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  • 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 […]

  • Make discoveries from public data (GEO, SRA and more) using QIAGEN Ingenuity Pathway Analysis

    Virtual - Americas - EST , United States

    You asked for it, and we’re here to deliver. We are hosting a comprehensive training on effectively using sample-level public data and metadata from sources like GEO, SRA, TCGA, GTEx, Blueprint, CCLE and others through QIAGEN Ingenuity Pathway Analysis (IPA) and the IPA Analysis Match Explorer feature. We’ll walk you through use cases involving biomarker […]

  • Public single-cell RNA-seq data investigation using QIAGEN OmicSoft and Ingenuity Pathway Analysis

    Virtual - Americas - EST , United States

    Single-cell RNA-sequencing (scRNA-seq) is widely used to investigate tissue heterogeneity, identify novel cell types, study pathogenic mechanisms, develop targeted therapy (including immunotherapy) and more. Accordingly, a tremendous amount of scRNA-seq data has been deposited to public domains like GEO. In this training, you will learn how to · Locate public single-cell studies of interest using […]

  • Featured

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

    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 […]