Electronic Medical Records (EMR) Integration

Integrating clonoSEQ ordering and reporting

Adaptive offers EMR integration for most platforms, allowing providers to electronically order clonoSEQ and view results in line with other relevant treatment information.

Benefits of EMR Integration

Leverage integration for a seamless ordering experience and streamlined clinical decision-making.

Test results are shared directly with patients via your EMR’s portal. Integrated results are available sooner.

Save time and improve order accuracy. Streamline order placement and view results alongside relevant treatment information.

Quicker turnaround times and a more efficient pathology workflow. EMR integration with Adaptive reduces administrative overhead.

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If you currently place lab orders in your Epic system, this integration is available for no additional cost

  • Our partnership enables all Epic customers to easily integrate clonoSEQ orders and results within their existing workflows.
  • Epic Aura integration takes 8-12 weeks with a clear project plan and experienced project team.

Leverage discrete data to make informed clinical decisions

EMR Integration

We are committed to ensuring critical information for patient care is available for decision making. That’s why we send all our results to Epic’s Care Everywhere network and Carequality.

Getting Started:

Fill out our Product Inquiry Form to get started or email our team: emrsupport@adaptivebiotech.com

One of our Integration Specialists will reach out to gather additional information as needed.

The Adaptive team will coordinate with you to outline project goals, participants, and timelines.

For Additional Support:

Call 1-888-552-8988, opt. 1 from 5:30 am to 5 pm PT, Monday through Friday, or email clinicalservices@adaptivebiotech.com.

Adaptive Biotechnologies
Attention: CLIA Clinical Laboratory
1165 Eastlake Avenue E
Seattle, WA 98109

Monday–Saturday
8 am to 5 pm PT

View our CAP accreditation and our CLIA license.

Biological specimens can be received and accessioned on the days and times above.
Samples cannot currently be received on Sundays.

Epic, Aura, and Care Everywhere are trademarks of Epic Systems Corporation


This page is intended for a US-based audience.

clonoSEQ® is available as an FDA-cleared in vitro diagnostic (IVD) test service provided by Adaptive Biotechnologies to detect measurable residual disease (MRD) in bone marrow from patients with multiple myeloma or B-cell acute lymphoblastic leukemia (B-ALL) and blood or bone marrow from patients with chronic lymphocytic leukemia (CLL). Additionally, clonoSEQ is available for use in other lymphoid cancers and specimen types as a CLIA-validated laboratory developed test (LDT). To review the FDA-cleared uses of clonoSEQ, visit clonoSEQ.com/technical-summary.