Clinical whole genome sequencing at a price that empowers adoption today - Fabric Genomics

Clinical whole genome sequencing at a price that empowers adoption today

Includes interpretation & reporting for as low as $1,000*

Setting a new standard, Broad Institute launches $1K sample-to-report clinical whole genome services powered by Fabric Genomics AI interpretation engine offering hospitals, research institutions, and commercial organizations a solution to procure the highest quality clinical testing that leverages whole genome sequencing at a cost that enables widespread adoption for diagnostic accuracy.

A novel combination. A paradigm shift.

These combined services offer healthcare providers, and their patients, greater access to high-complexity clinical whole genome testing which can have a profound impact on health outcomes, as well as providing genome-wide data for future research purposes.

Broad Clinical Lab - Fabric Genomics Integration

What's included ...

  • Samples are processed through Broad’s CLIA Certified, and CAP accredited lab (CRSP)
  • State-of-the-art clinical interpretation leveraging Fabric’s AI platform
  • Data is interpreted by an experienced team of clinical variant scientists
  • Clinical reports reviewed and signed out by Broad’s board-certified lab directors

To find out more information about this clinical WGS service please email

There is a need for clinical WGS testing at a larger scale to improve patient outcomes, support clinical utility measures, and ultimately enable widespread reimbursement. We are excited to be able to offer this new end-to-end clinical service that we have developed using the Fabric Genomics platform.

* Pricing subject to minimum sample number commitment. Offer currently valid in the U.S. only.

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