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Research & Discovery
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Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
Pharmaceutical Development
Biomarker and Indication Selection
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Trial Accrual and Drug Market Plans
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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...
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Oncology
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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...
Clinical Testing Solutions
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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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QIAGEN Ingenuity Pathway Analysis
QIAGEN OmicSoft Land Explorer
QIAGEN DiseaseLand
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QIAGEN CLC Genomics Server
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ANNOVAR
QIAGEN Ingenuity Pathway Analysis
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QCI Interpret for Hereditary Diseases
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Gene Variant Databases
COSMIC (Catalogue of Somatic Mutations in Cancer)
HSMD (Human Somatic Mutation Database)
HGMD (Human Gene Mutation Database)
Clinical QKB (Clinical QIAGEN Knowledge Base)
Real-World Insights Portfolio
Knowledge and Databases
Gene Variant Databases
COSMIC (Catalogue of Somatic Mutations in Cancer)
HSMD (Human Somatic Mutation Database)
HGMD (Human Gene Mutation Database)
Clinical QKB (Clinical QIAGEN Knowledge Base)
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QIAGEN DiseaseLand
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QIAGEN Single Cell Land
QIAGEN Genetics Solution
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QIAseq panels | QIAGEN Digital Insights
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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QIAGEN Discovery Bioinformatics Services
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Clinical Analysis and Interpretation Services
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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Webinars and Events
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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