FFPE tissue blocks were collected for each fresh-frozen tumor which underwent multiomic profiling and were used for pathology review, IHC (MYF-4, H3K7me3, S100, and Sox10) and additional molecular characterization [i.e., ploidy assay and multiregional whole-exome sequencing (WES)]. FFPE H&E slides from available blocks were reviewed by a pathologist to identify the block most representative (i.e., morphologically similar) to the frozen material which underwent multiomic profiling. These H&E sections were digitally scanned (40×) at each pathology hub by the Deep Lens Biomedical Imaging Team and uploaded to the VIPER digital pathology platform (Deep Lens, Inc.). Multiregional 500× exome sequencing was performed on 5 samples each from 36 FFPE NF1-related MPNST specimens to assess intratumor heterogeneity.