The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Unsupervised Learning of Visual Features through Spike Timing Dependent Plasticity
Open accessAbstract
Spike timing dependent plasticity (STDP) is a learning rule that modifies synaptic strength as a function of the relative timing of pre- and postsynaptic spikes. When a neuron is repeatedly presented with similar inputs, STDP is known to have the effect of concentrating high synaptic weights on afferents that systematically fire early, while postsynaptic spike latencies decrease. Here we use this learning rule in an asynchronous feedforward spiking neural network that mimics the ventral visual pathway and shows that when the network is presented with natural images, selectivity to intermediate-complexity visual features emerges. Those features, which correspond to prototypical patterns that are both salient and consistently present in the images, are highly informative and enable robust object recognition, as demonstrated on various classification tasks. Taken together, these results show that temporal codes may be a key to understanding the phenomenal processing speed achieved by the visual system and that STDP can lead to fast and selective responses.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fukushima, K. (1980) · Biological Cybernetics · doi:10.1007/bf00344251 · Cited by 5,759
Speed of processing in the human visual system
Thorpe, S., Fize, D., & Marlot, C. (1996) · Nature · doi:10.1038/381520a0 · Cited by 3,538
Self-citationHierarchical models of object recognition in cortex
Riesenhuber, M., & Poggio, T. (1999) · Nature Neuroscience · doi:10.1038/14819 · Cited by 3,309
On the Uniform Convergence of Relative Frequencies of Events to Their Probabilities
Vapnik, V. N., & Chervonenkis, A. Y. (1971) · Theory of Probability & Its Applications · doi:10.1137/1116025 · Cited by 2,448
Shape representation in the inferior temporal cortex of monkeys
Logothetis, N. K., Pauls, J., & Poggio, T. (1995) · Current Biology · doi:10.1016/s0960-9822(95)00108-4 · Cited by 963
Learning invariance from transformation sequences
Földiák, P. (1991) · Neural Computation · doi:10.1162/neco.1991.3.2.194 · Cited by 661
Visual features of intermediate complexity and their use in classification
Ullman, S., Vidal-Naquet, M., & Sali, E. (2002) · Nature Neuroscience · doi:10.1038/nn870 · Cited by 600
Cited by
HATS: Histograms of Averaged Time Surfaces for Robust Event-Based Object Classification
Sironi, A., Brambilla, M., Bourdis, N., Lagorce, X., & Benosman, R. (2018) · 2018 IEEE/CVF Conference on Computer Vision and Pattern Recognition · doi:10.1109/cvpr.2018.00186 · Cited by 486
Computing with Spiking Neuron Networks
Paugam-Moisy, H., & Bohte, S. (2012) · Handbook of Natural Computing · doi:10.1007/978-3-540-92910-9_10 · Cited by 272
Bio-Inspired Stochastic Computing Using Binary CBRAM Synapses
Suri, M., Querlioz, D., Bichler, O., Palma, G., Vianello, E., Vuillaume, D., Gamrat, C., & DeSalvo, B. (2013) · IEEE Transactions on Electron Devices · doi:10.1109/ted.2013.2263000 · Cited by 229
Tsanov, M., & Manahan-Vaughan, D. (2008) · The Neuroscientist · doi:10.1177/1073858408315655 · Cited by 65
Learning and disrupting invariance in visual recognition with a temporal association rule
Isik, L., Leibo, J. Z., & Poggio, T. (2012) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2012.00037 · Cited by 38
Metadata
- Authors
- Masquelier, T., & Thorpe, S. J.
- Venue
- PLoS Computational Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2007-02-16
- Volume
- 3
- Issue
- 2
- Pages
- e31
- ISSN
- 1553-734X (ISSN-L)
- 1553-7358
- OpenAlex
- W2007815184
- Cited by
- 548
- References
- 7
- FWCI
- 6.19
- Type
- journal article
- Language
- en
- Open access
- gold
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Unsupervised Learning of Visual Features through Spike Timing Dependent Plasticity. https://app.cochat.ai/papers/10.1371/journal.pcbi.0030031
- The paper
- Masquelier, T., & Thorpe, S. J. (2007). Unsupervised Learning of Visual Features through Spike Timing Dependent Plasticity. PLoS Computational Biology. https://doi.org/10.1371/journal.pcbi.0030031
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.