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  • Shed light on inherited mutations and solve hereditary investigations with QCI Interpret

    Featured

    In this webinar, we will demonstrate how QCI Interpret can improve your diagnostic yield for hereditary disorders. QCI Interpret is a clinical decision support platform that leverages augmented molecular intelligence to streamline the interpretation workflow. It uses the most extensive, globally trusted and manually curated molecular knowledge and bibliography evidence to provide you with the […]

  • Proteomics and phosphoproteomics data interpretation using QIAGEN Ingenuity Pathway Analysis

    Virtual - Americas - EST , United States

    In this live QIAGEN Ingenuity Pathway Analysis (IPA) training, we’ll focus on interpreting proteomics and phosphoproteomics datasets. In this tutorial, we’ll guide you through steps and workflows to address your questions related to interpreting proteomics and phosphoproteomics datasets using QIAGEN IPA, such as: • How should I format the data before uploading to IPA? • […]

  • How to improve your existing pipeline for somatic mutation analysis, interpretation and reporting: Part 1

    We are excited to bring thought leaders, NGS experts, lab directors, variant scientists, clinicians, and oncologists under one virtual roof at our second annual Clinical Oncology Summit hosted on April 27 and May 18, 2023. The two-part, content-rich event will feature invited lectures from lab directors and clinical geneticists, thought-provoking discussions on the future of […]

  • QIAGEN Ingenuity Pathway Analysis (IPA) for grant writing and publications with new features

    Virtual - Americas - EST , United States

    QIAGEN Ingenuity Pathway Analysis (IPA) represents a robust resource to aid in the process of writing grants publications. Driven by a wealth of manually-curated molecular interactions and associations in the QIAGEN Knowledge Base together with pre-analyzed public ‘omics data for hundreds of thousands of samples from QIAGEN OmicSoft Lands, IPA provides biological insights regardless of […]

  • Como anotar variantes somáticas e avaliar a prevalência delas com um único banco de dados

    Virtual - Portugal , Portugal

    Dentro das aplicações oncológicas, a habilidade de identificar alterações genéticas potencialmente acionáveis e explorar as vulnerabilidades moleculares do câncer está se tornando cada vez mais difícil. Um novo banco de dados desenvolvido pela QIAGEN, o HSMD, contém mais de 2 décadas de conteúdo com curadoria especializada e dados da QIAGEN Knowledge Base com mais de […]

  • Single-cell RNA-seq data analysis and interpretation

    Virtual - Americas - EST , United States

    Explore how to analyze and interpret your own single-cell RNA-seq (scRNA-seq) data using QIAGEN CLC Genomics Workbench and QIAGEN Ingenuity Pathway Analysis (IPA). In this 90-minute training, you’ll learn how […]

  • How to improve your existing pipeline for somatic mutation analysis, interpretation and reporting: Part 2

    We are excited to bring thought leaders, NGS experts, lab directors, variant scientists, clinicians, and oncologists under one virtual roof at our second annual Clinical Oncology Summit hosted on April 27 and May 18, 2023. The two-part, content-rich event will feature invited lectures from lab directors and clinical geneticists, thought-provoking discussions on the future of […]

  • IPA deeper 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 […]