Next-generation sequencing (NGS) techniques have improved to a point where whole-genome sequencing (WGS) and whole-exome sequencing (WES) are viable testing options for a range of diagnostic applications. However, analyzing, interpreting, and applying such large quantities of genomic data remains a challenge. Before large-panel genetic testing becomes a routine part of clinical care, diagnostic labs must first address the complexity and consistency of NGS test interpretation.
Download this application note from QIAGEN to learn how incorporating automation tools and software solutions can accelerate and standardize NGS analysis for clinical diagnostics.
