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    Gene set enrichment, target validation and more using high quality biomedical literature findings

    Virtual - Americas - EST , United States

    This 60-minute session will teach you how to effectively use a relationship database for various applications. QIAGEN Biomedical Knowledge Base (Biomedical KB), a database containing high-quality relationship literature findings, the same database backing Ingenuity Pathway Analysis/IPA) will be used, but learnings can also be applied to similar databases. The following points will be discussed: • […]

  • Germline and Somatic Variant Investigation using COSMIC, HGMD and QCI-IT

    Virtual - Americas - EST , United States

    The accurate identification and annotation of germline and somatic variants rely on the accuracy and depth of reference databases that contain information about the genetic variants, any associated phenotype, and their clinical implications. By combining COSMIC, HGMD and QIAGEN QCI-IT, scientists can annotate gene variants using the world’s most comprehensive and up-to-date curated scientific evidence […]

  • DNA-seq analyses (whole genome, whole exome, panel) using QIAGEN CLC Genomics Workbench

    Virtual - Americas - EST , United States

    In this training, we’ll go over how to easily perform DNA-seq analyses (for whole genome, whole exome, panel and similar) easily and effectively using QIAGEN CLC Genomics Workbench. Together, we’ll explore: • Read mapping • Variant calling (SNPs, mutations, Indels and more) • Annotations and filters • Genome Browser Please bring any questions you may […]

  • IPA deep dive: miRNA investigation using QIAGEN Ingenuity Pathway Analysis (IPA)

    Virtual - Americas - EST , United States

    In this 90-minute training session, you will learn how to identify target mRNAs for your miRNAs of interest and associate them with pathways, diseases, biological functions, tissues and cell types. We’ll cover topics such as: • How to analyze miRNA-seq datasets alone or both miRNA and corresponding mRNA datasets together • How to use QIAGEN […]

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

    Virtual - Americas - EST , United States

    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 […]