Whole brain alignment of spatial transcriptomics between humans and mice with BrainAlign.
Biao ZhangShuqin ZhangTinghu ZhangPublished in: Nature communications (2024)
The increasing utilization of mouse models in human neuroscience research places higher demands on computational methods to translate findings from the mouse brain to the human one. In this study, we develop BrainAlign, a self-supervised learning approach, for the whole brain alignment of spatial transcriptomics (ST) between humans and mice. BrainAlign encodes spots and genes simultaneously in two separated shared embedding spaces by a heterogeneous graph neural network. We demonstrate that BrainAlign could integrate cross-species spots into the embedding space and reveal the conserved brain regions supported by ST information, which facilitates the detection of homologous regions between humans and mice. Genomic analysis further presents gene expression connections between humans and mice and reveals similar expression patterns for marker genes. Moreover, BrainAlign can accurately map spatially similar homologous regions or clusters onto a unified spatial structural domain while preserving their relative positions.
Keyphrases
- gene expression
- high fat diet induced
- neural network
- endothelial cells
- single cell
- resting state
- genome wide
- white matter
- dna damage
- poor prognosis
- machine learning
- dna methylation
- mouse model
- functional connectivity
- dna repair
- healthcare
- induced pluripotent stem cells
- insulin resistance
- cerebral ischemia
- oxidative stress
- pluripotent stem cells
- genome wide identification
- blood brain barrier
- binding protein