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DTSTART;TZID=America/New_York:20240326T110000
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SUMMARY:Agilent Alissa to QCI Interpret: How can your lab reduce the stress and complexity of transitioning to a new clinical informatics platform?
DESCRIPTION:In 2023\, Agilent announced the discontinuation of their Alissa Interpret clinical informatics platform by the end of 2024. As a result\, many of their current customers need to transition to a new variant interpretation and reporting software within a tight timeframe. However\, when evaluating new interpretation solutions\, clinical labs must consider a variety of factors\, including: \n\nContent quality for clinical reporting\nFlexibility to adapt current workflows to a new platform\nRetaining historical content and comments\nEase of personnel training\n\nIn this webinar\, learn about QCI Interpret\, a panel- and sequencer-agnostic clinical informatics platform for NGS variant interpretation and reporting of germline and somatic tests. Our experts will address the concerns of current Agilent Alissa users and discuss what sets QCI Interpret apart from other interpretation solutions. In addition\, we will show you how seamless it is to transition your historical data and comments into QCI Interpret\, as well as provide a live demonstration of the industry-leading and reliable software that has been used to analyze and interpret more than 3.5 million patient test cases worldwide. \n 
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/agilent-alissa-to-qci-interpret-how-can-your-lab-reduce-the-stress-and-complexity-of-transitioning-to-a-new-clinical-informatics-platform/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Clinical,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/QPRO-6432_WEBINAR_QCI_Conversion_March_16x9.jpg
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DTSTART;TZID=America/New_York:20240326T130000
DTEND;TZID=America/New_York:20240326T143000
DTSTAMP:20260410T041917
CREATED:20240219T134033Z
LAST-MODIFIED:20241024T183026Z
UID:10000733-1711458000-1711463400@staging.digitalinsights.supremeclients.com
SUMMARY:Single-Cell RNA-Seq\, Cell Hashing\, and Spatial Transcriptomics
DESCRIPTION:A slide illustrating some of the many result types/graphics you will be able to generate after this training. https://qiagen.showpad.com/share/jYTCDPNfz1SdIMPQPSPYS  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.  Using CLC Genomics Workbench\, you will learn how to perform secondary analysis on your single-cell RNA-seq data. Specifically\, you will learn how to: • Import your raw FASTQ or processed cell-matrix files • Use pre-configured but customizable pipelines/workflows for single-cell RNA-seq data • Generate high-resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries o Dimension reduction (UMAP\, t-SNE) plots o Differential expression tables for clusters\, cell types\, or a combination of both o Heat map o Dot plots o Violin plots • Learn how to use “Create Cell Annotations from Hashtags” for cell hashing\, as with CITE-seq • Dive into spatial transcriptomic analysis\, the latest feature in the single-cell RNA-seq module 
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/single-cell-rna-seq-cell-hashing-and-spatial-transcriptomics-2/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_1064_6_OmicSoft-Single-Cell-Lands_QDI7303_16x9-1.jpg
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