<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Mayo Clinic</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1268607</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Frontotemporal lobar degeneration (FTLD) is one of the leading causes of dementia in individuals younger than 65 years, with the aggregation of TDP-43 as one of the most common forms of FTLD. FTLD-TDP is clinically, genetically and pathologically heterogeneous, with GRN and C9orf72 as the most common genetic forms (although more than 50% of the cases are genetically unexplained), and A, B and C as the most common pathological subtypes. To investigate the molecular differences between the different forms of FTLD-TDP, we performed bulk RNA sequencing (RNAseq) and reduced representation bisulfite sequencing (RRBS) from different brain regions of FTLD-TDP patients and controls. The RNAseq dataset includes samples from the frontal cortex of 149 individuals, comprising 127 FTLD-TDP cases... (for more see dbGaP study page.)</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>RNA transcriptomic and DNA methylation landscape in FTLD-TDP and controls</name><description>RNA transcriptomic and DNA methylation landscape in FTLD-TDP and controls</description><dates><last_updated>2025-09-24</last_updated><first_public>2025-06-29</first_public></dates><accession>PRJNA1268607</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>