The EMJ Podcast: Hope for NSCLC patients
Listen in as two experts, a clinician and a cancer survivor, share their perspectives on the changing landscape of targeted therapies for NSCLC.
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Global Oncohematology Summit: Sep 13 and 14
Ready to address challenges impacting blood cancer diagnosis and monitoring? Take the I Can pledge and join the event.
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Your partner in oncohematology
We support your path to personalized blood cancer care and molecular research advancements with our comprehensive Sample to Insight solutions.
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Webinar: CDx commercialization
Join three international experts in our live webinar and discover how to prepare for successful CDx commercialization. Learn how to set up CDx testing in time for drug launch and Day-One patient access.
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The power of one
Comprehensive genomic profiling (CGP) is dramatically changing our understanding of many cancers. Our multimodal technology can maximize insights by simultaneously preparing DNA and RNA libraries from a single total nucleic acid sample.
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PIK3CA status matters
Want to detect actionable mutations in PIK3CA? Use our test to identify breast cancer patients that may be eligible for treatment with PIQRAY.
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Confidently detect FGFR mutations
Learn about our solution to confidently assess genomic alternations in the FGFR3 gene in bladder cancer.
"The Quest/QIAGEN partnership has allowed us to provide rapid and insightful information to our clinical colleagues, allowing us to better take care of their patients."
Dr. Frederick K. Rocke, Medical Director of Hematology/Oncology and Coogulation, Quest Diagnostics
"PIK3CA is the perfect example of how things should be done. All parties were optimally aligned to have the new test validated according to the very rigorous FDA standards."
Dr. Lawrence Weiss, Chief Medical Officer, NeoGenomics
Real-world lab experience
Our scientists continue to find innovative oncohematology solutions supporting labs throughout the world. Read our real-world lab experience and get advice to overcome workflow challenges and maximize blood cancer insights with fewer resources.
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Expert webinars at your fingertips
Want advice to overcome typical workflow challenges? Access our on-demand webinars that reveal useful tips and tricks and advice from the experts. Learn how our NGS solutions were able to support their research.
One simple workflow for lung cancer profiling
Want a panel to deliver comprehensive coverage of known and novel fusions as well as all relevant alterations? Our QIAseq Lung Multimodal Panel starts with total nucleic acids (DNA + RNA) and prepares targeted DNA and RNA libraries using a one-day, consolidated workflow.
Together, we’ll improve cancer care
Share your story using #TestCancer #TestYourPatients.
Every test matters. Every patient matters. Join us in improving biomarker testing and reducing the burden of cancer. Share your cancer story on social media using #TestCancer or #TestYourPatients. We’ll curate and display them on our social media wall here.