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Introduction
The BaseSpace® App TruSight Tumor 170 v1.0 analyzes sequencing reads from DNA and RNA libraries prepared using the TruSight Tumor 170 v1.0 sequencing panel. DNA libraries output variant call files for small variants and copy number variants. RNA libraries output fusions and splice variant call files. Results include user-friendly outputs for high confidence fusions and splice variants, and published fusion results. Analyses up to 16 samples, or 32 total libraries are supported.
For Research Use Only. Not for use in diagnostic procedures.