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X-WR-CALDESC:Events for Bioinformatics Software | QIAGEN Digital Insights
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DTSTART;TZID=America/New_York:20230323T110000
DTEND;TZID=America/New_York:20230323T120000
DTSTAMP:20260527T031821
CREATED:20230309T161946Z
LAST-MODIFIED:20241024T182845Z
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SUMMARY:How to simplify somatic NGS analysis & reduce literature review time by 90% with HSMD
DESCRIPTION:Across clinical oncology applications\, from molecular testing to cancer research\, the ability to identify potentially actionable genomic and genetic alterations to exploit the molecular vulnerabilities of cancer is a burgeoning field. Due to the sporadic nature of somatic cancers and the expansion of next-generation sequencing\, the number of variants detected through tumor testing is growing exponentially\, presenting a challenge to clinical cancer genetics professionals working to confidently identify meaningful mutations that could influence decision-making at point-of-care.\n\nJoin Chelsea Alexander\, a certified genetic counselor\, and Aarthi Goverdhan\, our lead oncology application development scientist\, for a live webinar on Thursday\, March 23rd at 11 AM EST to discover a new database that can streamline your somatic NGS analysis and significantly reduce your literature review time—by up to 90%!\n\nIn this webinar\, we will introduce you to the Human Somatic Mutation Database (HSMD)—a new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies. Available as a web-based application\, this expert-curated resource contains data from over 419\,000 real-world clinical oncology cases combined with insights from the QIAGEN Knowledge Base\, providing clinically observed variant frequencies across diseases\, and diving deep into gene-level\, alteration-level and disease-level information. Users can easily search and explore mutational characteristics across genes\, synthesize key findings from drug labels and professional guidelines\, explore clinical trials\, and receive detailed annotations for each observed variant. In addition\, users can interrogate a bibliography of over 170\,000 PubMed articles and access detailed alteration-specific summaries written by PhD scientists.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/how-to-simplify-somatic-ngs-analysis-reduce-literature-review-time-by-90-with-hsmd/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Clinical,Webinar
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DTSTART;TZID=America/New_York:20230323T130000
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DTSTAMP:20260527T031821
CREATED:20230307T163759Z
LAST-MODIFIED:20241024T182839Z
UID:10000607-1679576400-1679581800@staging.digitalinsights.supremeclients.com
SUMMARY:Multi-omics (metabolomics\, proteomics\, transcriptomics) analysis using QIAGEN Ingenuity Pathway Analysis
DESCRIPTION:This 90-minute training session is about how QIAGEN Ingenuity Pathway Analysis (IPA) allows visualization of molecular intricacy and variations at multiple levels such as transcriptome\, proteome\, and metabolome. Through a series of brief technical vignettes\, it is demonstrated how to: \n· Generate associations among molecular signatures obtained via integrating multi-omics data \n· Extract mechanisms from multi-omics data for precision medicine \n· Disease stratification based on multi-omics profiles \n· Map disease networks among targets and indications \n  \nClick here to register.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/multi-omics-metabolomics-proteomics-transcriptomics-analysis-using-qiagen-ingenuity-pathway-analysis-3/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
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