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.