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Robust representation of natural images by sparse and variable population of active neurons in visual cortex

https://doi.org/10.1101/300863
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00359-006-0117-6openalex-snapshot
How silent is the brain: is there a “dark matter” problem in neuroscience?
inferredcites →https://doi.org/10.1007/s10827-006-0003-9openalex-snapshot
A network that uses few active neurones to code visual input predicts the diverse shapes of cortical receptive fields
inferredcites →https://doi.org/10.1016/0959-4388(94)90059-0openalex-snapshot
Noise, neural codes and cortical organization
inferredcites →https://doi.org/10.1016/j.conb.2004.07.007openalex-snapshot
Sparse coding of sensory inputs
inferredcites →https://doi.org/10.1016/j.cub.2011.08.031openalex-snapshot
Reconstructing Visual Experiences from Brain Activity Evoked by Natural Movies
inferredcites →https://doi.org/10.1016/j.cub.2013.04.012openalex-snapshot
Locomotion Controls Spatial Integration in Mouse Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2008.11.004openalex-snapshot
Visual Image Reconstruction from Human Brain Activity using a Combination of Multiscale Local Image Decoders
inferredcites →https://doi.org/10.1016/j.neuron.2009.09.006openalex-snapshot
Bayesian Reconstruction of Natural Images from Human Brain Activity
inferredcites →https://doi.org/10.1016/j.neuron.2010.01.033openalex-snapshot
Modulation of Visual Responses by Behavioral State in Mouse Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2010.08.002openalex-snapshot
Broadly Tuned Response Properties of Diverse Inhibitory Neuron Subtypes in Mouse Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2011.07.026openalex-snapshot
A Resource of Cre Driver Lines for Genetic Targeting of GABAergic Neurons in Cerebral Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2011.12.004openalex-snapshot
Functional Specialization of Seven Mouse Visual Cortical Areas
inferredcites →https://doi.org/10.1016/s0042-6989(97)00121-1openalex-snapshot
The “independent components” of natural scenes are edge filters
inferredcites →https://doi.org/10.1016/s0165-0270(00)00218-1openalex-snapshot
A comparison of video and magnetic search coil recordings of mouse eye movements
inferredcites →https://doi.org/10.1016/s0896-6273(03)00022-9openalex-snapshot
Coding of Natural Scenes in Primary Visual Cortex
inferredcites →https://doi.org/10.1038/370140a0openalex-snapshot
Correlated neuronal discharge rate and its implications for psychophysical performance
inferredcites →https://doi.org/10.1038/381607a0openalex-snapshot
Emergence of simple-cell receptive field properties by learning a sparse code for natural images
inferredcites →https://doi.org/10.1038/nature03274openalex-snapshot
Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex
inferredcites →https://doi.org/10.1038/nature06713openalex-snapshot
Identifying natural images from human brain activity
inferredcites →https://doi.org/10.1038/nature09880openalex-snapshot
Functional specificity of local synaptic connections in neocortical networks
inferredcites →https://doi.org/10.1038/nature12015openalex-snapshot
The emergence of functional microcircuits in visual cortex
inferredcites →https://doi.org/10.1038/nature12354openalex-snapshot
Ultrasensitive fluorescent proteins for imaging neuronal activity
inferredcites →https://doi.org/10.1038/nature14182openalex-snapshot
Functional organization of excitatory synaptic strength in primary visual cortex
inferredcites →https://doi.org/10.1038/nmeth.1243openalex-snapshot
A genetically encoded calcium indicator for chronic in vivo two-photon imaging
inferredcites →https://doi.org/10.1038/nmeth706openalex-snapshot
Sulforhodamine 101 as a specific marker of astroglia in the neocortex in vivo
inferredcites →https://doi.org/10.1038/nn.2140openalex-snapshot
Population imaging of ongoing neuronal activity in the visual cortex of awake rats
inferredcites →https://doi.org/10.1038/nn.2467openalex-snapshot
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
inferredcites →https://doi.org/10.1038/nn.2620openalex-snapshot
Parallel processing of visual space by neighboring neurons in mouse visual cortex
inferredcites →https://doi.org/10.1038/nn.2842openalex-snapshot
Measuring and interpreting neuronal correlations
inferredcites →https://doi.org/10.1038/nn.3707openalex-snapshot
Population code in mouse V1 facilitates readout of natural scenes through increased sparseness
inferredcites →https://doi.org/10.1038/nn.3807openalex-snapshot
Information-limiting correlations
inferredcites →https://doi.org/10.1038/nn.4155openalex-snapshot
Neuronal activity is not required for the initial formation and maturation of visual selectivity
inferredcites →https://doi.org/10.1038/nn1895openalex-snapshot
Rapid learning in cortical coding of visual scenes
inferredcites →https://doi.org/10.1038/s41586-019-1346-5openalex-snapshot
High-dimensional geometry of population responses in visual cortex
inferredcites →https://doi.org/10.1068/p5321openalex-snapshot
A Biologically Inspired Algorithm for the Recovery of Shading and Reflectance Images
inferredcites →https://doi.org/10.1073/pnas.1406077111openalex-snapshot
Visual stimuli recruit intrinsically generated cortical ensembles
inferredcites →https://doi.org/10.1088/0954-898x/2/4/004openalex-snapshot
What determines the capacity of autoassociative memories in the brain?
inferredcites →https://doi.org/10.1098/rspb.1998.0303openalex-snapshot
Independent component filters of natural images compared with simple cells in primary visual cortex
inferredcites →https://doi.org/10.1101/300863openalex-snapshot
Robust representation of natural images by sparse and variable population of active neurons in visual cortex
inferredcites →https://doi.org/10.1109/34.541406openalex-snapshot
Image representation using 2D Gabor wavelets
inferredcites →https://doi.org/10.1109/cvprw.2003openalex-snapshot
2003 Conference on Computer Vision and Pattern Recognition Workshop
inferredcites →https://doi.org/10.1117/12.825882openalex-snapshot
Learning real and complex overcomplete representations from the statistics of natural images
inferredcites →https://doi.org/10.1126/science.1234330openalex-snapshot
Neural Decoding of Visual Imagery During Sleep
inferredcites →https://doi.org/10.1126/science.287.5456.1273openalex-snapshot
Sparse Coding and Decorrelation in Primary Visual Cortex During Natural Vision
inferredcites →https://doi.org/10.1152/jn.00594.2010openalex-snapshot
Sparse coding in striate and extrastriate visual cortex
inferredcites →https://doi.org/10.1152/jn.00747.2006openalex-snapshot
Heterogeneity in the Responses of Adjacent Neurons to Natural Stimuli in Cat Striate Cortex
inferredcites →https://doi.org/10.1152/jn.1987.58.6.1233openalex-snapshot
An evaluation of the two-dimensional Gabor filter model of simple receptive fields in cat striate cortex
inferredcites →https://doi.org/10.1152/jn.1995.73.2.713openalex-snapshot
Sparseness of the neuronal representation of stimuli in the primate temporal visual cortex
inferredcites →https://doi.org/10.1162/0899766054026639openalex-snapshot
How Close Are We to Understanding V1?
inferredcites →https://doi.org/10.1162/neco.1994.6.4.559openalex-snapshot
What Is the Goal of Sensory Coding?
inferredcites →https://doi.org/10.1371/journal.pone.0108697openalex-snapshot
Thy1-GCaMP6 Transgenic Mice for Neuronal Population Imaging In Vivo
inferredcites →https://doi.org/10.1523/jneurosci.0623-08.2008openalex-snapshot
Highly Selective Receptive Fields in Mouse Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.1660-15.2015openalex-snapshot
Spatial Correlations in Natural Scenes Modulate Response Reliability in Mouse Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.19-18-08036.1999openalex-snapshot
Reconstruction of Natural Scenes from Ensemble Responses in the Lateral Geniculate Nucleus
inferredcites →https://doi.org/10.1523/jneurosci.23-11-04746.2003openalex-snapshot
The Receptive-Field Organization of Simple Cells in Primary Visual Cortex of Ferrets under Natural Scene Stimulation
inferredcites →https://doi.org/10.1523/jneurosci.2974-11.2011openalex-snapshot
Local Diversity and Fine-Scale Organization of Receptive Fields in Mouse Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.3869-08.2009openalex-snapshot
The Sparseness of Neuronal Responses in Ferret Primary Visual Cortex
inferredcites →https://doi.org/10.3389/fncir.2011.00018openalex-snapshot
Representation of visual scenes by local neuronal populations in layer 2/3 of mouse visual cortex
inferredcites →https://doi.org/10.3389/neuro.11.010.2008openalex-snapshot
Generating stimuli for neuroscience using PsychoPy
inferredcites →https://doi.org/10.7554/elife.33370openalex-snapshot
Large-scale two-photon imaging revealed super-sparse population codes in the V1 superficial layer of awake monkeys

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1038/s41467-020-14645-xopenalex-snapshot
Natural images are reliably represented by sparse and variable populations of neurons in visual cortex
inferred← citeshttps://doi.org/10.1101/460659openalex-snapshot
Neural Sampling Strategies for Visual Stimulus Reconstruction fromTwo-photon Imaging of Mouse Primary Visual Cortex
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