Blog

After over a year of delayed developmental milestones, Baylor Genetics’ Whole Genome Sequencing (WGS) provided important genomic insights that supported Lainey’s care journey, leading to tailored physical therapy and a…

Cerebral palsy (CP) is one of the most common motor conditions in children and is an umbrella term for a group of conditions affecting movement and posture that can be…

At Baylor Genetics, behind every test result is a team of dedicated clinical professionals working to uncover answers that improve lives for our patients and families. We asked them to…

The 2025 American College of Medical Genetics and Genomics (ACMG) Annual Meeting spotlighted some of the most innovative research in rare disease diagnostics and mitochondrial medicine. Among the contributions from…

In recent years, Whole Genome Sequencing (WGS) and Whole Exome Sequencing (WES) have emerged as groundbreaking tools in the field of genomics, offering providers and patients new insights into the…

WHAT IS WHOLE EXOME SEQUENCING? Navigating the complexities of genetic and rare conditions from diagnosis to treatment can be challenging, especially when answers feel out of reach. Determining the genetic…

Healthcare inequality and access to genetic testing is a pervasive challenge across the United States, often most acute in underserved regions with high poverty rates, scarce medical resources, and diverse…

Whole Genome Sequencing (WGS) is at the forefront of comprehensive genetic testing, designed to analyze the entire genome to find an underlying genetic cause (etiology) relating to a patient’s medical…

A Powerful First-Tier Diagnostic Tool Every day counts in the neonatal and pediatric intensive care unit (NICU and PICU), where healthcare providers work tirelessly to both manage symptoms and identify…

Bridging the Gap: Addressing Inequalities in Access to Genetic Testing  In the United States (U.S.), the landscape of healthcare is complex, blending innovative technology with a web of economic, social,…

What Parents Should Know about Genetic Testing for Rare Disease in Intensive Care Settings INTRODUCTION Genetic testing can offer hope for many families that are navigating the complex reality of…

Unlocking Comprehensive Genetic Insights with RNAseq for WGS and WES Whole genome sequencing (WGS) and whole exome sequencing (WES) are comprehensive genetic tests that help improve patient care by enabling…