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Large-scale copy number alterations are enriched for synthetic viability in BRCA1/BRCA2 tumors.

Yingjie ZhuXin PeiArdijana NovajJeremy SettonDaniel BronderFatemeh DerakhshanPier SelenicaNiamh McDermottMehmet OrmanSarina PlumShyamal SubramanyanSara H BravermanBiko McMillanSonali SinhaJennifer MaAndrea GazzoAtif KhanSamuel BakhoumSimon N PowellJorge S Reis-FilhoYingjie Zhu
Published in: Genome medicine (2024)
This study provides a means to solve the tumor suppressor paradox by identifying synthetic viability interactions and causal driver genes affected by large-scale CNAs in human cancers.
Keyphrases
  • copy number
  • mitochondrial dna
  • genome wide
  • endothelial cells
  • dna methylation
  • breast cancer risk
  • gene expression
  • induced pluripotent stem cells
  • pluripotent stem cells
  • genome wide identification