All your Myriad Oncology testing and results in your preferred EMR

Order and manage both germline and tumor genomic tests right inside the EMR platform you already use. Fewer steps, faster turnaround, concordant results, and no more juggling multiple labs or tracking down fragmented reports.

Coming soon: expanded integration in OncoEMR®

With our comprehensive oncology-focused portfolio, expanding your Myriad Oncology ordering in OncoEMR isn’t just easier—it’s better for you and your patients.

NOTIFY ME WHEN LIVE

All-in-one ordering

Seamlessly order MyRisk® Hereditary Cancer Test, Precise Tumor® Molecular Profile Test, MyChoice® CDx HRD Myriad HRD Companion Diagnostic Test, and immunohistochemistry (IHC) testing for PD-L1 and Folate receptor alpha (FOLR1/FRα) in a single workflow.

Concordant results

With Myriad Oncology, you get concordant results across the entire patient journey, avoiding inconsistencies that arise when multiple labs interpret variants differently.

One-page summary

You’ll receive clear, clinically actionable insights delivered directly to your EMR, along with a treatment-focused summary sheet consolidating germline and tumor genomic information on a single page that is easy to read and easy to share with patients.

Faster turnaround

Speed up turnaround times and increase visibility across your care team. No more switching between portals and paper TRFs. No more juggling multiple labs or tracking down fragmented reports.

Guideline adherence

With ASCO recommending germline testing for all eligible patients regardless of tumor results, Myriad simplifies adherence to these guidelines, helping to ensure that no critical variant or therapy opportunity is missed.1

Myriad Oncology is integrated into these platforms

Myriad can support most EMR platforms you currently use. We offer native integration with most EMR platforms and can build customizable solutions for others.

ONCOEMR Logo
MyRisk® Hereditary Cancer Test product logo

Coming soon

MyChoice CDx Myriad HRD Companion Diagnostic Test logo
Precise Tumor® Molecular Profile Test logo
Epic Logo
MyRisk® Hereditary Cancer Test product logo

Coming soon

MyChoice CDx Myriad HRD Companion Diagnostic Test logo
Precise Tumor® Molecular Profile Test logo
Lumea Logo
MyRisk® Hereditary Cancer Test product logo
Prolaris Prostate Cancer Prognostic Test logo
iKnowMed Logo
MyRisk® Hereditary Cancer Test product logo
Athena health Logo
MyRisk® Hereditary Cancer Test product logo

What are the benefits of choosing Myriad Oncology tests?

With Myriad Oncology, results are clear, treatment-focused, and clinically-actionable—making it easier to personalize therapy decisions, identify clinical trials, and support patients with confidence, across the entire patient journey.

By choosing Myriad Oncology, you also get access to our unrivaled suite of services—from pre- and post-test education to billing and clinical support—at no added cost to your clinic or patients.

MyRisk® Hereditary Cancer Test product logo

The MyRisk test provides more answers for more patients by identifying up to 63% of variants other labs cannot definitively classify and offers the industry’s lowest reported rates of BRCA1/2 variants of uncertain significance (VUS) of 1.0%.2,3

Precise Tumor® Molecular Profile Test

The Precise Tumor test utilizes combined DNA and RNA sequencing to detect more fusion and splice variants compared to DNA-only tests, increasing patient eligibility for targeted therapies and clinical trials.4-7

MyChoice CDx Myriad HRD Companion Diagnostic Test

The MyChoice CDx test helps you expand access to PARP inhibitors by identifying 34% more HRD-positive ovarian cancer patients than other tests that only use %LOH.8

Speak with our team about integrating Myriad Oncology into your EMR of choice.

Get started with Myriad Oncology

Request more information about how Myriad’s Oncology solutions can benefit you/your patients.


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Explore the Myriad Oncology tests and services

References:

  1. Tung N, Ricker C, Messersmith H, et al. Selection of Germline Genetic Testing Panels in Patients With Cancer: ASCO Guideline. J Clin Oncol. 2024;42(21):2599-2615.
  2. Gradishar W, Johnson K, Brown K, et al. Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory. Oncologist. 2017;22(7):797-803.
  3. Mundt E, McGreevy K, Nix P, Cummings S. Myriad’s Multidisciplinary Approach and Consistent Investment in Variant Classification for Clinical Decision Making [White paper]. Myriad Genetics. 2025. .
  4. Benayed R, Offin M, Mullaney K, et al. High Yield of RNA Sequencing for Targetable Kinase Fusions in Lung Adenocarcinomas with No Mitogenic Driver Alteration Detected by DNA Sequencing and Low
  5. Tumor Mutation Burden. Clin Cancer Res. 2019;25(15):4712-4722.
  6. Wong W, Son J, Tang T, et al. Methods for identifying patients with tropomyosin receptor kinase (TRK) fusions. Pathol Oncol Res. 2020;26(3):1385-1399.
  7. Yang Y, Qin G, Li Y, et al. A performance comparison of commonly used assays to detect RET fusions. Clin Cancer Res. 2020;26(24):6547-6556.
  8. Radonic T, Fukuda K, Lang C, et al. RET FISH analysis is a sensitive but highly unspecific method for RET fusions in lung cancer. J Thorac Oncol. 2021;16(2):270-276.
  9. Mills GB, Timms KM, Perry M, et al. Comparison of Genomic Instability Scores for Predicting PARP Activity in Ovarian Cancer. Poster presented at the 2020 SGO Annual Meeting on Women’s Cancer.