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BEGIN:VEVENT
DTSTART;TZID=America/Halifax:20240926T130000
DTEND;TZID=America/Halifax:20240926T143000
DTSTAMP:20260403T205537
CREATED:20240814T192314Z
LAST-MODIFIED:20241024T183059Z
UID:10000794-1727355600-1727361000@staging.digitalinsights.supremeclients.com
SUMMARY:Investigating biomarkers with bulk and single-cell RNA-seq expression data
DESCRIPTION:QIAGEN Ingenuity Pathway Analysis (IPA) is designed to help you analyze and compare different types of 'omics data. In this webinar\, we’ll compare bulk RNA-seq and single-cell RNA-seq data to identify common regulators/targets and see how those regulators/targets associate with your phenotype of interest. We will also use sample-level public data to validate gene expression of common genes in tissues and/or cell type of interest. \nYou'll learn how to: \n\nGenerate a Comparison Analysis for bulk and single-cell RNA-seq\nIdentify significant common genes with the Compare feature\nBuild a custom network associating common genes to a phenotype\nExamine sample- and cell-level expression in OmicSoft content
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/compare-bulk-rnaseq-and-single-cell-rnaseq-expression-data-for-biomarkers-investigation/
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:20241003T130000
DTEND;TZID=America/Halifax:20241003T150000
DTSTAMP:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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:20260403T205537
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
BEGIN:VEVENT
DTSTART;VALUE=DATE:20241105
DTEND;VALUE=DATE:20241110
DTSTAMP:20260403T205537
CREATED:20240923T190008Z
LAST-MODIFIED:20241024T183125Z
UID:10000811-1730764800-1731196799@staging.digitalinsights.supremeclients.com
SUMMARY:QIAGEN at ASHG 2024
DESCRIPTION:Meet QIAGEN at the 2024 American Society of Human Genetics (ASHG) Annual Meeting\nThis year at the 2024 American Society of Human Genetics (ASHG) Annual Meeting\, QIAGEN will showcase our Sample to Insight solutions for human genetics and inherited disease applications. From digital PCR technologies and actionable exome panels to 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 solutions are revolutionizing genetic testing. \nLearn more and schedule a VIP meeting with our experts at ASHG 2024 here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-at-ashg-2024/
CATEGORIES:Clinical,Event
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/pexels-noelace-16108565-scaled-1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20241106T130000
DTEND;TZID=UTC:20241106T150000
DTSTAMP:20260403T205537
CREATED:20241015T172634Z
LAST-MODIFIED:20241024T183126Z
UID:10000814-1730898000-1730905200@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 how to: \n\nUpload multiple dataset types (e.g.\, RNA-seq\, proteomics\, metabolomics) and perform interactive core/pathway analysis in IPA\nInterpret 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-3/
LOCATION:Virtual - Americas - EST\, United States
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:20241107T110000
DTEND;TZID=UTC:20241107T130000
DTSTAMP:20260403T205537
CREATED:20240923T171152Z
LAST-MODIFIED:20241024T183121Z
UID:10000808-1730977200-1730984400@staging.digitalinsights.supremeclients.com
SUMMARY:Exclusive Interactive Workshop: Master Clinical Variant Interpretation with QCI Interpret for Oncology
DESCRIPTION:An exclusive hands-on workshop to try QCI Interpret for Oncology\nFor US-based labs interested in learning more about QCI Interpret for Oncology\, QIAGEN’s clinical decision support software for variant interpretation and reporting\, we are hosting an exclusive\, interactive virtual workshop where you can access and demo the software for free. Each attendee will be given a temporary license and a VCF file to run a case on the industry-leading software. Through a guided session\, you will be able to see first-hand how QCI Interpret works\, with full exploration of the software’s capabilities and features. \nIn this workshop\, you will see how QCI Interpret: \n• Dynamically computes pathogenicity and actionability based on the ACMG and AMP/ASCO/CAP guidelines for every variant in all cancer types with full transparency. \n• Provides access to over 500\,000 pre-formulated\, oncologist-reviewed variant interpretation summaries to build customizable\, oncologist-ready reports. \n• Effortlessly streamlines case reviews by automatically selecting reportable variants\, along with tailored treatments and trials. \nOnly 40 spots available. Must apply by October 25\, 2024. \nThis workshop is an exclusive event limited to a select number of participants. To register\, you must provide a work email and be selected by QIAGEN to attend. The workshop will be hosted on a US server and no customer data will be involved. \nLearn more and register here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/exclusive-interactive-workshop-master-clinical-variant-interpretation-with-qci-interpret-for-oncology/
CATEGORIES:Clinical,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_5731_NGS_QCI_s-1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Dubai:20241107T130000
DTEND;TZID=Asia/Dubai:20241107T143000
DTSTAMP:20260403T205537
CREATED:20241015T174009Z
LAST-MODIFIED:20241024T183126Z
UID:10000815-1730984400-1730989800@staging.digitalinsights.supremeclients.com
SUMMARY:Support Session for IPA Certification
DESCRIPTION:Join us for a 90-minute LIVE group session designed to address different technical questions regarding IPA certification. QIAGEN IPA scientists will answer different IPA related technical questions and clarify various topics per requests of IPA certification participants. If possible\, please register for this session and let us know your questions by November 4\, 2024. \nPlease note: \n\nWe strongly encourage you to submit your questions ahead of time through this registration form.\nWhile questions submitted through this registration ahead of time will be prioritized\, we will try to answer as many questions as possible in these 90 min.\nThe purpose of this session is NOT for QIAGEN scientist to answer IPA certification exam questions but rather explain concepts surrounding these questions. Example\, for exam question asking how many molecules are mapped vs unmapped in the exam dataset\, the QIAGEN scientist will not give you the number but if asked\, will go over relevant steps of the data upload process.\nOnly those who signed up for IPA certification are invited to this session.\n\nQuestions we have so far: \n\nExplain course structure and exam related details.\nGo over recent update (RNA-seq analysis portal\, new pathways\, GWAS etc.) and cover this in context of this course.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/support-session-for-ipa-certification/
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:20241112T130000
DTEND;TZID=America/Halifax:20241112T143000
DTSTAMP:20260403T205537
CREATED:20240919T155400Z
LAST-MODIFIED:20241024T183120Z
UID:10000806-1731416400-1731421800@staging.digitalinsights.supremeclients.com
SUMMARY:Discover biomarkers\, validate targets and identify variants with QDI software
DESCRIPTION:Learn how to leverage solutions from QIAGEN Digital Insights to discover biomarkers\, validate targets\, and identify variants. \nAttendees will learn to: \n\nLocate public studies of interest using OmicSoft DiseaseLand\nInvestigate expression of genes of interest across different treatments\, disease states\, etc.\nIdentify variants of interest for candidate biomarkers and targets using Human Gene Mutation Database (HGMD)\nLeverage the QIAGEN Knowledgebase in Ingenuity Pathway Analysis (IPA) to explore and extend findings from OmicSoft DiseaseLand and HGMD\nAccess data from OmicSoft\, HGMD and IPA in ways that are helpful for data scientists
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/discover-biomarkers-validate-targets-and-identify-variants-with-qdi-software/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_1188_7_QDI_QDI_OmicSoft.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20241113T100000
DTEND;TZID=America/New_York:20241113T110000
DTSTAMP:20260403T205537
CREATED:20241023T175035Z
LAST-MODIFIED:20241024T183129Z
UID:10000821-1731492000-1731495600@staging.digitalinsights.supremeclients.com
SUMMARY:Webinar: Pharmacogenomics - One tool to decode drug response to variation in the genome
DESCRIPTION:Each year\, more than 134 million patients experience adverse drug events\, causing 2.4 million deaths worldwide. What if there was a better way to develop and prescribe safer\, more effective drugs based on the unique genetic information of every individual? \nIn this webinar\, learn about a game-changing solution for labs and pharmaceutical companies to rapidly and confidently translate complex pharmacogenomics (PGx) data into evidence-backed insights to inform therapeutic outcomes. QIAGEN Pharmacogenomic Insights (PGXI) is a new expert-curated knowledgebase solution that provides comprehensive access to verified and up-to-date data from multiple PGx sources\, including the FDA\, CPIC\, DPWG\, PharmVar\, and PubMed. Built upon a legacy platform used to deliver more than 1.6 million PGx annotations for more than 250 clinical research laboratories\, PGXI seamlessly integrates into existing or new workflows to automate the annotation of PGx data from all platforms\, including NGS and arrays. Within minutes\, users can retrieve a custom output of relevant information\, including relevant conditions associated with queried genes of interest\, relevant drug-gene associations\, and curated literature evidence for alleles in question. \nIn this webinar\, you will learn: \n\nHow PGXI can help your lab efficiently and consistently identify medications associated with adverse effects.\nWhat expert-curated content sources are available in PGXI\, eliminating the need to consult multiple databases and saving you significant time and money.\nHow to use PGXI to seamlessly scale your PGXI workflow and stay at the cutting edge of PGx research.\n\nPlus\, if eligible\, webinar attendees can try PGXI for free with an exclusive trial offer from QIAGEN. There’s an easier and faster way to translate PGx data into insights. Don’t miss this opportunity to elevate and transform your PGx program. \nLearn more and register here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/webinar-a-game-changer-for-pharmacogenomics-one-tool-to-decode-drug-response-to-variation-in-the-genome/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1419_4_QDI_QCI_PGXI_Launch.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Halifax:20241114T130000
DTEND;TZID=America/Halifax:20241114T143000
DTSTAMP:20260403T205537
CREATED:20240919T162936Z
LAST-MODIFIED:20241024T183120Z
UID:10000807-1731589200-1731594600@staging.digitalinsights.supremeclients.com
SUMMARY:Checkpoint inhibitor and immuno-oncology investigation leveraging curated high-quality public ‘omics data
DESCRIPTION:While there is great interest in the scientific community to investigate drug targets and biomarkers from public immune-oncology data\, such investigation is hindered by the difficulty in finding and combining related datasets to perform large-scale meta-analyses. This webinar will focus on how high-quality curated genomic repositories such as QIAGEN OmicSoft Lands immediately allows in-depth investigations across diverse data sources (GEO\, CPTAC\, TCGA\, GTEx and more) to discover and validate candidate checkpoint inhibitor drug targets and biomarkers. \nYou will learn how to do the following in the graphical user interface and through APIs: \n\nEasily identify relevant samples using extensive manually curated clinical metadata\nVisualize and identify checkpoint inhibition biology-related drug target and biomarkers expression patterns using expression data (RNA-seq\, scRNA-seq\, proteomics etc.)\nReveal how the expression of a group of biomarkers (or genes/proteins of interest) correlates in normal and disease tissue
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/checkpoint-inhibitor-and-immuno-oncology-investigation-leveraging-curated-high-quality-public-omics-data/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1063_9_OmicSoft-Single-Cell-Lands_028687_16x9-1-1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20241119T080000
DTEND;TZID=UTC:20241123T170000
DTSTAMP:20260403T205537
CREATED:20240923T190720Z
LAST-MODIFIED:20241024T183125Z
UID:10000812-1732003200-1732381200@staging.digitalinsights.supremeclients.com
SUMMARY:QIAGEN at AMP 2024
DESCRIPTION:Meet QIAGEN at the 2024 Association for Molecular Pathology (AMP) Annual Meeting\nThis year at the 2024 Association for Molecular Pathology (AMP) Annual Meeting\, 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. \nLean more and schedule a VIP meeting with our experts at AMP 2024 here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-at-amp-2024/
CATEGORIES:Clinical,Event
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1385_7_QDI_QCI_Skyline_Vancouver_pexels2416602.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Dubai:20241119T130000
DTEND;TZID=Asia/Dubai:20241119T143000
DTSTAMP:20260403T205537
CREATED:20241015T174847Z
LAST-MODIFIED:20241024T183126Z
UID:10000816-1732021200-1732026600@staging.digitalinsights.supremeclients.com
SUMMARY:Investigating genomic variants using QIAGEN CLC Genomics Workbench\, QCI Interpret-Translational (QCII-T)\, and Ingenuity Pathway Analysis (IPA)
DESCRIPTION:Discovery of new genes implicated in hereditary diseases or cancer progression is challenging and advancing rapidly with an increase in the amount of cohort data to analyze from next generation sequencing (NGS) data to associations between gene variants and diseases\, and finally to biological mechanisms of these gene variants. Combining QIAGEN CLC Genomics Workbench\, QCII-T\, and IPA\, scientists can analyze sequencing data obtained from a variety of NGS technologies\, annotate gene variants using the world’s most comprehensive and up-to-date curated scientific evidence\, and find biological connections in gene variants with manually curated scientific findings. Get valuable and reliable insights for your research project and speed up your discoveries by using a streamlined NGS analysis workflow. \nIn this webinar\, attendees will have the opportunity to: \n\nLearn how to import whole genome or exome sequencing data into QIAGEN CLC Genomics Workbench and use the ultra-fast LightSpeed Module that delivers end-to-end NGS FASTQ to VCF pipeline;\nExplore capabilities in QCII-T which can enable scientists to accelerate discoveries from hereditary or tumor cohort analyses to find associations between gene variants and diseases;\nLearn how to use IPA and its manually curated content among other integrated scientific evidence to uncover novel biological mechanisms underlying these gene variants.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/investigating-genomic-variants-using-qiagen-clc-genomics-workbench-qci-interpret-translational-qcii-t-and-ingenuity-pathway-analysis-ipa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Event
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=Asia/Dubai:20241120T130000
DTEND;TZID=Asia/Dubai:20241120T140000
DTSTAMP:20260403T205537
CREATED:20241015T175057Z
LAST-MODIFIED:20241023T210126Z
UID:10000817-1732107600-1732111200@staging.digitalinsights.supremeclients.com
SUMMARY:New feature: Insights with IPA Interpret
DESCRIPTION:Unlock actionable insights in your biological data by streamlining your data interpretation with IPA Interpret. \nThe newest feature of your trusted pathway analysis software\, QIAGEN IPA\, includes: \n\nContent powered by IPA's extensive\, manually curated knowledge base and aided by AI\nEasy-to-share reports and updated visualizations to facilitate collaboration and dissemination of research findings\nEasy access from your favorite web browser\, no additional software or hardware needed
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/new-feature-insights-with-ipa-interpret/
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=Asia/Dubai:20241121T130000
DTEND;TZID=Asia/Dubai:20241121T140000
DTSTAMP:20260403T205537
CREATED:20241015T175251Z
LAST-MODIFIED:20241023T210055Z
UID:10000818-1732194000-1732197600@staging.digitalinsights.supremeclients.com
SUMMARY:New feature: Navigating datasets with OmicSoft Explorer
DESCRIPTION:Meet OmicSoft Explorer\, a new feature included with your QIAGEN IPA/OmicSoft subscriptions. See how you can find ‘omics datasets to inform your next experiments or support your grant proposals. \nWith OmicSoft Explorer\, you can: \n\nSearch over 10\,000 disease-relevant datasets for clinical\, in vitro\, normal tissue and more\nReveal top differentially expressed genes from over 200\,000 experiments\nDiscover experiments that include your gene of interest\nExplore underlying biology through IPA Interpret
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/new-feature-navigating-datasets-with-omicsoft-explorer/
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/New_York:20250107T130000
DTEND;TZID=America/New_York:20250107T150000
DTSTAMP:20260403T205537
CREATED:20241218T221447Z
LAST-MODIFIED:20241218T221447Z
UID:10000822-1736254800-1736262000@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. \nRegister for the event.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-ipa-new-user-training-5/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
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/New_York:20250109T130000
DTEND;TZID=America/New_York:20250109T143000
DTSTAMP:20260403T205537
CREATED:20241218T221811Z
LAST-MODIFIED:20241218T222329Z
UID:10000823-1736427600-1736433000@staging.digitalinsights.supremeclients.com
SUMMARY:Support Session for IPA Certification
DESCRIPTION:Join us for a 90-minute LIVE group session designed to address different technical questions regarding IPA certification. QIAGEN IPA scientists will answer different IPA related technical questions and clarify various topics per requests of IPA certification participants.\n \nPlease note: \n\nWe strongly encourage you to submit your questions ahead of time through this registration form.\nWhile questions submitted through this registration ahead of time will be prioritized\, we will try to answer as many questions as possible in these 90 min.\nThe purpose of this session is NOT for QIAGEN scientist to answer IPA certification exam questions but rather explain concepts surrounding these questions. For example\, if you ask how many molecules are mapped vs unmapped in the exam dataset\, the QIAGEN scientist will go over relevant steps of the data upload process rather than give you the number directly.\nOnly those who signed up for IPA certification are invited to this session.\nQuestions we have so far:\n\nExplain course structure and exam related details.\n\n\nGo over recent update (RNA-seq analysis portal\, new pathways\, GWAS etc.) and cover this in context of this course.\n\nRegister for the event.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/support-session-for-ipa-certification-3/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
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/New_York:20250114T130000
DTEND;TZID=America/New_York:20250114T143000
DTSTAMP:20260403T205537
CREATED:20241218T222028Z
LAST-MODIFIED:20241218T222323Z
UID:10000824-1736859600-1736865000@staging.digitalinsights.supremeclients.com
SUMMARY:Sanger sequencing\, alignment\, cloning\, primer design and more using QIAGEN CLC Main and Genomics Workbench
DESCRIPTION:This training will be relevant to both QIAGEN Main and Genomics workbench users and prospects who are interested in below analytics. \n\nAlignment and tree construction\nSanger sequencing analysis\nCloning and primer design\nOther molecular biology tools\n\nRegister for the event.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/sanger-sequencing-alignment-cloning-primer-design-and-more-using-qiagen-clc-main-and-genomics-workbench/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
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/New_York:20250116T130000
DTEND;TZID=America/New_York:20250116T143000
DTSTAMP:20260403T205537
CREATED:20241218T222418Z
LAST-MODIFIED:20241218T222550Z
UID:10000825-1737032400-1737037800@staging.digitalinsights.supremeclients.com
SUMMARY:Discoveries from deeply curated TCGA expression data using OmicSoft Studio
DESCRIPTION:While there is great interest in the scientific community to investigate drug targets and biomarkers from public immune-oncology data sources such as The Cancer Genome Atlas (TCGA)\, such investigation is hindered by difficulties in finding and combining related datasets to perform large-scale meta-analyses. This webinar will focus on how high-quality curated genomic repositories such as QIAGEN OmicSoft Lands immediately allows in-depth investigations across diverse data sources (GEO\, CPTAC\, TCGA\, GTEx and more) to discover and validate candidate checkpoint inhibitor drug targets and biomarkers. \nYou will discover how to: \n\nUse sample IDs to create a custom dataset from the deeply curated TCGA collection available within OmicSoft Lands\nEasily download count information for each sample across all genes and create a local or server project\nCalculate differential expression using metadata of interest\nGenerate volcano\, PCA/PCOA\, heatmap\, expression and other plots for scientific discoveries\nUpload the data to Ingenuity Pathway Analysis for hypothesis generation\n\nRegister for the event.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/discoveries-from-deeply-curated-tcga-expression-data-using-omicsoft-studio/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1212_8_QDI_QDI_BKB_Original_62142.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250120T140000
DTEND;TZID=America/New_York:20250120T153000
DTSTAMP:20260403T205537
CREATED:20241218T222750Z
LAST-MODIFIED:20241218T222750Z
UID:10000826-1737381600-1737387000@staging.digitalinsights.supremeclients.com
SUMMARY:Single-cell RNA-seq\, cell hashing and spatial transcriptomics
DESCRIPTION:In this training\, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files. \nUsing CLC Genomics Workbench\, you will learn how to perform secondary analysis on your single cell RNA-seq data. Specifically\, you will learn how to: \n\nImport your raw FASTQ or processed cell-matrix files.\nUse pre-configured but customizable pipelines/workflows for single cell RNA-seq data.\nGenerate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries\, including dimension reduction (UMAP\, t-SNE) plots\, differential expression table for clusters\, cell types or both\, heat maps\, dot plots and violin plots.\nLearn how to use “Create Cell Annotations from Hashtags” for cell hashing (i.e.\, CITE-seq).\nDive into spatial transcriptomic analysis\, the latest feature in the single cell RNA-seq module.\n\nRegister for the event.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/single-cell-rna-seq-cell-hashing-and-spatial-transcriptomics-4/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
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/New_York:20250121T130000
DTEND;TZID=America/New_York:20250121T140000
DTSTAMP:20260403T205537
CREATED:20241218T222943Z
LAST-MODIFIED:20241218T222943Z
UID:10000827-1737464400-1737468000@staging.digitalinsights.supremeclients.com
SUMMARY:Identifying critical drug-to-disease pathways using high-quality curated literature and ‘omics data
DESCRIPTION:In the drug discovery pipeline\, evaluating multiple pathways between a drug target and disease is crucial for identifying potential therapeutic approaches. By examining overlapping pathways between competing drugs\, researchers can uncover novel drug targets\, while isoform-specific findings may elucidate unexpected clinical trial outcomes. Filtering these pathways with real-world expression and proteomics data is essential to validate new hypotheses and avoid pursuing non-viable leads. \nLeveraging tools such as Neo4j\, Python\, and R\, powered by curated databases like the QIAGEN Biomedical Knowledge Base and OmicSoft Lands\, enables scientists to efficiently explore potential mechanisms of action during both target discovery and later stages of drug development. \nAttendees will learn to: \n\nApply pathfinding algorithms to navigate our comprehensive knowledge graph.\nQualify drug candidates using curated scRNA-Seq expression data and detailed cell type annotations.\nExpand\, filter\, prioritize\, and refine lists of biomarkers and drug targets through various advanced approaches.\n\nRegister for the event.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/identifying-critical-drug-to-disease-pathways-using-high-quality-curated-literature-and-omics-data/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1212_8_QDI_QDI_BKB_Original_62142.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250123T130000
DTEND;TZID=America/New_York:20250123T140000
DTSTAMP:20260403T205537
CREATED:20241218T223130Z
LAST-MODIFIED:20241218T223130Z
UID:10000828-1737637200-1737640800@staging.digitalinsights.supremeclients.com
SUMMARY:Tissue-specific target identification using QIAGEN OmicSoft high-quality ‘omics data
DESCRIPTION:Disease pathogenesis is often context-dependent\, specifically on tissue expression profiles within a given disease context. However\, tissue expression profile of drug targets or potential targets is often difficult to ascertain. In this webinar\, we will dive deep into the wealth of available deeply curated high quality ‘omics data (RNA-seq\, scRNA-seq and more) in the OmicSoft Lands database using APIs to achieve the following: \n\nDemonstrate how to obtain a disease gene signature of interest.\nCompare the constitutive expression profile of that gene set across different tissues.\nFind tissues with similar expression profiles.\nGenerate a hypothesis relating two tissue specific diseases to each other for the purpose of indication expansion.\n\nRegister for the event.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/tissue-specific-target-identification-using-qiagen-omicsoft-high-quality-omics-data/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1212_8_QDI_QDI_BKB_Original_62142.jpg
END:VEVENT
END:VCALENDAR