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Upcoming webinars

  • SARS-CoV-2 NGS surveillance & epidemiology with QIAGEN Digital Insights - May 11

    This one-hour event will summarize our solutions for genomics research, environmental testing, and epidemiological study of SARS-CoV-2 NGS data. Including: Local and high-performance cloud (GCE) deployment • Workflows for analyzing SARS-CoV-2 data using CLC Genomics software and focused approaches such as QIAseq SARS-CoV-2 Primer and Ion AmpliSeq SARS-CoV-2 panel...

    May. 11 | 01:00PM ET | 10:00 AM PT

  • How to scale your expanded carrier screening workflow by 80% - May 13

    Learn how your genetic testing lab can scale your expanded carrier screening workflow by up to 80%. Eliminate manural curation. Accelerate variant interpretation. Report with confidence....

    May. 13 | 11:00AM SGT l 11:00 AM CEST l 11:00 AM EDT

  • RNA sequence analysis using PacBio and Illumina reads from a host-pathogen interaction - May 18

    Learn from an expert in plant genetics and bioinformatics about expression analysis using short and long reads in a host-pathogen interaction. Click here to register....

    May. 18 | 01:00PM ET | 10:00 AM PT

  • Uncovering Genomic Evidence of SARS-CoV-2 Infection and Reinfection - May 19

    Is it possible to become reinfected with SARS-CoV-2? If so, how can we identify and confirm reinfection?  What tools can we use to better identify prevalent and emerging strains of SARS-CoV-2? Click here to find out more....

    May. 19 | 12:00PM EDT l 09: 00 AM PDT

  • Calling, annotating and investigating genomic variants using QIAGEN CLC Genomics Workbench and QCII-T - May 27

    Join us for a 90-minute training where attendees will learn how to call SNPs, MNPs and structural variants (insertions, deletions, inversions and copy number variants) using QIAGEN CLC Genomics Workbench. In addition, we will demonstrate how to annotate these variants using both QIAGEN CLC Genomics Workbench and QIAGEN Clinical Insight Interpret Translational (QCII-T)...

    May. 27 | 01:00PM ET | 10:00 AM PT

  • Advancing Personalized Oncology with Transcriptomic Profiling and Mechanistic Modeling - June 8

    In this webinar, Moritz Schütte, head of next-generation sequencing data analysis at Alacris, will explore the advantages of RNA sequencing alone or in combination with whole-exome sequencing as part of a precision oncology workflow. Click here to register....

    Jun. 08 | 10:00AM Eastern Daylight Time

Upcoming Trainings

  • QIAGEN Ingenuity Pathway Analysis (IPA) New user training - May 18

    Join us for a 90-minute training session aimed towards new users on QIAGEN IPA. Users will learn how to: • Upload their dataset (RNA-seq, scRNA-seq, proteomics, metabolomics and more) and perfor...

    May. 18
    01:00PM ET | 10:00 AM PT

  • Single-cell RNA-seq: Analysis and interpretation of user and public data - May 20

    In this 90-minute training, attendees will learn how to analyze and interpret their own single-cell RNA-seq (scRNA-seq) data as well as public data using a combination of QIAGEN CLC Genomics Workbench...

    May. 20
    01:00PM ET l 10:00 AM PT

Upcoming events

May. 20 - May. 20 | Virtual Event

May. 20 - May. 20 | Virtual Event

Jun. 29 - Jun. 30 | Virtual Event

On-demand Webinars

  • On-demand web seminar: Scaling your bioinformatics with QIAGEN CLC Genomics Server and Cloud Engine

      By attending this webinar, you will learn how to use QIAGEN Digital Insight’s enterprise solutions to extend the powerful QIAGEN CLC Genomics Workbench platform to tackle even the greatest bioinformatics challenges....

  • On-demand webinar: Multi-omic changes in the postnatal mouse heart identified by QIAGEN Ingenuity Pathway Analysis (IPA) and QIAGEN OmicSoft

    Multi-omics experiments allow researchers to make important discoveries in ways that have never before been possible. However, integrating these data into a broader biological context can be challenging and time consuming when using standard resources. At QIAGEN, we have introduced an innovative solution to this challenge: The market-leading QIAGEN Ingenuity Pathway A...

  • On-demand webinar: Get insights into the bioinformatics analysis of Nanopore sequencing data for SARS-CoV-2

    The study of the COVID-19 pandemic often involves sequencing the SARS-CoV-2 virus using Illumina, Nanopore, IonTorrent and Sanger technologies alone or in combination. Depending on the sampling and library preparation method used, this can involve metatranscriptomic data of varying viral content. In this webinar tutorial, you will learn about: Best practices for ...

  • On-demand webinar: Tumor mutational burden analysis using QIAGEN CLC Genomics Workbench

    QIAGEN offers two analysis solutions for data acquired using QIAseq Kits. The GeneGlobe Analysis Center is our web-based portal with fixed, ready-to-use pipelines, while QIAGEN CLC Genomics Workbench is our onpremise solution providing ready-to-use workflows, which are fully configurable. QIAGEN CLC Genomics Workbench is a user-friendly bioinformatics software solutio...

  • On-demand webinar: Discover hidden relationships in your toxicological studies with QIAGEN IPA

    QIAGEN Ingenuity Pathway Analysis (IPA) reveals the hidden upstream drivers and downstream outcomes in your toxicogenomics datasets. Put those results into context using Analysis Match with over 50,000 pre-analyzed datasets for human, mouse and rat. Explain the causes and effects in your studies so you can generate hypotheses to develop better drugs, biomarkers and mo...

  • On-demand web seminar: Enabling high-throughput genomic surveillance of emerging SARS-CoV-2 strains

    Join our webinar to discover a scalable workflow for SARS-CoV-2 whole genome sequencing to accelerate detection of variants such as B.1.1.7 and B.1.351. In this new webinar, we will describe how QIAGEN’s QIAseq SARS-CoV-2 integrated workflow combines QIAseq chemistries and CLC Genomics Analysis software to deliver a scalable, high-performance solution for sequencing...

  • On-demand webinar: Investigation of Somatic and Germline Variants by COSMIC, HGMD and QIAGEN Databases

    Identifying and studying actionable variants is of great interest to many investigators. In this webinar, COSMIC, HGMD and QIAGEN database will be introduced for annotation and investigation of both somatic and germline variants. Attendees will learn how to use QIAGEN Clinical Insight Interpret Translational (QCI-IT) to identify key actionable variants from whole geno...

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