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Calling, annotating and investigating genomic variants using QIAGEN CLC Genomics Workbench and QCII-T – May 27

Date: 2021/05/27 Duration: 01:30:00 Presented by: Sumana Chintalapudi, Ph.D., Field Application Scientist, QIAGEN Digital insights

Join us for a 90-minute training where attendees will learn how to call SNPs, MNPs and structural variants (insertions, deletions, inversions and copy number variants) using QIAGEN CLC Genomics Workbench. In addition, we will demonstrate how to annotate these variants using both QIAGEN CLC Genomics Workbench and QIAGEN Clinical Insight Interpret Translational (QCII-T).

Click here to register.