Panel Discussion | October 26, 2023 Overcoming challenges for incorporating large genomic panels in precision oncology practice
Willis Tower | 1:20-1:55 PM (CST) Presented by Dr. Sheryl Elkin, Chief Scientific Officer of QIAGEN Digital Insights, and Alana Nunes, Customer Solutions Manager at QIAGEN
Learn more about our precision oncology solutions
This year at Precision Oncology and Diagnostics 2023, QIAGEN will be showcasing our clinical insights solutions for precision oncology NGS testing. Learn more about our software, services and databases, and receive complimentary demos and sign-up for free trials. Our experts will be available to chat with you an answer any questions you may have. We look forward to seeing you in Chicago!
Featured solutions at Precision Oncology and Diagnostics
QIAGEN offers a range of precision oncology solutions to meet your varying needs.
Workflow solutions to meet your needs
For clinical labs that need to complete their NGS oncology workflow with downstream secondary and/or tertiary analysis. QCI Interpret for Oncology is a clinical decision support platform for variant analysis, interpretation and reporting. Learn more here.
Wish you had more variant scientists? QCI Precision Insights (formerly N-of-One) is a professional clinical variant interpretation service for precision oncology.
Powered by a world-class team of molecular biologists and oncologists,
Delivers concise clinical evidence for each biomarker in the context of the cancer sub-type, listing information on the mutation’s molecular characteristics, roles in disease, and therapeutic, prognostic, and diagnostic implications.
Users receive a ready to use expert-assembled report content with detailed assessments of variants, written summaries of evidence with references, treatments, and geographically matched clinical trials.
For clinical labs who have an existing NGS workflow for precision oncology but want to optimize their pipeline with high-quality variant databases. COSMIC is a somatic database that can be used to help variant scientists identify biomarkers and annotate variants, whereas HSMD is a somatic database can be used at the end of the workflow to help validate biomarkers and better assess their biological and clinical relevance. Learn more here.
Build your workflow
Clinical decision support software for precision oncology
For labs that need to complete their NGS oncology workflow with downstream secondary and/or tertiary analysis.
QCI Interpret for Oncology
Clinical decision support software with on-demand professional variant interpretation services for precision oncology NGS testing
For labs that need to optimize their NGS oncology workflow with high-quality, expert-curated somatic databases.
Human Somatic Mutation Database (HSMD)
Great for Clinicians, Clinical Geneticists, and Molecular Tumor Boards: Expert-curated resource contains content from over 490,000 real-world clinical oncology cases to validate biomarkers and better assess their biological and clinical relevance.
Great for Variant Scientists, Bioinformaticians, and Clinicians: The world’s largest and most comprehensive resource for somatic mutations to help identify biomarkers and annotate variants for genomic reports.
