Webinars and events

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Single-cell RNA-seq data analysis and interpretation

Virtual - Americas - EST , United States

Explore how to analyze and interpret your own single-cell RNA-seq (scRNA-seq) data using QIAGEN CLC Genomics Workbench and QIAGEN Ingenuity Pathway Analysis (IPA). In this 90-minute training, you’ll learn how to: • Start with FASTQ, cell matrix file and/or differential expression file for scRNA-seq data • Either automate or customize your analysis pipeline/workflow, depending on […]

Whole genome sequencing (WGS), rapid WGS and ultra-rapid WGS for hereditary disorders – where speed matters

Virtual - Americas - EST , United States

QIAGEN CLC LightSpeed Module delivers an ultra-fast, end-to-end hereditary NGS FASTQ to VCF pipeline. LightSpeed takes raw FASTQ files generated by paired-end 150 bp sequencing protocols and performs quality trimming, adapter trimming, read mapping, deduplication, local realignment, QC and germline variant calling. More details: https://qiagen.showpad.com/share/Tue4ZxKsjAFetyoswbTfE Cloud module: QIAGEN CLC Genomics Cloud computing software allows you […]

Checkpoint inhibitors in the context of biomarkers, drug targets and pathways

Virtual - Americas - EST , United States

In this training, we will focus on how you can use QIAGEN Omicsoft Studio and QIAGEN Ingenuity Pathway Analysis (IPA) to discover new biomarkers, validate (or study) drug targets and identify novel mechanisms of action with your own and/or public checkpoint inhibitor datasets from resources like GEO, SRA, TCGA and more. In this training, you’ll […]

How to improve your existing pipeline for somatic mutation analysis, interpretation and reporting: Part 2

Virtual - EMEA - CET

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 […]

Pathway and network analysis on different types of lists with QIAGEN IPA

Virtual - Americas - EST , United States

You may not have a typical transcriptomics dataset (i.e., a list of genes with differential expression), yet, you’d like to analyze a list of IDs. In this training, we will explore how to perform pathway and network analysis for lists of IDs in QIAGEN IPA. Examples of lists that we’ll explore include: • A gene/protein/metabolite […]

How to improve your existing pipeline for somatic mutation analysis, interpretation and reporting: Part 2

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 […]

IPA deeper dive: miRNA investigation using QIAGEN Ingenuity Pathway Analysis (IPA)

Virtual - Americas - EST , United States

In this 90-minute training session, you will learn how to identify target mRNAs for your miRNAs of interest and associate them with pathways, diseases, biological functions, tissues and cell types. We’ll cover topics such as: - How to analyze miRNA-seq datasets alone, or both miRNA and corresponding mRNA datasets together - How to use QIAGEN […]

Acceda rápidamente a amplios conocimientos para interpretar variantes somáticas con la HSMD

Virtual - Argentina , Argentina

Dentro de las aplicaciones oncológicas, la capacidad de identificar alteraciones genéticas potencialmente accionables y explorar las vulnerabilidades moleculares del cáncer es cada vez más difícil. Una nueva base de datos desarrollada por QIAGEN, la HSMD, contiene más de 2 décadas de contenido curado por expertos y datos de la QIAGEN Knowledge Base con más de […]

Roman Testing Conference

Romania Cluj-Napoca, Romania

In 2023, we want to hear stories of improved communication and bridging gaps. Of technology used to harness the power of agility. Of process improvements, impediments removal and common goals. About changing attitudes, ways of working and minds. We want to hear stories of failure or win, standing up against change or championing it. What you […]

Sample to Insight at LightSpeed: A barrier-breaking workflow for inherited disease NGS testing

Virtual - Americas - EST , United States

Get a first-hand look at QIAGEN’s new Sample to Insight Hereditary solution. By attending this webinar, you will: Learn more about each workflow component. Hear from experts in the field as they discuss how this technology advances the diagnosis and management of inherited diseases. Examine real-world case studies demonstrating the clinical utility and cost-effectiveness of […]

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 […]

On-demand Webinars

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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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{"webinar_date":"2024-05-02 01:00:00","start_month":"May","start_day":"02","start_date":"20240502","start_time":"01:00","end_month":"","end_day":"","end_date":"","webinar_end_date":"","title":"Network construction and customization with QIAGEN Ingenuity Pathway Analysis","content":"This in-depth training focuses on effectively constructing a network, with or without a dataset (RNA-seq, proteomics, etc.), and easily modifying it \u2013 all within Ingenuity Pathway Analysis.\n\nIn this interactive training, attendees will learn how to:\n\n\u2022 Construct a network from scratch or open a network\/pathway of interest from their analysis or the Ingenuity Knowledge Base\n\u2022 Effectively use tools present in the Build and Overlay menus to add molecules (genes\/proteins, chemicals, metabolites), biological processes\/diseases of their interest and more\n\u2022 Modify the network (e.g., to keep only a specific type of relationship like activation, phosphorylation, protein-protein binding and more)\n\u2022 Perform in silico prediction (e.g., if a drug, siRNA or CRISPR were to reduce the activity of a gene\/protein, how will it impact the remaining genes\/proteins\/diseases in that network)\n\u2022 Export high-resolution graphics or tabular relationships and make the created network usable in future pathway analysis","duration":"01:00:00","presenter":"","featured":"","slug":"network-construction-and-customization-with-qiagen-ingenuity-pathway-analysis-2","url":"https:\/\/tv.qiagenbioinformatics.com\/video\/100159561\/network-construction-and","description_webinars":"","category_select":"26199","time_start":"PM ET l 10:00 AM PT"}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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{"webinar_date":"2024-05-14 01:00:00","start_month":"May","start_day":"14","start_date":"20240514","start_time":"01:00","end_month":"","end_day":"","end_date":"","webinar_end_date":"","title":"QIAGEN Biomedical KB-HD: data- and analytics-driven drug discovery","content":"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 more applications.\n\nIn this webinar, we will introduce Biomedical KB-HD and how it allows its users to tackle applications that are not feasible with the Ingenuity Pathway Analysis graphical user interface or can be done faster and with more flexibility programmatically. We will demonstrate queries such as\n\n\u2022 Quickly find the shortest connections between genes\/proteins\/metabolites of interest in the context of specific disease through queries\n\u2022 Systematically build a network given a short list of genes\/proteins\/metabolites\/chemicals\n\u2022 Recreate a drug mechanism of action","duration":"01:00:00","presenter":"","featured":"","slug":"qiagen-biomedical-kb-hd-data-and-analytics-driven-drug-discovery-2","url":"https:\/\/tv.qiagenbioinformatics.com\/video\/101070223\/qiagen-biomedical-kb-hd-data-and","description_webinars":"","category_select":"26199","time_start":"PM ET l 10:00 AM PT"}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...
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{"webinar_date":"2024-05-16 01:00:00","start_month":"May","start_day":"16","start_date":"20240516","start_time":"01:00","end_month":"","end_day":"","end_date":"","webinar_end_date":"","title":"Leveraging the power of API-based omics (RNA-seq, proteomics and more) queries for discovery","content":"\n

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 data via the QIAGEN OmicSoft APIs. These OmicSoft APIs provide a powerful and flexible platform for discovering, retrieving, filtering, analyzing and visualizing multi-omic data. You can learn how to access the OmicSoft APIs and programmatically leverage extensive metadata to perform custom analyses and identify targets of interest.<\/p>\n\n\n\n

Topics to be covered in this webinar:<\/p>\n\n\n\n

\u2022 Leveraging curated metadata to structure queries (metadata refers to cell type, tissue, disease, drug treatment etc., associated with public data)
\u2022 Finding multiple samples with the same metadata and creating cohorts
\u2022 Identifying expression and correlation
\u2022 Performing gene set enrichment analysis
\u2022 Testing cell specificity with custom aggregation<\/p>\n","duration":"01:00:00","presenter":"","featured":"","slug":"leveraging-the-power-of-api-based-omics-rna-seq-proteomics-and-more-queries-for-discovery","url":"https:\/\/tv.qiagenbioinformatics.com\/video\/101070251\/leveraging-the-power-of-api-based","description_webinars":"","category_select":"26199","time_start":"PM ET l 10:00 AM PT"}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...
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{"webinar_date":"2024-05-16 01:00:00","start_month":"May","start_day":"16","start_date":"20240516","start_time":"01:00","end_month":"","end_day":"","end_date":"","webinar_end_date":"","title":"Clinician\u2019s Roundtable: Interpreting genomic test results for precision oncology","content":"\n

You\u2019re invited to attend the 2024 Clinician\u2019s 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 labs must overcome challenges in genomic test interpretation to ensure maximum clinical utility of molecular profiling results. At this event, hear from clinicians at leading universities and organizations as they present real-world case studies of how molecular pathology labs can improve test turnaround, standardize test interpretation, and deliver comprehensive genomic reports with personalized diagnostic, prognostic, and therapeutic information for each patient.<\/p>\n\n\n\n

The free-to-attend virtual event will consist of four educational parts:<\/strong><\/p>\n\n\n\n

1.    Case Presentations:<\/strong> Clinicians from Dana Farber Cancer Institute and the National Cancer Institute will present cases of how their labs have overcome challenges in genomic test interpretation.<\/p>\n\n\n\n

2.    Live Q&A Session:<\/strong> Attendees will have the opportunity to ask the clinicians questions about their experiences implementing precision oncology programs at their institutions.<\/p>\n\n\n\n

3.    Solution Showcase:<\/strong> In a brief presentation, experts from QIAGEN Digital Insights will showcase our leading Sample to Insight solutions for molecular tumor profiling.<\/p>\n\n\n\n

4.    Future Forecast:<\/strong> The event will conclude with a short presentation about how molecular tumor profiling will change in the next five years and how labs can leverage new technologies to improve patient care.<\/p>\n","duration":"01:00:00","presenter":"","featured":"","slug":"clinicians-roundtable-interpreting-genomic-test-results-for-precision-oncology","url":"https:\/\/tv.qiagenbioinformatics.com\/video\/100892343\/clinicians-roundtable-interpreting","description_webinars":"","category_select":"26199","time_start":"PM ET l 10:00 AM PT"}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...
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{"webinar_date":"2024-05-22 01:00:00","start_month":"May","start_day":"22","start_date":"20240522","start_time":"01:00","end_month":"","end_day":"","end_date":"","webinar_end_date":"","title":"Scale up NGS bioinformatics analysis throughput with CLC Genomics Server and Cloud solutions","content":"\n

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 used to customize workflows and send analyses for batch execution. We will also highlight analysis automation solutions, use of third-party dockers, audit trails and user management \u2013 all of which are available with the CLC Genomics Server software.<\/p>\n\n\n\n

You will learn to:
\u2022 Customize template workflows to meet your NGS analysis requirements
\u2022 Set up a CLC Genomics Cloud environment on AWS
\u2022 Submit workflows to run on internal servers or AWS and retrieve results from these analyses
\u2022 Use third-party dockers and automate workflow execution<\/p>\n","duration":"01:00:00","presenter":"","featured":"","slug":"scale-up-ngs-bioinformatics-analysis-throughput-with-clc-genomics-server-and-cloud-solutions","url":"https:\/\/tv.qiagenbioinformatics.com\/video\/101070251\/leveraging-the-power-of-api-based","description_webinars":"","category_select":"26199","time_start":"PM ET l 10:00 AM PT"}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 ...
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{"webinar_date":"2024-05-23 01:00:00","start_month":"May","start_day":"23","start_date":"20240523","start_time":"01:00","end_month":"","end_day":"","end_date":"","webinar_end_date":"","title":"Streamline H5N1 and other microbial samples with CLC Genomics Workbench","content":"\n

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.<\/p>\n\n\n\n

Using viral samples, you will learn how to:<\/p>\n\n\n\n

\u2022 Utilize molecular biology tools such as primer design, cloning, alignment and tree construction and Sanger sequencing analysis
\u2022 Profile the virus present in a sample and automatically generate read mappings, detect variants, annotate consensus sequences, BLAST annotated consensus sequence genes and build phylogenetic trees for top hits and their close relatives
\u2022 Microbial genomics analysis including OTU clustering, taxonomic profiling and functional analysis
\u2022 Additional topics of interest based on registration feedback<\/p>\n\n\n\n

QIAGEN CLC Genomics Workbench is a user-friendly bioinformatics software solutions for genomics, transcriptomics, epigenomics and metagenomics analysis in one program.<\/p>\n","duration":"01:00:00","presenter":"","featured":"","slug":"streamline-h5n1-and-other-microbial-samples-with-clc-genomics-workbench","url":"https:\/\/tv.qiagenbioinformatics.com\/video\/101491433\/streamline-h5n1-and-other-microbial","description_webinars":"","category_select":"26199","time_start":"PM ET l 10:00 AM PT"}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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