QIAGEN CLC Genomics
DNA-seq (whole genome, whole exome, DNA-panel) analyses using QIAGEN CLC Genomics Workbench
270 views
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.
Related videos
QIAGEN CLC Genomics
QIAGEN CLC Genomics Workbench 20 – scalable desktop software for NGS data analysis
In this webinar, Leif Schauser, Ph.D., Director Product Management Genome...
QIAGEN CLC Genomics
De novo assembly, BLAST and genome finishing using QIAGEN CLC Genomics Workbench
This webinar will introduce users to the tools available for short reads...
QIAGEN CLC Genomics
16S/18S/ITS sequencing analysis using CLC Genomics Workbench
QIAGEN CLC Microbial Genomics Module provides tools and workflows for a broad...
QIAGEN CLC Genomics
Single-cell RNA-seq analysis made easy - February 24
Single-cell gene expression analysis starting from either FASTQ or expression...