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Introduction
The BaseSpace Sequence Hub® Whole Genome Sequencing App uses the following enhanced modules to analyze sequencing data:
| • | Isaac for aligning and read mapping. |
| • | Strelka for variant calling single nucleotide variants (SNVs) and small indels. |
| • | Manta for structural variant and large indels calling. |
| • | Canvas for copy number variation analysis. |
For Research Use Only. Not for use in diagnostic procedures.