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X-WR-CALNAME:Bioinformatics Software | QIAGEN Digital Insights
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X-WR-CALDESC:Events for Bioinformatics Software | QIAGEN Digital Insights
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SUMMARY:Third Annual Clinical Hereditary Disease Diagnostics Summit "Exome experts: Improving the interpretation and integration of exome testing in routine clinical care"
DESCRIPTION:Industry leaders discuss how to improve the speed\, precision and cost-effectiveness of clinical exome testing for newborn screening and rare and undiagnosed diseases \nClinical exome testing is revolutionizing the diagnosis of rare and inherited diseases. Its ability to quickly pinpoint the genetic causes of complex conditions has made it a critical component of personalized medicine\, leading to earlier diagnoses\, targeted treatments and improved patient outcomes. However\, without the right strategies\, databases and informatics tools\, clinical exome testing remains inaccessible for many small to mid-sized laboratories. \nThe Third Annual Clinical Hereditary Disease Diagnostics Summit hosted by QIAGEN Digital Insights will examine the incredible opportunities—and challenges—of brining clinical exome testing in-house. Join industry leaders as they discuss how labs\, regardless of size\, budget and experience\, can integrate exome testing into routine clinical care with transformative impact for providers and their patients. \nFeatured topics will include: \n\nEmerging trends and recent technological advancements in genetic testing\nOvercoming challenges of interpreting complex genetic data from genome\, exome\, and next-generation sequencing panels\nHow to integrate genetic testing into clinical practice with consideration of efficiency\, cost\, and ethics\nFuture directions for the field and how to prepare your lab for innovation
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/exome-experts-improving-the-interpretation-and-integration-of-exome-testing-in-routine-clinical-care/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Clinical,Webinar
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DTSTART;TZID=America/Halifax:20240926T130000
DTEND;TZID=America/Halifax:20240926T143000
DTSTAMP:20260610T125818
CREATED:20240814T192314Z
LAST-MODIFIED:20241024T183059Z
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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
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