Statistical Learning of Serial Visual Transitions by Neurons in Monkey Inferotemporal Cortex
Open accessAbstract
If monkeys repeatedly, over the course of weeks, view displays in which two images appear in fixed sequence, then neurons of inferotemporal cortex (ITC) come to exhibit prediction suppression. The response to the trailing image is weaker if it follows the leading image with which it was paired during training than if it follows some other leading image. Prediction suppression is a plausible neural mechanism for statistical learning of visual transitions such as has been demonstrated in behavioral studies of human infants and adults. However, in the human studies, subjects are exposed to continuous sequences in which the same image can be both predicted and predicting and statistical dependency can exist between nonadjacent items. The aim of the present study was to investigate whether prediction suppression in ITC develops under such circumstances. To resolve this issue, we exposed monkeys repeatedly to triplets of images presented in fixed order. The results indicate that prediction suppression can be induced by training not only with pairs of images but also with longer sequences.
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ES effects in macaque IT neurons emerge at early latencies (~150 ms).
“These effects were sensitive to transitional statistics (e.g., the transition from Stimulus A to Stimulus B being more probable than from B to A), 90 , 91 persisted after controlling for RS, 88 , 89 and emerged at early latencies (∼150 ms). 88 , 90 , 91 , 92”
From Evaluating the neurophysiological evidence for predictive processing as a model of perception (2020) · cites this paper as [91]
ES effects in macaque IT neurons are sensitive to transitional statistics.
“These effects were sensitive to transitional statistics (e.g., the transition from Stimulus A to Stimulus B being more probable than from B to A), 90 , 91 persisted after controlling for RS, 88 , 89 and emerged at early latencies (∼150 ms). 88 , 90 , 91 , 92”
From Evaluating the neurophysiological evidence for predictive processing as a model of perception (2020) · cites this paper as [91]
There is conflicting evidence regarding whether IT neurons are sensitive to statistical regularities present in nonadjacent stimuli from a sequence of images or whether these suppression effects are determined by the immediately preceding stimulus.
“There is also conflicting evidence regarding whether IT neurons are sensitive to statistical regularities present in nonadjacent stimuli from a sequence of images 91 or whether these suppression effects are determined by the immediately preceding stimulus. 89 , 96”
From Evaluating the neurophysiological evidence for predictive processing as a model of perception (2020) · cites this paper as [91]
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Cites
Statistical learning by 8-month-old infants
Saffran, J. R., Aslin, R. N., & Newport, E. L. (1996) · Science · doi:10.1126/science.274.5294.1926 · Cited by 5,659 · see citing works
Visual statistical learning in infancy: evidence for a domain general learning mechanism
Kirkham, N. Z., Slemmer, J. A., & Johnson, S. P. (2002) · Cognition · doi:10.1016/s0010-0277(02)00004-5 · Cited by 1,072 · see citing works
Expectation (and attention) in visual cognition
Summerfield, C., & Egner, T. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.06.003 · Cited by 950 · see citing works
Variability and Detection of Invariant Structure
Gómez, R. (2002) · Psychology Science · doi:10.1111/1467-9280.00476 · Cited by 898 · see citing works
The Automaticity of Visual Statistical Learning.
Turk‐Browne, N. B., Junge, J. A., & Scholl, B. J. (2005) · Journal of Experimental Psychology General · doi:10.1037/0096-3445.134.4.552 · Cited by 817 · see citing works
Neuronal correlate of visual associative long-term memory in the primate temporal cortex
Miyashita, Y. (1988) · Nature · doi:10.1038/335817a0 · Cited by 741 · see citing works
Learning at a distance I. Statistical learning of non-adjacent dependencies.
Newport, E., & Aslin, R. (2004) · Cognitive Psychology · doi:10.1016/s0010-0285(03)00128-2 · Cited by 735 · see citing works
Statistical learning of higher-order temporal structure from visual shape sequences.
Fiser, J., & Aslin, R. (2002) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037//0278-7393.28.3.458 · Cited by 641 · see citing works
A neuronal model of predictive coding accounting for the mismatch negativity.
Wacongne, C., Changeux, J.-P., & Dehaene, S. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5003-11.2012 · Cited by 542 · see citing works
Statistical learning and language acquisition
Romberg, A. R., & Saffran, J. R. (2010) · WIREs Cognitive Science · doi:10.1002/wcs.78 · Cited by 517 · see citing works
Statistical learning of higher-order temporal structure from visual shape sequences.
Fiser, J., & Aslin, R. Ν. (2002) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.28.3.458 · Cited by 505 · see citing works
Statistical Learning in a Natural Language by 8-Month-Old Infants
Pelucchi, B., Hay, J. F., & Saffran, J. R. (2009) · Child Development · doi:10.1111/j.1467-8624.2009.01290.x · Cited by 476 · see citing works
Stimulus Predictability Reduces Responses in Primary Visual Cortex
Alink, A., Schwiedrzik, C. M., Kohler, A., Singer, W., & Muckli, L. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3730-10.2010 · Cited by 435 · see citing works
Statistical Learning: From Acquiring Specific Items to Forming General Rules
Aslin, R. N., & Newport, E. L. (2012) · Current Directions in Psychological Science · doi:10.1177/0963721412436806 · Cited by 348 · see citing works
Statistical learning of visual transitions in monkey inferotemporal cortex
Meyer, T., & Olson, C. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112895108 · Cited by 325 · see citing works
Self-citationDistant melodies: statistical learning of nonadjacent dependencies in tone sequences.
Creel, S. C., Newport, E., & Aslin, R. (2004) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037/0278-7393.30.5.1119 · Cited by 313 · see citing works
Visual statistical learning in the newborn infant
Bulf, H., Johnson, S. P., & Valenza, E. (2011) · Cognition · doi:10.1016/j.cognition.2011.06.010 · Cited by 281 · see citing works
Predictive coding of music – Brain responses to rhythmic incongruity
Vuust, P., Østergaard, L., Pallesen, K. J., Bailey, C. J., & Roepstorff, A. (2008) · Cortex · doi:10.1016/j.cortex.2008.05.014 · Cited by 277 · see citing works
Unsupervised Natural Experience Rapidly Alters Invariant Object Representation in Visual Cortex
Li, N., & DiCarlo, J. J. (2008) · Science · doi:10.1126/science.1160028 · Cited by 263 · see citing works
Testing assumptions of statistical learning: Is it long-term and implicit?
Kim, R. S., Seitz, A. R., Feenstra, H., & Shams, L. B. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.06.030 · Cited by 256 · see citing works
Pearce, M. T., Ruiz, M. H., Kapasi, S., Wiggins, G. A., & Bhattacharya, J. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.019 · Cited by 248 · see citing works
Experience-dependent sharpening of visual shape selectivity in inferior temporal cortex.
Freedman, D. J., Riesenhuber, M., Poggio, T., & Miller, E. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj100 · Cited by 241 · see citing works
Learned spatiotemporal sequence recognition and prediction in primary visual cortex
Gavornik, J. P., & Bear, M. F. (2014) · Nature Neuroscience · doi:10.1038/nn.3683 · Cited by 227 · see citing works
Responses of Macaque Perirhinal Neurons during and after Visual Stimulus Association Learning
Erickson, C. A., & Desimone, R. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-23-10404.1999 · Cited by 221 · see citing works
Multidimensional visual statistical learning.
Turk‐Browne, N. B., Isola, P., Scholl, B. J., & Treat, T. A. (2008) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.34.2.399 · Cited by 163 · see citing works
Statistical Learning of Adjacent and Non-Adjacent Dependencies among Non-Linguistic Sounds
Gebhart, A. L., Newport, E., & Aslin, R. (2009) · Psychonomic Bulletin & Review · doi:10.3758/pbr.16.3.486 · Cited by 157 · see citing works
Phonology impacts segmentation in online speech processing
Onnis, L., Monaghan, P., Richmond, K., & Chater, N. (2005) · Journal of Memory and Language · doi:10.1016/j.jml.2005.02.011 · Cited by 135 · see citing works
Improved Methods for Statistical Modelling of Monophonic Music
Pearce, M. T., & Wiggins, G. A. (2004) · Journal of New Music Research · doi:10.1080/0929821052000343840 · Cited by 131 · see citing works
Dien, J., Frishkoff, G. A., Cerbone, A. B., & Tucker, D. M. (2002) · Cognitive Brain Research · doi:10.1016/s0926-6410(02)00147-7 · Cited by 91 · see citing works
James, C. E., Britz, J., Vuilleumier, P. O., Hauert, C.-A., & Michel, C. M. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.06.025 · Cited by 81 · see citing works
Howard, J. H., Howard, D. V., Dennis, N. A., & Kelly, A. J. (2008) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/a0012797 · Cited by 80 · see citing works
The Effect of Conditional Probability of Chord Progression on Brain Response: An MEG Study
Kim, S., Kim, J. S., & Chung, C. K. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017337 · Cited by 61 · see citing works
Image familiarization sharpens response dynamics of neurons in inferotemporal cortex
Meyer, T., Walker, C. P. R., Cho, R. Y., & Olson, C. R. (2014) · Nature Neuroscience · doi:10.1038/nn.3794 · Cited by 59 · see citing works
Self-citationRollenhagen, J. E., & Olson, C. R. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00158.2005 · Cited by 59 · see citing works
Self-citationContext Familiarity Enhances Target Processing by Inferior Temporal Cortex Neurons
Mruczek, R. E. B., & Sheinberg, D. L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2106-07.2007 · Cited by 43 · see citing works
Gonzalez-Gomez, N., & Nazzi, T. (2013) · Journal of Speech, Language and Hearing Research · doi:10.1044/1092-4388(2012/12-0138 · Cited by 33 · see citing works
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Dehaene, S., Meyniel, F., Wacongne, C., Wang, L., & Pallier, C. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.019 · Cited by 478 · see citing works
Evaluating the neurophysiological evidence for predictive processing as a model of perception
Walsh, K. S., McGovern, D. P., Clark, A., & O'Connell, R. G. (2020) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14321 · Cited by 333 · see citing works
Conway, C. M. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.01.032 · Cited by 272 · see citing works
Human Inferences about Sequences: A Minimal Transition Probability Model
Meyniel, F., Maheu, M., & Dehaene, S. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005260 · Cited by 137 · see citing works
Kremláček, J., Kreegipuu, K., Tales, A., Astikainen, P., Põldver, N., Näätänen, R., & Stefanics, G. (2016) · Cortex · doi:10.1016/j.cortex.2016.03.017 · Cited by 138 · see citing works
Encoding of Stimulus Probability in Macaque Inferior Temporal Cortex
Bell, A. H., Summerfield, C., Morin, E. L., Malecek, N. J., & Ungerleider, L. G. (2016) · Current Biology · doi:10.1016/j.cub.2016.07.007 · Cited by 118 · see citing works
Statistical Learning Signals in Macaque Inferior Temporal Cortex
Kaposvari, P., Kumar, S., & Vogels, R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhw374 · Cited by 91 · see citing works
Brain signatures of a multiscale process of sequence learning in humans
Maheu, M., Dehaene, S., & Meyniel, F. (2019) · eLife · doi:10.7554/elife.41541 · Cited by 98 · see citing works
Encoding of predictable and unpredictable stimuli by inferior temporal cortical neurons
Kumar, S., Kaposvari, P., & Vogels, R. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01135 · Cited by 75 · see citing works
Problems with visual statistical learning in developmental dyslexia
Sigurdardottir, H. M., Daníelsdóttir, H. B., Gudmundsdottir, M., Hjartarson, K. H., Þórarinsdóttir, E. Á., & Kristjansson, A. K. (2017) · Scientific Reports · doi:10.1038/s41598-017-00554-5 · Cited by 75 · see citing works
Kikuchi, Y., Attaheri, A., Wilson, B., Rhone, A. E., Nourski, K. V., Gander, P. E., Kovach, C. K., Kawasaki, H., Griffiths, T. D., Howard, M. A., et al. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2000219 · Cited by 60 · see citing works
Ramachandran, S., Meyer, T., & Olson, C. R. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00091.2015 · Cited by 38 · see citing works
Self-citationThe Role of Visual Factors in Dyslexia
Kristjansson, A. K., & Sigurdardottir, H. M. (2023) · Journal of Cognition · doi:10.5334/joc.287 · Cited by 37 · see citing works
Feuerriegel, D., Churches, O. F., Coussens, S. W., & Keage, H. A. D. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.12.029 · Cited by 38 · see citing works
Structured sequence learning across sensory modalities in humans and nonhuman primates
Milne, A. E., Wilson, B., & Christiansen, M. H. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.11.016 · Cited by 38 · see citing works
Computational and neural mechanisms of statistical pain learning
Mancini, F., Zhang, S., & Seymour, B. (2022) · Nature Communications · doi:10.1038/s41467-022-34283-9 · Cited by 36 · see citing works
Descending pathways generate perception of and neural responses to weak sensory input
Metzen, M. G., Huang, C. G., & Chacron, M. J. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005239 · Cited by 35 · see citing works
den Ouden, C., Zhou, A., Mepani, V., Kovács, G., Vogels, R., & Feuerriegel, D. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120347 · Cited by 32 · see citing works
The Visual System's Internal Model of the World
Lee, T. S. (2015) · Proceedings of the IEEE · doi:10.1109/jproc.2015.2434601 · Cited by 28 · see citing works
Prediction suppression and surprise enhancement in monkey inferotemporal cortex
Ramachandran, S., Meyer, T., & Olson, C. R. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00136.2017 · Cited by 29 · see citing works
Self-citationRemembering the Past to See the Future
Rust, N. C., & Palmer, S. E. (2021) · Annual Review of Vision Science · doi:10.1146/annurev-vision-093019-112249 · Cited by 24 · see citing works
Temporal continuity shapes visual responses of macaque face patch neurons
Russ, B. E., Koyano, K. W., Day‐Cooney, J., Perwez, N., & Leopold, D. A. (2023) · Neuron · doi:10.1016/j.neuron.2022.12.021 · Cited by 23 · see citing works
Perceptual suppression of predicted natural images
Denison, R. N., Sheynin, J., & Silver, M. A. (2016) · Journal of Vision · doi:10.1167/16.13.6 · Cited by 22 · see citing works
A multimodal cortical network of sensory expectation violation revealed by fMRI
Grundei, M., Schmidt, T. T., & Blankenburg, F. (2023) · Human Brain Mapping · doi:10.1002/hbm.26482 · Cited by 18 · see citing works
Adaptation in the visual system: Networked fatigue or suppressed prediction error signalling?
Feuerriegel, D. (2024) · Cortex · doi:10.1016/j.cortex.2024.06.003 · Cited by 25 · see citing works
Statistical Learning Signals for Complex Visual Images in Macaque Early Visual Cortex
Vergnieux, V., & Vogels, R. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00789 · Cited by 16 · see citing works
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Esmailpour, H., Raman, R., & Vogels, R. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac265 · Cited by 15 · see citing works
Beukema, P., & Verstynen, T. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.11.014 · Cited by 15 · see citing works
Zhou, Y. J., Pérez-Bellido, A., Haegens, S., & de Lange, F. P. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01511 · Cited by 12 · see citing works
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Macaques preferentially attend to intermediately surprising information
Wu, S., Blanchard, T. C., Meschke, E. X., Aslin, R. Ν., Hayden, B. Y., & Kidd, C. (2022) · Biology Letters · doi:10.1098/rsbl.2022.0144 · Cited by 13 · see citing works
A Long Timescale Stimulus History Effect in the Primary Visual CortexPreprint
Kim, H., Homann, J., Tank, D. W., & Berry, M. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/585539 · Cited by 9 · see citing works
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Loidolt, M., Rudelt, L., & Priesemann, V. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.15.297580 · Cited by 9 · see citing works
Online measurement of learning temporal statistical structure in categorization tasks
Sáringer, S., Fehér, Á., Sáry, G., & Kaposvári, P. (2022) · Memory & Cognition · doi:10.3758/s13421-022-01302-5 · Cited by 7 · see citing works
den Ouden, C., Kashyap, M., Kikkawa, M., & Feuerriegel, D. (2025) · Psychophysiology · doi:10.1111/psyp.70076 · Cited by 10 · see citing works
Traveling waves shape neural population dynamics enabling predictions and internal model updatingPreprint
Mohanta, S., Cleveland, D., Afrasiabi, M., Rhone, A. E., Górska, U., Borkenhagen, M. J. C., Sanders, R. D., Boly, M., Nourski, K. V., & Saalmann, Y. B. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.09.574848 · Cited by 5 · see citing works
van Kerkoerle, T., Pape, L., Ekramnia, M., Feng, X., Tasserie, J., Dupont, M., Li, X., Jarraya, B., Vanduffel, W., Dehaene, S., et al. (2024) · eLife · doi:10.7554/elife.87380.2.sa0 · Cited by 4 · see citing works
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Puneeth, N., & Arun, S. P. (2016) · Scientific Reports · doi:10.1038/srep30808 · Cited by 4 · see citing works
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Feuerriegel, D. (2023) · doi:10.31234/osf.io/73hb4 · Cited by 4 · see citing works
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Pedersen, R. (2024) · Synthese · doi:10.1007/s11229-024-04787-6 · Cited by 3 · see citing works
Wilson, B., & Petkov, C. I. (2018) · Interaction Studies Social Behaviour and Communication in Biological and Artificial Systems · doi:10.1075/is.17038.wil · Cited by 3 · see citing works
Prior probability cues bias sensory encoding with increasing task exposure
Walsh, K. S., McGovern, D. P., Dully, J., Kelly, S. P., & O’Connell, R. G. (2024) · eLife · doi:10.7554/elife.91135.3 · Cited by 2 · see citing works
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Adaptation of the inferior temporal neurons and efficient visual processing
Yamane, Y. (2024) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2024.1398874 · Cited by 2 · see citing works
Wyrick, D. G., Cain, N., Larsen, R. S., Lecoq, J. A., Valley, M. T., Ahmed, R., Bowlus, J., Boyer, G., Caldejon, S., Casal, L., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.02.543483 · Cited by 2 · see citing works
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Dissociation of sensory facilitation and decision bias in statistical learning
Simard, F., & Pack, C. C. (2015) · Visual Cognition · doi:10.1080/13506285.2015.1085477 · Cited by 1 · see citing works
Incidental learning of predictive temporal context within cortical representations of visual shape
Kakaei, E., & Braun, J. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00278
Brain areas for reversible symbolic reference, a potential singularity of the human brainPreprint
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Finnie, P. S. B., Bear, M. F., & Cooke, S. F. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21079-1
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Liberto, D., & de Marco, G. (2017) · Arrow@dit (Dublin Institute of Technology)
Cortical and behavioral signatures of response binding during sequential skill learning
Beukema, P. (2018) · D-Scholarship@Pitt (University of Pittsburgh)
Wilson, B., & Petkov, C. I. (2020) · Benjamins current topics · doi:10.1075/bct.112.20wil
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- Authors
- Meyer, T., Ramachandran, S., & Olson, C. R.
- Affiliations
- Center for the Neural Basis of Cognition (US)
- University of Pittsburgh (US)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2014-07-09
- Volume
- 34
- Issue
- 28
- Pages
- 9332-9337
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC4087210
- OpenAlex
- W1991888778
- Cited by
- 70
- References
- 35
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 20 · 2023: 11 · 2022: 4 · 2021: 1 · 2020: 5 · 2019: 4 · 2018: 3 · 2017: 9 · 2016: 6 · 2015: 4
- FWCI
- 3.50
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Pennsylvania Department of Health (P41RR03631)
- National Institutes of Health (NIH P50, EY08098, MH084053)
- National Institute of Mental Health (P50MH084053, K08MH080329)
- National Eye Institute (R01EY018620, P30EY008098)
- National Center for Research Resources (P41RR003631)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Keywords
- statistical learning, inferotemporal cortex, monkey visual cortex, image sequences, neural prediction, visual learning
- MeSH terms
- Animals, Cues, Data Interpretation, Statistical, Discrimination Learning, Female, Inhibition, Psychological, Macaca mulatta, Male, Models, Neurological, Neural Inhibition, Pattern Recognition, Visual, Photic Stimulation, Temporal Lobe, Visual Cortex, Models, Statistical
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 ›
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