QIAGEN CLC Genomics
DNA-seq (whole genome, whole exome, DNA-panel) analyses using QIAGEN CLC Genomics Workbench
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In this training, we’ll go over how to easily perform DNA-seq (specifically whole genome, whole exome, DNA-panel and similar) analyses easily and effectively using QIAGEN CLC Genomics Workbench.
Together, we’ll explore:
• Read mapping
• Variant calling (SNPs, mutations, Indels and more)
• Annotations and filters
• Genome browser view
Please bring any questions you may have, and we will answer them during this training.
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