tv.qiagenbioinformatics.com

00:29

Turn any 'omics dataset into actionable insights with...

tv.qiagenbioinformatics.com ·

2026/06/24

QIAGEN Ingenuity Pathway Analysis (IPA) is a tertiary analysis platform that:- Predicts the activity of pathways, diseases, genes and more- Validates your results against existing research- Interprets your ‘omics data into clear, action-oriented insightsReady to turn your ‘omics data into discoveries? See how you can leverage expert-curated, AI-augmented knowledge for actionable ‘omics insights → https://digitalinsights.qiagen.com/ipa

en-us

00:57

Turn any 'omics dataset into actionable insights with...

tv.qiagenbioinformatics.com ·

2026/06/24

QIAGEN Ingenuity Pathway Analysis (IPA) is a tertiary analysis platform that:- Predicts the activity of pathways, diseases, genes and more- Validates your results against existing research- Interprets your ‘omics data into clear, action-oriented insightsReady to turn your ‘omics data into discoveries? See how you can leverage expert-curated, AI-augmented knowledge for actionable ‘omics insights → https://digitalinsights.qiagen.com/ipa

en-us

53:09

Franklin by QIAGEN for Hereditary Cancer Variant...

tv.qiagenbioinformatics.com ·

2026/06/18

Accurate variant interpretation is critical in hereditary cancer genetics, but it’s often complex due to conflicting data and evolving clinical context. In this webinar, Molecular Geneticist Dr. Ana Krivokuca will lead a live, case-based demonstration using Franklin by QIAGEN, showing how the platform's structured workflows, ACMG criteria and integrated data can support confident, transparent interpretations while addressing uncertainty and real-world clinical decision-making.You will learn:-How to

en-us

01:00:01

Reduce Discovery Risk Using Comorbidity Data, Omics...

tv.qiagenbioinformatics.com ·

2026/06/09

Comorbidity data can reveal unexpected and insightful connections between diseases. Understanding shared risks and underlying mechanisms are critical for informing patient care, yet these analyses often present significant challenges for researchers.Using a case study on the correlation between asthma and inflammatory bowel disease (IBD) in women, this webinar will demonstrate how comorbidity data can be integrated with harmonized omics datasets and knowledge graph–based analytical

en-us

56:03

Identify drug target receptors and investigate their...

tv.qiagenbioinformatics.com ·

2026/06/07

Biomedical KB-HD analysis in Neo4j enables researchers to explore complex relationships between drugs, targets and diseases using a comprehensive biomedical knowledge graph. Explore how to use this expert-curated data to identify promising disease biomarkers and examine their targets for various applications, using GLP-1, diabetes and Alzheimer’s disease as an example.You will learn:-To query BKB-HD in Neo4j to identify relevant drug candidates-To investigate connected biology by linking drugs,

en-us

46:00

Influenza Strain Typing Made Easy with QIAGEN CLC...

tv.qiagenbioinformatics.com ·

2026/06/03

Influenza is a highly contagious disease that affects humans and multiple animal hosts. Since influenza viruses are prone to major genetic changes, continuous research is critical for global public health, enabling scientists to anticipate and mitigate the impact of this rapidly evolving pathogen.Our webinar will show how you can analyze and interpret influenza virus sequencing data using QIAGEN CLC Genomics Workbench. Using the Microbial Genomics Module, we will explore influenza strain typing on

en-us

01:32:57

Get Hands-on with Franklin + HGMD – May 28 (Spanish)

tv.qiagenbioinformatics.com ·

2026/06/03

Welcome to one of our exclusive, hands-on virtual workshops to exploreFranklin + HGMD Professional— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll analyze areal-world caseinvolving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform

en-us

01:44:36

Get Hands-on with Franklin + HGMD – May 27 (Portuguese)

tv.qiagenbioinformatics.com ·

2026/06/03

Welcome to one of our exclusive, hands-on virtual workshops to exploreFranklin + HGMD Professional— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll analyze areal-world caseinvolving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform

en-us

01:29:02

Exploration of deeply curated single-cell data with...

tv.qiagenbioinformatics.com ·

2026/06/03

QIAGEN OmicSoft Explorer is your portal to thousands of deeply curated and integrated ‘omics datasets. In this hands-on workshop, we will explore projects with cell-level data and use it to investigate relevant studies, diseases or genes of interest using curated metadata terms. See how you can use OmicSoft Explorer by itself or with Ingenuity Pathway Analysis (IPA) to accelerate biological insights.You will learn:• To search for a project based on user-defined metadata and explore dimension

en-us

01:30:59

Simplify bulk and single-cell ATAC-seq analysis with...

tv.qiagenbioinformatics.com ·

2026/06/03

ATAC-seq is a powerful technique for assessing chromatin accessibility and identifying regulatory regions across the genome. From bulk ATAC-seq for population-level findings to single-cell ATAC-seq (scATAC-seq) to resolve chromatin accessibility at the individual cell level, these approaches lend deeper insights into gene regulation and cell state.QIAGEN CLC Genomics Workbench Premium provides researchers with a single, flexible platform for the analysis of both bulk ATAC-seq and scATAC-seq data. In

en-us

01:32:39

Multi-omics (metabolomics, proteomics,...

tv.qiagenbioinformatics.com ·

2026/06/03

This 90-minute training session will show you how QIAGEN Ingenuity Pathway Analysis (IPA) helps visualize molecular intricacies and variations at multiple levels, such as transcriptome, proteome and metabolome. Through a series of brief technical vignettes, we will demonstrate how to:- Generate associations among molecular signatures obtained via integrating multi-omics data- Extract mechanisms from multi-omics data for precision medicine- Disease stratification based on multi-omics profiles- Map

en-us

36:45

Beyond enrichment Causal discovery powered by Neo4j &...

tv.qiagenbioinformatics.com ·

2026/05/29

One click from your target gene to disease drivers, drug candidates and causal evidence. The Neo4j & QIAGEN solution transforms causal biomedical knowledge from QIAGEN Discovery KB+ into an interactive discovery surface. Learn how to query biomarkers, navigate causal networks and find drug repositioning candidates, provenance and natural language summaries included.

en-us

10:23

QIAGEN and NVIDIA collaboration to advance AI driven...

tv.qiagenbioinformatics.com ·

2026/05/29

NVIDIA and QIAGEN are collaborating to bring trustworthy, contextual AI to drug discovery. By integrating NVIDIA's accelerated computing and the BioNeMo platform with QIAGEN Digital Insights' manually curated biomedical knowledge graphs, cited in over 70,000 peer-reviewed publications; the collaboration aims to transform how disease mechanisms, therapeutic targets, and biomarkers are identified. Using a graph-based AI approach built on G-Retriever, the solution delivers 5–10x better performance than

en-us

04:53

Predict activity of regulators and biological...

tv.qiagenbioinformatics.com ·

2026/05/27

Single cell experiment viewer (SCEV) enables researchers to explore single-cell experiments in an interactive visual environment, overlaying curated cell metadata and gene expression patterns to reveal biologically meaningful cell states. By applying IPA’s embedding model of causal relationships, SCEV predicts upstream regulators and downstream functions that are likely active in specific cells or cell populations, helping users move from visualization to mechanistic interpretation.

en-us

53:42

Scale up NGS bioinformatics analysis throughput with...

tv.qiagenbioinformatics.com ·

2026/05/25

Explore how CLC Genomics Server enables the transition from ad hoc bioinformatics analyses to a scalable, centrally managed and production-ready infrastructure. We will show how the platform supports:- Secure and centralized compute environments- Controlled deployment of validated workflows- Multi-user access with governance and audit trails- Integration within existing IT and virtualized environmentsGain insights into how a genomics server framework improves reproducibility, reduces operational

en-us

35:38

Beyond the Surface: Applying NGS to Advance Cosmetic R&D

tv.qiagenbioinformatics.com ·

2026/05/20

As cosmetic science advances, consumers are demanding products better tailored to their specific concerns. What if you could decode skin biology and translate it into targeted cosmetic innovation?Next-generation sequencing (NGS) is deepening our understanding of skin biology by enabling comprehensive, high-throughput analysis of DNA and RNA to identify key genetic and transcriptomic markers associated with skin function and response. From fundamental processes and pathways to validating product

en-us

44:02

T cell receptor repertoire analysis: Unraveling new...

tv.qiagenbioinformatics.com ·

2026/05/19

Understanding the inner workings of the adaptive immune system is critical to new strategies for combatting cancer and infectious diseases. In this webinar led by Drs. Mazza, Mazzotti and de Souza, we will explore T-cell receptor (TCR) repertoire analysis from start to finish, examining the different steps, approaches and data analysis implications.Join us to gain a deeper understanding of the molecular mechanisms of the adaptive immune system, discover the various applications of TCR repertoire

en-us

38:15

Accelerating hereditary variant interpretation: HGMD...

tv.qiagenbioinformatics.com ·

2026/05/19

“Reliable AI”? Sounds like a contradiction, but with HGMD in Franklin, it’s possible.By combining HGMD Pro’s comprehensive, expert-curated hereditary variant content and Franklin’s AI workflows and user-friendly interface, accelerated hereditary variant interpretation is now within closer reach. Whether you’re in diagnostics, research or bioinformatics, you will gain practical insights into a simplified genomic analysis workflow.You will learn to:Access HGMD data directly within Franklin by

en-us

34:46

Grazing for insights: Leveraging regulatory...

tv.qiagenbioinformatics.com ·

2026/05/19

Neutrophils, known for killing microbes, can be both beneficial and harmful during a tuberculosis (TB) infection. While neutrophils kill the bacteria early on, they also contribute to chronic inflammation and lung tissue destruction. However, recent studies show that these roles are associated with different subsets of neutrophils: regulatory ones that display major histocompatibility complex (MHC)-II and the classical MHC-II- neutrophils.In this webinar, Dr. Aude Remot from Université de Tours,

en-us

01:31:57

Get Hands-on with Franklin + HGMD

tv.qiagenbioinformatics.com ·

2026/05/19

Our exclusive, hands-on virtual workshops will exploreFranklin + HGMD Professional:a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll analyze areal-world caseinvolving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical

en-us

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