Owing to a revolution in NGS technologies, massive amounts of somatic mutations were identified in the past decade. The Cancer Genome Atlas or TCGA, is a landmark cancer genomics program to molecularly characterized over 20,000 primary cancer and matched normal samples spanning 33 cancer types. This joint effort between NCI and the National Human Genome Research Institute began in 2006, bringing together researchers from diverse disciplines and multiple institutions. TCGA has generated over 2.5 petabytes of genomic, epigenomic, transcriptomic, and proteomic data. The data, which has already led to improvements in our ability to diagnose, treat, and prevent cancer, will remain publicly available for anyone in the research community to use.
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