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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
Cohort Stratification and CDx Design
Molecular Profiling
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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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...
Know your biomarkers: PRKD1 linked to head and neck cancer?
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A new cancer gene, PRKD1, has been identified as defining a subset of head and neck cancers. Learn more about its role in oncogenesis and ac...
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QIAGEN Ingenuity Pathway Analysis
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QIAGEN CLC Genome Finishing Module
QIAGEN CLC Microbial Genomics Module
QIAGEN CLC Main Workbench
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QIAGEN Ingenuity Pathway Analysis
QIAGEN OmicSoft Land Explorer
QIAGEN DiseaseLand
QIAGEN GeneticsLand
QIAGEN OncoLand
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QIAGEN CLC Genomics Server
CLC Server Command Line Tools
QIAGEN CLC Genomics Cloud Engine
QIAGEN OmicSoft Suite
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QCI Secondary Analysis
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QCI Interpret Translational
ANNOVAR
QIAGEN Ingenuity Pathway Analysis
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QIAGEN CLC Genomics
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QCI Interpret for Hereditary Diseases
QCI Interpret for Oncology
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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
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HGMD (Human Gene Mutation Database)
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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
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
QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings – All Regions – Jul. 12 to Jul. 13
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Join us for a 90-minute training session for new users of QIAGEN IPA.
50 to 500 genes: Scale-up to comprehensive genomic profiling – Jun 29
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Learn how to overcome unique challenges of CGP, including how to identify incidental germline findings, interpret co-occurring variants, and...
FASTQ to final report: An ultra-fast workflow for comprehensive genomic profiling – Jul 14
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Join us to learn how DNAnexus and QIAGEN Digital Insights are partnering to develop an agnostic, end-to-end workflow for CGP that goes from ...
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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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