Article
Lessons from the deep study of rare tumours.
The Journal of pathology - 1 Jul 2011
Thomas David M
Abstract excerpt
Next-generation sequencing technologies are having an enormous impact on mapping mutations in cancer. However, it is unclear to what extent mutations in genes are shared between cancer types, and to what extent these are unique to different cancers. While the mapping of mutations is almost saturated in common cancer types, the study of rare tumours offers surprising insights into pathways that are deranged in...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
