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Detecting copy number variants with QIAGEN CLC Genomics Workbench


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Learn how to use the copy number variant (CNV) detection tool in the QIAGEN CLC Genomics Workbench to examine your exome and targeted resequencing data.

Our live demo will cover:

• Using the CNV detection algorithm for exome and targeted resequencing data

• Adding the CNV detection tool to workflows

• Visualizing your results

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