At CCMG 2024, we will be showcasing our Sample to Insight solutions for exome testing. Get a preview of the workflow by downloading a free sample report.
This year at the Canadian College of Medical Geneticists (CCMG) Annual Meeting, QIAGEN will be showcasing our Sample to Insight solutions for whole genome, exome, and large panel sequencing for rare and inherited disease applications.
Visit booth #18 to 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 CCMG 2024.
NGS platform-agnostic solution that contains all the necessary components to construct libraries from enriched genomic targets
Agnostic hardware and cloud-based service for NGS secondary analysis solutions for oncology and inherited disease applications
Automated variant interpretation and reporting platform powered by AI-enabled literature searches and state-of-the-art manual curation.
The largest, manually curated resource for finding disease-causing mutations
In-depth database providing detailed information on clinical trials and therapeutic outcomes
