For nearly 50 years, we’ve advanced the field of precision diagnostics with a clear mission:
to Empower Patients, Healthcare Providers, & Partners
with trusted insights, translating scientific innovations into accessible clinical solutions.
From pioneers in genetic testing to leaders setting today’s standards in modern genomics, we’ve consistently delivered deeper answers that improve care for every patient we serve.
Guided by our vision to unlock the power of genomics to transform healthcare, we are committed to delivering meaningful answers to complex genetic disorders when they matter most.
We offer a full spectrum of comprehensive genetic tests and diagnostic services—from clinical-grade genomic sequencing to expert interpretation.
Our tests—including Whole Genome and Whole Exome Sequencing, targeted panels, and specialized assays—combined with unmatched clinical expertise, uncover deeper insights across specialties, including rare disease, pediatric genetics, reproductive health, hereditary cancer, metabolic disorders, and more.
CA, MD, PA, RI
Grounded in clinical integrity, each result is interpreted by our world-class team of PhDs, MDs, laboratory directors, and genetic counselors—translating complex genomic data into clear, actionable insights that support confident decision-making and help patients and families find the answers that matter.
Comprehensive Care, Every Step of the Way
Full end-to-end support—from sequencing to interpretation—to deliver answers that turn complexity into clarity.
Clinical Support
Our full-service team of clinical geneticists, genetic counselors, and client service professionals guides you from order to report—ensuring reliable, personalized support throughout the testing journey.
Post-Test Genetic Counseling
Patients with positive or uncertain Whole Exome Sequencing results may receive counseling with a certified genetic counselor to interpret findings and guide next steps. (Restrictions apply.)
Physician-Initiated Reanalysis
As genomic knowledge evolves, physicians can request reanalysis of patient data in light of new evidence, offering renewed opportunities for meaningful answers.
Expert-Led Review
ABMGG-certified Baylor College of Medicine faculty serve as Medical Directors, reviewing every report. This ensures unmatched clinical oversight, expertise, and the highest standards of quality.
Patient Financial Assistance
Our dedicated team helps patients understand insurance coverage, explore qualifying financial support options, and manage out-of-pocket costs.
Phlebotomy Services
When access to a blood draw is limited, we can help locate convenient phlebotomy options to prevent testing delays. (Restrictions apply.)
Artificial Intelligence
Our proprietary analysis pipeline leverages industry-leading AI to rapidly prioritize candidate variants, using trusted databases and curated literature to uncover underlying causes.
Undiagnosed Diseases Network (UDN)
As the sole sequencing core for the NIH UDN, Baylor Genetics uses rare disease data from uncharacterized conditions to provide deeper insight and more definitive diagnostic support for complex cases.
Multiple Testing Formats
Comparator testing (Duo, Trio, Quad) analyzes patients alongside biological relatives for more accurate interpretation. Rapid testing delivers clinical reports in as little as 5 days.
Epic Aura EMR Integration
Organizations using Epic Aura can order Whole Genome Sequencing and view results directly in the EHR—enabling faster, more informed clinical decisions.
Research Leadership
We advance genomics through publications in the New England Journal of Medicine and Genome Medicine, and presentations at the American College of Medical Genetics and Genomics, the American Society of Human Genetics, the National Society of Genetic Counselors, and other major scientific meetings.