Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 17 von 10855

Details

Autor(en) / Beteiligte
Titel
Chromatin structure-based prediction of recurrent noncoding mutations in cancer
Ist Teil von
  • Nature genetics, 2016-11, Vol.48 (11), p.1321-1326
Ort / Verlag
United States: Nature Publishing Group
Erscheinungsjahr
2016
Quelle
MEDLINE
Beschreibungen/Notizen
  • Recurrence is a hallmark of cancer-driving mutations. Recurrent mutations can arise at the same site or affect the same gene at different sites. Here we identified a set of mutations arising in individual samples and altering different cis-regulatory elements that converge on a common gene via chromatin interactions. The mutations and genes identified in this fashion showed strong relevance to cancer, in contrast to noncoding mutations with site-specific recurrence only. We developed a prediction method that identifies potentially recurrent mutations on the basis of the features shared by mutations whose recurrence is observed in a given cohort. Our method was capable of accurately predicting recurrent mutations at the level of target genes but not mutations recurring at the same site. We experimentally validated predicted mutations in distal regulatory regions of the TERT gene. In conclusion, we propose a novel approach to discovering potential cancer-driving mutations in noncoding regions.

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX