Baylor Genetics to Highlight Multimodal Solutions for Rare Disease Diagnostics at Festival of Genomics, Biodata & AI

Baylor Genetics to Highlight Multimodal Solutions for Rare Disease Diagnostics at Festival of Genomics, Biodata & AI

Baylor Genetics will be participating in the Festival of Genomics, Biodata & AI, taking place June 3–4 in Boston, bringing together leaders advancing genomic medicine.

Dr. Christine Eng, Chief Medical Officer and Chief Quality Officer at Baylor Genetics, will present “Innovative Multimodal Solutions for Rare Disease Diagnostics” on June 3 from 2:40–3:10 PM (Innovation Stage).

The session will highlight how Baylor Genetics integrates Whole Genome Sequencing (WGS) with complementary technologies—including RNA Sequencing, long-read sequencing, and optical genome mapping—to identify complex variants that conventional approaches may miss. Through real-world case examples, attendees will learn how this patient-centered, multimodal approach helps deliver more answers and guide patient care.

Learn more about our genome-first, multimodal approach here.

About Baylor Genetics

Baylor Genetics is a leading diagnostic genomics partner offering a full spectrum of comprehensive genetic tests and diagnostic services, from clinical-grade genomic sequencing to expert interpretation, 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, pharmacogenomics and many other specialized testing options. Located in Houston’s Texas Medical Center, Baylor Genetics serves clients in 50 states.

PR Contact
SVM PR
[email protected]
(401) 490-9700

image_print