Bioinformatics Software | QIAGEN Digital Insights

How clinical labs can confidently assess cancer-associated variants with real-world data and expert-curated genomic evidence
2023-11-16 13:00 - 14:00 (America/Halifax) | Virtual - Americas - EST, United States
Across various stages of the clinical oncology workflow, from panel design to genomic testing and molecular tumor boards, the identification and validation of actionable genomic alterations is critical. The advent of next-generation sequencing (NGS) has led to an exponential increase in the number of variants detected in tumor testing, posing a challenge for clinical cancer genetics professionals seeking to confidently discern clinically relevant mutations that can guide patient care decisions.

Join Dr. Umadevi Thirumurthi, Associate Director of Global Product Management for Oncology at QIAGEN Digital Insights as she discusses how the Human Somatic Mutation Database (HSMD), an expert-curated somatic variant database, can enhance your clinical NGS workflow.

Attendees will learn how HSMD:

Can be used to design targeted panels, streamline somatic variant analysis, and support molecular tumor board decisions;
Provides access to data from over 419,00 real-world oncology cases and human-certified expert curation
Enables users to effortlessly explore mutational characteristics across genes, synthesize critical information from drug labels and professional guidelines, investigate ongoing clinical trials, and access comprehensive annotations for each observed variant

Easily process your FASTQ files
2023-11-15 13:00 - 14:30 (America/New_York) | Virtual - Americas - EST, United States
Do you ever get stuck processing raw FASTQ data or cell matrix data from your RNA-seq, scRNA-seq or other NGS assays using? Are you interested in creating a differential expression table that’s compatible with the QIAGEN Ingenuity Pathway Analysis (IPA) software you use? In this training, you’ll learn how to use QIAGEN CLC Genomics Workbench to easily process your FASTQ files and generate differential expression tables without using command line tools. We’ll also explore how you can generate other desired outputs, such as volcano plots, heatmaps, PCA/PCOA plots and more.
You can delve into more information about QIAGEN CLC Genomics Workbench here:
https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-genomics-workbench/

IPA deeper dive: miRNA investigation using QIAGEN Ingenuity Pathway Analysis (IPA)
2023-11-14 13:00 - 14:30 (America/New_York) | 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 IPA without a dataset, using miRNA IDs - Introduction to databases and curated content specific to miRNA - How to effectively apply various filters and functionalities to identify biomarkers, key targets and novel biological mechanisms

AMP 2023
2023-11-14 - 2023-11-18 | Salt Lake City, Salt Lake City, UT, United States
AMP is the leading organization in the field of molecular diagnostics, and our annual meeting is widely considered the “premier gathering” of molecular professionals. As always, we will explore how cutting-edge technology and developments in molecular testing continue to have a major and direct impact on patient care. The AMP 2023 Program Committee is planning an impressive program to spark dialogue and engagement amongst attendees and exhibitors from around the world, and we look forward to welcoming you to discuss the latest in molecular diagnostics and network with friends and colleagues.

Isolate typing, strain identification and antimicrobial resistance analyses using QIAGEN CLC Genomics Workbench
2023-11-09 13:00 - 14:30 (America/New_York) | Virtual - Americas - EST, United States
QIAGEN CLC Genomics Workbench provides tools and workflows for a broad range of bioinformatics applications, including microbiome analysis, isolate characterization through SNP and K-mer trees using NGS data, and antimicrobial resistance characterization. CLC Genomics Workbench is widely used for analyses of bacterial, viral and eukaryotic (fungal) genomes and metagenomes. We’ll cover these topics in the training: I. Overview of different tools within MGM application and research areas supported II. Focused review of isolate typing and characterization a. Importing data b. Utilization of metadata c. Downloading and managing references i. Database of Isolates/ Resistances/ MLST d. Walk through of Type a Known Species workflow i. Review details for each Isolate e. Creating SNP profiles to specific reference f. Generate a SNP tree for isolate comparison g. Export tabular and high-quality graphical outputs in wide range of file formats

Part 2: AI-Powered Hereditary Disease Diagnostics: Closing the Gap in Clinical Exome Completeness
2023-11-09 10:00 - 12:00 UTC | Virtual Global Event (Times shown in EST)
Clinical exome sequencing (CES) is increasingly being adopted by small and mid-sized laboratories to diagnose genetic diseases, aid treatment decisions, and provide prognostic information. However, the exponential increase in genetic data generated from exome and genome panels poses significant workflow challenges. The ability to prioritize potentially pathogenic variants from large datasets and identify the few candidate variants becomes more difficult. This issue is further amplified in cases where labs must use deep phenotyping of patients and compare that to reference genotype-phenotype knowledge associated with each candidate variant. To overcome these challenges, labs are beginning to implement Artificial Intelligence (AI) in their variant analysis, interpretation and reporting workflows.
Join us for our 2023 Clinical Hereditary Disease Diagnostics Summit, a free-to-attend, two-part event exploring the opportunities and limitations of AI in hereditary disease diagnostics. Designed to help clinical diagnostic labs learn how to safely apply AI to exome and genome sequencing workflows, the content-rich event will feature invited lectures from lab directors and clinical geneticists, thought-provoking discussions on the future of hereditary disease diagnostics, as well as educational presentations on the latest databases and AI-powered software for germline secondary and tertiary analysis.
Part II: Roundtable discussion with genomics experts – November 9, 2023
A panel discussion featuring experts in the field of clinical genomics that will explore the challenges and opportunities in the future of inherited disease diagnostic testing.
For the list of speakers and session information, visit our event page here.

New user training: Large dataset analysis and knowledge base queries using QIAGEN Ingenuity Pathway Analysis (IPA)
2023-11-07 13:00 - 15:00, 2023-10-04 13:00 - 15:00 (America/New_York) | Virtual - Americas - EST, United States
Join us for a 120-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 different experimental conditions (treatments, time points, single-cell clusters, disease types and more) and identify similarities and contrasts
• Generate a network even without a dataset or experimental design for hypothesis generation
For those with IPA license,
To install IPA before or after this training, please use below installer.
https://qiagen.showpad.com/share/CBv30blCPKFDUYHRWtAvI

How to scale-up comprehensive genomic profiling and deliver confident variant interpretations with QCI Interpret for Oncology
2023-11-07 13:00 - 14:00 (America/Halifax) | Virtual Global Event (Times shown in EST)
As gene panels increase in size, comprehensive genomic profiling and variant interpretation becomes more complex and time-consuming, which places tremendous burden on labs needing to scale and grow case volume. QIAGEN Clinical Insights (QCI) Interpret for Oncology is a clinical decision support platform powered by augmented molecular intelligence that enables rapid, evidence-powered comprehensive genomic profiling at scale. QCI Interpret for Oncology is supported by the world’s most comprehensive, manually curated knowledge base and dynamically computes variant classifications according to AMP/ASCO/CAP and ACMG/AMP guidelines with transparency. Users also get access to over 500,000 pre-formulated, oncologist-reviewed variant interpretation summaries and can build customizable, oncologist-ready reports with the latest diagnostic and prognostic information, as well as biomarker-directed therapeutic information and clinical trial recommendations. With its latest release, QCI Interpret for Oncology adds several new capabilities that further enhances the platform’s scalability and flexibility, and enables users to significantly reduce variant research and review time.
In this webinar, attendees will learn how QCI Interpret for Oncology enables you to:

Navigate from VCF to final report with speed, precision, and confidence;
Easily issue report addendums without the need for re-running a VCF;
Streamline structural variant filtering based on user set thresholds and hence reduce the time and effort needed to eliminate noise and identify truly relevant variants for reporting;
Utilize built-in AI capabilities to identify all the literature, case reports, drug therapies, and clinical studies relevant to a patient’s tumor type with just one-click.

The epididymis: Balancing the burden and responsibility of fertility
2023-11-02 13:00 - 14:00 (America/Halifax) | Virtual Global Event (Times shown in EST)
The responsibility of fertility is disproportionately placed on women, who bear most of the health, emotional and financial burdens. Infertility is rapidly rising, with one in six Australian couples seeking assisted reproductive technologies to help them start a family, and over 50% of cases involving a male factor. Despite these contributions, we still don’t fully understand the mechanisms that create competent sperm for fertilization, which occurs during their transit from the epididymis, a highly specialized region of the male reproductive tract.
To address this knowledge gap, we used high-resolution tandem mass spectrometry and in-silico analyses to characterize proteome-wide changes in mouse sperm. We studied changes associated with their transit through the epididymis and elicited in response to capacitation stimuli, such as maturation initiated upon contact with the female reproductive tract.
In this webinar, you’ll learn about:

The unprecedented depth of >6000 proteins and 14,586 site-specific phosphorylation events across these sperm populations that we discovered using QIAGEN Ingenuity Pathway Analysis (IPA)
How sperm shed over 56% of their proteins during this process, producing a refined fertilization-competent cell
How this reduced proteomic complexity of sperm coincides with the activation of certain functions, such as sperm motility and capacitation
Key proteins and kinases we identified through selective pharmacological inhibition that regulate sperm function
The role of RHOA on mature spermatozoa to reduce the rate of acrosome reaction by about 40%

Our data represent an essential paradigm shift in our understanding of male fertility regulation. They will contribute to important advancements in developing non-hormonal male contraceptives and robust sperm selection biomarkers for infertile men.

RNA-seq Analysis Portal - Analysis of QIAseq miRNA datasets
2023-11-01 15:00 - 16:00 UTC | Virtual - EMEA - CET
In this webinar, we will introduce how to analyze and explore your QIAseq miRNA data in RNA-seq Analysis Portal.
During the webinar, we will answer the following questions: • Which sample kits are supported by RNA-seq Analysis Portal? • How to upload your data to RNA-seq Analysis Portal? • How to start an analysis? • How to create a project? • How to create an experiment for differential expression? • How to inspect your experiment and quality control of your dataset? • How to view and filter differential expression results? • How to export your results?
Bring any questions you may have and we will answer them during the webinar.

ASHG 2023
2023-11-01 - 2023-11-05 | Washington, DC, United States
This year at the American Society for Human Genetics (ASHG) 2023 Annual Meeting, QIAGEN will be showcasing our Sample to Insight solutions for human genetics at booth #902. Learn more about our products and solutions and receive complimentary demos of our bioinformatic software and databases. Our experts will be available to chat with you and answer any questions you may have. We look forward to seeing you at ASHG 2023.

Real-World Applications of Clinical Metagenomic Sequencing in Cancer and Infectious Disease Diagnostics
2023-10-25 13:00 - 14:00 (America/New_York) | Virtual - Americas - EST, United States
Clinical metagenomic next-generation sequencing (mNGS), the comprehensive analysis of microbial and host DNA and RNA in samples from patients, is rapidly moving from research to clinical laboratories. This emerging approach is changing the diagnosis and treatment of diseases, with applications in a range of areas, including oncology, human host gene expression (transcriptomics), and antimicrobial infections and resistance.
In this webinar, Elif Dagdan, the director of the Center for Medical Genetics at Augusta Hospital Bochum in Bochum, Germany, will discuss real-world applications of using clinical mNGS to improve diagnostics of cancer and infectious diseases. The talk will also feature challenges and opportunities of using mNGS in disease diagnostics and how Dagdan’s lab uses clinical variant interpretation and reporting software from Qiagen to detect and characterize pathogenic somatic variants.
Dagdan will discuss:
How mNGS can be used to assess homologous recombination deficiency (HRD) status in patients with ovarian cancer.
How mNGS can be used to assess cell-free microbial DNA via liquid biopsy to aid in early-stage lung cancer diagnosis.
How mNGS can improve the accuracy and speed of infectious disease diagnostics, with a use-case on cardiovascular infections in intensive care units.

What's new in QIAGEN IPA Fall Release 2023?
2023-10-25 11:00 - 12:00 (America/New_York) | Virtual - Americas - EST, United States
Interested in learning about new features and functionalities that have been added to IPA lately?
During this webinar, we will highlight the updates from the QIAGEN IPA Fall Release and from previous releases from this year. Topics, amongst others, will be
• Newly added findings and pathways
• Reactome pathways
• Artificial intelligence approves to pathways
• More precise matches in Analysis Match
• Cell type prediction
• New queueing view for checking your analysis status
Bring any questions you may have and we will answer them during the webinar.
IPA release notes are available via the following webpage: https://digitalinsights.qiagen.com/products/qiagen-ipa/latest-improvements/current-line/

What's new in QIAGEN IPA Fall Release 2023?
2023-10-25 09:30 - 10:30 (Europe/Paris) | Virtual - EMEA - CET

Multi-omics (metabolomics, proteomics, transcriptomics) analysis using QIAGEN Ingenuity Pathway Analysis
2023-10-24 13:00 - 14:30 (America/New_York) | Virtual - Americas - EST, United States
This 90-minute training session is about how QIAGEN Ingenuity Pathway Analysis (IPA) allows visualization of molecular intricacy and variations at multiple levels such as transcriptome, proteome, and metabolome. Through a series of brief technical vignettes, it is demonstrated 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 disease networks among targets and indications

A breakthrough for rare disease: Completing the Clinical exome gap!
2023-10-19 11:00 - 12:00 UTC | Virtual Global Event (Times shown in EST)
In its latest release, QCI Interpret for Hereditary extends its market-leading content with further advancements in Artificial Intelligence (AI) for enhanced capabilities in clinical exome NGS testing. Now, with the addition of AI-derived literature references for rare disease genes, QCI Interpret provides complete exome coverage, on top of the existing unrivalled manually curated content and bibliography.
In this webinar, we will demonstrate how QCI Interpret is expanding its literature coverage enabling easy and efficient variant filtering workflow, based on bibliography and on patient’s phenotype. This new feature provides greater control over bibliography context, allowing users to only look at publications where the causative variant is associated with a specific disease. In addition, the release provides AI-enhanced phenotype-driven ranking. Using this approach that has been trained using thousands of solved cases, QCI Interpret for Hereditary Diseases provides superior overall candidate ranking for causative variants in rare diseases. The new variant-ranking approach is enhanced by taking into account additional variant related variables supported also by AI, as well as the patient’s symptoms, and all of the manually curated literature in the QIAGEN Knowledge Base to give the best possible chance of reaching an accurate diagnosis.
Learning objectives:

Learn about QCI Interpret’ s new AI bibliography content providing expanded clinical exome coverage, due to the combination of the AI-derived literature references with QIAGEN’s unrivalled manual curation.
Learn about QCI Interpret gives users the best possible chance of reaching an accurate diagnosis by providing phenotype-driven ranking that considers the detected mutations, the patient’s symptoms, and all the content in the QIAGEN Knowledge Base.
View live demonstration of unique features in QCI Interpret, which can drastically reduce the time spent on solving a case, resulting in faster turnaround time and an accurate assessment of a case.

RNA-seq data analysis and interpretation using QIAGEN CLC and QIAGEN IPA
2023-10-17 13:00 - 15:00 (America/New_York) | Virtual - Americas - EST, United States
This 120-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 and generate gene and transcript counts and QC reports displaying % mapped reads, knee plots, etc.
• Generate visualizations of results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams and others
• Easily customize RNA-seq workflows
• Export publication-quality graphics, tables and reports
• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways
Explore the types of analyses and visualizations you’ll learn to generate (slides from previous training): https://qiagen.showpad.com/share/qiZLmCUS32GZNM1B4llMf

Integrating deeply curated omics data with APIs for biomarkers and drug-target investigation
2023-10-17 09:00 - 10:00 (Europe/Paris) | Virtual - EMEA - CET
This webinar is for data scientists and bioinformaticians working in biopharma who need extensive high-quality omics data for target discovery efforts. Learn how to programmatically discover, retrieve, filter, aggregate, and analyze omics data from QIAGEN’s extensive repositories of deeply-curated multi-omics data. Attendees will learn how to leverage extensive metadata to find and combine datasets of interest, find and test signatures, and perform custom analyses to reveal patterns relevant to disease. Join us to learn how QIAGEN OmicSoft Lands API can revolutionize your data analysis workflows and help you make more informed decisions.

Exploring pan-cancer immunomodulators for biomarker discovery and validation using TCGA and public single-cell data
2023-10-12 13:00 - 14:30 (America/New_York) | Virtual - Americas - EST, United States
Cancer outcome is influenced by both the tumor microenvironment and host immune response. Using QIAGEN OmicSoft Studio to access public data from The Cancer Genome Atlas (TCGA) and our human Single Cell Lands collection, you’ll learn how to:
• View host immune response clusters across TCGA samples
• Identify differentially expressed immunomodulators across sample groups
• Visualize single-cell dimension reduction maps and overlay expression data
• Identify potential biomarkers whose expression correlates or anti-correlates with target genes
• Validate new biomarkers using custom queries and TCGA survival data

Part 1: AI-Powered Hereditary Disease Diagnostics: Closing the Gap in Clinical Exome Completeness
2023-10-12 10:00 - 12:00 UTC | Virtual Global Event (Times shown in EST)
Clinical exome sequencing (CES) is increasingly being adopted by small and mid-sized laboratories to diagnose genetic diseases, aid treatment decisions, and provide prognostic information. However, the exponential increase in genetic data generated from exome and genome panels poses significant workflow challenges. The ability to prioritize potentially pathogenic variants from large datasets and identify the few candidate variants becomes more difficult. This issue is further amplified in cases where labs must use deep phenotyping of patients and compare that to reference genotype-phenotype knowledge associated with each candidate variant. To overcome these challenges, labs are beginning to implement Artificial Intelligence (AI) in their variant analysis, interpretation and reporting workflows.
Join us for our 2023 Clinical Hereditary Disease Diagnostics Summit, a free-to-attend, two-part event exploring the opportunities and limitations of AI in hereditary disease diagnostics. Designed to help clinical diagnostic labs learn how to safely apply AI to exome and genome sequencing workflows, the content-rich event will feature invited lectures from lab directors and clinical geneticists, thought-provoking discussions on the future of hereditary disease diagnostics, as well as educational presentations on the latest databases and AI-powered software for germline secondary and tertiary analysis.
Part I: Educational talks – October 12, 2023
An education session exploring the latest databases, software, and services for germline secondary and tertiary NGS analysis. Topics will include:

How labs can achieve clinical exome completeness with AI-enriched and manually curated content
How labs can apply enhanced phenotype-driven ranking in clinical cases
How labs can safely use a “smart” approach to AI to reach the best possible chance of reaching a diagnosis

QIAGEN Biomedical Knowledge Base: Data- and analytics-driven drug discovery
2023-10-10 11:00 - 12:00 UTC | Virtual - Americas - EST, United States
Biomedical relationships knowledge is now 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.
In this one-hour training, you’ll get an introduction to QIAGEN Biomedical Knowledge Base. You’ll learn how to tackle applications you can’t achieve with the QIAGEN Ingenuity Pathway Analysis (IPA) graphical user interface, or which can be done quicker and with more flexibility when performed programmatically. You’ll learn how to perform queries such as:
• Quickly find the shortest connections between genes/proteins/metabolites of interest in the context of a specific disease
• Systematically build a network using a short list of genes/proteins/metabolites/chemicals
• Recreate a drug mechanism of action
Please note: Based on the feedback we receive from you, the registrants, we may modify the topics we cover to ensure we discuss material that’s most relevant to you.

Scale up NGS bioinformatics analysis throughput with QIAGEN CLC Genomics cloud computing
2023-10-05 11:00 - 12:00 UTC | Virtual - Americas - EST, United States
Scale your NGS analysis to match your sequencing throughput using our QIAGEN CLC Genomics cloud solution. In this webinar, you’ll learn about the flexible and powerful setup for running your NGS sequence analyses on Amazon Web Services (AWS). You’ll learn how to use QIAGEN CLC Genomics Workbench to customize workflows and send analyses to AWS Batch for execution. Together we’ll also explore analysis automation solutions, third-party dockers, audit trails and user management, all of which are available with QIAGEN CLC Genomics Server software.
Together, we’ll explore how to:
• Customize template workflows to meet your NGS analysis requirements
• Set up a QIAGEN CLC Genomics cloud environment on AWS
• Submit workflows to run on AWS and to retrieve results from these analyses.
• Use third-party dockers and automate workflow execution

Circulating Tumor Cell Detection and Analysis to Support Malignancy Designation, Tumor-of-Origin Identification, and Treatment Selection
2023-10-05 10:00 - 11:00 (America/New_York) | Virtual - Americas - EST, United States
Circulating tumor cells (CTCs) are cells that leave the primary tumor and are intravasated into the blood circulation system. A subset of those make it to other organs and are responsible for metastasis. iCellate’s CellMate platform is a CTC-based liquid biopsy for cancer cell enrichment, detection, and biomarker analysis via a simple blood draw.
In this seminar, you’ll learn:

From Helena Silva Cascales, senior scientist at iCellate Medical AB, how the isolation of whole-tumor cells provides a more comprehensive biomarker analysis, including genomic sequencing and multiplexed protein expression analysis.
From Kashyap Dave, principal scientist at iCellate Medical AB, how DNA from single CTCs can be amplified, sequenced, and analyzed to support malignancy designation and tissue of origin identification using classification analyses under development within Qiagen CLC Genomics Workbench.

Introduction to QIAGEN CLC Genomics Workbench & Getting Started
2023-10-04 11:00 - 12:00 (Asia/Kolkata) | Virtual - India, India
In this training, we will introduce you to QIAGEN CLC Genomics Workbench, including a live demo of the basic features and main functionalities.
During the training, we’ll cover:
• A general overview of the Workbench user interface
• Easy installation on Windows, Mac and Linux
• Plugin installation, e.g., Biomedical Genomics Analysis plugin
• Reference Data Management
• Working with reads from various NGS platforms
• Running individual tools and workflows
• Batch processing of data
• Data visualization using Track List/Genome Browser
• How to export of data and share workflows
• Q&A

Supercharge your AI in drug discovery with high-quality biomedical data
2023-10-03 13:00 - 14:00 (America/New_York) | Virtual - Americas - EST, United States
If you’re working in pharma or biotech, you likely rely on artificial intelligence (AI) to help you identify new drug targets or plausible biomarkers for disease within large data sets. Yet AI alone isn't enough. A large proportion of Biomedical data have errors and are unstructured. For AI models to provide reliable insights, the underlying data must be of ‘high quality’, meaning it’s accurate, comprehensive, up-to-date and standardized.
Jesper Ryge (Idorsia Pharmaceuticals), Alex Jarasch (Neo4j) and Venkatesh Moktali (QIAGEN Digital Insights) come together to showcase the practical applications of high-quality biomedical relationships data from the QIAGEN Biomedical Knowledge Base (BKB) to accelerate, improve and transform research in drug discovery and pharmaceutical development. By applying AI to a gene-disease knowledge graph, they identify promising drug targets and key mechanisms underlying diseases. A brief introduction to Neo4j shows how graph-centric analysis and visualizations facilitate the effective exploration of large knowledge graphs like BKB. This integration of high-quality curated data, AI-driven analysis and advanced visualization provides valuable insights and accelerates the progress of precision medicine.
In this webinar, you’ll learn how you can:

Build disease interactomes using protein-protein interactions
Identify high-quality drug targets using inferred causal interactions
Choose targets with the least likelihood of adverse outcomes by leveraging the depth of the data in BKB
Formulate plausible hypotheses using state-of-the-art graph visualization

Don't miss this chance to learn how to supercharge your AI toolbox to transform your drug discovery.

Supercharge your AI in drug discovery with high-quality biomedical data
2023-10-03 13:00 - 14:00 (Europe/Paris) | Virtual - EMEA - CET

Impulsionando sus análisis con el software QIAGEN IPA: Cómo nuestros clientes utilizan nuestra herramienta para complementar su investigación
2023-09-28 12:00 - 13:30 (America/Sao_Paulo) | Virtual - Argentina, Argentina
En este seminario web, usuarios de QIAGEN IPA mostrarán cómo les ha ayudado en su investigación nuestro software de análisis e interpretación de datos de expresión génica.

Los principales temas tratados serán:
• Aplicaciones de QIAGEN IPA en Biología de la Reproducción
• Aplicaciones de QIAGEN IPA en la simulación de vías de transducción dependientes de proteínas de membrana

Venga y descubra cómo QIAGEN IPA puede impulsar sus análisis.

HGMD Pro: La solution complète pour évaluer et classer les variants issus des workflows NGS héréditaires avec une seule base de données
2023-09-28 10:00 - 11:00 (Europe/Paris) | Virtual - EMEA - CET
Rejoignez-nous le 28 septembre pour découvrir comment HGMD Pro (Human Gene Mutation Database Professional) peut rationaliser vos recherches et analyses génétiques à travers diverses approches NGS. HGMD est une base de données de référence avec des mesures expertes de conservation et de contrôle de la qualité pour garantir l'exactitude et la fiabilité de ces données. Les utilisateurs gagnent du temps en éliminant le besoin de recoupement manuel des informations. Avec plus de 410 000 mutations pathogènes collectées et intégrées à partir de milliers de publications scientifiques, HGMD Pro est la source la plus complète de mutations germinales humaines disponible, organisée par des experts. HGMD est également indépendant des plateformes d’analyse secondaire utilisées, ce qui permet une intégration facile dans votre pipeline d'analyse existant.

Introduction to Phosphorylation Analyses in QIAGEN Ingenuity Pathway Analysis (IPA)
2023-09-27 11:00 - 12:00 (America/New_York) | Virtual - Americas - EST, United States
In this training, we’ll introduce how you can analyze and interpret your phosphoproteomics data in QIAGEN IPA. Using an example phosphoproteomics dataset, we will answer questions such as:
• How can I format the data before uploading it into QIAGEN IPA?
• How do I set up the analysis?
• Which upstream kinases are implicated in the observed phosphoproteomics changes?
• What are the targets of a particular upstream kinase and how do their levels of phosphorylation change over time?
• How do the levels of phosphorylation change for proteins on Canonical Pathways over time?
• Which biological predictions trend in a time-dependent manner during the time course?
• How do the biological predictions from phosphoproteomics compare with a related transcriptomics dataset?
Learn more about QIAGEN Ingenuity Pathway Analysis and sign up for a trial:
https://qiagen.showpad.com/share/RC7IWOoVJnSsEd5w9LjiA
