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COSMIC, the Catalogue Of Somatic Mutations In Cancer (https://cancer.sanger.ac.uk/cosmic) is the world’s largest and most comprehensive resource on somatic mutations and other molecular alterations causing every form of human cancer.
Integrating COSMIC into your NGS pipeline accelerates cancer sample analysis by rapidly prioritizing cancer driver mutations, distinguishing VUSes, and determining if an alteration is common or rare in the cancer type of interest.
The database’s contents are primarily obtained from scientific literature and trustworthy online sources like the TCGA and ICGC. During thorough & exhaustive manual curation by a team of experienced post-doctoral experts, all available information about mutations and tumour samples (e.g., disease type, demographic data, treatments) are collected, standardised, and integrated into the database. And to help users navigate its immense dataset, COSMIC offers an ever-expanding portfolio of specialised projects that each present a distinct dataset or view of the data.
COSMIC is updated 3 times a year with substantial new content and functionality. Our most recent release (v94) describes over 71 million somatic mutation events across almost 1.5M tumour samples, detailing mutation patterns in every human gene and regulatory region across multiple mutation mechanisms.
Essential to precision oncology research, COSMIC is fully available through QIAGEN. (https://digitalinsights.qiagen.com/products-overview/cosmic/).
Who should attend?
Cancer scientists and clinical developers (pharmaceutical, diagnostic, academic), bioinformatic scientists, developers & solution providers.
What to expect?
Speakers
Dr. Simon Forbes
Head of COSMIC
Wellcome Sanger Institute, Cambridge, UK
Dr. Zbyslaw Sondka
Senior Scientist, COSMIC
Wellcome Sanger Institute, Cambridge, UK
56:37 minutes
Tags: clinical, cosmic, databases, oncology, webinar