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X-WR-CALNAME:Bioinformatics Software | QIAGEN Digital Insights
X-ORIGINAL-URL:https://staging.digitalinsights.supremeclients.com
X-WR-CALDESC:Events for Bioinformatics Software | QIAGEN Digital Insights
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20230606
DTEND;VALUE=DATE:20230609
DTSTAMP:20260506T062108
CREATED:20230504T134649Z
LAST-MODIFIED:20241024T182859Z
UID:10000639-1686009600-1686268799@staging.digitalinsights.supremeclients.com
SUMMARY:Roman Testing Conference
DESCRIPTION: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 changed. What you learned from it. \nWe are looking to build a program offering a wide variety of inspiring talks and hands-on workshops. The conference will span over 3 days with the first two days consisting of one- and two-day workshops and training. On the third day we will have a classic multi-track setup with a variety of keynotes and talks. We will also be trying out a few exciting concepts that we will share more information about along the way.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/roman-testing-conference-jun-6-8/
LOCATION:Romania\, Cluj-Napoca\, Romania
CATEGORIES:Clinical,Event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230607T110000
DTEND;TZID=UTC:20230607T123000
DTSTAMP:20260506T062108
CREATED:20230511T112735Z
LAST-MODIFIED:20241024T182900Z
UID:10000640-1686135600-1686141000@staging.digitalinsights.supremeclients.com
SUMMARY:Unlocking the power of API-based 'omics queries
DESCRIPTION:If you're a data scientist or bioinformatician working in biopharma\, here's your chance to explore an advanced and comprehensive way to access and analyze high-quality 'omics data. The QIAGEN OmicSoft API provides a powerful and flexible platform for easy data discovery\, retrieval\, filtering\, analysis and visualization. In this webinar\, you'll learn how to leverage the OmicSoft API to access vast amounts of multi-omics data and perform custom analyses. We will also highlight the capabilities of the OmicSoft API to query across data sources to obtain a complete picture of the available 'omics data for any given disease. \nJoin us to learn how OmicSoft API can revolutionize your data analysis workflows and help you make more informed decisions for your drug and target discovery projects. \nIn this webinar\, we'll discuss how to: \n\nAvoid the pitfalls of poorly labeled data\nUse the OmicSoft API to accelerate queries and promote consistency\nPerform multi' omics data analysis to reveal patterns and prioritize hypotheses\nLeverage curated metadata\, including sample clinical data\, to structure queries\nDrive efficiency in your drug discovery and bioinformatics programs\n\nDon't miss this chance to learn how to unlock the power of API-based 'omics queries.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/unlocking-the-power-of-api-based-omics-queries-jun-7/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/faefb219-97c3-467a-b5aa-4c5f12517be6.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230608T110000
DTEND;TZID=UTC:20230608T120000
DTSTAMP:20260506T062108
CREATED:20230525T145821Z
LAST-MODIFIED:20241024T182901Z
UID:10000645-1686222000-1686225600@staging.digitalinsights.supremeclients.com
SUMMARY:Sample to Insight at LightSpeed: A barrier-breaking workflow for inherited disease NGS testing
DESCRIPTION:Get a first-hand look at QIAGEN’s new Sample to Insight Hereditary solution. By attending this webinar\, you will: \n\nLearn more about each workflow component.\nHear from experts in the field as they discuss how this technology advances the diagnosis and management of inherited diseases.\nExamine real-world case studies demonstrating the clinical utility and cost-effectiveness of the solution.\n\nIf your lab needs a fast\, cost-effective\, ultra-precise workflow for germline NGS testing\, you do not want to miss this webinar.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/sample-to-insight-at-lightspeed-a-barrier-breaking-workflow-for-inherited-disease-ngs-testing/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Clinical,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/16x9.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230608T130000
DTEND;TZID=UTC:20230608T143000
DTSTAMP:20260506T062108
CREATED:20230418T131657Z
LAST-MODIFIED:20241024T182859Z
UID:10000637-1686229200-1686234600@staging.digitalinsights.supremeclients.com
SUMMARY:Antimicrobial resistance (AMR) and multi-locus sequence typing (MLST) using QIAGEN CLC Genomics Workbench
DESCRIPTION: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).\nIn this training\, we’ll cover:\n• Introduction to AMR\, MLST and relevant databases\n• QIAGEN Microbial Insight - Antimicrobial Resistance database (QMI-AR)\n• Importing data and downloading needed databases\n• Finding resistance with nucleotide DB\, PointFinder and ShortBRED\n• Integrating AMR with MLST\n• Exporting high-resolution graphics and result tables
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/antimicrobial-resistance-amr-and-multi-locus-sequence-typing-mlst-using-qiagen-clc-genomics-workbench/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20230610
DTEND;VALUE=DATE:20230614
DTSTAMP:20260506T062108
CREATED:20230525T162924Z
LAST-MODIFIED:20241024T182903Z
UID:10000646-1686355200-1686700799@staging.digitalinsights.supremeclients.com
SUMMARY:ESHG 2023
DESCRIPTION:Learn about our Sample to Insight solutions for inherited disorders\n\n\n\n\n\nThis 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. \nLearn 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 ESHG 2023.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/eshg-2023/
LOCATION:Glasgow\, Glasgow\, Scotland\, United Kingdom
CATEGORIES:Clinical,Event
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_1305_1_QDI_QCI_Glasgow_GI519375418.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230613T130000
DTEND;TZID=UTC:20230613T143000
DTSTAMP:20260506T062108
CREATED:20230418T130426Z
LAST-MODIFIED:20241024T182857Z
UID:10000636-1686661200-1686666600@staging.digitalinsights.supremeclients.com
SUMMARY:Investigation of inflammatory conditions public data for biomarker and drug target discovery using QIAGEN OmicSoft and IPA
DESCRIPTION: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:\n• Rapidly query and identify public datasets that fit our search criteria\n• Discover and validate biomarker expression in disease tissue\, different treatments and response groups\n• Identify a list of biomarkers specific to a condition (non-responders\, disease-specific\, cell-type specific and more)\n• Confirm condition-specific biomarkers through gene expression heatmaps\n• Investigate biological mechanisms through network study \nAdditional QIAGEN Digital Insights scientists will be on the call to answer your questions and help with other inquiries\, such as how to install the software\, etc.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/investigation-of-inflammatory-conditions-public-data-for-biomarker-and-drug-target-discovery-using-qiagen-omicsoft-and-ipa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230615T130000
DTEND;TZID=UTC:20230615T143000
DTSTAMP:20260506T062108
CREATED:20230315T133249Z
LAST-MODIFIED:20241024T182845Z
UID:10000616-1686834000-1686839400@staging.digitalinsights.supremeclients.com
SUMMARY:RNA-seq data analysis and interpretation using QIAGEN CLC and QIAGEN IPA
DESCRIPTION: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). \nFor RNA-seq data\, you will learn how to:\n• Import FASTQ files\, cell matrix files and metadata and how to download references\n• Map reads to a reference genome and generate gene and transcript counts and QC reports displaying % mapped reads\, knee plots\, etc.\n• Generate visualizations of results\, such as heatmaps\, differential expression tables\, PCA/PCOA plots\, Venn diagrams and others\n• Easily customize RNA-seq workflows\n• Export publication-quality graphics\, tables and reports\n• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways \nExplore the types of analyses and visualizations you’ll learn to generate (slides from previous training): https://qiagen.showpad.com/share/qiZLmCUS32GZNM1B4llMf
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/rna-seq-data-analysis-and-interpretation-using-qiagen-clc-and-qiagen-ipa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20230620T100000
DTEND;TZID=Europe/Paris:20230620T113000
DTSTAMP:20260506T062108
CREATED:20230516T164243Z
LAST-MODIFIED:20241024T182901Z
UID:10000643-1687255200-1687260600@staging.digitalinsights.supremeclients.com
SUMMARY:Interpretieren Sie somatische Varianten einfach und schnell mit HSMD
DESCRIPTION:Verpassen Sie nicht die Gelegenheit\, das bestgehütete Geheimnis von somatischen NGS-Tests kennenzulernen.\nDie 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 und Frameshifts zu bieten\, die "klinisch beobachtet" oder aus wissenschaftlichen Publikationen kuratiert wurden.\nAm 20. Juni werden unsere Experten Ihnen in einer Demonstation die neue Datenbank vorstellen und Ihnen ihre Funktionen\, Fähigkeiten und Anwendungen vorstellen.\nIn diesem Webinar werden Sie lernen:\n• Woher HSMD seine Daten zieht\n• Wie Sie HSMD für verschiedene Anwendungen wie Forschung\, molekulare Tests und pharmazeutische Entwicklung nutzen und anwenden können\n• Wie Sie eine kostenlose\, 5-tägige Testversion von HSMD für Ihr Labor erhalten können
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/interpretieren-sie-somatische-varianten-einfach-und-schnell-mit-hsmd/
LOCATION:Virtual - Germany\, Germany
CATEGORIES:Clinical,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230620T130000
DTEND;TZID=UTC:20230620T143000
DTSTAMP:20260506T062108
CREATED:20230516T154328Z
LAST-MODIFIED:20241024T182900Z
UID:10000641-1687266000-1687271400@staging.digitalinsights.supremeclients.com
SUMMARY:QIAGEN IPA Deeper Dive: Making most out of user’s core analysis and new features
DESCRIPTION: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. \nThat’s why we’ve designed this training to focus on thesetopics and more: \n· What are the different result types produced by an IPA core analysis? \n· What are the differences between causal network vs. mechanistic network vs. regulator effects? \n· How do you predict molecular activity in IPA? What is a Z-score? \n· What is the new bubble plot feature? \n· How can I edit\, expand and modify the network the way I want it? For example\, add a disease or gene(s) of interest\, remove certain connections\, etc?
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-ipa-deeper-dive-making-most-out-of-users-core-analysis-and-new-features/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230622T110000
DTEND;TZID=UTC:20230622T123000
DTSTAMP:20260506T062108
CREATED:20230516T164935Z
LAST-MODIFIED:20241024T182901Z
UID:10000644-1687431600-1687437000@staging.digitalinsights.supremeclients.com
SUMMARY:Scale your comprehensive genomic profiling workflow with superior automated variant interpretation
DESCRIPTION: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.  \nIn this webinar\, learn about QIAGEN Clinical Insight (QCI) Interpret for Oncology\, a clinical decision support platform that has been trusted to analyze and interpret more than 3 million patient molecular profiles worldwide. Unlike other commercial solutions\, QCI Interpret for Oncology is powered by augmented molecular intelligence and offers in-software access to a team of variant scientists to assist you with rare or novel variant research\, curation\, and interpretation. The platform connects to the QIAGEN Knowledge Base—the highest quality genomic knowledge base in the industry—and dynamically computes variant classifications according to AMP/ASCO/CAP and ACMG/AMP guidelines. To help you further scale and reduce hands-on time\, QCI Interpret for Oncology provides over 410\,000 variant interpretation summaries that have all been reviewed by oncologists. This enables you to quickly build custom reports for your oncologists and their patients with the latest diagnostic and prognostic information\, as well as biomarker-directed therapy and clinical trial recommendations. \nBy attending this webinar\, you will: \nReceive a step-by-step guide of how to go from VCF to final report using QCI Interpret for Oncology\nLearn about the platform’s automated variant classification process\nLearn how QIAGEN uses augmented molecular intelligence to enhance our expert curation process\nSee first-hand how to build a custom report with an opportunity to submit your own VCF file for a sample report
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/scale-your-comprehensive-genomic-profiling-workflow-with-superior-automated-variant-interpretation/
CATEGORIES:Clinical,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230627T130000
DTEND;TZID=UTC:20230627T143000
DTSTAMP:20260506T062108
CREATED:20230516T155417Z
LAST-MODIFIED:20241024T182900Z
UID:10000642-1687870800-1687876200@staging.digitalinsights.supremeclients.com
SUMMARY:De novo assembly\, BLAST and genome finishing using QIAGEN CLC Genomics Workbench
DESCRIPTION: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. \nParticipants will learn the following: \no Download and install needed plugins.\no Import data required for the analysis.\no Run the de novo assembly workflow.\no For long reads\, improve a de novo assembly by polishing with short\, high-quality reads.\no Map reads to a reference and visualize an assembly.\no For long reads\, correct raw long reads for further analysis.\no Use BLAST to investigate the contigs.\no Analyze and assemble contigs through Genome Finishing tools.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/de-novo-assembly-blast-and-genome-finishing-using-qiagen-clc-genomics-workbench/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
END:VEVENT
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