作者: Christina Curtis , Sohrab P Shah , Suet-Feung Chin , Gulisa Turashvili , Oscar M Rueda
DOI: 10.1038/NATURE10983
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摘要: The elucidation of breast cancer subgroups and their molecular drivers requires integrated views of the genome and transcriptome from representative numbers of patients. We present an integrated analysis of copy number and gene expression in a discovery and validation set of 997 and 995 primary breast tumours, respectively, with long-term clinical follow-up. Inherited variants (copy number variants and single nucleotide polymorphisms) and acquired somatic copy number aberrations (CNAs) were associated with expression in∼ …