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  • 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 own single-cell RNA-seq data using QIAGEN CLC Genomics Workbench, starting with either FASTQ or matrix files.  Using CLC Genomics Workbench, you will learn how to perform […]

  • Multi-omics (metabolomics, proteomics, transcriptomics) analysis using QIAGEN Ingenuity Pathway Analysis

    Virtual - Americas - EST , United States

    This 90-minute training session will show you how QIAGEN Ingenuity Pathway Analysis (IPA) visualizes molecular intricacies and variations at the transcriptome, proteome and metabolome levels. Through a series of brief technical vignettes, you will learn how to: • Generate associations among molecular signatures obtained by integrating multi-omics data  • Extract mechanisms from multi-omics data for precision medicine  • […]

  • How to scale-up comprehensive genomic profiling and deliver confident variant interpretations with QCI Interpret for Oncology

    Virtual - Americas - EST , United States

    In this webinar, attendees will learn how QCI Interpret for Oncology enables you to: Navigate from VCF to final report with speed, precision, and confidence; Easily issue report addendums without the need for re-running a VCF; Streamline structural variant filtering based on user-set thresholds and hence reduce the time and effort needed to eliminate noise […]

  • 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 […]

  • 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 applications. Learn more about our products and solutions and receive complimentary demos of our bioinformatic software and databases. Our experts will be available to chat […]

  • Integrating deeply curated omics data with APIs for biomarkers and drug target investigation

    Virtual - Americas - EST , United States

    This webinar is for data scientists and bioinformaticians who need extensive high-quality omics data to target discovery efforts. Learn how to programmatically discover, retrieve, filter, aggregate and analyze omics (RNA-seq, scRNA-seq, microarray, proteomics etc.) data from QIAGEN’s comprehensive repository of deeply curated multi-omics data. Attendees will learn how to leverage extensive metadata to find and […]

  • 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 […]

  • 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 […]