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Meet The Families In Need
In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.
From Our Founder’s Heart: Dr. Brandon Colby's Story
Dr. Brandon Colby, founder of Sequencing.com, navigated through a challenging childhood plagued by a mysterious health condition—extensive blistering on his feet and hands, with no diagnosis in sight despite countless medical consultations and tests. His significant discovery was made possible by merging whole genome sequencing with the innovative Next-Gen Disease Screen (NGDS), a combination beyond the capability of any other existing test. This powerful approach finally uncovered the genetic culprit: a mutation in the KRT14 gene.
This breakthrough not only provided Dr. Colby with much-needed clarity but also allowed him and his wife to make informed decisions about their family's future, understanding the implications of their genetic makeup. Dr. Colby's experience highlights the transformative impact of NGDS, showcasing its potential to replace fear and uncertainty with empowerment and precise genetic knowledge.
Meet The Families In Need
In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.
Meet The Families In Need
In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.
Meet The Families In Need
In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.
Made Possible With Whole Genome Sequencing
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.
0.1%
100%
Of Your Genome
Of Your Genome
Free Shipping + HSA/FSA Eligible
5 Health Reports Included
Made possible with Whole Genome Sequencing
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.
0.1%
100%
Of Your Genome
Of Your Genome
Made Possible With Whole Genome Sequencing
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.
0.1%
100%
Of Your Genome
Of Your Genome
What people are saying
Lillian L.
"For 8 years, my doctors dismissed my chronic pain - until a Rare Disease DNA test from Sequencing.com finally led to the diagnosis I’d been searching for."
Katherine F.
"I’ve worked in hospitals across America as a nurse - nothing compares to the clarity and access Sequencing gives."
Tia W.
"Being able to self-order genetic testing for Ehlers-Danlos Syndrome changed everything, Sequencing empowered me to rule out other hypermobile conditions and finally feel in charge of my health."
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This Rare Disease Month, take a step toward clarity with whole genome sequencing, screening for 15,000+ genetic conditions, medication reactions, and inherited risks.
Helping families in need
In honor of Rare Disease Day, Sequencing is partnering with Dr. Hodes, the medical director of JDC’s Ethiopia Spine and Heart project, to provide whole genome sequencing to families who otherwise wouldn’t be able to get the critical information DNA can provide. Many of these patients face the same diagnostic odyssey seen around the world:
- 1 in 10 people worldwide live with a rare disease.
- 80% of rare diseases are linked to genetics, yet most go undiagnosed for years.
- It takes an average of 7 years for individuals with rare diseases to find answers and the right support.
We’re proud to support the work of Dr. Hodes and others, helping to bring life-changing genetic insight to families who’ve been waiting far too long.
More Insights From DNA You Already Have
Free DNA upload. AI-powered analysis. New insights from data you already have.
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Answers today. Health intelligence for life.
This Rare Disease Month, take a step toward clarity with whole genome sequencing, screening for 15,000+ genetic conditions, medication reactions, and inherited risks.
Our Difference
Products
Explore Reports
DNA Education
Support
More Insights From DNA You Already Have
Free DNA upload. AI-powered analysis. New insights from data you already have.
Rare Disease Month Sale | Up to 50% off + free shipping
Rare Disease Month Sale
Up to 50% off + free shipping
Rare Disease Month Sale
Up to 50% off + free shipping
Rare Disease Month Sale | Up to 50% off + free shipping
