English
Contact Sales
QIAGEN Webshop
Resellers
MyCLC
Search
Search
Solutions
Discovery and Research
Biomarker and Target Discovery
Single-Cell Genomics
Microbial/Metagenomics
Gene Regulation
Variant Analysis
SARS-CoV-2 Solutions
Research & Discovery
–
Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
Data Sciences
Data and Pipeline Management
Clinical NGS Testing
Oncology
Solid Tumors
Hematological Malignancies
Hereditary Cancers
Inherited Disorders
Rare & Undiagnosed Diseases
Carrier Screening
Cardiac Disorders
Arrhythmias
Cardiomyopathies
Partner Program
Single-Cell Genomic Solutions
–
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
–
Easily accelerate biomarker and target discovery by exploring and interpreting your data with intuitive, visual biomarker identification too...
Clinical Testing Solutions
–
Deliver patient-specific reports for any NGS panel in minutes with on-demand, expert-curated content and professional interpretation service...
Products
Applications
Secondary Analysis Tools
QIAGEN CLC Workbench Premium
QIAGEN CLC Main Workbench
QIAGEN CLC Module and Plugin Overview
QIAGEN CLC Genome Finishing Module
QIAGEN CLC Microbial Genomics Module
QIAGEN CLC Genomics
QIAGEN CLC Genomics Workbench
Clinical Insights
NGS Secondary Analysis
QCI Secondary Analysis (Cloud-Based)
Clinical Interpretation & Reporting
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)
Interpretation and Visualization
QIAGEN Ingenuity Pathway Analysis
QIAGEN OmicSoft
QIAGEN OmicSoft Suite
Enterprise NGS Solutions
QIAGEN CLC Genomics Server
QIAGEN CLC Server Command Line Tools
QIAGEN CLC Genomics Cloud Engine
QIAGEN OmicSoft Suite
Sample to Insight Solutions
Human Gene Mutations Database (HGMD)
–
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
–
QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow.
Knowledge Bases
QIAGEN Biomedical Knowledge Base
Gene Variant Databases
COSMIC (Catalogue of Somatic Mutations in Cancer)
HSMD (Human Somatic Mutation Database)
HGMD (Human Gene Mutation Database)
‘Omics Database
QIAGEN Biomedical Knowledge Base
QIAGEN DiseaseLand
QIAGEN GeneticsLand
QIAGEN OncoLand
QIAGEN Single Сell Land
ATCC Cell Line Land
QIAGEN OmicSoft Land Explorer
Services
QIAGEN Discovery Bioinformatics Services
Clinical Analysis and Interpretation Services
Catalogue of Somatic Mutations in Cancer (COSMIC)
–
Explore the impact of somatic mutations in human cancer with the world’s largest and most comprehensive resource
QCI Interpret One
–
Oncology variant interpretation just got more precise. Introducing QCI Interpret One, clinical decision support software with professional i...
QIAGEN IPA
–
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)
–
A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies.
QIAGEN OmicSoft
–
Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration
Resources
News
Press Releases
Blog
Science
Case Studies
Technical Information
Public Citations
Citation Guidelines
Allele Frequency Community
SARS-CoV-2 Resources
Webinars and Events
Clinical Oncology Summit: Part 1 – Part 2 – June 16 (North America) and June 21 (Europe) | Customer I…
–
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
–
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
–
In this webinar, we will walk through examples from variant interpretation scientists who have derived great value from consulting HGMD in t...
Support
Technical Support
QIAGEN CLC Tutorials
Contact Support
FAQs
Product Manuals
Latest Improvements
Maintenance and Support
Training
IPA Training
Upcoming Webinars
Webinar Recordings
Technical Information
Downloads
Product Downloads
Module and Plugin Downloads
Example Data
3d Graphics Support
System Requirements
Licensing
License transfer
MyCLC
On-demand webinar: Discover hidden relationships in your toxicological studies with QIAGEN IPA
–
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
–
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
–
In this on-demand webinar, we will introduce you to the Human Somatic Mutation Database (HSMD)—a new somatic database developed by QIAGEN.
About
QIAGEN Digital Insights
About Us
Contact
Careers
QIAGEN Corporate
Request a Trial
Product Login
Contact
Shop
How to Purchase
Contact Sales
QIAGEN Webshop
Resellers
MyCLC
Search
Search
QCI Interpret Translational
ANNOVAR
Pharmaceutical Development
–
Whether searching for clinically applicable biomarkers, designing a new companion diagnostic (CDx), or honing your study accrual and go-to-m...
Maintenance in progress
