ArticleNature neuroscience2026
Functional bipartite invariance in mouse primary visual cortex receptive fields.
Article in Nature neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Deep learning-driven characterization of single cell tuning in primate visual area V4 supports topological organization.bioRxiv : the preprint server for biology · 2025Article
- Direction of motion decoding in mouse V1: Neuron predictive power relates to functional connectivity organization.bioRxiv : the preprint server for biology · 2025Article
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- Foundation model of neural activity predicts response to new stimulus types and anatomy.bioRxiv : the preprint server for biology · 2024Article
- Closed-loop experiments and brain machine interfaces with multiphoton microscopy.Neurophotonics · 2024Review
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31 authors.
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Abstract
Sensory systems support generalization by representing features that persist under input variation; however, identifying the neuronal basis of these invariances remains difficult due to high-dimensional and nonlinear neural computations. Here we leverage the inception loop paradigm, iterating between large-scale recordings, predictive models and in silico experiments with in vivo verification, to characterize neuronal invariances in mouse primary visual cortex (V1). We synthesize varied exciting inputs (VEIs), dissimilar images that drive target neurons. These VEIs revealed a new bipartite invariance: one subfield encodes a shift-tolerant high-frequency texture and the other encodes a fixed low-frequency pattern. This division aligns with object boundaries defined by spatial frequency differences in highly activating images, suggesting a contribution to segmentation. Analysis of the MICrONS dataset revealed a hierarchy of excitatory neurons in mouse V1 layers 2/3: postsynaptic neurons exhibited greater invariance than their presynaptic inputs, while neurons with lower invariance formed more connections. Together, these results provide insights and scalable methodology for mapping neuronal invariances.
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