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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;TZID=America/Halifax:20241003T130000
DTEND;TZID=America/Halifax:20241003T150000
DTSTAMP:20260610T031408
CREATED:20240919T152232Z
LAST-MODIFIED:20241024T183117Z
UID:10000803-1727960400-1727967600@staging.digitalinsights.supremeclients.com
SUMMARY:QIAGEN IPA new user training
DESCRIPTION:Are you new to QIAGEN Ingenuity Pathway Analysis (IPA) or interested in expanding your skill set? Join us as we learn more on large dataset analysis and knowledge base queries using QIAGEN IPA. \nYou’ll learn to: \n\nUpload multiple dataset types (e.g.\, RNA-seq\, proteomics\, metabolomics) and perform interactive core/pathway analysis in IPA\nLearn how to interpret different results\, including pathways\, key regulators\, impact on biological functions/diseases and more\nCompare different experimental conditions (e.g.\, single-cell clusters\, disease types) and identify similarities and contrasts\nGenerate a network for hypothesis generation\, even without a dataset or experimental design\n\nAlready have an IPA license? Install IPA and start using it now. \nLearn more about IPA or request a free trial.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-ipa-new-user-training-2/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_9978_QDI_IPA_Gi609807396_16x9_Medium-720px_50570.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20241007T140000
DTEND;TZID=UTC:20241007T153000
DTSTAMP:20260610T031408
CREATED:20240919T151918Z
LAST-MODIFIED:20241024T183115Z
UID:10000802-1728309600-1728315000@staging.digitalinsights.supremeclients.com
SUMMARY:RNA-seq data analysis and interpretation with Sankey plot update
DESCRIPTION:For RNA-seq data\, you will learn how to: \n\nImport FASTQ files\, cell matrix files and metadata and how to download references\nMap reads to a reference genome and generate gene and transcript counts and QC reports displaying % mapped reads\, knee plots\, etc.\nGenerate visualizations of results\, such as heatmaps\, differential expression tables\, PCA/PCOA plots\, Venn diagrams\, sankey plot and others\nEasily customize RNA-seq workflows\nExport publication-quality graphics\, tables and reports\nSend differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/rna-seq-data-analysis-and-interpretation-with-sankey-plot-update-3/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_9978_QDI_IPA_Gi609807396_16x9_Medium-720px_50570.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Halifax:20241008T130000
DTEND;TZID=America/Halifax:20241008T140000
DTSTAMP:20260610T031408
CREATED:20240919T151623Z
LAST-MODIFIED:20241024T183114Z
UID:10000801-1728392400-1728396000@staging.digitalinsights.supremeclients.com
SUMMARY:How to triage drug targets with curated\, causal relationships data
DESCRIPTION:In the rapidly evolving landscape of drug discovery\, the ability to integrate high-quality research findings into knowledge graphs is paramount. For over twenty years\, our scientists have curated the relationships between genes\, drugs\, diseases\, and pathways to power Ingenuity Pathway Analysis. Now\, these data are available via our QIAGEN Biomedical KB-HD\, which provides direct access to flat files\, SQL APIs in Python and R\, and the ability to export knowledge graph objects for analysis in Neo4j. In this talk\, we will explore how to use this rich data resource to: \n\naggregate relevant findings across our comprehensive disease and gene ontologies\ncross-reference clinical trial results to focus your research on genes upstream or downstream of known drug targets\nfilter causal relationships by the directionality of observed effects\ncombine the above methods to accelerate the drug discovery process\n\nBy demonstrating the underlying database live\, we will show how the high-quality curated biomedical knowledge bases can be rapidly deployed\, as well as how the underlying schema and ontologies could serve as a scaffold for integrating your own research. Overall\, this demonstration will show the critical role of knowledge graphs in finding viable drug targets while avoiding potential adverse outcomes and toxicity.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/how-to-triage-drug-targets-with-curated-causal-relationships-data/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/08/S_1212_8_QDI_QDI_BKB_Original_62142.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20241010T110000
DTEND;TZID=UTC:20241010T120000
DTSTAMP:20260610T031408
CREATED:20240930T165834Z
LAST-MODIFIED:20241024T183125Z
UID:10000813-1728558000-1728561600@staging.digitalinsights.supremeclients.com
SUMMARY:Webinar: Streamline your hereditary diseases interpretation workflow with QCI Interpret
DESCRIPTION:Learn how QCI Interpret\, clinical decision support software for variant interpretation and reporting\, can help your lab rapidly identify pathogenic variants\, improve diagnostic yields\, and significantly reduce test turnaround time for hereditary diseases. Attendees will receive a demonstration of QCI Interpret’s unique capabilities and advanced features for germline variant interpretation with example workflows for carrier screening and whole-exome sequencing panels. Key highlights will include how your lab can expedite variant interpretation by leveraging the most extensive\, manually curated knowledge base\, dynamically compute pathogenicity based on ACMG guidelines for every variant with full transparency\, and leverage QCI Interpret’s proprietary augmented molecular intelligence approach to literature curation and variant classification to streamline your interpretation workflow. \nIn this webinar\, attendees will: \n\nReceive a demonstration of QCI Interpret’s analysis and interpretation workflows for hereditary diseases using targeted and extended gene panels\, including whole-genome and whole-exome sequencing.\nLearn about QIAGEN’s proprietary expert curation process for the knowledge base in QCI Interpret.\nExplore unique time-saving features within QCI Interpret\, including phenotype-driven ranking and automation of ACMG guidelines.\nUnderstand how QCI Interpret supports copy number variant (CNV) interpretation and reporting with bibliographic coverage of over 60\,000 CNV case reports.\n\n\n\n\nSpeaker: \n\n\n\n\nElias Hage\, PhD\nAssociate Director\, Global Product Management\nQIAGEN Digital Insights\n\n\nElias Hage\, PhD\, is the Associate Director of Global Product Management for Hereditary Disease and Oncology Applications at QIAGEN Digital Insights (QDI). In this role\, he oversees the development\, management\, and optimization of QDI software\, databases and services for genomic analysis and interpretation of hereditary disease and oncology cases. Prior to joining QDI\, Dr. Hage served as a Global Product Manager at Agilent Technologies\, where he managed the Genomics division flagship SaaS application (Alissa Interpret) and supported its usage globally in both research and IVD settings. Dr. Hage obtained his Ph.D. in virology and genomics from Hannover Medical School in Belgium.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/webinar-streamline-your-hereditary-diseases-interpretation-workflow-with-qci-interpret/
LOCATION:Virtual Global Event (Times shown in EST)
CATEGORIES:Clinical,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_1327_8_QDI_QCI_Hereditary_Gi1346512014.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20241014
DTEND;VALUE=DATE:20241017
DTSTAMP:20260610T031408
CREATED:20240923T184432Z
LAST-MODIFIED:20241024T183124Z
UID:10000809-1728864000-1729123199@staging.digitalinsights.supremeclients.com
SUMMARY:QIAGEN at VEPTC 2024
DESCRIPTION:Meet QIAGEN at the Variant Effect Prediction Training Course (VEPTC)\nThis year at the 2024 Variant Effect Prediction Training Course (VEPTC)\, QIAGEN will be showcasing our industry-leading next-generation sequencing (NGS) variant analysis\, interpretation and reporting solutions. Trusted to analyze and interpret more than 4 million NGS patient test cases\, QIAGEN Clinical Insight (QCI) is the industry’s leading clinical decision support platform by volume. Find out why nobody does variant analysis and interpretation better than QIAGEN at VEPTC 2024. \nLearn more and schedule a VIP meeting with our experts at VEPTC 2024 here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-at-veptc-2024-2/
LOCATION:Palermo\, Italy
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/pexels-inmaculada-pena-567266-14213525-scaled-1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Halifax:20241016T130000
DTEND;TZID=America/Halifax:20241016T150000
DTSTAMP:20260610T031408
CREATED:20240919T151233Z
LAST-MODIFIED:20241024T183113Z
UID:10000800-1729083600-1729090800@staging.digitalinsights.supremeclients.com
SUMMARY:Gene therapy applications through knowledge graph explorations
DESCRIPTION:In gene therapy space\, there is great interest in discovering new gene editing targets as well as identifying new indications for known targets though exploration of vector biology and studying biological mechanism underlying disease pathology. In this webinar\, we will focus on how recently introduced Biomedical KB-AI can enable and accelerate such investigation. QIAGEN Biomedical KB-AI uses generative AI to identify novel relationships and patterns that may be missed by traditional methods and can provide a more comprehensive view of the biological landscape. Participants will learn about: \n\nBiomedical KB-AI and its structure\nHow to easily search and filter results for vector system of interest through subgraph\nHow to thoroughly interrogate the subgraph to look for similarity between diseases and targets that can be targeted by vectors of interest\nHow to effectively use knowledge graph for drug repurposing applications
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/gene-therapy-applications-through-knowledge-graph-explorations/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/08/S_1212_8_QDI_QDI_BKB_Original_62142.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20241016T140000
DTEND;TZID=UTC:20241016T150000
DTSTAMP:20260610T031408
CREATED:20241015T225810Z
LAST-MODIFIED:20241024T183127Z
UID:10000819-1729087200-1729090800@staging.digitalinsights.supremeclients.com
SUMMARY:Master HGMD Professional: Virtual Training Session
DESCRIPTION:Back by popular demand\, our live\, interactive HGMD Professional sessions are designed to help you master the skills needed to navigate and use the industry-leading database like an expert. Offered on two dates—October 16\, 2024\, and October 23\, 2024—these virtual training sessions will show you how to effectively leverage the extensive features and functionalities of HGMD Professional compared to its public counterpart. \nAttendees will learn how to: \n\n\n\n\n\nDistinguish clinically relevant variants from variants of unknown significance (VUS)\n\n\n\n\n\n\nCurate genes using HGMD Professional’s accurate\, up-to-date evidence\n\n\n\n\n\n\nIdentify the predominant genetic variant in a specific gene to understand the genetic mechanisms underlying associated diseases\n\n\n\n\n\n\nUse batch search vs advanced search when you need to query a large number of mutations or variants at once.\n\n\n\n  \nCan't make Session 1? Register for Session 2 on October 23 here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/master-hgmd-professional-virtual-training-session-1/
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/HGMD-2024.3-002.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Halifax:20241017T130000
DTEND;TZID=America/Halifax:20241017T143000
DTSTAMP:20260610T031408
CREATED:20240919T153150Z
LAST-MODIFIED:20241024T183118Z
UID:10000804-1729170000-1729175400@staging.digitalinsights.supremeclients.com
SUMMARY:Introducing the RNA-seq Analysis Portal in QIAGEN IPA
DESCRIPTION:Get to know the RNA-seq Analysis Portal\, a cloud-based platform you can access from within QIAGEN Ingenuity Pathway Analysis (IPA) that helps you analyze your RNA-seq expression data. Its predefined analysis pipelines let you calculate expression levels and identify differential expression and significant pathways\, regulators\, diseases and functions in just a few steps. The graphical views and interactive plots enable seamless exploration and refinement of your RNA-seq analysis results. \nIn this training you will learn how to: \n\nUpload your own expression data (example raw FASTQ files) or start with a public dataset\nPerform RNA-seq analysis and generate outputs such as heatmap\, differential expression table\, volcano plot and more\nExport graphical and tabular results\n\nLearn more about the IPA RNA-seq Analysis Portal.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/introducing-the-rna-seq-analysis-portal-in-qiagen-ipa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/CILLU_0221_LS_GG_RNA_seq_analysis.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20241023T100000
DTEND;TZID=UTC:20241023T110000
DTSTAMP:20260610T031408
CREATED:20241015T232603Z
LAST-MODIFIED:20241024T183127Z
UID:10000820-1729677600-1729681200@staging.digitalinsights.supremeclients.com
SUMMARY:Master HGMD Professional: Virtual Training Session
DESCRIPTION:Back by popular demand\, our live\, interactive HGMD Professional sessions are designed to help you master the skills needed to navigate and use the industry-leading database like an expert. This virtual training session will show you how to effectively leverage the extensive features and functionalities of HGMD Professional compared to its public counterpart. \nAttendees will learn how to: \n\n\n\n\n\nDistinguish clinically relevant variants from variants of unknown significance (VUS)\n\n\n\n\n\n\nCurate genes using HGMD Professional’s accurate\, up-to-date evidence\n\n\n\n\n\n\nIdentify the predominant genetic variant in a specific gene to understand the genetic mechanisms underlying associated diseases\nUse batch search vs advanced search when you need to query a large number of mutations or variants at once.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/master-hgmd-professional-virtual-training-session/
CATEGORIES:Clinical,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/HGMD-2024.3-002.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Halifax:20241024T130000
DTEND;TZID=America/Halifax:20241024T143000
DTSTAMP:20260610T031408
CREATED:20240919T153809Z
LAST-MODIFIED:20241024T183119Z
UID:10000805-1729774800-1729780200@staging.digitalinsights.supremeclients.com
SUMMARY:2024 update: Long reads analysis with QIAGEN CLC Genomics Workbench
DESCRIPTION:This webinar will introduce users to the long read support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench. \nParticipants will learn how to: \n\nDownload and install needed plugins\nImport data required for the analysis\nPerform long read de novo assembly\nMap reads to a reference and visualize an assembly\nUse BLAST to investigate the contigs\nUse additional long read tools: polish with short reads\, structural variant calling\nUse genome finishing tools: analyze and assemble contigs\nUse analytical tools: RNA-seq analysis for long reads\, classify long read amplicons for metagenomics
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/2024-update-long-reads-analysis-with-qiagen-clc-genomics-workbench/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_1040_8_QDI_CLC_GWBv21_Gi470306612_16x9_Large-1200px_53596-768x432-1-1-1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20241029
DTEND;VALUE=DATE:20241031
DTSTAMP:20260610T031408
CREATED:20240923T185323Z
LAST-MODIFIED:20241024T183124Z
UID:10000810-1730160000-1730332799@staging.digitalinsights.supremeclients.com
SUMMARY:QIAGEN at the Precision Medicine Forum Berlin
DESCRIPTION:Meet QIAGEN at the Precision Medicine Forum Berlin\nThis year at the 2024 Precision Medicine Forum Berlin\, QIAGEN will showcase our barrier-breaking Sample to Insight Oncology solution. Combining targeted DNA and multimodal pan-cancer panels\, one of the fastest and cheapest secondary analysis solutions in the market\, and industry-leading variant interpretation and reporting software trusted to analyze and interpret over 4 million NGS patient test cases worldwide\, our Sample to Insight Oncology solution is revolutionizing precision oncology testing. \nLearn more and register here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-at-the-precision-medicine-forum-berlin/
LOCATION:Berlin\, Germany
CATEGORIES:Clinical,Event
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1385_5_QDI_QCI_Slyline_Berlin_pexels19297608-2.jpg
END:VEVENT
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