BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Bioinformatics Software | QIAGEN Digital Insights - ECPv6.15.20//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:UTC
BEGIN:STANDARD
TZOFFSETFROM:+0000
TZOFFSETTO:+0000
TZNAME:UTC
DTSTART:20220101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=UTC:20230419T110000
DTEND;TZID=UTC:20230419T120000
DTSTAMP:20260504T063723
CREATED:20230317T121304Z
LAST-MODIFIED:20241024T182849Z
UID:10000622-1681902000-1681905600@staging.digitalinsights.supremeclients.com
SUMMARY:Shed light on inherited mutations and solve hereditary investigations with QCI Interpret
DESCRIPTION:In this webinar\, we will demonstrate how QCI Interpret can improve your diagnostic yield for hereditary disorders. QCI Interpret is a clinical decision support platform that leverages augmented molecular intelligence to streamline the interpretation workflow. It uses the most extensive\, globally trusted and manually curated molecular knowledge and bibliography evidence to provide you with the best possible opportunity to solve every case. By demonstrating the different features and series of use-cases\, we will show you how QCI Interpret guarantees a comprehensive and thorough investigation of every case for all types of genetic variation\, including copy number variants (CNVs). This will allow you to provide precise answers to patients and their families\, while also reducing test turnaround time from hours to minutes. \nLearning objectives: \n\nLearn about QCI Interpret’s analysis and interpretation workflow for hereditary diseases using targeted and extended gene panels\, including WES/WGS\nLearn about QCI Interpret and QIAGEN’s expert curation process based on the latest ACMG carrier screening guidelines\nView demonstrations of unique features in QCI Interpret\, including how to input symptoms relevant to a case and receive relationships to candidate diseases and mutated genes using the Phenotype Network Analysis feature and triage mode of variant assessment.\nLearn how QCI Interpret supports CNV interpretation and reporting with bibliographic coverage of over 60\,000 CNV case reports"
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/shed-light-on-inherited-mutations-and-solve-hereditary-investigations-with-qci-interpret/
CATEGORIES:Clinical,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/WEBINAR_QCI_RockReleaseWebinar_0323_16x9.jpg
END:VEVENT
END:VCALENDAR