Molecular Diagnostics - Fabric Genomics

Launching NGS Testing Has Never Been Easier

Kick off your testing program in as little as 4 weeks.

Analysis is no longer a bottleneck

Next generation sequencing is rapidly transforming
health care, but the complexity of data analysis can
be a stumbling block for labs without in-house
bioinformaticians.

Fabric Enterprise empowers labs by offering
automated, fast and highly-accurate AI algorithms
for common genomic panel tests.

Hereditary Cancers

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Cardiac Conditions

Neurodegeneration

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Carrier Screening

Don't miss out on reimbursement

NGS panel testing is highly profitable. Learn how you can save time cost, and personnel by running multiple tests on a single assay

Learn how to multiply your profits

Smart algorithms and efficient clinical workflows reduce interpretation costs for NGS tests by ~50-75%

We’ll help you set up panel testing at all stages

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Step 1

Our implementation team will help you finalize your test launch plan

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Step 2

We set up Fabric Enterprise for your lab including clinical workflows

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Step 3

Collect samples
and sequence

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Step 4

Fully automated interpretation
delivers reports in minutes

Step 5

Our team of clinical experts assists in finalizing interpretation and drafting reports, as needed

Still not sure?

Get the facts on affordable NGS panel testing in these Case Studies

Fabric Genomics Clinical NGS Resource Series on Avoiding the common mistakes labs make when launching hereditary cancer panel tests
Mistakes to avoid
Fabric Genomics Solution Datasheet on Hereditary Cancer Testing
Hereditary Panels
Fabric Genomics Solution Datasheet on Interpretation of Next-Generation Sequencing Panels
Launching and Scaling

Ready to
get started?