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Explore our powerful solutions for the analysis and interpretation of single-cell gene expression analysis and genomics.
Stop looking for a needle in a haystack
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Easily accelerate biomarker and target discovery by exploring and interpreting your data with intuitive, visual biomarker identification too...
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Deliver patient-specific reports for any NGS panel in minutes with on-demand, expert-curated content and professional interpretation service...
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Solve more cases faster, with data you can trust using HGMD Professional, the gold standard for identifying inherited disease-causing mutati...
QIAGEN CLC Genomics Workbench
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QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow.
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Catalogue of Somatic Mutations in Cancer (COSMIC)
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Explore the impact of somatic mutations in human cancer with the world’s largest and most comprehensive resource
QCI Interpret One
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Oncology variant interpretation just got more precise. Introducing QCI Interpret One, clinical decision support software with professional i...
QIAGEN IPA
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Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems
Human Somatic Mutation Database (HSMD)
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A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies.
QIAGEN OmicSoft
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Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration
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Clinical Oncology Summit: Part 1 – Part 2 – June 16 (North America) and June 21 (Europe) | Customer I…
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A free-to-attend, two-part virtual event exploring how diagnostic labs can lower the barrier to adopt large cancer genomic profiling.
Updates and Improvement in QIAGEN CLC Genomics Workbench – Feb. 22
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Join this webinar to learn ways to take advantage of the latest improvements to QIAGEN CLC Genomics Workbench 22 and get an overview of the ...
How to streamline your variant classification workflow – Jan. 20
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In this webinar, we will walk through examples from variant interpretation scientists who have derived great value from consulting HGMD in t...
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MyCLC
On-demand webinar: Discover hidden relationships in your toxicological studies with QIAGEN IPA
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Watch this informative past webinar on how QIAGEN IPA can help you dig deeper into your toxicogenomic studies!
On-demand Webinar: How you can simplify your NGS secondary analysis workflow to 5 easy steps
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Find out how you can simplify your NGS secondary analysis workflow to 5 easy steps using QCI Secondary Analysis, a new cloud-based service f...
On-demand webinar: Harnessing insight from real-world oncology cases : introducing HSMD
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In this on-demand webinar, we will introduce you to the Human Somatic Mutation Database (HSMD)—a new somatic database developed by QIAGEN.
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QCI Interpret Translational
ANNOVAR
Pharmaceutical Development
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Whether searching for clinically applicable biomarkers, designing a new companion diagnostic (CDx), or honing your study accrual and go-to-m...
Institute for Clinical Genetics
Institute for Clinical Genetics
Driving discoveries, creating ideas
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