• Webinar: Pharmacogenomics - One tool to decode drug response to variation in the genome

    Each year, more than 134 million patients experience adverse drug events, causing 2.4 million deaths worldwide. What if there was a better way to develop and prescribe safer, more effective drugs based on the unique genetic information of every individual? In this webinar, learn about a game-changing solution for labs and pharmaceutical companies to rapidly […]

  • QIAGEN at AMP 2024

    Meet QIAGEN at the 2024 Association for Molecular Pathology (AMP) Annual Meeting This year at the 2024 Association for Molecular Pathology (AMP) Annual Meeting, QIAGEN will showcase our barrier-breaking Sample to […]

  • New feature: Insights with IPA Interpret

    Virtual - Americas - EST , United States

    Unlock actionable insights in your biological data by streamlining your data interpretation with IPA Interpret. The newest feature of your trusted pathway analysis software, QIAGEN IPA, includes: Content powered by […]

  • New feature: Navigating datasets with OmicSoft Explorer

    Meet OmicSoft Explorer, a new feature included with your QIAGEN IPA/OmicSoft subscriptions. See how you can find ‘omics datasets to inform your next experiments or support your grant proposals. With […]

  • QIAGEN IPA new user training

    Virtual - Americas - EST , United States

    Are you new to QIAGEN Ingenuity Pathway Analysis (IPA) or interested in expanding your skill set? Join us as we learn more on large dataset analysis and knowledge base queries […]

  • Support Session for IPA Certification

    Virtual - Americas - EST , United States

    Join us for a 90-minute LIVE group session designed to address different technical questions regarding IPA certification. QIAGEN IPA scientists will answer different IPA related technical questions and clarify various […]

  • Single-cell RNA-seq, cell hashing and spatial transcriptomics

    Virtual - Americas - EST , United States

    In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files. Using […]