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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
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DTSTART:20220101T000000
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BEGIN:VEVENT
DTSTART;TZID=UTC:20231019T110000
DTEND;TZID=UTC:20231019T120000
DTSTAMP:20260411T033328
CREATED:20230912T164135Z
LAST-MODIFIED:20241024T182938Z
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SUMMARY:A breakthrough for rare disease: Completing the Clinical exome gap!
DESCRIPTION:In its latest release\, QCI Interpret for Hereditary extends its market-leading content with further advancements in Artificial Intelligence (AI) for enhanced capabilities in clinical exome NGS testing. Now\, with the addition of AI-derived literature references for rare disease genes\, QCI Interpret provides complete exome coverage\, on top of the existing unrivalled manually curated content and bibliography. \nIn this webinar\, we will demonstrate how QCI Interpret is expanding its literature coverage enabling easy and efficient variant filtering workflow\, based on bibliography and on patient’s phenotype. This new feature provides greater control over bibliography context\, allowing users to only look at publications where the causative variant is associated with a specific disease. In addition\, the release provides AI-enhanced phenotype-driven ranking. Using this approach that has been trained using thousands of solved cases\, QCI Interpret for Hereditary Diseases provides superior overall candidate ranking for causative variants in rare diseases. The new variant-ranking approach is enhanced by taking into account additional variant related variables supported also by AI\, as well as the patient’s symptoms\, and all of the manually curated literature in the QIAGEN Knowledge Base to give the best possible chance of reaching an accurate diagnosis. \nLearning objectives: \n\nLearn about QCI Interpret’ s new AI bibliography content providing expanded clinical exome coverage\, due to the combination of the AI-derived literature references with QIAGEN’s unrivalled manual curation.\nLearn about QCI Interpret gives users the best possible chance of reaching an accurate diagnosis by providing phenotype-driven ranking that considers the detected mutations\, the patient’s symptoms\, and all the content in the QIAGEN Knowledge Base.\nView live demonstration of unique features in QCI Interpret\, which can drastically reduce the time spent on solving a case\, resulting in faster turnaround time and an accurate assessment of a case.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/a-breakthrough-for-rare-disease-completing-the-clinical-exome-gap/
LOCATION:Virtual Global Event (Times shown in EST)
CATEGORIES:Clinical,Webinar
ATTACH;FMTTYPE=image/jpeg:https://staging.digitalinsights.supremeclients.com/wp-content/uploads/2024/05/S_1327_7_QDI_QCI_Hereditary_Summit.jpg
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