Expanse Genomics

The future of medicine. Right now.

For health systems of all sizes, the path to precision medicine is here. Our integrated, end-to-end solution gives providers access to patients’ genetic data — and the clinical decision support tools they need to apply it.

When physicians have meaningful genetic data, along with the tools for interpretation, at the point of care, they can deliver the right treatment, to the right patient, the first time.

Genomics Demo

Announcement for Physicians
Sign up for a FREE category 1 CME customer event in April:
Genomics in the Era of the Electronic Medical Record

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Pharmacogenomics is a reality.

Leveraging First Databank, Expanse Genomics guides clinicians with clear and concise recommendations. It’s embedded with pharmacogenomic decision support, including hundreds of known genomic interactions.

Referencing an individual’s genetic profile when creating pharmaceutical therapies optimizes drug efficacy while mitigating the risk of adverse reactions or dosing errors.

A solution to today’s workarounds.

To access genetic data in most EHRs, physicians launch separate applications, search PDF files, copy and paste data back into the patient record, and consult with genetic specialists — all before making their clinical decision. No wonder they find accessing this information so frustrating and inefficient.

Expanse Genomics allows physicians to perform all aspects of their genetic workflow within the EHR. When needed, it isolates the relevant genetic data and provides clinical decision support, with clear, concise, and actionable guidance that physicians can easily interpret.


Physician orders genetic test in Expanse.

No More:

  • launching separate systems
  • manually entering genetic test orders
  • returning to the EHR to document test orders.


Reference lab conducts test and returns results.

No More:

  • results returned in flat files (typically PDFs) and encoded as free text.


Results are displayed intuitively within patient chart.

No More:

  • searching for relevant results
  • test results displayed in disparate formats based on test vendor and test type.


Specimen is collected and sent to reference lab.

No More:

  • manually tying specimens to genetic tests ordered.


Expanse imports and parses data into patient record.

No More:

  • results stored as document links that launch in a separate viewer.


Embedded clinical decision support with pharmocogenomics.

No More:

  • searching through documents for analysis
  • translating genetic results into patient-friendly language
  • trial and error prescribing — drug and dosing recommendations based on patients’ unique genetic profiles.
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Dr. William Dailey Headshot

“We are thrilled to be one of the first to implement Expanse Genomics. The solution is going to expand our possibilities for delivering precision medicine at our organization and enhance our connectivity with commercial labs. It’s also going to elevate our ability to analyze and parse results into discrete, actionable data displayed directly in the patient charts.”

Dr. William Dailey, CMIO

Golden Valley Memorial Hospital

Learn how Expanse Genomics can help your organization tap into the power of genomic medicine to deliver more effective and personalized patient care.

Sign Up For The Expanse Patient Care Webinar