WHAT IS AMBRYSHARE?

It’s a chance to unlock the promise of the human genome project by breaking the mold of data hoarding.

AmbryShare is a program based on Ambry’s commitment to sequence and share aggregate, anonymized genomic data from patients with disease, to understand the genetic basis of all human disease. It is comprised of three key pieces: The AmbryShare database, scientific community, and patients. Like an ecosystem, we need all these pieces to work together to help bring understanding to the relationships between genetics and human disease.

WANT TO GET INVOLVED?

Register with AmbryShare to help stop data hoarding and unlock the promise of the human genome project.

I am... A Patient or Advocate

Select this if you are a patient or other individual who wants to learn more about genetic diseases.

Get Involved
I am... A Medical Professional

Select this if you are a doctor or clinician and would like to view and use the database to search for variants and help with clinical care.

Get Involved
I am... A Researcher

Select this if you are a researcher and would like to view the database or to download the dataset to target your search for disease solutions.

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