Baylor Genetics

Baylor Genetics’ long‑read sequencing within Whole Genome Sequencing enables advanced analysis of complex STRs—expanding our coverage from 29 to 58 genes associated with neurologic, neuromuscular, and other disorders. Learn more: baylorgenetics.com/wgs2026/ #Genomics

Lisa Salz, Sr. MSL, Baylor Genetics, highlights how rWGS improves diagnosis in critically ill infants with cardiac conditions. A retrospective study found rWGS identified findings in ~25% of cases—often variants missed by standard tests—reinforcing its value in high-acuity care.

At #ACMGMtg26, we joined Kira Dineen of DNA Today to discuss advances in precision diagnostics to explore how combining WGS with optical genome mapping, long-read sequencing, & RNA sequencing can provide deeper insights into complex cases: dnapodcast.com/episodes/2026/…

What if your clinical genome test could do more? Today at #ACMGMtg26, we shared how enhanced WGS—paired with optical genome mapping, long-read sequencing, & RNA Sequencing—can unlock deeper insights for complex rare disease cases. Learn more: baylorgenetics.com/wgs2026/ #ACMG26

If you’re at #ACMGMtg26, swing by booth 1017 to learn about how Baylor Genetics’ multimodal approach can support clinical decision-making for patients with complex rare disease. We’re looking forward to meeting you! #Multimodal #Genomics #ACMG #ACMG26 @theacmg

Happening today at #ACMGMtg26! Baylor Genetics shares how enhanced WGS with optical genome mapping, long‑read sequencing & RNA‑Seq delivers deeper insights for complex rare disease cases. Learn more: baylorgenetics.com/news/baylor-ge… #LongReadSequencing #OpticalGenomeMapping

Hello, Baltimore! If you’re attending #ACMGMtg26, swing by the exhibit hall and engage with our team about work in precision diagnostics. Visit us at booth 1017 to grab a coffee and learn more: baylorgenetics.com/news/baylor-ge…

If you’re attending the #ACMGMtg26 Opening Reception tonight, we’d love to connect! Visit us at booth 1017 & learn more: baylorgenetics.com/news/baylor-ge… #ACMGMtg26  #Genomics

Sometimes answers require going beyond standard sequencing. Our enhanced WGS—featuring OGM & #LongReadSequencing—provides deeper insight into complex structural variants, expanded STR analysis, & FMR1 methylation analysis for Fragile X syndrome: baylorgenetics.com/wgs2026/

What if your clinical genome test could do more? Our enhanced WGS now includes optical genome mapping, targeted long‑read sequencing, alongside RNA‑Seq, delivering deeper insights to support faster, more precise diagnoses: baylorgenetics.com/news/baylor-ge… #OGM #LongReadSequencing

Shortening the diagnostic odyssey for rare & complex disease requires genomic innovation that can truly scale—across technologies, workflows, & the healthcare ecosystem. Learn more in this Fast Company byline from Kengo Takishima, our Chairman & CEO: fastcompany.com/91498078/how-t…

RNA Sequencing is changing the way we diagnose rare diseases. On the DNA Today Podcast, Kira Dineen speaks with our CMO, Dr. Christine Eng, about how RNA-seq helps resolve VUS, detect splicing abnormalities, & shorten the diagnostic odyssey: bit.ly/3N8Gkvw

Baylor Genetics is seeking a Senior Genetic Counselor to provide advanced clinical leadership and oversight. Manage complex cases, serve as a trusted advisor, and mentor the next generation of genetic counselors—Apply today: recruiting2.ultipro.com/BAY1006BML/Job… #Hiring

At #ACMGMtg26, March 10–14, Baylor Genetics will present new research highlighting how advanced genomic testing is uncovering insights across rare & complex conditions. Visit us at booth 1017 to connect with us! Learn more: baylorgenetics.com/news/baylor-ge… #ACMG26

Join us at #ACMGMtg26, March 10–14, and see how Baylor Genetics is utilizing multimodal genomic testing to close critical gaps in rare disease diagnosis. Visit Booth 1017 to connect with our experts. Learn more: baylorgenetics.com/conferences/ac… #ACMG26 #Genomics

This #WomensHistoryMonth, we honor the women who broke barriers in science and celebrate our team of scientists, doctors, genetic counselors, researchers, administrators, & lab professionals. Every day, they help shape the future of precision diagnostics.

When other testing fell short for Kelly’s son, Baylor Genetics identified a FOXP4 variant linked to neurodevelopmental disorders—bringing clarity to guide his care. Read their story: bit.ly/3Oyulb5 #RareDiseaseDay

Collaboration, data‑driven innovation, & patient‑centered design are shaping precision diagnostics. In this Fast Company byline, Kengo Takishima, our Chairman & CEO, shares how genomic sequencing can shorten the diagnostic odyssey & improve outcomes: fastcompany.com/91498078/how-t…

Join us at #ACMGmtg26 for a platform presentation on the diagnostic yield of Rapid Whole Genome Sequencing (rWGS) in critically ill infants with cardiac indications. Learn more: baylorgenetics.com/conferences/ac… #ACMG26 #Genomics

At #ACMGmtg26, Baylor Genetics will highlight how #multimodal & #multiomic data drive more informed results for rare disease. Dr. Christine Eng & Chris Sands will discuss these innovative approaches that help deliver clearer answers, faster. Learn more: baylorgenetics.com/conferences/ac…