Baylor Genetics

Every diagnosis has the potential to change a patient's path forward.

This Spinal Muscular Atrophy (SMA) Awareness Month, we recognize the power of genetic testing to help identify SMA earlier, inform clinical decision-making, and connect patients and families with the care and support they need.

Join us in raising awareness, advancing research, and expanding access to genetic testing. Together we can help improve outcomes for the SMA community.

Targeted reflex RNA Sequencing can uncover answers beyond the genome.

In a retrospective analysis of more than 3,200 Whole Genome and Whole Exome sequencing cases, RNA-Seq led to variant reclassification in 42% of completed cases, resulting in a genetic or likely genetic diagnosis for 25 patients. Among cases with positive RNA-Seq results, clinical management changed in 71% of cases, underscoring its potential clinical impact.

Join Dr. Christine Eng, Chief Medical Officer and Chief Quality Officer, for the GenomeWeb-hosted webinar, When the Genome isn't Enough: Closing Rare Disease Gaps with RNA Sequencing, to learn how RNA-Seq can help improve diagnostic outcomes.

Register today: https://event.on24.com/wcc/r/5425767/A92063BE488169672B0928A34E813197?partnerref=baylor

Our values come to life through the people who live them.

This month, we're proud to recognize team members whose dedication, collaboration, innovation, and commitment to excellence make a meaningful impact across Baylor Genetics.

Join us in celebrating our Core Values honorees for the impact they make every day.

We're proud to announce that Baylor Genetics has received the Bronze Award for Technical Innovation of the Year at the 2026 Stevie® Awards for Technology Excellence for our Innovative Multimodal Solutions for Rare Disease Diagnostics.

This recognition reflects our commitment to advancing rare disease diagnostics with cutting-edge genomic technologies, including Whole Genome Sequencing, to help clinicians uncover answers for patients and families seeking a diagnosis.

Every innovation at Baylor Genetics is driven by our mission to shorten the diagnostic odyssey and improve patient care. We're honored to have our work recognized alongside some of today's leading technology innovations.

Learn more about the Stevie Awards for Technology Excellence: https://tech.stevieawards.com/

Every answer starts with a conversation.

Join us in recognizing Genetic Testing Action Day, a day dedicated to raising awareness about the power of genetic testing and helping providers and families take the next step toward answers.

Early conversations about genetic testing can help patients with unexplained symptoms or suspected rare diseases move closer to a diagnosis and more informed care decisions.

Help spread awareness, share your story, or encourage someone to ask about genetic testing. Together, we can help more people find the answers they deserve.

We're hiring!

Baylor Genetics is looking for a Senior Infrastructure Engineer to help support and strengthen the systems that power our clinical laboratory operations and genomics pipeline.

In this role, you'll help ensure the performance, security, and resilience of critical infrastructure while enabling the technologies that support patients, providers, and laboratory teams every day.

If you thrive in complex environments and are passionate about building and maintaining high-performing systems, we'd love to hear from you. Apply today: https://recruiting2.ultipro.com/BAY1006BML/JobBoard/0669eed3-5441-4f8e-a7b1-c5df596a4dfe/OpportunityDetail?opportunityId=33c42b00-9b5e-40f6-9411-4ca99c45b09d

Many patients with suspected rare genetic diseases remain undiagnosed after genome sequencing, often due to variants of uncertain significance.

Join Dr. Christine Eng, Chief Medical Officer and Chief Quality Officer, on August 24 for a GenomeWeb-hosted webinar, When the Genome Isn't Enough: Closing Rare Disease Gaps with RNA Sequencing, to explore how RNA-Seq can provide functional evidence that helps clarify uncertain variants and improve diagnostic outcomes.

Register today to learn how Baylor Genetics can help uncover answers beyond the genome: https://event.on24.com/wcc/r/5425767/A92063BE488169672B0928A34E813197?partnerref=baylor

Today we celebrate Gregor Mendel, the father of genetics, whose curiosity and groundbreaking research laid the foundation for modern genomics.

His experiments with pea plants revealed the basic laws of inheritance, providing insights that continue to guide genetic research, testing, and precision diagnostics more than 150 years later.

At Baylor Genetics, we strive to advance the future of genetic testing and patient care, and recognize the enduring influence of Mendel’s discoveries and their impacts.

Greetings from the Southeastern Regional Genetics Group (SERGG) Annual Meeting!

Our team is proud to be part of the conversation around the future of genomics, including the evolving role of whole genome and exome sequencing in clinical care.

Be sure to stop by our booth to connect with the Baylor Genetics team. Learn more: www.baylorgenetics.com