To all our CKB CORE users, don’t miss the latest new features now available! Register for a free CORE account here and then login for access. Feel free to contact us at ckbsupport@genomenon.com if you have any questions!
Cancer Knowledgebase logo. White letters 'CKB' in light blue circle next to text Cancer Knowledgebase in black.  Under this reads 'Powered by Genomenon' in dark blue text.

CKB is a dynamic digital resource for interpreting complex cancer genomic profiles in the context of protein impact, therapies, and clinical trials. CKB CORE is the public access version we have been providing to the community since 2016. CKB CORE contains all the content associated with 50 genes that are commonly found on cancer hotspot panels. New and updated content is pushed out daily and viewable genes are available on a quarterly rotating schedule.

News
Mar 3, 2025 - Exciting news for our CKB CORE users! We have new features available in CORE! If you're interested in having access to these features, you can register for a free account here, and then login. Let us know if you have any questions and/or comments by emailing ckbsupport@genomenon.com.

Feb 12, 2025 - Interested in using the Advanced Search options in CKB, but not sure when and how to use them? Then check out this tutorial to learn how you can quickly identify potential treatments and appropriate clinical trials based on specific molecular criteria. Please feel free to reach out to us with any questions/comments or request a live demo! ckbsupport@genomenon.com 

Jan 13, 2025 - To our CORE users, it's time for the quarterly update to the gene list! This quarter's theme includes genes relevant to immuno-oncology. Check out the latest blog here to start exploring these valuable insights: https://lnkd.in/dbXf_bCr! If you have any questions, please feel free to reach out to us at ckbsupport@genomenon.com.
Check out   CKB BOOST for content extending to 2100+ genes.


Explore the Mastermind Genomic Intelligence Platform

Access article information on over 26 million variants, as well as curated germline variant content, and discover valuable gene and variant summary information to streamline your analysis and deepen your insights.