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In this training, we’ll go over how to easily perform DNA-seq analyses (for whole genome, whole exome, panel and similar) 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
Please bring any questions you may have, and we will answer them during this training. To learn more about CLC Genomics Workbench or request for a trial:
https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/?cmpid=CM_QDI_DISC_042024webinars-DNAseq
