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  • Leveraging the power of API-based omics (RNA-seq, proteomics and more) queries for discovery


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    There is a strong interest in the scientific community to use public (GEO, SRA, TCGA, LINCS, etc.) omics (RNA-seq, scRNA-seq, microarray, proteomics, etc.) data for a variety of discoveries. This […]

  • Clinician’s Roundtable: Interpreting genomic test results for precision oncology

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    You’re invited to attend the 2024 Clinician’s Roundtable, a virtual event where medical directors and oncologists will discuss how to better interpret genomic test results to tailor treatment strategies for […]

  • Isolate typing, strain identification and anti-microbial resistance analyses using CLC Genomics Workbench


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    QIAGEN CLC Genomics Workbench provides tools and workflows for a broad range of bioinformatics applications, including microbiome analysis, isolate characterization through SNP and K-mer trees using NGS data, and antimicrobial […]

  • Scale up NGS bioinformatics analysis throughput with CLC Genomics Server and Cloud solutions

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    More and more biopharma and academic groups are looking to process a large number of samples simultaneously or for a quicker turnaround time. This webinar will introduce a flexible and […]

  • Streamline H5N1 and other microbial samples with CLC Genomics Workbench


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    In this training, you will learn how to analyze viral samples using QIAGEN CLC Genomics Workbench. This webinar will focus on bioinformatics workflows and data interpretation using H5N1 as an […]

  • Discovery from public data (GEO, SRA and more) using Ingenuity Pathway Analysis


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    Per public demand, we are hosting a comprehensive training on how to effectively use sample level public data and metadata from sources like GEO, SRA, TCGA, GTEx, Blueprint, CCLE and […]

  • HGMD Pro in action: Search, curate and classify genetic variants - Session 1


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    In this live, interactive training session, our technical expert will show you how the Human Gene Mutation Database (HGMD) Professional can help you get better variant data faster. You will […]

  • Investigating genomic variants using QIAGEN CLC Genomics Workbench, QCI Interpret Translational (QCIIT), and QIAGEN Ingenuity Pathway Analysis (IPA)


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    Discovering new genes implicated in hereditary diseases or cancer progression is challenging yet advancing rapidly due to the increase in next-generation sequencing (NGS) cohort data. These data analyses produce insights […]

  • QIAGEN Ingenuity Pathway Analysis (IPA) new user training


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    Large dataset analysis and exploring the knowledge base using QIAGEN Ingenuity Pathway Analysis (IPA) Join us for a 120-minute training session for new users of QIAGEN IPA. In this training, […]

  • Geneset enrichment, target Validation and more through programmatically utilizing high quality biomedical literature findings


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    In this 60-minute session, the trainer will go over how to effectively utilize a relationship database for below applications. In this case, QIAGEN Biomedical Knowledgebase (Biomedical KB – a database […]

  • How is AI Changing Pharma R&D?

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    AI has begun to transform and accelerate every step of the drug development lifecycle from target identification to drug discovery and clinical trial design. However, the rapid development and adoption […]

  • How decentralized and small labs can adopt high-throughput NGS analysis with limited time and resource investment

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    Next-generation sequencing (NGS) has rapidly gained popularity as a diagnostic testing approach due to its unparalleled ability to comprehensively analyze genetic information with high throughput and precision. However, decentralized and […]