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Antimicrobial resistance (AMR) and multi-locus sequence typing (MLST) using QIAGEN CLC Genomics Workbench

Virtual - Americas - EST , United States

You asked for it by popular demand, and we’re here to deliver. In this training, we’ll cover how antimicrobial resistance (AMR) is used for isolation or can be easily integrated with other functionalities such as multi-locus sequence typing (MLST). In this training, we’ll cover: • Introduction to AMR, MLST and relevant databases • QIAGEN Microbial […]

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ESHG 2023

Glasgow Glasgow, Scotland, United Kingdom

Learn about our Sample to Insight solutions for inherited disorders This year at the European Society for Human Genetics (ESHG) 2023 Annual Meeting, QIAGEN will be at booth #472 premiering our new barrier-breaking Sample to Insight workflow for inherited disease NGS testing—a fast, cheap, ultra-precise panel to report pipeline. Learn more about our products and solutions […]

Investigation of inflammatory conditions public data for biomarker and drug target discovery using QIAGEN OmicSoft and IPA

Virtual - Americas - EST , United States

In this 90-minute training on QIAGEN OmicSoft and Ingenuity Pathway Analysis (IPA), we’ll cover how to easily query inflammatory conditions related to public data (GEO, SRA and more) to: • Rapidly query and identify public datasets that fit our search criteria • Discover and validate biomarker expression in disease tissue, different treatments and response groups […]

RNA-seq data analysis and interpretation using QIAGEN CLC and QIAGEN IPA

Virtual - Americas - EST , United States

This 90-minute training will teach you how to easily analyze and interpret RNA-seq data using QIAGEN CLC Genomics Workbench software and QIAGEN Ingenuity Pathway Analysis (IPA). For RNA-seq data, you will learn how to: • Import FASTQ files, cell matrix files and metadata and how to download references • Map reads to a reference genome […]

Interpretieren Sie somatische Varianten einfach und schnell mit HSMD

Virtual - Germany , Germany

Verpassen Sie nicht die Gelegenheit, das bestgehütete Geheimnis von somatischen NGS-Tests kennenzulernen. Die von QIAGEN entwickelte neue Datenbank namens HSMD enthält über 2 Jahrzehnte von Experten kuratierte Inhalte aus der QIAGEN Knowledge Base und Daten aus über 300.000 realen Onkologie-Fällen, um tiefgreifende Einblicke in die genaue Funktion und Handlungsfähigkeit von kleinen Varianten wie SNVs, Indels […]

QIAGEN IPA Deeper Dive: Making most out of user’s core analysis and new features

Virtual - Americas - EST , United States

Many of you who use QIAGEN Ingenuity Pathway Analysis (IPA) have requested a deeper dive into the IPA core analysis (also known as expression analysis - performed on RNA-seq, scRNA-seq, proteomics and many other ‘omics data). You’ve specifically requested to cover topics like causal networks, regulator effects, etc., in more detail. That’s why we’ve designed […]

Scale your comprehensive genomic profiling workflow with superior automated variant interpretation

Automating and scaling a comprehensive genomic profiling workflow can be a tedious and challenging process that requires lots of time and resources. However, an intelligent clinical decision support platform and on-demand expert support services can make all the difference. In this webinar, learn about QIAGEN Clinical Insight (QCI) Interpret for Oncology, a clinical decision support […]

De novo assembly, BLAST and genome finishing using QIAGEN CLC Genomics Workbench

Virtual - Americas - EST , United States

This webinar will introduce users to the tools available for short reads (Illumina) as well as long reads (Oxford Nanopore, Pac Bio) de novo assembly in QIAGEN CLC Genomics Workbench. It will also go over other useful functionalities such as BLAST and genome finishing. Participants will learn the following: o Download and install needed plugins. […]

Insights into cancer genomics via COSMIC v98

Virtual - Americas - EST , United States

Our understanding of cancer mechanisms, genetics and complexities continues to expand rapidly. Without a streamlined, standardized and easy to understand organizational system to keep track of this plethora of knowledge, potentially crucial data can effectively be lost. Trusted by scientists for nearly 20 years, COSMIC is the world’s largest, most comprehensive, expert-curated resource for exploring […]

Pathogen detection and variant analysis using hybrid capture technology and QIAGEN CLC Genomics Workbench

Virtual - Americas - EST , United States

The detection and surveillance of pathogens such as respiratory viruses, sexually transmitted pathogens, adventitious agents and antimicrobial-resistant bacteria are increasingly important in healthcare settings and environmental monitoring. The COVID-19 pandemic highlighted the importance of identifying and differentiating variants of concern. By applying the lessons learned from the COVID-19 pandemic to other pathogens of interest, it’s […]

Target exploration and cell line selection for drug discovery

Virtual - Americas - EST , United States

Cancer cell line models have been a cornerstone of cancer research for decades. Profiling cancer cell lines is a powerful tool to identify gene alterations or cancer-related pathways and to discover potential drug targets. This training will focus on using QIAGEN OmicSoft Lands and Ingenuity Pathway Analysis (IPA) as guides to select cell lines and […]

Investigating genomic variants using QIAGEN CLC Genomics Workbench, QCI Interpret-Translational (QCII-T), and QIAGEN Ingenuity Pathway Analysis (IPA)

Virtual - Americas - EST , United States

Discovering new genes implicated in hereditary diseases or cancer progression is challenging yet advancing rapidly due to the increase in next-generation sequencing (NGS) cohort data. These data analyses produce insights into associations between gene variants and diseases and the biological mechanisms of these gene variants. By combining QIAGEN CLC Genomics Workbench, QCII-T and QIAGEN IPA, […]

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Exome experts: Improving the interpretation and integration of exome testing in routine clinical care

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, […]

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Streamline H5N1 and other microbial samples with CLC Genomics Workbench

In 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: […]

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Scale up NGS bioinformatics analysis throughput with CLC Genomics Server and Cloud solutions

More 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 […]

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Leveraging the power of API-based omics (RNA-seq, proteomics and more) queries for discovery

There 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 […]

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Clinician’s Roundtable: Interpreting genomic test results for precision oncology

You’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 […]

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QIAGEN Biomedical KB-HD: data- and analytics-driven drug discovery

Ingenuity 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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Network construction and customization with QIAGEN Ingenuity Pathway Analysis
This in-depth training focuses 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 network/pathway of interest from their analysis or the Ingenuity Knowl...
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QIAGEN Biomedical KB-HD: data- and analytics-driven drug discovery
Ingenuity 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, a...
WATCH NOW
Clinician’s Roundtable: Interpreting genomic test results for precision oncology
You’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 medici...
WATCH NOW
Leveraging the power of API-based omics (RNA-seq, proteomics and more) queries for discovery
There 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, exper...
WATCH NOW
Scale up NGS bioinformatics analysis throughput with CLC Genomics Server and Cloud solutions
More 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 Workbench can be ...
WATCH NOW
Streamline H5N1 and other microbial samples with CLC Genomics Workbench
In 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: • Utilize molec...
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Sample to Insight
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