The BaseSpace™ App TruSight™ Tumor 170 v2.0 analyzes sequencing reads from DNA and RNA libraries prepared using the TruSight Tumor 170 sequencing panel. DNA libraries output variant call files for small variants, EGFR complex variants, copy number variants, and a microsatellite instability score. RNA libraries output fusions and splice variant call files. Results include user-friendly outputs for high confidence fusions and splice variants. Analysis of up to 16 biosamples is supported.