<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Lakhani Lab, UQ Centre for Clinical Research, The University of Queensland</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1168525</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Metaplastic breast cancer (MpBC) is a rare and aggressive form of breast cancer. Characteristically heterogeneous, MpBC are defined by the presence of various morphological elements, typically biphasic, with epithelial (e.g. non-special type (NST), squamous) and mesenchymal (e.g. spindle, chondroid, osteoid) components. The established clonality of the different components, favours an evolution model encompassing either a multipotent progenitor, or a linear metaplastic conversion. Our study defines the micro-methylome and a spatial transcriptomic profile in MpBC, and identifies potential drivers associated with tumor heterogeneity that supports the conversion model of metaplasia and warrants further functional analysis. Overall design: This submission includes only methylation arrays. Illumina Human Methylation EPIC BeadChip used for FFPE-origin DNA.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Integrated Methylation and Spatial Transcriptomic Profiling of Metaplastic Breast Cancer identifies putative master regulators of intratumoral heterogeneity</name><description>Integrated Methylation and Spatial Transcriptomic Profiling of Metaplastic Breast Cancer identifies putative master regulators of intratumoral heterogeneity</description><dates><last_updated>2025-09-24</last_updated><first_public>2025-08-14</first_public></dates><accession>PRJNA1168525</accession><cross_references><GEO>GSE278722</GEO><taxon>9606</taxon></cross_references></HashMap>