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X-WR-CALDESC:Events for Bioinformatics Software | QIAGEN Digital Insights
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DTSTART;TZID=America/New_York:20230404T130000
DTEND;TZID=America/New_York:20230404T143000
DTSTAMP:20260503T184351
CREATED:20230307T180301Z
LAST-MODIFIED:20241024T182844Z
UID:10000613-1680613200-1680618600@staging.digitalinsights.supremeclients.com
SUMMARY:New user training: Large dataset analysis and knowledge base queries using QIAGEN Ingenuity Pathway Analysis (IPA)
DESCRIPTION:Join us for a 90-minute training session for new users of QIAGEN IPA. \nIn this training\, you’ll learn how to:\n• Upload your dataset (RNA-seq\, scRNA-seq\, proteomics\, metabolomics and more) and perform interactive core/pathway analysis in IPA\n• Understand the different result types produced (pathways\, key regulators\, impact on biological functions/diseases and more)\n• Compare different experimental conditions (treatments\, time points\, single-cell clusters\, disease types and more) and identify similarities and contrasts\n• Generate a network even without a dataset or experimental design for hypothesis generation \nFor those with IPA license\,\nTo install IPA before or after this training\, please use below installer.\nhttps://qiagen.showpad.com/share/CBv30blCPKFDUYHRWtAvI
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/new-user-training-large-dataset-analysis-and-knowledge-base-queries-using-qiagen-ingenuity-pathway-analysis-ipa-2/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230405T110000
DTEND;TZID=UTC:20230405T120000
DTSTAMP:20260503T184351
CREATED:20230329T120420Z
LAST-MODIFIED:20241024T182849Z
UID:10000623-1680692400-1680696000@staging.digitalinsights.supremeclients.com
SUMMARY:Can you trust AI for germline variant curation? A Stanford University case study
DESCRIPTION:In this webinar\, we examine a new study by Stanford University that analyzes the accuracy\, consistency\, and comprehensiveness of automated and manual germline variant curation. The study compares the quality of data from Stanford’s Automatic VAriant evidence DAtabase (AVADA) to the Human Gene Mutation Database (HGMD)\, an expert-curated resource for human inherited disease mutations. \nBy attending this webinar\, you will: \n\nAnalyze a series of use-cases comparing the performance of AI-driven variant curation to manual approaches\nReceive a virtual demonstration of how HGMD presents mutation data\, including how the database provides genomic coordinates\, Human Genome Variation Society (HGVS) nomenclatures for variants\, citations from key publications\, and where a variant is described in a paper or supplemental text\nLearn how HGMD simplifies literature review and supports CNV interpretation\nReceive a complimentary 5-day trial of HGMD Professional
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/can-you-trust-ai-for-germline-variant-curation-a-stanford-university-case-study/
CATEGORIES:Clinical,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230411T130000
DTEND;TZID=UTC:20230411T143000
DTSTAMP:20260503T184351
CREATED:20230315T133702Z
LAST-MODIFIED:20241024T182846Z
UID:10000617-1681218000-1681223400@staging.digitalinsights.supremeclients.com
SUMMARY:Pathogen detection in wastewater samples using QIAGEN CLC Genomics Workbench
DESCRIPTION:In this 90-minute training\, you will learn how to easily analyze wastewater samples to detect pathogens (SARS-COV2\, etc.) using QIAGEN CLC Genomics Workbench software. \nYou will learn how to:\n• Importing reads\n• Open and modify prebuilt workflow (analysis pipeline)\n• Install and execute workflow\n• Review QC reports\n• Perform genome visualization\n• Export the consensus sequence in FASTA format to upload to Pangolin\n• Create a SNP tree of the consensus sequence and overlay Pangolin information\n• Export graphical and tabular results
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/pathogen-detection-in-wastewater-samples-using-qiagen-clc-genomics-workbench/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230413T110000
DTEND;TZID=UTC:20230413T120000
DTSTAMP:20260503T184351
CREATED:20230329T120940Z
LAST-MODIFIED:20241024T182850Z
UID:10000624-1681383600-1681387200@staging.digitalinsights.supremeclients.com
SUMMARY:Take your genome research to the next level with QCI Interpret Translational
DESCRIPTION:Learn how QCI Interpret Translational can get your research to the next level by providing you all the necessary analysis tools with the world’s most comprehensive and up-to-date curated scientific evidence. Get valuable and reliable insights for your research project and speed up your discoveries by using a streamlined NGS analysis workflow in a user-friendly interface without needing bioinformatics expertise. \nIn this webinar\, attendees will have the opportunity to: \n\nExplore capabilities which can enable them to accelerate discoveries from hereditary or tumor cohort analyses\nDiscover interactive tools with current and comprehensive associations between gene variants and diseases\nLearn how these resources are supported by unique curated content among other integrated scientific evidence
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/take-your-genome-research-to-the-next-level-with-qci-interpret-translational/
CATEGORIES:Clinical,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230413T130000
DTEND;TZID=UTC:20230413T143000
DTSTAMP:20260503T184351
CREATED:20230315T134055Z
LAST-MODIFIED:20241024T182848Z
UID:10000618-1681390800-1681396200@staging.digitalinsights.supremeclients.com
SUMMARY:Make discoveries from public data (GEO\, SRA and more) using QIAGEN Ingenuity Pathway Analysis
DESCRIPTION:You asked for it\, and we’re here to deliver. We are hosting a comprehensive training on effectively using sample-level public data and metadata from sources like GEO\, SRA\, TCGA\, GTEx\, Blueprint\, CCLE and others through QIAGEN Ingenuity Pathway Analysis (IPA) and the IPA Analysis Match Explorer feature. We’ll walk you through use cases involving biomarker discovery\, drug target investigation\, studying survival in custom patient cohorts\, multi-gene correlation and more. \nWe’ll cover topics like:\n• How is a gene of interest expressed across different conditions?(‘conditions’ refers to diseases\, disease subtypes\, treatments\, cell types\, cell lines and more)\n• Is there a correlation in expression for two genes or biomarkers of user interest for a given condition?\n• Can we compare more than two genes in a heatmap?\n• For a given condition of interest\, can we derive a list of genes (for example\, genes specific to a disease\, treatment or cell type)?\n• Can we generate custom cohorts of patients (for example\, TP53 wt vs. mutant or PDCD1 high vs. low expression) and then create survival curves representing those cohorts? Can we generate a p-value to see if there is a significant difference?\n• Can we detect the expression of a gene in different cell types from single-cell data?
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/make-discoveries-from-public-data-geo-sra-and-more-using-qiagen-ingenuity-pathway-analysis/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230418T130000
DTEND;TZID=UTC:20230418T143000
DTSTAMP:20260503T184351
CREATED:20230315T134308Z
LAST-MODIFIED:20241024T182848Z
UID:10000619-1681822800-1681828200@staging.digitalinsights.supremeclients.com
SUMMARY:Public single-cell RNA-seq data investigation using QIAGEN OmicSoft and Ingenuity Pathway Analysis
DESCRIPTION:Single-cell RNA-sequencing (scRNA-seq) is widely used to investigate tissue heterogeneity\, identify novel cell types\, study pathogenic mechanisms\, develop targeted therapy (including immunotherapy) and more. Accordingly\, a tremendous amount of scRNA-seq data has been deposited to public domains like GEO. \nIn this training\, you will learn how to \n· Locate public single-cell studies of interest using QIAGEN Omicsoft Single Cell Lands \n· Study different cell types by dimension reduction plots (for example\, t-SNE\, UMAP) \n· Investigate expression of genes of interest across different cell types (Violin plots\, overlay expression on cluster) \n· Identify key pathways and regulators from scRNA-seq data using QIAGEN Ingenuity Pathway Analysis (IPA)
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/public-single-cell-rna-seq-data-investigation-using-qiagen-omicsoft-and-ingenuity-pathway-analysis/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230419T110000
DTEND;TZID=UTC:20230419T120000
DTSTAMP:20260503T184351
CREATED:20230317T121304Z
LAST-MODIFIED:20241024T182849Z
UID:10000622-1681902000-1681905600@staging.digitalinsights.supremeclients.com
SUMMARY:Shed light on inherited mutations and solve hereditary investigations with QCI Interpret
DESCRIPTION:In this webinar\, we will demonstrate how QCI Interpret can improve your diagnostic yield for hereditary disorders. QCI Interpret is a clinical decision support platform that leverages augmented molecular intelligence to streamline the interpretation workflow. It uses the most extensive\, globally trusted and manually curated molecular knowledge and bibliography evidence to provide you with the best possible opportunity to solve every case. By demonstrating the different features and series of use-cases\, we will show you how QCI Interpret guarantees a comprehensive and thorough investigation of every case for all types of genetic variation\, including copy number variants (CNVs). This will allow you to provide precise answers to patients and their families\, while also reducing test turnaround time from hours to minutes. \nLearning objectives: \n\nLearn about QCI Interpret’s analysis and interpretation workflow for hereditary diseases using targeted and extended gene panels\, including WES/WGS\nLearn about QCI Interpret and QIAGEN’s expert curation process based on the latest ACMG carrier screening guidelines\nView demonstrations of unique features in QCI Interpret\, including how to input symptoms relevant to a case and receive relationships to candidate diseases and mutated genes using the Phenotype Network Analysis feature and triage mode of variant assessment.\nLearn how QCI Interpret supports CNV interpretation and reporting with bibliographic coverage of over 60\,000 CNV case reports"
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/shed-light-on-inherited-mutations-and-solve-hereditary-investigations-with-qci-interpret/
CATEGORIES:Clinical,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/WEBINAR_QCI_RockReleaseWebinar_0323_16x9.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230425T130000
DTEND;TZID=UTC:20230425T143000
DTSTAMP:20260503T184351
CREATED:20230315T134937Z
LAST-MODIFIED:20241024T182848Z
UID:10000620-1682427600-1682433000@staging.digitalinsights.supremeclients.com
SUMMARY:Proteomics and phosphoproteomics data interpretation using QIAGEN Ingenuity Pathway Analysis
DESCRIPTION:In this live QIAGEN Ingenuity Pathway Analysis (IPA) training\, we’ll focus on interpreting proteomics and phosphoproteomics datasets. \nIn this tutorial\, we’ll guide you through steps and workflows to address your questions related to interpreting proteomics and phosphoproteomics datasets using QIAGEN IPA\, such as:\n• How should I format the data before uploading to IPA?\n• How do I set up the analysis?\n• Which upstream kinases are implicated in the observed phosphoproteomics changes?\n• What are the targets of a particular upstream kinase and how do their levels of phosphorylation change over the time course?\n• What are the targets on a particular Canonical Pathway and how do their levels of phosphorylation change over time?\n• Which biological predictions trend in a time-dependent manner during the time course?\n• How do the biological predictions from phosphoproteomics compare with a related transcriptomics dataset? \nAdditional QIAGEN Digital Insights (QDI) scientists will be on the call to answer questions and help with other inquiries\, such as how to install the software\, etc. \nFor those with a QIAGEN IPA license\n• To install IPA before or after the training\, please use the below installer.\nhttps://qiagen.showpad.com/share/CBv30blCPKFDUYHRWtAvI\n• If you haven’t done core analysis in IPA before\, we recommend you review below video/slides before the training (however\, this is not required).\no IPA beginner training recording: https://qiagen.showpad.com/share/t2cGMdF3NjVucBA0b9tIT \no IPA step-by-step guide w/ data format (slide 9) and upload (slide 28) instructions: https://qiagen.showpad.com/share/VjizSLJVBw1qfV
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/proteomics-and-phosphoproteomics-data-interpretation-using-qiagen-ingenuity-pathway-analysis/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230427T100000
DTEND;TZID=UTC:20230427T120000
DTSTAMP:20260503T184351
CREATED:20230329T121854Z
LAST-MODIFIED:20241024T182850Z
UID:10000625-1682589600-1682596800@staging.digitalinsights.supremeclients.com
SUMMARY:How to improve your existing pipeline for somatic mutation analysis\, interpretation and reporting: Part 1
DESCRIPTION:We are excited to bring thought leaders\, NGS experts\, lab directors\, variant scientists\, clinicians\, and oncologists under one virtual roof at our second annual Clinical Oncology Summit hosted on April 27 and May 18\, 2023. \nThe two-part\, content-rich event will feature invited lectures from lab directors and clinical geneticists\, thought-provoking discussions on the future of comprehensive genomic profiling\, and educational presentations on the latest databases\, software\, and services for somatic secondary and tertiary analysis. Designed to help clinical diagnostic labs understand how they can optimize their current pipelines for somatic NGS analysis\, interpretation and reporting\, the Clinical Oncology Summit is a must-attend event for labs who need to reduce turnaround time\, improve operational costs\, and scale for higher throughput. \nMeet the speakers and view the full agenda here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/how-to-improve-your-existing-pipeline-for-somatic-mutation-analysis-interpretation-and-reporting-part-1/
CATEGORIES:Clinical,Event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230427T130000
DTEND;TZID=UTC:20230427T143000
DTSTAMP:20260503T184351
CREATED:20230316T151730Z
LAST-MODIFIED:20241024T182849Z
UID:10000621-1682600400-1682605800@staging.digitalinsights.supremeclients.com
SUMMARY:QIAGEN Ingenuity Pathway Analysis (IPA) for grant writing and publications with new features
DESCRIPTION:QIAGEN Ingenuity Pathway Analysis (IPA) represents a robust resource to aid in the process of writing grants publications. Driven by a wealth of manually-curated molecular interactions and associations in the QIAGEN Knowledge Base together with pre-analyzed public ‘omics data for hundreds of thousands of samples from QIAGEN OmicSoft Lands\, IPA provides biological insights regardless of whether you have your own data or not. In the absence of your own data\, IPA provides a resource to query existing molecular knowledge from the literature or public ‘omics data\, build networks in silico\, and review results from pre-analyzed public studies. With data\, you can dig deeply into the biological meaning of your results through the identification of key pathways\, regulatory molecules and functional changes as well as understand how your study relates to other published studies. \nJoin us for a 90-min training session where you will learn: \n• Ways to query IPA’s vast collection of curated literature and ‘omics data\n• How molecules relate to phenotypes and functions\n• Build your own networks and predict activity changes\n• Ways to explore a library of over 100\,000 precomputed IPA analyses pulled from public ‘omics data\n• How to format your dataset and set up an analysis\n• How to deeply interrogate key Canonical Pathway\n• How to predict regulators which are causing your expression changes\n• How to contextualize the result of your analysis by comparing your results to internal and public data\n• Ways to generate the necessary tables and figures for your manuscript
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-ingenuity-pathway-analysis-ipa-for-grant-writing-and-publications-with-new-features/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
END:VCALENDAR