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Meet QIAGEN at Precision Oncology and Diagnostics 2023

October 26-27, 2023 | Chicago, IL

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 at booth #XXX. 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!

Panel Discussion | October 26, 2023
Overcoming challenges for incorporating large genomic panels in precision oncology practice

Willis Tower | 3:45 - 4:45 PM
Presented by Dr. Sheryl Elkin, Chief Scientific Officer of QIAGEN Digital Insights, and Alana Nunes, Customer Solutions Manager at QIAGEN

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.

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.

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.

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

The industry’s only automated FASTQ to final report solution for oncology NGS testing powered by AI-enabled literature searches and state-of-the-art manual curation

Optimize your workflow

Expert-curated somatic databases

For labs that need to optimize their NGS oncology workflow with high-quality, expert-curated somatic databases.

Catalogue of Somatic Mutations in Cancer (COSMIC)

The world’s largest and most comprehensive resource for somatic mutations to help identify biomarkers and annotate variants for genomic reports (great for variant scientists and for performing variant assessment).

Human Somatic Mutation Database
(HSMD)

Expert-curated resource contains content from over 419,000 real-world clinical oncology cases to validate biomarkers and better assess their biological and clinical relevance (great for Molecular Tumor Boards).

Supplement your workflow

Professional variant interpretation services for precision oncology

For labs that need to supplement their current workflow with the additional support of virtual variant scientists.

QCI Precision Insights (formerly N-of-One)

Professional variant interpretation services for precision oncology to help your lab grow caseload without requiring additional personnel.

Meet with our experts

Schedule your complimentary consultation or demo