Research into the tumor evolution and genomic architecture of gliomas has revealed significant insights into the complexity of these malignancies. One study utilized murine models of IDH-wild-type glioblastoma to characterize the spatiotemporal genomic architecture of multifocal glioblastomas (M-GBMs). The findings indicated the existence of a common ancestor (CA) with a less aggressive phenotype, which subsequently evolved into genetically divergent malignant gliomas across different brain regions. This study employed advanced methodologies, including serial MRI, 3D reconstruction, whole-genome sequencing, and single-cell phylogenetic tree construction, to identify two distinct types of tumor evolution: Type 1, characterized by the growth of a single mass, and Type 2, marked by multifocal masses. Both types exhibited loss of Pten and chromosome 19, alongside PI3K/Akt pathway activation, highlighting the genetic underpinnings of glioma heterogeneity (ref: Li doi.org/10.1038/s41467-020-17382-3/). Another significant contribution to this theme is the development of Somalier, a tool designed for rapid relatedness estimation in cancer studies. This tool addresses the challenges of detecting sample mix-ups in genomic studies, particularly when analyzing multiple spatial or longitudinal biopsies. By focusing on somatic variants, Somalier enhances the accuracy of genomic comparisons, which is crucial for understanding tumor evolution and ensuring the integrity of genomic data (ref: Pedersen doi.org/10.1186/s13073-020-00761-2/). Together, these studies underscore the intricate dynamics of glioma evolution and the importance of robust methodologies in genomic research.