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For Europe: Easy and fast somatic variant calling, interpretation and reporting

Date: 2020/06/02 Duration: 01:00:00 Presented by: QIAGEN Digital Insights

Do you want to learn how to easily perform user-friendly secondary analysis? Does your lab require reliable, up-to-date variant interpretation? Would you like to standardize your variant interpretation workflow from FASTQ to report? Join us for a 60-minute live demonstration where we will show you in the language of your choice (English, German, French or Italian) how to accomplish everything mentioned above.

This live demonstration will introduce the QIAGEN CLC Genomics Workbench and how to generate variant profiles in a Variant Call Format (VCF), starting from next-generation sequencing (NGS) data.  We will provide examples of data generated from QIAseq library preps, although it works with any kit provider. Then, the variant profiles will be interpreted using QIAGEN Clinical Insight Interpret (QCI-I), a web-based tool that prioritizes and classifies variants based on a given biological context and professional guidelines, respectively, to generate an exportable report containing the most clinically relevant mutations related to a given disease.

During the live demo we will cover:

QIAGEN CLC Genomics Workbench

  • How to import data
  • Available references and plugins
  • Individual tools versus analysis workflows
  • How to run samples in batch
  • Data visualization
  • How to export data

QIAGEN Clinical Insight Interpret (QCI-I)

  • The QIAGEN Knowledge Base
  • How to upload data
  • Variant classification using professional guidelines
  • Clinical report generation

After the webinar, there will a brief Q&A session, where QIAGEN Digital Insights will be able to provide you with trial licenses to both CLC Genomics Workbench and QCI-I to allow you to explore the solutions and run a limited number of tests with your own samples.