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  • Featured

    Expert Roundtable: Advances in Genomic Testing for Rare Disease Diagnostics

    Over the past decade, whole-exome and whole-genome sequencing have transformed the diagnosis of patients with suspected rare genetic diseases. However, despite recent advancements, a large number of patients with rare genetic diseases remains undiagnosed for years because they have limited access to comprehensive genomic testing. In this virtual roundtable of leading rare disease experts, panelists […]

  • How to transition from Agilent Alissa Interpret to a new platform

    Agilent Alissa to QCI Interpret: How can your lab reduce the stress and complexity of transitioning to a new clinical informatics platform?

    Virtual - Americas - EST , United States

    In 2023, Agilent announced the discontinuation of their Alissa Interpret clinical informatics platform by the end of 2024. As a result, many of their current customers need to transition to a new variant interpretation and reporting software within a tight timeframe. However, when evaluating new interpretation solutions, clinical labs must consider a variety of factors, […]

  • Single-Cell RNA-Seq, Cell Hashing, and Spatial Transcriptomics

    Virtual - Americas - EST , United States

    A slide illustrating some of the many result types/graphics you will be able to generate after this training. https://qiagen.showpad.com/share/jYTCDPNfz1SdIMPQPSPYS  Description: In this training, you will learn how to analyze and interpret your […]

  • 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, […]

  • Featured

    Human Genome Meeting 2024

    Rome, Italy Rome, Italy

    This year at the Human Genome Meeting (HGM), QIAGEN will be showcasing our Sample to Insight solutions for whole genome, exome, and large panel sequencing for oncology and inherited disease […]

  • Featured

    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 […]