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Introduction

Introduction

The BaseSpace® App Whole Genome Sequencing v5.0 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, and copy number anomalies analysis.
• Manta for structural variant and large indels calling.
• Canvas for copy number variation analysis.

Compatible Libraries

Workflow Requirements

Versions

Reference Genomes

App Workflow

For Research Use Only. Not for use in diagnostic procedures. 

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