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  • QIAGEN Biomedical Knowledge Base: data- and analytics-driven drug discovery


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    Ingenuity pathway analysis (IPA) which is currently cited in tens of thousands of publications and used by large number of biopharmaceuticals is backed by QIAGEN Biomedical Knowledgebase. Accordingly, Biomedical relationships […]

  • Mitigating Variability in Somatic Variant Interpretation with Live Q&A


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    Next-generation sequencing (NGS) oncology panels are becoming integral in hospital and academic settings to guide patient treatment and enrollment in clinical trials. But as NGS is increasingly used in precision […]

  • 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

    Featured
    Virtual Global Event (Times shown in EST)

    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 cancer patients. As the role of the Molecular Tumor Board (MTB) becomes increasingly important in the implementation of evidence-based precision cancer medicine programs, molecular pathology […]

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

    Virtual - Americas - EST , United States

    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 resistance characterization. CLC Genomics Workbench is widely used for analyses of bacterial, viral and eukaryotic (fungal) genomes and metagenomes. Topics covered in this webinar include: […]

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

    Featured
    Virtual - Americas - EST , United States

    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 powerful setup for running your NGS sequence analyses through servers or Amazon Web Services (AWS), depending on user preference. We will demonstrate how CLC Genomics […]

  • Streamline H5N1 and other microbial samples with CLC Genomics Workbench

    Virtual - Americas - EST , United States

    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 example, but similar analysis can be done with other viral and microbial (bacteria, fungus and more) samples. Using viral samples, you will learn how to: […]

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

    Virtual - Americas - EST , United States

    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 other sources through Ingenuity Pathway Analysis (IPA) and IPA Analysis Match Explorer feature. The trainer will walk through use cases in realms of biomarker discovery, […]

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

    Virtual - Americas - EST , United States

    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 learn how to: • Differentiate between clinically significant variants and variants of unknown significance (VUS) • Use batch search vs. advanced search, including their differences […]

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

    Virtual - Americas - EST , United States

    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 into associations between gene variants and diseases and the biological mechanisms of these gene variants. By combining QIAGEN CLC Genomics Workbench, QCIIT and QIAGEN IPA, […]

  • QIAGEN Ingenuity Pathway Analysis (IPA) new user training

    Virtual - Americas - EST , United States

    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, you’ll learn how to: • Upload your dataset (RNA-seq, scRNA-seq, proteomics, metabolomics and more) and perform interactive core/pathway analysis in IPA • Understand the different […]

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

    Virtual - Americas - EST , United States

    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 containing high-quality relationship literature findings, the same database backing Ingenuity Pathway Analysis/IPA) will be used, but learning can possibly be applied to similar databases as […]