BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Bioinformatics Software | QIAGEN Digital Insights - ECPv6.15.17.1//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-ORIGINAL-URL:https://staging.digitalinsights.supremeclients.com
X-WR-CALDESC:Events for Bioinformatics Software | QIAGEN Digital Insights
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20230312T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20231105T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20240310T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20241103T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20250309T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20251102T060000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20241113T100000
DTEND;TZID=America/New_York:20241113T110000
DTSTAMP:20260419T024824
CREATED:20241023T175035Z
LAST-MODIFIED:20241024T183129Z
UID:10000821-1731492000-1731495600@staging.digitalinsights.supremeclients.com
SUMMARY:Webinar: Pharmacogenomics - One tool to decode drug response to variation in the genome
DESCRIPTION:Each year\, more than 134 million patients experience adverse drug events\, causing 2.4 million deaths worldwide. What if there was a better way to develop and prescribe safer\, more effective drugs based on the unique genetic information of every individual? \nIn this webinar\, learn about a game-changing solution for labs and pharmaceutical companies to rapidly and confidently translate complex pharmacogenomics (PGx) data into evidence-backed insights to inform therapeutic outcomes. QIAGEN Pharmacogenomic Insights (PGXI) is a new expert-curated knowledgebase solution that provides comprehensive access to verified and up-to-date data from multiple PGx sources\, including the FDA\, CPIC\, DPWG\, PharmVar\, and PubMed. Built upon a legacy platform used to deliver more than 1.6 million PGx annotations for more than 250 clinical research laboratories\, PGXI seamlessly integrates into existing or new workflows to automate the annotation of PGx data from all platforms\, including NGS and arrays. Within minutes\, users can retrieve a custom output of relevant information\, including relevant conditions associated with queried genes of interest\, relevant drug-gene associations\, and curated literature evidence for alleles in question. \nIn this webinar\, you will learn: \n\nHow PGXI can help your lab efficiently and consistently identify medications associated with adverse effects.\nWhat expert-curated content sources are available in PGXI\, eliminating the need to consult multiple databases and saving you significant time and money.\nHow to use PGXI to seamlessly scale your PGXI workflow and stay at the cutting edge of PGx research.\n\nPlus\, if eligible\, webinar attendees can try PGXI for free with an exclusive trial offer from QIAGEN. There’s an easier and faster way to translate PGx data into insights. Don’t miss this opportunity to elevate and transform your PGx program. \nLearn more and register here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/webinar-a-game-changer-for-pharmacogenomics-one-tool-to-decode-drug-response-to-variation-in-the-genome/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/10/S_1419_4_QDI_QCI_PGXI_Launch.jpg
END:VEVENT
END:VCALENDAR