Baylor Genetics

Diagnosing ataxia isn’t simple. Patients may present with diverse neurological, mitochondrial & neurodevelopmental symptoms. Genome sequencing can help capture multiple variant types in one test, helping find answers in ~1/3 of cases. #GenomeSequencing #Ataxia

In @HCIToday, Baylor Genetics' Chairman & CEO Kengo Takishima shares how earlier insights drive faster diagnoses, more precise care, and lower long-term costs. Read the full article: healthcareittoday.com/2026/05/12/the… #Genomics #GenomeSequencing

Baylor Genetics is #hiring a Project Manager of Digital Project Management to lead digital initiatives that support innovation across our organization. Your leadership will help support the future of digital transformation in healthcare: recruiting2.ultipro.com/BAY1006BML/Job… #JobSearch

Meet Joel Kaufman, CFO at Baylor Genetics, leading financial strategy that powers innovation, strengthens operations, and expands access to answers for providers and patients. Learn more about our team: baylorgenetics.com/people/ #Leadership #Excellence

Patients deserve more than data—they deserve clear, actionable answers. That starts with a genome-first approach. For nearly 50 years, Baylor Genetics has empowered patients, providers, & partners through comprehensive testing & expert interpretation: baylorgenetics.com

Long diagnostic odyssey? Our genomic technologies are helping bring answers. In our latest discussion with Kira Dineen of @DNATodayPodcast, we explore what’s next in precision diagnostics: dnapodcast.com/episodes/2026/… #Genomics #GenomeSequencing

This Mothers Day, we honor moms navigating the rare disease journey—advocates, experts, and champions for their children. At Baylor Genetics, we’re proud to support families seeking answers. Learn about Kelly’s story: linkedin.com/pulse/mothers-… #MothersDay #RareDisease

This week, we recognize #WorldPICUAwarenessWeek and the teams caring for critically ill children. “Take Care of Those Who Care”—because caregiver well-being supports patient safety. Baylor Genetics is proud to support clinicians when clarity matters most. baylorgenetics.com

At Baylor Genetics, we believe more answers are possible. Our enhanced WGS integrates optical genome mapping, long‑read + RNA sequencing—now with FMR1 methylation analysis for Fragile X. More precise insights. Better care. Learn more: baylorgenetics.com/wgs2026/ #LongReadSequening

Genomic knowledge doesn’t stand still, and neither should a patient’s results. Morgan Driver of Baylor Genetics highlights why Whole Genome Sequencing or Whole Exome Sequencing reanalysis matters and how updated findings can impact a patient’s diagnosis. #Genomics

#CysticFibrosis is one of the most common inherited conditions, yet many people don’t know they carry an affected CFTR variant. GeneAware™ carrier screening helps identify risk earlier and guide decisions: baylorgenetics.com/geneaware/ #CysticFibrosisAwareness #GeneAware

Behind every undiagnosed condition is a patient who needs answers. On #UndiagnosedDay, we recognize the patients still searching, & the clinicians helping them. We're proud to partner with the UDN, evaluating 3,400+ participants with WGS/WES. Learn more: baylorgenetics.com

Last week at #PLUGS2026, Baylor Genetics shared data showing how early #GenomeSequencing can shorten the diagnostic odyssey, reduce uninformative testing, improve care decisions, & lower long‑term costs, & advance better outcomes. Learn more: baylorgenetics.com/whole-genome-s…

National #DNADay celebrates the discovery of the double helix & the breakthroughs behind modern genomics. At Baylor Genetics, we build on a legacy that began at Baylor College of Medicine, decoding DNA to deliver clear, actionable answers: baylorgenetics.com #NationalDNADay

Stop by our booth & learn how our WGS is evolving—enhanced with optical #genome mapping, long read sequencing, RNA-Seq—delivering insight into complex cases & supporting informed care decisions: baylorgenetics.com 📍20th Annual Virginia State Genetics Education Conference

Behind every test result is a lab team making precision diagnostics possible. Fan Xia shares how our lab teams play a central role in advancing precision diagnostics by supporting providers with high‑quality data & partnering across the healthcare ecosystem. #LabWeek #Lab4Life

We’re at the #MNGCA Spring Education Conference—stop by our booth to learn how Baylor Genetics’ Whole Genome Sequencing, enhanced with long‑read, RNA sequencing & optical genome mapping, supports informed, patient‑centered care. baylorgenetics.com #GeneChat

Baylor Genetics is seeking a Senior Specimen Management Specialist to oversee the handling, processing, and tracking of biological samples across our laboratory operations. Apply now: recruiting2.ultipro.com/BAY1006BML/Job… #Hiring

What if your clinical genome testing could do more? Our enhanced #WholeGenomeSequencing brings together multiple genomic modalities, automatically reflexed when appropriate, to help uncover clinically insights that standard sequencing alone may miss: baylorgenetics.com/wgs2026/

Baylor Genetics' Whole Genome Sequencing can help uncover clinically meaningful findings that standard approaches may miss. Our WGS test, which now includes long‑read sequencing & optical genome mapping, supports key enhancements to analysis. Learn more: baylorgenetics.com