BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Bioinformatics Software | QIAGEN Digital Insights - ECPv6.16.2//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Bioinformatics Software | QIAGEN Digital Insights
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:20230101T000000
END:STANDARD
END:VTIMEZONE
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;VALUE=DATE:20240513
DTEND;VALUE=DATE:20240516
DTSTAMP:20260611T171352
CREATED:20240418T145504Z
LAST-MODIFIED:20241024T183036Z
UID:10000752-1715558400-1715817599@staging.digitalinsights.supremeclients.com
SUMMARY:International Symposium of Variants 2024
DESCRIPTION:
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/international-symposium-of-variants-2024/
LOCATION:Porto\, Porto\, Portugal
CATEGORIES:Clinical,Event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20240515T133000
DTEND;TZID=America/New_York:20240515T143000
DTSTAMP:20260611T171352
CREATED:20240508T132337Z
LAST-MODIFIED:20241024T183039Z
UID:10000759-1715779800-1715783400@staging.digitalinsights.supremeclients.com
SUMMARY:Mitigating Variability in Somatic Variant Interpretation with Live Q&A
DESCRIPTION:Next-generation sequencing (NGS) oncology panels are becoming integral in hospital and academic settings to guide patient treatment and enrollment in clinical trials. But as NGS is increasingly used in precision oncology and an unprecedented amount of genomic information is uncovered\, there is an industry-wide issue of standardization: a high degree of variability in variant interpretation currently exists across laboratories. \nInconsistencies in variant interpretation among laboratories can create confusion for clinicians and their patients\, leaving them unable to confidently use genetic information to manage healthcare decisions. In this live panel discussion\, experts in NGS testing and clinical informatics explore the issues surrounding the standardization of variant interpretation and consider how interpretation guidelines and clinical decision support (CDS) software can help to mitigate variability between laboratories. \nTopics of discussion will include: \n• Findings of a peer-reviewed study comparing the accuracy and consistency of variant assessments from commercial CDS software to the internal variant interpretation methods of eight laboratories. \n• Causes of inter-laboratory inconsistency in variant interpretation and how to mitigate variability. \n• The benefits of having an up-to-date\, high-quality knowledge base to produce consistent\, evidence-based clinical classifications.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/mitigating-variability-in-somatic-variant-interpretation-with-live-qa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Clinical,Event
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_1327_8_QDI_QCI_Hereditary_Gi1346512014.jpg
END:VEVENT
END:VCALENDAR