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Introduction
The BaseSpace™ Sequence Hub Tumor Normal App performs subtractive variant calling to detect somatic variants in a matched pair of tumor and normal samples. The app uses the following enhanced tools for analyzing sequencing data:
| • | Strelka for somatic small variants. |
| • | Manta for large indel and structural variant calls. |
| • | Canvas for somatic copy number variant (CNV) calls. |
For Research Use Only. Not for use in diagnostic procedures.