110P Clinical validation of a 50-gene hotspot NGS panel in Asian patients with solid tumors

Abstract

The advent of next-generation sequencing (NGS) technologies had seen rapid adoption by clinical laboratories. Herein, we report the clinical validation data of a laboratory developed test-APEX Tissue (MiRXES), which enables simultaneous detection of single-nucleotide variants (SNVs), insertions/deletions (InDels), copy number amplifications and fusions through both DNA and RNA sequencing.