• Isolate Typing, Strain Identification and Anti-Microbial Resistance Analyses Using QIAGEN CLC Genomics Workbench

    Virtual - Americas - EST , United States

    QIAGEN CLC Genomics Workbench provides tools and workflows for a broad range of bioinformatics applications, including microbiome analysis, isolate characterization through SNP and K-mer trees using NGS data, and antimicrobial resistance characterization. CLC Genomics Workbench is widely used for analyses of bacterial, viral and eukaryotic (fungal) genomes and metagenomes. Topics covered in this webinar include: […]

  • Biomarker discovery and disease pathology investigation using QIAGEN OmicSoft and Ingenuity Pathway Analysis

    Virtual - Americas - EST , United States

    In this training, attendees will learn how to harness curated ‘omics datasets in OmicSoft DiseaseLand and curated research findings in IPA to discover new potential biomarkers. Using a neurological disorder as a case study, we will: • Search public RNA-Seq datasets for tissue- and disease-specific differential expression in brain • Identify genes whose expression correlates […]

  • IPA deeper dive: Generating novel discoveries in IPA - even when you don’t have data

    Virtual - Americas - EST , United States

    Take a deeper dive into the discovery capabilities of QIAGEN IPA. In this training, you will learn how to: • Leverage the IPA knowledge base to generate hypotheses regarding novel biological mechanisms, discover biomarkers and targets as well as design experiments. • Generate interactive networks using genes, chemicals and diseases of interest • Search and […]

  • Lowering NGS analysis cost at lightspeed

    Virtual - Americas - EST , United States

    Advances in next-generation sequencing (NGS) technologies over the years have significantly decreased the cost of whole genome (WGS) and whole exome (WES) applications, such that they are considered the standard of care within multiple healthcare organizations. Arguably, the most significant NGS challenges lie within data analysis and interpretation. Various parameters such as sensitivity, specificity, cost […]

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

    Virtual - Americas - EST , United States

    This 90-minute training session is about how QIAGEN Ingenuity Pathway Analysis (IPA) allows visualization of molecular intricacy and variations at multiple levels such as transcriptome, proteome, and metabolome. Through a series of brief technical vignettes, it is demonstrated how to: · Generate associations among molecular signatures obtained via integrating multi-omics data · Extract mechanisms from […]

  • Accéder rapidement à une connaissance exhaustive pour l’interprétation des variants somatiques avec HSMD

    L’interprétation et la classification des variants somatiques demeurent un challenge alors que le nombre de gènes testés continue d’augmenter faisant apparaitre de nouvelles altérations. Ces nouveaux variants dont l’impact clinique est encore inconnu nécessitent une recherche d’information croisée à partir de nombreuses sources. Déterminer la classification d’un variant peut donc s’avérer longue et fastidieuse. La […]

  • New user training: Large dataset analysis and knowledge base queries using QIAGEN Ingenuity Pathway Analysis (IPA)

    Virtual - Americas - EST , United States

    Join us for a 90-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 […]

  • Can you trust AI for germline variant curation? A Stanford University case study

    In this webinar, we examine a new study by Stanford University that analyzes the accuracy, consistency, and comprehensiveness of automated and manual germline variant curation. The study compares the quality of data from Stanford’s Automatic VAriant evidence DAtabase (AVADA) to the Human Gene Mutation Database (HGMD), an expert-curated resource for human inherited disease mutations. By […]

  • Pathogen detection in wastewater samples using QIAGEN CLC Genomics Workbench

    Virtual - Americas - EST , United States

    In this 90-minute training, you will learn how to easily analyze wastewater samples to detect pathogens (SARS-COV2, etc.) using QIAGEN CLC Genomics Workbench software. You will learn how to: • Importing reads • Open and modify prebuilt workflow (analysis pipeline) • Install and execute workflow • Review QC reports • Perform genome visualization • Export […]

  • Take your genome research to the next level with QCI Interpret Translational

    Learn how QCI Interpret Translational can get your research to the next level by providing you all the necessary analysis tools with the world’s most comprehensive and up-to-date curated scientific evidence. Get valuable and reliable insights for your research project and speed up your discoveries by using a streamlined NGS analysis workflow in a user-friendly […]