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Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
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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...
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Single-Cell Genomic Solutions
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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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Human Gene Mutations Database (HGMD)
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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
QIAGEN OmicSoft
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Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration
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.
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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.
Human vs. AI: Why manual curation is irreplaceable in clinical genomics – Jun. 2
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When it comes to variant curation, is AI capable of replacing human expertise? Find out on June 2 in our live expert webinar.
QIAGEN Ingenuity Pathway Analysis (IPA): Deep-dive trainings – All Regions – May. 24 to Jun. 28
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As requested by many users, QIAGEN Digital Insights team is excited to introduce QIAGEN Ingenuity Pathway Analysis (IPA) deep-dive trainings...
QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings – All Regions – Jun. 7 to Jun. 15
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Join us for a 90-minute training session for new users of QIAGEN IPA.
Human vs. AI: Why manual curation is irreplaceable in clinical genomics – Jun. 2
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In this webinar, we’ll walk you through a series of use-cases where our manually-curated database, HGMD, outperforms AI solutions.
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MyCLC
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.
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: 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!
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Institute for Clinical Genetics
Institute for Clinical Genetics
Driving discoveries, creating ideas
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