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Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
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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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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...
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 ...
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QIAGEN CLC Workbench Premium
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ANNOVAR
QIAGEN Ingenuity Pathway Analysis
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QCI Interpret for Hereditary Diseases
QCI Interpret for Oncology
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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
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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
RNA-seq data analysis and interpretation using QIAGEN CLC and QIAGEN IPA – Apr. 6
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Learn how to easily analyze and interpret RNA-seq data using QIAGEN CLC Genomics Workbench software and QIAGEN Ingenuity Pathway Analysis.
Shed light on inherited mutations and solve hereditary investigations with QCI Interpret – Apr. 19
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Learn how QCI Interpret can improve your diagnostic yield for hereditary disorders, reducing test turnaround time from hours to minutes!
Pathogen detection in wastewater samples using QIAGEN CLC Genomics Workbench – Apr. 11
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In this 90-minute training, you will learn how to easily analyze wastewater samples to detect pathogens using QIAGEN CLC Genomics Workbench.
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On-demand webinar: Investigation of Somatic and Germline Variants by COSMIC, HGMD and QIAGEN Databases
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Identifying and studying actionable variants is of great interest to many investigators. In this webinar, COSMIC, HGMD and QIAGEN database w...
On-demand Webinar: Whole exome sequencing (WES) helps understand exceptional survival in rare sarcoma…
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In this webinar, we present a unique case study of a treatment-naïve patient with aggressive metastatic uLMS with multiple pulmonary metast...
On-demand Webinar: CRISPR data analysis and interpretation using QIAGEN IPA and CLC Genomics Workbench
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QIAGEN Digital Insights is hosting this 90-minute training focused on analyzing CRISPR high-throughput sequencing data using QIAGEN CLC Geno...
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