Comprehensive genetic diagnosis of acute myeloid leukemia by

Comprehensive genetic diagnosis of acute myeloid leukemia by next-generation sequencing by Elisabeth K. M. Mack, André Marquardt, Danny Langer, Petra Ross, Alfred Ultsch, Michael G. Kiehl, Hildegard I. D. Mack, Torsten Haferlach, Andreas Neubauer, and Cornelia Brendel haematol Volume 104(2): 277 -287 January 31, 2019 © 2019 by Ferrata Storti Foundation

Comprehensive genetic diagnosis of acute myeloid leukemia by next-generation sequencing. Elisabeth K. M. Mack et al. Haematologica 2019; 104: 277 -287 © 2019 by Ferrata Storti Foundation

Calculated chromosome banding and in silico-generated reference karyotypes. Elisabeth K. M. Mack et al. Haematologica 2019; 104: 277 -287 © 2019 by Ferrata Storti Foundation

Patients’ samples and karyotypes. Elisabeth K. M. Mack et al. Haematologica 2019; 104: 277 -287 © 2019 by Ferrata Storti Foundation

Detection of whole chromosome gains and losses by copy number variation karyotyping. Elisabeth K. M. Mack et al. Haematologica 2019; 104: 277 -287 © 2019 by Ferrata Storti Foundation

Detection of partial chromosome losses and gains by copy number variation karyotyping. Elisabeth K. M. Mack et al. Haematologica 2019; 104: 277 -287 © 2019 by Ferrata Storti Foundation

Sensitivity of copy number variation karyotyping. Elisabeth K. M. Mack et al. Haematologica 2019; 104: 277 -287 © 2019 by Ferrata Storti Foundation