Ambry Genetics

Ambry Genetics As a company built by scientists, genetic counselors and physicians, Ambry, a Tempus company, is your partner in genetics and genomics.

As a company built by scientists, genetic counselors and physicians, we are your partner in genetics and genomics.

Pathogenic variants confer risk across a continuum. In this Research for your Practice, we explore why categorizing a va...
09/02/2026

Pathogenic variants confer risk across a continuum. In this Research for your Practice, we explore why categorizing a variant as moderate risk or reduced penetrance is a data-driven decision and should
not be viewed as a limitation of uncertainty, but rather as a step forward in diagnostic precision. https://hubs.ly/Q04wh4Hx0

In this week's , Frankie Fann, MS, CGC, breaks down NF2 and its association with NF2-related schwannomatosis. htt...
09/01/2026

In this week's , Frankie Fann, MS, CGC, breaks down NF2 and its association with NF2-related schwannomatosis.
https://hubs.ly/Q04w23Qf0

Ambry's comprehensive hereditary cancer and rare disease genetic testing portfolios now have extended access through Epi...
08/28/2026

Ambry's comprehensive hereditary cancer and rare disease genetic testing portfolios now have extended access through Epic Aura via the Tempus compendium.
Embedding genetic testing into the EHR aligns with guidance from the American College of Medical Genetics and Genomics and has been shown to streamline provider workflows by reducing order time and cutting results management time.
With this integration, providers can
- order genetic tests and receive results within their existing electronic health record (EHR) workflow, including ExomeNext®
- order duo and trio exome testing directly through Epic Aura and other EHR platforms for more comprehensive family-based analysis
- share genetic test results through MyChart, giving patients easier access to their information while keeping results connected to their broader medical record
- help ensure everyone involved in a patient’s care is working from the same, up‑to‑date information.

Explore real case examples demonstrating how patients benefitted from long‑read whole genome sequencing and learn more a...
08/26/2026

Explore real case examples demonstrating how patients benefitted from long‑read whole genome sequencing and learn more about this collaborative effort:
https://hubs.ly/Q04vp_rc0

Jessica Scott, MGC, CGC, explores the TSC1 gene and its association with Tuberous Sclerosis Complex (TSC) in this week's...
08/25/2026

Jessica Scott, MGC, CGC, explores the TSC1 gene and its association with Tuberous Sclerosis Complex (TSC) in this week's . https://hubs.ly/Q04v9bNr0

Genetic testing isn’t a one-time assessment—our understanding of DNA evolves as science advances. Ambry’s Patient for Li...
08/21/2026

Genetic testing isn’t a one-time assessment—our understanding of DNA evolves as science advances. Ambry’s Patient for Life™ program keeps your patients’ results up to date by automatically reanalyzing eligible tests and notifying you of important changes. No retesting needed.
Learn more at https://hubs.ly/Q04tBXqY0

How do Patient Advocates help families? Morgan Turpin explains how being part of a community helped her family:"It's tru...
08/19/2026

How do Patient Advocates help families? Morgan Turpin explains how being part of a community helped her family:
"It's true that [Dravet Syndrome] does not have a cure, but knowing his diagnosis has opened an entire world to us that we didn't know about before. We found an online community and a cause to support: the Dravet Syndrome Foundation. They fund research into treatment options and therapies and family support for Dravet Syndrome. We've connected with countless other parents across the country (some in other countries across the world) whose children have Dravet Syndrome and we have been able to develop community with them ... The most invaluable thing we've done is connect with other families ... Sometimes you get families who have never met another Dravet family. That connection is completely vital."

How can you get involved as a patient advocate?Noelle Carbognin, Lynch Syndrome Previvor, explains how she participates ...
08/19/2026

How can you get involved as a patient advocate?
Noelle Carbognin, Lynch Syndrome Previvor, explains how she participates in advocacy in her local community: "I am passionate about awareness and access to hereditary cancer testing and appropriate cancer screening. I have remained active in raising colon cancer awareness in my community through fitness fundraisers, social media, supporting local health systems’ events and most importantly through connection. I welcome the opportunity to connect with others about my story and theirs."

Patient Advocacy Day is August 19. Ambry recognizes and appreciates our patients and caregivers who advocate for their h...
08/19/2026

Patient Advocacy Day is August 19. Ambry recognizes and appreciates our patients and caregivers who advocate for their health. We are dedicated to providing genetic testing support and education so they and their families can make informed decisions about their healthcare journey.

08/18/2026

What are the benefits of germline genetic testing? It can…
- Reveal inherited risks for certain cancers long before symptoms appear.
- Enable proactive screenings.
- Suggest risk-reducing options.
- Lead to early detection, when cancers may be easier to treat.
By routinely assessing which patients may be at increased hereditary risk, healthcare providers can identify individuals who may benefit from earlier, more frequent, or advanced cancer screening. Watch the video to see how the ripple effect extends to families.

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