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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.
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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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From Variant Calling to Biological Insights – A Lynch Syndrome Case Study – Dec. 7
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In this webinar, we present a case study on Lynch syndrome (LS), a hereditary condition characterized by a high risk of colorectal cancer, e...
How community hospital labs can perform comprehensive genomic profiling – Dec. 10
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In this webinar, we will discuss how community hospital labs can perform comprehensive genomic profiling faster and with greater accuracy an...
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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QIAGEN Ingenuity Pathway Analysis
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QIAGEN CLC Microbial Genomics Module
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ANNOVAR
QIAGEN Ingenuity Pathway Analysis
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Gene Variant Databases
COSMIC (Catalogue of Somatic Mutations in Cancer)
HSMD (Human Somatic Mutation Database)
HGMD (Human Gene Mutation Database)
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Gene Variant Databases
COSMIC (Catalogue of Somatic Mutations in Cancer)
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HGMD (Human Gene Mutation Database)
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QIAGEN DiseaseLand
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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.
Services Overview
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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QIAGEN Ingenuity Pathway Analysis (IPA): Deep-dive trainings – All Regions Dec. 8 to Dec. 15
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As requested by many users, your QIAGEN Digital Insights team is excited to introduce QIAGEN Ingenuity Pathway Analysis (IPA) deep-dive trai...
QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings – All Regions – Dec. 7 to Dec. 14
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Join us for a 90-minute training session for new users of QIAGEN IPA.
Rapid, evidence-based reporting of oncology NGS tests at scale – Dec. 3
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Connected to the world’s most comprehensive, manually curated knowledge base that is updated weekly, QCI Interpret One dynamically compute...
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MyCLC
Overcoming Challenges of Copy Number Variant Interpretation – Dec. 15
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In this webinar, we will introduce a genomic variant analysis, interpretation and reporting solution that is being used by major labs and po...
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...
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