Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations

Authors: Boris Noyvert, A Mesut Erzurumluoglu, Dmitriy Drichel, Steffen Omland, Till F M Andlauer, Stefanie Mueller, Lau Sennels, Christian Becker, Aleksandr Kantorovich, Boris A Bartholdy, Ingrid Brænne, Julio Cesar Bolivar-Lopez, Costas Mistrellides, Gillian M Belbin, Jeremiah H Li, Joseph K Pickrell, Jatin Arora, Yao Hu, Boehringer Ingelheim – Global Computational Biology and Digital Sciences, Clive R Wood, Jan M Kriegl, Nikhil Podduturi, Jan N Jensen, Jan Stutzki, Zhihao Ding