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DNA-seq analyses (whole genome, whole exome, panel) using QIAGEN CLC Genomics Workbench
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
01:37:07 minutes
Tags: dna-seq
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