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Identification of significantly mutated regions across cancer types highlights a rich landscape of functional molecular alterations

Cancer sequencing studies have primarily identified cancer-driver genes by the accumulation of protein-altering mutations. An improved method would be annotation-independent, sensitive to unknown distributions of functions within proteins, and inclusive of non-coding drivers. We employed density-bas...

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Bibliografiska uppgifter
I publikationen:Nat Genet
Huvudupphovsmän: Araya, Carlos L., Cenik, Can, Reuter, Jason A., Kiss, Gert, Pande, Vijay S., Snyder, Michael P., Greenleaf, William J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2015
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4731297/
https://ncbi.nlm.nih.gov/pubmed/26691984
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3471
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