SAVANA: reliable analysis of somatic structural variants and copy number aberrations in clinical samples using long-read sequencing
Hillary Elrick, Carolin M. Sauer, Jose Espejo Valle-Inclán, Katherine E. Trevers, M. Tanguy, Sonia Zumalave, Solange De Noon, Francesc Muyas, Rita Cascão, Ângela Afonso, Alistair G. Rust, Fernanda M Amary, Roberto Tirabosco, Adam P Giess, Timothy M. Freeman, , Isidro Cortés‐Ciriano
SAVANA improves detection of somatic structural variants and copy number aberrations in cancer using long-read sequencing with higher sensitivity and specificity than existing tools.
Nature Methods · May 28, 2025Peer-reviewedCancer Biology