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Secondary Analysis
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QIAGEN CLC Genomics
QCI Secondary Analysis (Cloud-Based)
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ANNOVAR
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QCI Interpret for Hereditary Diseases
QCI Interpret for Oncology
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Sample to Insight Solutions
QCI Interpret for Oncology
The most advanced end-to-end solution for oncology NGS analysis, interpretation and reporting
Ingenuity Pathway Analysis (IPA)
Analyze, compare and contextualize your NGS data with the leading pathway analysis application
Knowledge Bases
Biomedical Knowledge Bases
Gene Variant Databases
COSMIC (Catalogue of Somatic Mutations in Cancer)
HSMD (Human Somatic Mutation Database)
HGMD (Human Gene Mutation Database)
PGXI (Pharmacogenomic Insights)
'Omics Databases
QIAGEN DiseaseLand
QIAGEN OncoLand
QIAGEN Single Cell Land
ATCC Cell Line Land
QIAGEN OmicSoft Land Explorer
Biomedical Knowledge Base-AI
Find novel connections missed by traditional methods, hiding in over 640M biomedical relationships
Services
Discovery Bioinformatics Services
Clinical Analysis and Interpretation Services
QCI Precision Insights
Biomedical Knowledge Bases
Access critical drug discovery data, save time and explore novel biomedical relationships
QCI Precision Insights
A professional clinical interpretation service that translates molecular data specific to each patient into insights and therapeutic options
Biomedical Knowledge Base-HD
Directly access over 10M high-quality biological findings
QIAGEN receives European IVDR certification for QIAGEN Clincal Insight Interpret
Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration
Which secondary analysis solution is right for you?
Use our decision tree to find out which secondary analysis solution is right for your lab
Solutions
Discovery and Research
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Target Discovery
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Single-Cell Genomics
Microbial/Metagenomics
Gene Regulation
Variant Analysis
SARS-CoV-2 Solutions
OmicSoft NGS Data Analysis
Explore and compare data across 700K+ disease studies with a cloud-based NGS analysis suite
Data Sciences
Data and Pipeline Management
OmicSoft OncoLand
Explore high-quality, preprocessed genomics data with our oncology database
Webinar: How decentralized and small labs can adopt high-throughput NGS analysis
Discover a new secondary analysis solution for oncology & inherited disease applications for high-throughput use with any clincal NGS data
Clinical NGS Testing
Oncology
Solid Tumors
Hematological Malignancies
Hereditary Cancers
Inherited Disorders
Rare & Undiagnosed Diseases
Carrier Screening
Cardiac Discorders
Arrhythmias
Cardiomyopathies
Sample to Insight solutions
View our NGS workflows for labs of all sizes and experience - and find the right fit for you
Partner Program
Biomarker and Target Discovery
Augment your biomarker discovery research with 20M findings & 700K preprocessed ` omics samples
Rare and Undiagnosed Diseases
Finding a diagnosis for rare diseases is often a race against time. QDI is helping provide answers where none were available before
Clinical Testing Solutions
Deliver partient-specific reports for any NGS panel in minutes with on-demand, expert-curated content & professional interpretation services
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SARS-CoV-2 Resources
Knowledge Bases Blog: Using trusted cancer data can accelerate drug discovery and development
See our expert curation processes and how data curated this way helps biopharma research
Latest IPA Blog: Free pathway analysis - How much do you really save?
Discover why you need pathway analysis tools that provide rich, directional relationships
Latest Blog: Immune Repertoire Analysis Showdown: Speed, Ease, Accuracy
Find out which B-cell receptor reconstruction tool takes the crown
Webinar: Investigating genomic variants with QDI Software
Learn to analyze various types of NGS data with CLC Genomics Workbench, QCII Translational and IPA
Blog: How COSMIC & HSMD support different phases of cancer drug discovery and development
Learn how expert-curated cancer data can help biopharma researchers identify & validate drug targets faster & optimize clinical trial design
Support
Technical Support
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VIdeo: Introduction to QCI Interpret for Oncology
Check out this introductory video to QCI Interpret for Oncology, a CDS software that will allow you to confidently interpret NGS variants
Lateset improvements: IPA
See the newest improvements and updates in the IPA 2024R1 Release
Training
IPA Training
Omicsoft Training
QIAGEN CLC Tutorials
Webinar: Leveraging the QIAGEN Knowledge Graph for insights into drug repurposing
This webinar shows how to predict novel drug-disease relationships and construct networks that capture relevant supporting evidence
Webinar: HGMD Pro in action: Search, curate and classify genetic variants - Session 2
Learn how HGMD Professional can help you get better variant data faster
Downloads
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Somatic knowledge bases for clinical NGS testing
Expert-curated content for accelerated analysis of cancer mutations in clincal NGS testing
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MyCLC
Somatic knowledge bases for biopharmaceutical research
Expert-curated content for the discovery and development of precision cancer therapies
Human Gene Mutation Database (HGMD) Professional
Improve diagnostics with the largest expert-curated source of hereditary disease-causing mutations
Latest improvements: OmicsSoft Lands
See the latest improvements and updates in the Lands 2024R1 Release
Video: Introduction to QCI for Hereditary Disorders
Check out this introductory video to QCI Interpret for Hereditary Disorders, industry's only automated FASTQ to final report solution
Press Release: QIAGEN enchances bioinformatics workflows with new secondary analysis solultion
QIAGEN launches QCI Secondary Analysis, a cloud-based solution enabling high-throughput secondary analysis with clincal NGS data
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