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X-WR-CALDESC:Events for Bioinformatics Software | QIAGEN Digital Insights
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DTSTART:20230101T000000
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DTSTART;TZID=UTC:20241119T080000
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CREATED:20240923T190720Z
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SUMMARY:QIAGEN at AMP 2024
DESCRIPTION:Meet QIAGEN at the 2024 Association for Molecular Pathology (AMP) Annual Meeting\nThis year at the 2024 Association for Molecular Pathology (AMP) Annual Meeting\, QIAGEN will showcase our barrier-breaking Sample to Insight Oncology solution. Combining targeted DNA and multimodal pan-cancer panels\, one of the fastest and cheapest secondary analysis solutions in the market\, and industry-leading variant interpretation and reporting software trusted to analyze and interpret over 4 million NGS patient test cases worldwide\, our Sample to Insight Oncology solution is revolutionizing precision oncology testing. \nLean more and schedule a VIP meeting with our experts at AMP 2024 here.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/qiagen-at-amp-2024/
CATEGORIES:Clinical,Event
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DTSTART;TZID=Asia/Dubai:20241119T130000
DTEND;TZID=Asia/Dubai:20241119T143000
DTSTAMP:20260610T064604
CREATED:20241015T174847Z
LAST-MODIFIED:20241024T183126Z
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SUMMARY:Investigating genomic variants using QIAGEN CLC Genomics Workbench\, QCI Interpret-Translational (QCII-T)\, and Ingenuity Pathway Analysis (IPA)
DESCRIPTION:Discovery of new genes implicated in hereditary diseases or cancer progression is challenging and advancing rapidly with an increase in the amount of cohort data to analyze from next generation sequencing (NGS) data to associations between gene variants and diseases\, and finally to biological mechanisms of these gene variants. Combining QIAGEN CLC Genomics Workbench\, QCII-T\, and IPA\, scientists can analyze sequencing data obtained from a variety of NGS technologies\, annotate gene variants using the world’s most comprehensive and up-to-date curated scientific evidence\, and find biological connections in gene variants with manually curated scientific findings. Get valuable and reliable insights for your research project and speed up your discoveries by using a streamlined NGS analysis workflow. \nIn this webinar\, attendees will have the opportunity to: \n\nLearn how to import whole genome or exome sequencing data into QIAGEN CLC Genomics Workbench and use the ultra-fast LightSpeed Module that delivers end-to-end NGS FASTQ to VCF pipeline;\nExplore capabilities in QCII-T which can enable scientists to accelerate discoveries from hereditary or tumor cohort analyses to find associations between gene variants and diseases;\nLearn how to use IPA and its manually curated content among other integrated scientific evidence to uncover novel biological mechanisms underlying these gene variants.
URL:https://staging.digitalinsights.supremeclients.com/webinars-and-events/investigating-genomic-variants-using-qiagen-clc-genomics-workbench-qci-interpret-translational-qcii-t-and-ingenuity-pathway-analysis-ipa/
LOCATION:Virtual - Americas - EST\, United States
CATEGORIES:Discovery,Event
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