured In
DNA
RESOURCES
COMPANY
Get Whole Genome Sequencing to Get The Full Picture
Traditional DNA tests obtain less than 0.1% of your genome. That’s enough to track your genetic ancestry but not much more. Whole Genome Sequencing analyzes 100% of your genome to provide the accurate insights you need to make better-informed decisions about your health.
0.1%
100%
Of Your Genome
Of Your Genome
Get Whole Genome Sequencing to Get The Full Picture
Traditional DNA tests obtain less than 0.1% of your genome. That’s enough to track your genetic ancestry but not much more. Whole Genome Sequencing analyzes 100% of your genome to provide the accurate insights you need to make better-informed decisions about your health.
0.1%
100%
Of Your Genome
Of Your Genome
Ready To Get Sequenced?
Start by ordering the world’s most comprehensive DNA test kit.
Whole Genome Sequencing
Rare Disease Bundle
$399 $639
Privacy First Data Protection
We don’t sell or share your data with anyone.
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).
Whole Genome Sequencing Premium Expedited Bundle
$1,999 $2,739
Full Access to All Raw Genome Data and Analyzed Data:
3 billion genetic variants
30x genome sequencing depth
All chromosomes fully sequenced including the mitochondrial and Y chromosomes
100% of your genome
30x genome sequencing depth
3 Months PREMIUM Genome Plan ($100 Value)
INCLUDES
Wellness and Longevity Report View
Privacy Forever Data Protection
We don’t sell or share your data with anyone.
Free Telomere Length Analysis
Ready To Get Sequenced?
Start by ordering the world’s most comprehensive DNA test kit.
Whole Genome Sequencing
Rare Disease Bundle
$399 $639
Privacy First Data Protection
We don’t sell or share your data with anyone.
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).
Whole Genome Sequencing Premium Expedited Bundle
$1,999 $2,739
Full Access To All Raw Genome Data And Analyzed Data:
3 billion genetic variants
All 30,000 genes sequenced
All chromosomes fully sequenced incl. the mitochondrial and Y chromosomes
100% of your genome
30x genome sequencing
3 Months PREMIUM Genome Plan ($100 Value)
INCLUDES
Wellness and Longevity View
Privacy Forever Data Protection
We don’t sell or share your data with anyone.
Free Telomere Length Analysis
Included Reports with Bundle Purchase
Receive more relevant healthcare with personalized medicine based on your DNA.
Enable your physician to know which medications work best for you.
Improve the health of future generations by helping researchers identify mutations that cause genetic disorders.
Detect genetic variants that increase your predisposition to preventable conditions and diseases
Receive more relevant healthcare with personalized medicine based on your DNA
Enable your physician to know which medications work best for you
Improve the health of future generations by helping researchers identify mutations that cause genetic disorders
Brandon Colby, MD
Founder, CEO
“Waiting for test results that can normally take up to three months can be nerve wracking, especially if someone is dealing with a health issue that may have genetic implications or they suspect that they may have a genetic disease. The sooner they can access their own genome, the quicker they can gain insights to optimize their strategies for the best health and wellness outcomes.”
Zero Delay With Personalized Care
Existing sequencing services process samples in batches across multiple locations to cut costs, which results in an 8- to 12-week processing time. Premium Expedited samples are all processed in Temple City, CA, using a highly optimized flow for individual sample processing.
Revealing More Complex Regions of the Genome
Beyond a faster turnaround time, personalized sample care allows us to focus sequencing for comprehensive reads. Sequencing them successfully often requires multiple sequencing passes, which are not available with regular batch processing.
Brandon Colby, MD
Founder, CEO
“Waiting for test results that can normally take up to three months can be nerve wracking, especially if someone is dealing with a health issue that may have genetic implications or they suspect that they may have a genetic disease. The sooner they can access their own genome, the quicker they can gain insights to optimize their strategies for the best health and wellness outcomes.”
Our Tests Vs Our Competitors
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.
Our Tests Vs Our Competitors
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.
Transform your DNA data into clear, actionable insights with our enhanced reports, developed by leading scientists throughout the world and curated by Sequencing's bioinformatics team to meet the highest scientific standards.
What's The Same
What's The Difference
Benefits
30x Clinical-Grade Whole Genome Sequencing
Data files: FASTQ, BAM (GRCH38 aligned), and VCF (SNVs/SNPs, INDELs, CNVs, SVs, Mitochondrial)
Batch Processing
Standardize Quality Control for 30x Sequencing
Multi Lab + Shipping required to reach next step
8-12 weeks sequencing time
Cost efficient sequencing service to obtain whole genome data for health applications
Data can be used to run all reports on Sequencing.com’s marketplace
Whole Genome Sequencing
30x Clinical-Grade Whole Genome Sequencing
Data files: FASTQ, BAM (GRCH38 aligned), and VCF (SNVs/SNPs, INDELs, CNVs, SVs, Mitochondrial)
Individualize Processing
Additional Sequencing Passes for added data in complex genome regions
Single Lab + One Location no shipping time added at each step
2-3 weeks sequencing time
Fastest consumer whole genome sequencing on the market
30x sequencing guaranteed but on average sequencing depth could go up to 40x due to individualized quality control
Whole Genome Sequencing
Premium Expedited
How Do Our Kits Compare?
Our DNA testing kits at a glance.
Zero Delay With Personalized Care
Existing sequencing services process samples in batches across multiple locations to cut costs, which results in a 8- to 12-week processing time. Premium Expedited samples are all processed in Temple City, CA, using a highly optimized flow for individual sample processing.
Revealing More Complex Regions of the Genome
Beyond a faster turnaround time, personalized sample care allows us to focus sequencing for comprehensive reads. Sequencing them successfully often requires multiple sequencing passes, which are not available with regular batch processing.
How Do Our Kits Compare?
Whole Genome Sequencing
Individualize Processing
2-3 weeks sequencing time
30x Clinical-Grade Whole Genome Sequencing
Data files: FASTQ, BAM (GRCH38 aligned), and VCF (SNVs/SNPs, INDELs, CNVs, SVs, Mitochondrial)
Whole Genome Sequencing Premium Expedited
Our DNA testing kits at a glance.
Batch Processing
30x Clinical-Grade Whole Genome Sequencing
Data files: FASTQ, BAM (GRCH38 aligned), and VCF (SNVs/SNPs, INDELs, CNVs, SVs, Mitochondrial)
8-12 weeks sequencing time