Multiscale transcriptomic organization of the human brain with DigitalBrain

Journal: bioRxiv
Published Date:

Abstract

The human brain varies across anatomical regions, cell types, development, ageing and disease states, yet existing single-cell transcriptomic resources remain fragmented and difficult to integrate into a unified biological model. Here we present DigitalBrain, a human brain-specific atlas and foundation-model framework for organizing diverse and fragmented human brain transcriptomic data across scales. We first built DigitalBrain-Atlas, a harmonized whole-brain single-cell resource comprising 16.35 million transcriptomes from 2,143 donors across 165 brain regions, spanning the human lifespan and multiple neurological and clinical conditions. We then developed DigitalBrain-M1, a Transformer-based model that jointly encodes gene identity and expression magnitude to learn a shared embedding space for cells and genes. Across held-out datasets, DigitalBrain supported robust single-cell integration, clustering and cell-type annotation while preserving major biological structure and reducing technical fragmentation. Beyond these benchmarks, the learned embeddings revealed emergent large-scale hierarchical organization of the human brain, linking anatomically distinct regions into higher-order patterns consistent with known functional systems. Applied to human hippocampal aging, DigitalBrain identified cell-type-specific aging sensitive gene sets, identified dentate gyrus granule cells as a particularly age-sensitive population, and discovered selective reorganization of gene programs related to synaptic transmission, postsynaptic structure, membrane excitability and axon guidance during aging. Cross-dataset convergence was strongest at the level of functional modules and recurrent aging sensitive genes. Together, these results demonstrate DigitalBrain as a brain-specific framework for mapping human brain organization across scales, and as an early step towards a complete virtual organ for the human brain.

Authors

  • An
  • J.; Hu
  • X.; Jiang
  • Y.; Jiang
  • M.; Qiu
  • S.; Liu
  • G.; Wei
  • X.; Wang
  • Y.; Lin
  • J. Q.; Wang
  • C.; Lu
  • M.

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