Confidential 30x whole genome sequencing with a 2-3 week turnaround.
Detect genetic variants that increase your predisposition to preventable conditions and diseases.
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.
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
Why Whole Genome Sequencing?
How It Works
Confidential 30x whole genome sequencing with a 2-3 week turnaround.
DNA
RESOURCES
COMPANY
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
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
Start by ordering the world’s most comprehensive DNA test kit.
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).
Start by ordering the world’s most comprehensive DNA test kit.
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).
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
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.
“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.”
Existing sequencing services process samples in batches across multiple locations to cut costs, which results in a 10- to 12-week processing time. Premium Expedited samples are all processed in Temple City, CA, using a highly optimized flow for individual sample processing.
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.
Existing sequencing services process samples in batches across multiple locations to cut costs, which results in an 10- to 12-week processing time. Premium Expedited samples are all processed in Temple City, CA, using a highly optimized flow for individual sample processing.
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.
“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.”
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
10-12 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
Ultra Rapid
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)
Our DNA testing kits at a glance.
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)
10-12 weeks sequencing time
Ultra Rapid Whole Genome Sequencing WGS Bundle
$1,999 $4,519
Genetic Analysis Included:
Full Access To All Raw Genome Data & Analyzed Data:
3 billion genetic variants
All 30,000 genes sequenced
All chromosomes fully sequenced including the mitochondrial & Y chromosomes
100% of your genome
30x genome sequencing depth
Annual Premium Genome Plan
Whole Genome Sequencing
Cardiovascular Health
Brain Health
Cancer Risk
Rare Disease Screening
(15,000+ Diseases + EDS)
Carrier Screening
Autoimmune Disorders
Digestive Disorders & Gut Health
Neurological Health
Metabolic & Endocrine Health
Musculoskeletal Health
Skin Health
Respiratory Health
Reproductive & Hormonal Health
Medication & Drug Response
Growth & Bone Health
Nutritional & Metabolic Health
Ultra Rapid Whole Genome Sequencing WGS Bundle
$1,999 $4,519
Full Access To All Raw Genome Data & Analyzed Data:
3 billion genetic variants
All 30,000 genes sequenced
All chromosomes fully sequenced incl. the mitochondrial & Y chromosomes
100% of your genome
30x genome sequencing
Genetic Analysis Included:
Whole Genome Sequencing
Annual Premium Genome Plan
Cardiovascular Health
Brain Health
Cancer Risk
Rare Disease Screening
(15,000+ Diseases + EDS)
Carrier Screening
Autoimmune Disorders
Digestive Disorders & Gut Health
Neurological Health
Metabolic & Endocrine Health
Musculoskeletal Health
Skin Health
Respiratory Health
Reproductive & Hormonal Health
Medication & Drug Response
Growth & Bone Health
Nutritional & Metabolic Health
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.
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.
Free Shipping + HSA/FSA Eligible
Free Shipping
HSA/FSA Eligible
+
Ultra Rapid
Whole Genome Sequencing