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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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DTSTART:20220101T000000
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BEGIN:VEVENT
DTSTART;TZID=UTC:20230711T110000
DTEND;TZID=UTC:20230711T123000
DTSTAMP:20260504T160417
CREATED:20230619T140741Z
LAST-MODIFIED:20241024T182917Z
UID:10000652-1689073200-1689078600@staging.digitalinsights.supremeclients.com
SUMMARY:Insights into cancer genomics via COSMIC v98
DESCRIPTION:Our understanding of cancer mechanisms\, genetics and complexities continues to expand rapidly. Without a streamlined\, standardized and easy to understand organizational system to keep track of this plethora of knowledge\, potentially crucial data can effectively be lost. Trusted by scientists for nearly 20 years\, COSMIC is the world’s largest\, most comprehensive\, expert-curated resource for exploring the impact of somatic mutations in human cancers.\n\nJoin Leonie Hodges\, Scientific Communications Officer for COSMIC\, for this webinar to take a journey through COSMIC’s mission\, the results of our latest curation focus and how we have developed our download files to improve accessibility and useability.\n\nThrough the lens of COSMIC v98\, participants of this session will:\n\nDelve into our manual curation and rigorous data annotation processes\, and how the resulting gold standard data enables users to experiment and innovate with confidence.\nGain insight into the motivations behind our curation focuses and the results of our latest focus: rare skin tumors\, including new tumor types/histologies\, a newly fully curated cancer gene and more.\nExplore the revamped COSMIC download files\, with particular focus on their interoperability\, accessibility and useability.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/insights-into-cancer-genomics-via-cosmic-v98/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Clinical,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/QPRO-4267_WEBINAR_QCI_Labroots_COSMIC_A_1x1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230711T130000
DTEND;TZID=UTC:20230711T143000
DTSTAMP:20260504T160417
CREATED:20230614T130043Z
LAST-MODIFIED:20241024T182911Z
UID:10000647-1689080400-1689085800@staging.digitalinsights.supremeclients.com
SUMMARY:Pathogen detection and variant analysis using hybrid capture technology and QIAGEN CLC Genomics Workbench
DESCRIPTION:The detection and surveillance of pathogens such as respiratory viruses\, sexually transmitted pathogens\, adventitious agents and antimicrobial-resistant bacteria are increasingly important in healthcare settings and environmental monitoring. The COVID-19 pandemic highlighted the importance of identifying and differentiating variants of concern. By applying the lessons learned from the COVID-19 pandemic to other pathogens of interest\, it’s clear there’s a widespread need for the ability to target sensitive variants using next-generation sequencing (NGS) enrichment strategies and to analyze NGS data. \nIn this training\, we'll use QIAGEN CLC Genomics Workbench to analyze NGS data generated from hybrid capture technology. Using data generated from QIAGEN HYB panels\, you'll learn how to import\, analyze and interpret NGS data. Specifically\, you’ll discover:\n1. How to import NGS data into QIAGEN CLC Genomics Workbench\n2. How to analyze the data using template workflows;\n3. How to interpret the results using the interactive graphics produced by the workflows;\n4. How to modify the template workflows to accommodate custom panels
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/pathogen-detection-and-variant-analysis-using-hybrid-capture-technology-and-qiagen-clc-genomics-workbench/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230713T130000
DTEND;TZID=UTC:20230713T143000
DTSTAMP:20260504T160417
CREATED:20230614T130505Z
LAST-MODIFIED:20241024T182913Z
UID:10000648-1689253200-1689258600@staging.digitalinsights.supremeclients.com
SUMMARY:Target exploration and cell line selection for drug discovery
DESCRIPTION:Cancer cell line models have been a cornerstone of cancer research for decades. Profiling cancer cell lines is a powerful tool to identify gene alterations or cancer-related pathways and to discover potential drug targets. This training will focus on using QIAGEN OmicSoft Lands and Ingenuity Pathway Analysis (IPA) as guides to select cell lines and translate insights gained from cell lines into discovering new possible drug targets. \nIn this 90-minute training\, we’ll explore how you can use our platforms to:\n• Select appropriate cancer cell lines for a variety of applications such as drug discovery\, precision disease modeling\, understanding gene function in cancer and immune-oncology research\n• Examine genes of interest across various ‘omics datasets to analyze changes in expression\, mutation\, hotspots and gene dependency data\n• Generate networks for hypotheses and test them in-silico to improve the translation of insights derived from cell line models to drug target identification\n• Analyze integrated public 'omics data and drug response phenotypes using cell line model systems by exploring data from the Library of Integrated Network-Based Cellular Signatures (LINCS)\n• Prioritize drug targets and profile phenotypic/downstream effects of drug action by overlaying public data on your own generated networks \nOur system uses millions of curated literature findings in the QIAGEN/ IPA Knowledge Base and the OmicSoft digital warehouse. This training is for those of you familiar with QIAGEN IPA\, as well as newcomers interested in learning more.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/target-exploration-and-cell-line-selection-for-drug-discovery/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230718T130000
DTEND;TZID=UTC:20230718T143000
DTSTAMP:20260504T160417
CREATED:20230614T131211Z
LAST-MODIFIED:20241024T182915Z
UID:10000649-1689685200-1689690600@staging.digitalinsights.supremeclients.com
SUMMARY:Investigating genomic variants using QIAGEN CLC Genomics Workbench\, QCI Interpret-Translational (QCII-T)\, and QIAGEN Ingenuity Pathway Analysis (IPA)
DESCRIPTION:Discovering new genes implicated in hereditary diseases or cancer progression is challenging yet advancing rapidly due to the increase in next-generation sequencing (NGS) cohort data. These data analyses produce insights into associations between gene variants and diseases and the biological mechanisms of these gene variants. \nBy combining QIAGEN CLC Genomics Workbench\, QCII-T and QIAGEN IPA\, you 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. Using a streamlined NGS analysis workflow\, you’ll get valuable and reliable insights for your research project and speed up your discoveries. \nIn this training\, you’ll:\n1. Learn to import whole genome or exosome sequencing data into QIAGEN CLC Genomics Workbench and use the ultra-fast LightSpeed Module that delivers an end-to-end NGS FASTQ to VCF pipeline\n2. Explore the capabilities in QCII-T which can help accelerate your discoveries from hereditary or tumor cohort analyses to find associations between gene variants and diseases\n3. Learn how to use QIAGEN 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-qiagen-ingenuity-pathway-analysis-ipa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230725T130000
DTEND;TZID=UTC:20230725T143000
DTSTAMP:20260504T160417
CREATED:20230614T132014Z
LAST-MODIFIED:20241024T182916Z
UID:10000650-1690290000-1690295400@staging.digitalinsights.supremeclients.com
SUMMARY:Delving into public single-cell RNA-seq data using QIAGEN OmicSoft and Ingenuity Pathway Analysis (IPA)
DESCRIPTION:Single-cell RNA-sequencing (scRNA-seq) is widely used to study tissue heterogeneity\, identify novel cell types\, study pathogenic mechanisms\, develop targeted therapies (including immunotherapy) and more. Accordingly\, scientists have deposited a tremendous amount of scRNA-seq data into public domains like GEO. \nIn this training\, you will learn how to: \n· Locate public single-cell studies of interest to you 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 IPA
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/delving-into-public-single-cell-rna-seq-data-using-qiagen-omicsoft-and-ingenuity-pathway-analysis-ipa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20230726T130000
DTEND;TZID=UTC:20230726T143000
DTSTAMP:20260504T160417
CREATED:20230614T133100Z
LAST-MODIFIED:20241024T182916Z
UID:10000651-1690376400-1690381800@staging.digitalinsights.supremeclients.com
SUMMARY:Metagenomics taxonomic profiling using QIAGEN CLC Genomics Workbench
DESCRIPTION:QIAGEN CLC Microbial Genomics Module provides tools and workflows for many various bioinformatics applications\, including microbiome analysis\, isolate characterization\, functional metagenomics and antimicrobial resistance characterization. The module supports the analysis of bacterial\, viral and eukaryotic (fungal) genomes and metagenomes. \nThis training focuses on amplicon-based taxonomic profiling (16S/18S/ITS sequencing OTU clustering). Specifically\, we’ll cover together: \n• An overview of the different tools within QIAGEN CLC Microbial Genomics Module and the research areas supported \n• Taxonomic profiling \n• Importing data \n• Utilization of metadata \n• Downloading and managing references \n• The OTU clustering workflow (analytical pipeline) \n• Downstream processing of abundance tables \n• Creating and exporting high-quality graphics
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/metagenomics-taxonomic-profiling-using-qiagen-clc-genomics-workbench/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Training
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