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 […]
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 […]
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 […]
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: • […]
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 […]
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 […]
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 […]
Per attendees’ requests from a recent training, we are hosting this in-depth training focused on effectively constructing a network, with or without a dataset (RNA-seq, proteomics, etc.), and easily modifying it – all within Ingenuity Pathway Analysis. In this interactive training, attendees will learn how to: • Construct a network from scratch or open a […]
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 result types produced (pathways, key regulators, impact on biological functions/diseases and more) • Compare […]
Industry leaders discuss how to improve the speed, precision and cost-effectiveness of clinical exome testing for newborn screening and rare and undiagnosed diseases Clinical exome testing is revolutionizing the diagnosis of rare and inherited diseases. Its ability to quickly pinpoint the genetic causes of complex conditions has made it a critical component of personalized medicine, […]
Watch NowIn this training, you will learn how to analyze viral samples using QIAGEN CLC Genomics Workbench. This webinar will focus on bioinformatics workflows and data interpretation using H5N1 as an example, but similar analysis can be done with other viral and microbial (bacteria, fungus and more) samples. Using viral samples, you will learn how to: […]
Watch NowMore and more biopharma and academic groups are looking to process a large number of samples simultaneously or for a quicker turnaround time. This webinar will introduce a flexible and powerful setup for running your NGS sequence analyses through servers or Amazon Web Services (AWS), depending on user preference. We will demonstrate how CLC Genomics […]
Watch NowThere is a strong interest in the scientific community to use public (GEO, SRA, TCGA, LINCS, etc.) omics (RNA-seq, scRNA-seq, microarray, proteomics, etc.) data for a variety of discoveries. This webinar, aimed at data scientists, bioinformaticians and similar roles in biopharma and academia, explores a comprehensive way of accessing and analyzing high-quality, expertly curated omics […]
Watch NowYou’re invited to attend the 2024 Clinician’s Roundtable, a virtual event where medical directors and oncologists will discuss how to better interpret genomic test results to tailor treatment strategies for cancer patients. As the role of the Molecular Tumor Board (MTB) becomes increasingly important in the implementation of evidence-based precision cancer medicine programs, molecular pathology […]
Watch NowIngenuity Pathway Analysis (IPA), currently cited in tens of thousands of publications and used by a large number of biopharmaceutical companies, is backed by QIAGEN Biomedical KB-HD. Accordingly, biomedical relationships knowledge has practically become required for innovative data- and analytics-driven drug discovery. It powers biomedical knowledge graph analysis, artificial intelligence (AI)-driven target identification and many […]
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