Discovery and Research
Calling, annotating and investigating genomic variants using QIAGEN CLC Genomics Workbench and QCII-T - May 27 2021
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In this training, we will discuss the following topics:
• Variant calling from FASTQ or BAM files using QIAGEN CLC Genomics Workbench
• Variant annotation using QIAGEN CLC Genomics Workbench and QCI-IT
• Filtering variants based on quality score, genetic analysis and biological context
• Identifying causal and actionable variants using the QIAGEN Knowledge Base (includes annotations from HGMD and COSMIC)
• Generating VCFs and tabular exports for further analysis in QIAGEN Ingenuity Pathway Analysis
Speaker: Sumana Chintalapudi, Ph.D., Field Application Scientist, QIAGEN Digital insights
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