Utilize Whole Genome Sequencing from our CAP-CLIA certified labs to access 100% of your DNA, providing essential insights for personalized treatment plans and improving overall family health management.
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The World's Most Comprehensive Rare Disease Screening
DNA
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COMPANY
Start by ordering the world’s most comprehensive DNA test kit.
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).
$399 $889
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
INCLUDES
Fatty Liver Foundation WGS Bundle
1 Month Premium Membership
1 Month SequencingAI Access
Health Scan
Genome Explorer
$399 $889
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
INCLUDES:
Health Scan
Fatty Liver Foundation WGS Bundle
Genome Explorer
1 Month SequencingAI Access
1 Month Premium Membership
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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HSA/FSA Eligible
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Engage with SequencingAI for in-depth conversational analysis of rare genetic conditions, delivering customized insights and strategies to enhance health outcomes.
Store and manage your family’s genetic information securely, enabling comprehensive health planning and decision-making for rare diseases in a HIPAA-compliant environment.
Discover unparalleled insights with the Next-Gen Disease Screen, featuring the most extensive disease inventory globally. Benefit from top-tier software for rare disease detection, precise health planning, and certified genetic counseling for personalized care.
Embark on a journey with Genome Explorer, the premier genetic search engine. Explore your genetic landscape in the context of the world's latest scientific discoveries and empower your health decisions.
Ensure you have access to the latest science in the context of your DNA with Health Scan. Stay at the forefront of rare disease genetics, with weekly and monthly updates to discoveries from around the world aligning your health strategy with the best information.
Utilize Whole Genome Sequencing from our CAP-CLIA certified labs to access 100% of your DNA, providing essential insights for personalized treatment plans and improving overall family health management.
Discover unparalleled insights with the Next-Gen Disease Screen, featuring the most extensive disease inventory globally. Benefit from top-tier software for rare disease detection, precise health planning, and certified genetic counseling for personalized care.
Embark on a journey with Genome Explorer, the premier genetic search engine. Explore your genetic landscape in the context of the world's latest scientific discoveries and empower your health decisions.
Ensure you have access to the latest science in the context of your DNA with Health Scan. Stay at the forefront of rare disease genetics, with weekly and monthly updates to discoveries from around the world aligning your health strategy with the best information.
Engage with SequencingAI for in-depth conversational analysis of rare genetic conditions, delivering customized insights and strategies to enhance health outcomes.
Store and manage your family’s genetic information securely, enabling comprehensive health planning and decision-making for rare diseases in a HIPAA-compliant environment.