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The accurate identification and annotation of germline and somatic variants rely on the accuracy and depth of reference databases that contain information about the genetic variants, any associated phenotype, and their clinical implications. By combining COSMIC, HGMD and QIAGEN QCI-IT, scientists can 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. The software and databases allow you to get valuable and reliable insights for your research project and speed up your discoveries related to disease-causing and disease-associated germline and somatic variants.
In this training, you will:
1. Learn about COSMIC, the world’s largest, most comprehensive, expert-curated resource for somatic mutations in human cancers, and how COSMIC can help you identify variants of interest for cancer research.
2. Hear about the breadth and depth of HGMD (Human Gene Mutation Database) and how HGMD can aid in your search for disease-causing and disease-associated germline mutations.
3. Explore the capabilities of QCI-IT, which can help accelerate your discoveries from hereditary or tumor cohort analyses, and find associations between gene variants and diseases from VCF files.
To learn more about the products or request for a trial:
COSMIC: https://digitalinsights.qiagen.com/products-overview/cosmic/?cmpid=CM_QDI_DISC_042024webinars
HGMD: https://digitalinsights.qiagen.com/products-overview/clinical-insights-portfolio/human-gene-mutation-database/?cmpid=CM_QDI_DISC_042024webinars
QCI-IT: https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/qci-interpret-translational/?cmpid=CM_QDI_DISC_042024webinars
