Comprehensive study of tumour single nucleotide polymorphism array data reveals significant driver aberrations and disrupted signalling pathways in human hepatocellular cancer.

Abstract excerpt

The authors describe an integrated method for analysing cancer driver aberrations and disrupted pathways by using tumour single nucleotide polymorphism (SNP) arrays. The authors new method adopts a novel statistical model to explicitly quantify the SNP signals, and therefore infers the genomic ab...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Algorithms
• Share to Carcinoma, Hepatocellular
• Share to Chromosome Aberrations