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Meet QIAGEN at ESHG 2023

June 10–13, 2023 | Glasgow, Scotland, UK

Learn about our Sample to Insight solutions for inherited disorders

This year at the European Society for Human Genetics (ESHG) 2023 Annual Meeting, QIAGEN will be at booth #472 premiering our new barrier-breaking Sample to Insight workflow for inherited disease NGS testing—a fast, cheap, ultra-precise panel to report pipeline.

Learn more about our products and solutions and receive complimentary demos of our bioinformatic software and databases. Our experts will be available to chat with you and answer any questions you may have. We look forward to seeing you at ESHG 2023.

Corporate Satellite Workshop | June 10th
"Tackling your genomic challenges: From pre-analytics to NGS interpretation"

Join us on Saturday, June 10th from 12:00 – 13:30 for a corporate satellite workshop where our experts will present a series of short talks on how you can overcome the barriers of whole exome sequencing implementation. Session is free to attend and lunch will be provided.

Sample to Insight inherited disease workflow solutions at ESHG 2023

NGS Platform-Agnostic Panel

NGS Secondary Analysis

Variant Interpretation and Reporting

Collection, Stabilization and Isolation

Automated Digital PCR Workflow

Gene and Variant Database

Where to catch QIAGEN at ESHG 2023


Tackling your genomic challenges: From pre-analytics to NGS interpretation for complex whole exome cases

Experts discusses challenges and opportunities of implementing whole-exome sequencing

Saturday, June 10 | 12:00 - 13:30 | Alsh 1, Level 0

Join us for a series of short talks on how you can overcome the barriers of whole-genome sequencing (WGS) and whole-exome sequencing (WES) implementation from pre-analytics to variant interpretation.

Topics include:

  • Non-invasive sample collection for population-scale WGS projects with a real-world use-case
  • How labs can improve efficiency and scalability in WES/WGS with an ultra-fast, automation-compatible sample-to-report workflow
  • Clinical geneticist shares how her lab streamlines and accelerates NGS variant interpretation with a software solution that leverages augmented molecular intelligence (AMI)

Dr. habil. ​​Luiza Handschuh

Deputy Director for Scientific Affairs, Institute of Bioorganic Chemistry, Polish Academy of Sciences

Anna Teubert, PhD

Head of Scientific Staff, Molecular Diagnostics, Amedes Genetics

Georgios Stamoulis, PhD

Director, Global Product Manager Hereditary, QIAGEN Digital Insights

Jolene Peddie

Trainee Clinical Scientist, East of Scotland Regional Genetics Service

Schedule a 1:1 VIP consult at ESHG 2023