SAVANA: reliable analysis of somatic structural variants and copy number aberrations in clinical samples using long-read sequencing
H. Elrick, C. M. Sauer, J. Espejo Valle-Inclan, K. Trevers, M. Tanguy, S. Zumalave, S. De Noon, F. Muyas, R. Cascao, A. Afonso, F. Amary, R. Tirabosco, A. Giess, T. Freeman, A. Sosinsky, , I. Cortes-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.
bioRxiv · Jul 25, 2024 · PreprintCancer Biology