See how tools like long read sequencing, RNA sequencing, MAVEs, and AI are ethically transforming WGS to make patients lives better.
All tagged Ambry Genetics
#303 RNA Analysis with Ambry Genetics
Dr. Rachid Karam explains how RNA testing increases diagnostic yield and reduces variants of uncertain significance in cancer and exomes.
#259 NSGC 2023 Recap and Reflections
Genetic Counselors Catherine Mayo and Kira Dineen discuss this year’s NSGC conference in Chicago including their favorite sessions.
#73 Jenna Guiltinan on Laboratory Genetic Counseling
Discuss classification of genetic variants including Variants of Unknown Significance (VUS)