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Baylor Genetics Hosts Webinar Highlighting the Power of Whole Genome Sequencing in Complex Pediatric Cases

Houston, August 14, 2025 -- Baylor Genetics, a clinical diagnostic laboratory at the forefront of genetic testing, today announced a clinical webinar highlighting pediatric cases in which Whole Genome Sequencing (WGS) delivered diagnostic insights that traditional genetic testing methods could not achieve.

What:

Baylor Genetics will host a 30-minute webinar, titled “From Symptoms to Sequencing: Diagnostic Insights from 3 Pediatric Genome Sequencing Cases,” presenting three pediatric cases, each involving a patient with a complex presentation and illustrating how a comprehensive sequencing approach enabled timely diagnosis and informed care decisions. The session will cover the following cases:

 

  • 4-year-old with neurological symptoms clarified using RNA sequencing data
  • 9-day-old NICU patient with respiratory insufficiency and motor disorder; diagnosed via uniparental disomy (UPD)
  • 4-year-old with global developmental delay and failure to thrive; novel noncoding variant identified

The American College of Medical Genetics found that WGS delivers a higher diagnostic yield compared to traditional genetic testing methods such as gene panels, chromosomal microarray, and exome sequencing. Attend this webinar to learn how Baylor Genetics is reducing time to diagnosis and improving clinical management through comprehensive sequencing, advanced multiomic analysis, artificial intelligence, and expert medical review, illustrated through three complex pediatric cases.

 

Who:

Lisa Salz, MS, CGC, Senior Medical Liaison, Baylor Genetics

Moderated by Jason Chibuk, MS, CGC, Vice President of Medical Affairs, Baylor Genetics

 

When:

Date: Tuesday, August 19, 2025

Time: 10:00 a.m. PT / 11:00 a.m. MT / 12:00 p.m. CT / 1:00 p.m. ET

Register here.

About Baylor Genetics  

Baylor Genetics is a leading diagnostic genomics partner offering a full spectrum of clinically relevant genetic testing, including Whole Genome Sequencing, Whole Exome Sequencing, and focused panels. Baylor Genetics combines rapid and comprehensive precision diagnostics options with the support of genetic counselors to help clinicians avoid a lengthy diagnostic odyssey for their patients, guide medical management, and ensure no patient with a genetic disorder gets left behind. Baylor Genetics’ testing menu covers family planning, pregnancy, neonatal and pediatric testing, oncology, and many other specialized testing options. Located in Houston’s Texas Medical Center, Baylor Genetics serves clients in 50 states and 16 countries. Learn more about what’s next.

  

Contact for Media Inquiries: 

SVM PR 
baylorgenetics@svmpr.com 
(401) 490-9700