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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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QCI Interpret for Oncology
Clinical decision support software powered by augmented molecular intelligence that helps clinical labs not only make faster decisions—but...
QCI Interpret for Hereditary Diseases
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?
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 CLC Workbench Premium
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QCI Interpret for Hereditary Diseases
QCI Interpret for Oncology
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HSMD (Human Somatic Mutation Database)
HGMD (Human Gene Mutation Database)
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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
NGS Variant Assessment
QCI Interpret Translational
ANNOVAR
Sample to Insight Solutions
Discovery & Research
Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
Discovery & Research
Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
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Gene Variant Databases
QIAGEN CLC Genomics Server
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ATCC Cell Line Land
QIAGEN Omicsoft Land Explorer
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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
QIAGEN IPA
Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems
QIAGEN OmicSoft
Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration
Human Somatic Mutation Database (HSMD)
A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies.
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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
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MyCLC
Latest Blog: Immune Repertoire Analysis Showdown: Speed, Ease, Accuracy
Find out which B-cell receptor reconstruction tool takes the crown
Latest Blog: Immune Repertoire Analysis Showdown: Speed, Ease, Accuracy
Find out which B-cell receptor reconstruction tool takes the crown
Latest Blog: Immune Repertoire Analysis Showdown: Speed, Ease, Accuracy
Find out which B-cell receptor reconstruction tool takes the crown
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Applications
Secondary Analysis
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)
Clinical QKB (Clinical QIAGEN Knowledge Base)
Interpretation and Vizulization
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
NGS Variant Assessment
QCI Interpret Translational
ANNOVAR
Sample to Insight Solutions
Discovery & Research
Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
Discovery & Research
Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
Knowledgebase
QIAGEN Biomedical Knowledge Base
Gene Variant Databases
QIAGEN CLC Genomics Server
QIAGEN CLC Server Command Line Tools
QIAGEN CLC Genomics Cloud Engine
QIAGEN OmicSoft Suite
'Omics Databases
QIAGEN Biomedical Knowledge Base
QIAGEN DiseaseLand
QIAGEN OncoLand
QIAGEN Single Cell Land
ATCC Cell Line Land
QIAGEN Omicsoft Land Explorer
Services
QIAGEN Discovery Bioinformatics Services
Clinical Analysis and Interpretation Services
Pharmaceutical Development Bioinformatic Services
QIAGEN IPA
Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems
QIAGEN OmicSoft
Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration
Human Somatic Mutation Database (HSMD)
A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies.
Technical Information
Dig into the details and get inspired!
Application notes
Workflows for extracting and analyzing microbiomes from whole-genome data of plant and animal species
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
LightSpeed – enabling affordable genome sequencing analysis at scale
Dynamics of microbial communities during coffee fermentation under different processing conditions
Reporting of NGS sequencing data in clinical practice
Determinants of Test Selection for Hereditary Cancer Risk Assessment
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
RNA-seq analysis using long and short reads from pathogen-infected plant tissues
Assembly and annotation of plastid genomes using QIAGEN CLC Genomics Workbench
Detection of FLT3 internal tandem duplications with QIAseq Targeted Panels and QIAGEN CLC Genomics Workbench analysis workflows
Improving structural annotation in complex genomes with QIAGEN CLC Genomics Workbench
CLC Server Command Line Tools: a powerful choice to optimize your analyses
Improving Microbiome Sequencing using QIAseq® 16S/ITS Panels
“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
QIAseq Targeted Panel Analysis
Example queries for HGMD MySQL Database
Whole genome functional annotation of Solanum lycopersicum
Comparative analysis of three bovine genomes
Comparative Analysis of Endophytic Bacterial Microbiomes in Grapevine
White papers
Know your biomarkers: How PRKD1 is linked to head and neck cancers (HNSCC)
How to integrate somatic and germline NGS into routine clinical oncology practice
Overcome the four common data challenges in clinical diagnostics
A strategy for evaluating genomic assemblies in QIAGEN CLC Genomics Workbench
Probabilistic Variant Caller 1.1
Discovering the functional potential of microbial communities through whole metagenome shotgun sequencing analysis
TET2 binds the androgen receptor and loss is associated with prostate cancer
A comprehensive analysis of coregulator recruitment, androgen receptor function and gene expression in prostate cancer
Characterizing the Microbiome through Targeted Sequencing of Bacterial 16S rRNA and Fungal ITS Regions
Dynamics in the airway microbiome in children with Cystic fibrosis as revealed by 16S rRNA gene sequencing
Chip-seq Analysis
Phenotype-Driven Ranking filter
Understanding Breast Cancer Subtypes by Jointly Interpreting Tumor Genomes and Transcriptomes
Challenges in Clinical Testing
De novo assembly
CLC read mapper
Transcription factor ChIP-seq
Copy number variant detection
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