Unscrambling cancer genomes via integrated analysis of structural variation and copy number
C. Shale, J. Baber, D. Cameron, M. Wong, M. J. Cowley, A. T. Papenfuss, E. Cuppen, P. Priestley
This paper introduces LINX, a tool for analyzing structural variation and copy number alterations in cancer genomes, revealing novel insights into oncogenic fusions and inactivation events.
bioRxiv · Dec 3, 2020Cancer Biology