Functional connectomics spanning multiple areas of mouse visual cortex
J. Alexander BaeiD, Mahaly Baptiste, Maya R. Baptiste, Caitlyn A. BishopiD, Ágnes L. BodoriD, Derrick BrittainiD, Victoria BrooksiD, JoAnn BuchananiD, Daniel J. BumbargeriD, Manuel CastroiD, Brendan CeliiiD, Erick Cobos, Forrest CollmaniD, Nuno Maçarico da CostaiD, Bethanny P. DanskiniD, Sven DorkenwaldiD, Leila ElabbadyiD, Paul G. FaheyiD, Tim P. FlissiD, Emmanouil FroudarakisiD, Jay GageriD, Clare Ruth GamliniD, William Gray-RoncaliD, Akhilesh HalageriiD, James Hebditch, , Chi ZhangiD
Abstract
To understand the brain we must relate neurons functional responses to the circuit architecture that shapes them. Here, we present a large functional connectomics dataset with dense calcium imaging of a millimeter scale volume. We recorded activity from approximately 75,000 neurons in primary visual cortex (VISp) and three higher visual areas (VISrl, VISal and VISlm) in an awake mouse viewing natural movies and synthetic stimuli. The functional data were co-registered with a volumetric electron microscopy (EM) reconstruction containing more than 200,000 cells and 0.5 billion synapses. Subsequent proofreading of a subset of neurons in this volume yielded reconstructions that include complete dendritic trees as well the local and inter-areal axonal projections that map up to thousands of cell-to-cell connections per neuron. Here, we release this dataset as an open-access resource to the scientific community including a set of tools that facilitate data retrieval and downstream analysis. In accompanying papers we describe our findings using the dataset to provide a comprehensive structural characterization of cortical cell types1-3 and the most detailed synaptic level connectivity diagram of a cortical column to date2, uncovering unique cell-type specific inhibitory motifs that can be linked to gene expression data4. Functionally, we identify new computational principles of how information is integrated across visual space5, characterize novel types of neuronal invariances6 and bring structure and function together to decipher a general principle that wires excitatory neurons within and across areas7, 8.
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