Building a next-gen software workflow for germline testing

10:00 - 10:30 am (CEST) | 1:00 - 1:30 pm (EST)

Simplify your secondary analysis from FASTQ to VCF in 5 steps 

• Variant calling, filtering and visualization: Structural variants, indels, point mutations
• Quality control reports
• Get started quickly with configurable pre-made workflows

10:30 - 11:00 am (CEST) | 1:30 - 2:00 pm (EST)

Solve every hereditary disorder case for all types of genetic mutations

• Why lab's need high-quality, deeply curated knowledge to skip the diagnostic odyssey 

• How you can interpret complex germlines cases and increase your diagnostic yield with QCI Interpret

• How QCI Interpret displays and interprets copy number variants

11:00 - 11:30 am (CEST) | 2:00 - 2:30 pm (EST)

Going beyond the exome

• Addressing current challenges in germline and exome analytics
• Solving complex germline cases with the most comprehensive content from QIAGEN Digital Insights

Attendees will gain:

• Insight into how leading laboratories address bottlenecks in their NGS data pipelines
• Tips on how to solve process inefficiencies of critical workflow components, including variant curation and interpreting rare or novel variants
• An outlook on how germline NGS analysis and interpretation will change in the next 5 years and how to remain at the forefront of innovation