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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.
Clinical NGS Testing
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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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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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Secondary Analysis
QIAGEN CLC Workbench Premium
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QIAGEN CLC Module and Plugin Overview
QIAGEN CLC Genome Finishing Module
QIAGEN CLC Microbial Genomics Module
QIAGEN CLC Genomics
QIAGEN CLC Genomics Workbench
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QIAGEN OmicSoft
QIAGEN OmicSoft Suite
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QIAGEN DiseaseLand
QIAGEN GeneticsLand
QIAGEN OncoLand
QIAGEN Single Сell Land
ATCC Cell Line Land
QIAGEN OmicSoft Land Explorer
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QIAGEN CLC Genomics Server
CLC Server Command Line Tools
QIAGEN CLC Genomics Cloud Engine
QIAGEN OmicSoft Suite
NGS Variant Assessment
QCI Interpret Translational
ANNOVAR
Clinical Insights
NGS Secondary Analysis
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QCI Interpret for Hereditary Diseases
QCI Interpret for Oncology
QCI Precision Insights
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 Biomedical Knowledge Base
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)
Integrated ‘Omics Data
QIAGEN DiseaseLand
QIAGEN OncoLand
QIAGEN Single Cell Land
QIAGEN Genetics Solution
Real-World Insights Portfolio
Sample to Insight Solutions
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
Clinical Analysis and Interpretation Services
Pharmaceutical Development Bioinformatic 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
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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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.
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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