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Discovery & Research
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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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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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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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QCI Interpret for Oncology
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Clinical decision support software powered by augmented molecular intelligence that helps clinical labs not only make faster decisions—but...
QCI Interpret for Hereditary Diseases
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Clinical decision support software powered by augmented molecular intelligence that gives clinical labs the best possible chance of solving ...
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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Secondary Analysis
QIAGEN CLC Workbench Premium
QIAGEN CLC Genomics Workbench
QIAGEN CLC Genome Finishing Module
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QIAGEN CLC Main Workbench
QIAGEN CLC Module and Plugin Overview
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QIAGEN Ingenuity Pathway Analysis
QIAGEN OmicSoft Suite
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QIAGEN Biomedical Knowledge Base
QIAGEN DiseaseLand
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ATCC Cell Line Land
QIAGEN OmicSoft Land Explorer
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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
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Gene Variant Databases
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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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Integrated ‘Omics Data
QIAGEN DiseaseLand
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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
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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
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
Webinar: Supercharge your AI in drug discovery with high-quality biomedical data – Oct. 3
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Learn how high-quality curated data, AI-driven analysis and advanced visualization accelerate the progress of precision medicine.
Webinar: QIAGEN Biomedical Knowledge Base: Data- and analytics-driven drug discovery – Oct. 10
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In this one-hour training, you’ll get an introduction to QIAGEN Biomedical Knowledge Base where you’ll learn how to perform various quer...
Webinar: Scale up NGS bioinformatics analysis throughput with CLC Genomics cloud computing – Oct. 5
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In this webinar, you’ll learn about the flexible and powerful setup for running your NGS sequence analyses on Amazon Web Services (AWS).
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MyCLC
On-demand webinar: Insights into cancer genomics via COSMIC v98
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Join this webinar with Leonie Hodges, Scientific Communications Officer for COSMIC, to take a journey through COSMIC’s mission and data an...
On-demand webinar: Pathogen detection and variant analysis using hybrid capture technology
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In this training, we\'ll use QIAGEN CLC Genomics Workbench to analyze NGS data generated from hybrid capture technology. Using data generate...
On-demand webinar: Target exploration and cell line selection for drug discovery
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This training focuses on using QIAGEN OmicSoft Lands and Ingenuity Pathway Analysis (IPA) as guides to select cell lines and translate insig...
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Technical Information
Dig into the details and get inspired!
Application notes
“External Applications”: adding functionalities to the CLC Genomics Server
A Sample to Insight® NGS solution for myeloid neoplasms: Redefined amplicon sequencing for low variant detection and interpretation
Assembly and annotation of plastid genomes using QIAGEN CLC Genomics Workbench
CLC Server Command Line Tools: a powerful choice to optimize your analyses
Comparative Analysis of Endophytic Bacterial Microbiomes in Grapevine
Comparative analysis of three bovine genomes
Detection of FLT3 internal tandem duplications with QIAseq Targeted Panels and QIAGEN CLC Genomics Workbench analysis workflows
Determinants of Test Selection for Hereditary Cancer Risk Assessment
Dynamics of microbial communities during coffee fermentation under different processing conditions
Example queries for HGMD MySQL Database
Identification of LOH on chromosome arms 1p and 19q for molecular classification of gliomas with QIAseq Targeted DNA Pro Panels and QIAGEN CLC Genomics Workbench
Improving Microbiome Sequencing using QIAseq® 16S/ITS Panels
Improving structural annotation in complex genomes with QIAGEN CLC Genomics Workbench
LightSpeed – enabling affordable genome sequencing analysis at scale
Methods and Challenges of Variant Annotation in Hereditary Cancer
Multi-Gene Panels in Hereditary Cancer: Cause for Caution?
Prevalence of Hereditary Cancer and Benefits of Multi-Gene Panel Testing
QIAseq Targeted Panel Analysis
Reporting of NGS sequencing data in clinical practice
RNA-seq analysis using long and short reads from pathogen-infected plant tissues
Whole genome functional annotation of Solanum lycopersicum
Workflows for extracting and analyzing microbiomes from whole-genome data of plant and animal species
White papers
A comprehensive analysis of coregulator recruitment, androgen receptor function and gene expression in prostate cancer
A strategy for evaluating genomic assemblies in QIAGEN CLC Genomics Workbench
Challenges in Clinical Testing
Characterizing the Microbiome through Targeted Sequencing of Bacterial 16S rRNA and Fungal ITS Regions
Chip-seq Analysis
CLC read mapper
Copy number variant detection
De novo assembly
Discovering the functional potential of microbial communities through whole metagenome shotgun sequencing analysis
Dynamics in the airway microbiome in children with Cystic fibrosis as revealed by 16S rRNA gene sequencing
How to integrate somatic and germline NGS into routine clinical oncology practice
Know your biomarkers: How PRKD1 is linked to head and neck cancers (HNSCC)
Overcome the four common data challenges in clinical diagnostics
Phenotype-Driven Ranking filter
Probabilistic Variant Caller 1.1
TET2 binds the androgen receptor and loss is associated with prostate cancer
Transcription factor ChIP-seq
Understanding Breast Cancer Subtypes by Jointly Interpreting Tumor Genomes and Transcriptomes