Scores on benchmarks
Model rank shown below is with respect to all public models.| .330 |
average_vision
rank 84
111 benchmarks |
|
| .274 |
neural_vision
rank 98
68 benchmarks |
|
| .297 |
V1
rank 98
31 benchmarks |
|
| .358 |
Allen2022_fmri_surface.V1
rank 36
2 benchmarks |
|
| .223 |
Allen2022_fmri_surface.V1-rdm
v1
[reference]
rank 41
|
|
|
||
| .494 |
Allen2022_fmri_surface.V1-ridge
v1
[reference]
rank 28
|
|
|
||
| .220 |
FreemanZiemba2013.V1-pls
v3
[reference]
rank 310
|
|
|
recordings from
102
sites in
V1
315 images
|
||
| .614 |
Hebart2023_fmri.V1-ridgecv
v3
rank 24
|
|
|
||
| .675 |
Marques2020
[reference]
rank 314
22 benchmarks |
|
| .862 |
V1-orientation
rank 197
7 benchmarks |
|
| .961 |
Marques2020_DeValois1982-pref_or
v1
rank 157
|
|
|
1152 images
|
||
| .762 |
Marques2020_Ringach2002-circular_variance
v1
rank 266
|
|
|
1152 images
|
||
| .921 |
Marques2020_Ringach2002-cv_bandwidth_ratio
v1
rank 52
|
|
|
1152 images
|
||
| .932 |
Marques2020_Ringach2002-opr_cv_diff
v1
rank 84
|
|
|
1152 images
|
||
| .845 |
Marques2020_Ringach2002-or_bandwidth
v1
rank 210
|
|
|
1152 images
|
||
| .875 |
Marques2020_Ringach2002-or_selective
v1
rank 298
|
|
|
1152 images
|
||
| .742 |
Marques2020_Ringach2002-orth_pref_ratio
v1
rank 260
|
|
|
1152 images
|
||
| .297 |
V1-receptive_field_size
rank 365
2 benchmarks |
|
| .595 |
Marques2020_Cavanaugh2002-surround_diameter
v1
[reference]
rank 163
|
|
|
2304 images
|
||
| .951 |
V1-response_magnitude
rank 22
3 benchmarks |
|
| .960 |
Marques2020_FreemanZiemba2013-max_noise
v1
[reference]
rank 11
|
|
|
450 images
|
||
| .952 |
Marques2020_FreemanZiemba2013-max_texture
v1
[reference]
rank 55
|
|
|
450 images
|
||
| .942 |
Marques2020_Ringach2002-max_dc
v1
rank 220
|
|
|
1152 images
|
||
| .574 |
V1-response_selectivity
rank 341
4 benchmarks |
|
| .944 |
Marques2020_FreemanZiemba2013-texture_selectivity
v1
[reference]
rank 5
|
|
|
450 images
|
||
| .573 |
Marques2020_FreemanZiemba2013-texture_variance_ratio
v1
[reference]
rank 349
|
|
|
450 images
|
||
| .779 |
Marques2020_Ringach2002-modulation_ratio
v1
rank 30
|
|
|
1152 images
|
||
| .489 |
V1-spatial_frequency
rank 393
3 benchmarks |
|
| .312 |
Marques2020_DeValois1982-peak_sf
v1
rank 396
|
|
|
2112 images
|
||
| .851 |
Marques2020_Schiller1976-sf_bandwidth
v1
[reference]
rank 192
|
|
|
2112 images
|
||
| .306 |
Marques2020_Schiller1976-sf_selective
v1
[reference]
rank 405
|
|
|
2112 images
|
||
| .888 |
V1-surround_modulation
rank 4
1 benchmark |
|
| .888 |
Marques2020_Cavanaugh2002-surround_suppression_index
v1
[reference]
rank 4
|
|
|
2304 images
|
||
| .665 |
V1-texture_modulation
rank 151
2 benchmarks |
|
| .566 |
Marques2020_FreemanZiemba2013-abs_texture_modulation_index
v1
[reference]
rank 162
|
|
|
450 images
|
||
| .764 |
Marques2020_FreemanZiemba2013-texture_modulation_index
v1
[reference]
rank 115
|
|
|
450 images
|
||
| .034 |
Coggan2024_fMRI.V1-rdm
v1
rank 170
|
|
|
24 images
|
||
| .174 |
Zerbe2026_fmri.V1
rank 104
3 benchmarks |
|
| .336 |
Zerbe2026_fmri.V1-ood-ridgecv
v1
rank 71
|
|
|
||
| .186 |
Zerbe2026_fmri.V1-rdm-pearson
v1
rank 60
|
|
|
||
| .314 |
V2
rank 56
8 benchmarks |
|
| .393 |
Allen2022_fmri_surface.V2
rank 10
2 benchmarks |
|
| .266 |
Allen2022_fmri_surface.V2-rdm
v1
[reference]
rank 34
|
|
|
||
| .520 |
Allen2022_fmri_surface.V2-ridge
v1
[reference]
rank 3
|
|
|
||
| .250 |
FreemanZiemba2013.V2-pls
v3
[reference]
rank 221
|
|
|
recordings from
103
sites in
V2
315 images
|
||
| .631 |
Hebart2023_fmri.V2-ridgecv
v3
rank 9
|
|
|
||
| .062 |
Coggan2024_fMRI.V2-rdm
v1
rank 148
|
|
|
24 images
|
||
| .231 |
Zerbe2026_fmri.V2
rank 97
3 benchmarks |
|
| .257 |
Zerbe2026_fmri.V2-rdm-pearson
v1
rank 22
|
|
|
||
| .438 |
Zerbe2026_fmri.V2-tau-ridgecv
v1
rank 8
|
|
|
||
| .285 |
V4
rank 93
13 benchmarks |
|
| .345 |
Allen2022_fmri_surface.V4
rank 14
2 benchmarks |
|
| .217 |
Allen2022_fmri_surface.V4-rdm
v1
[reference]
rank 38
|
|
|
||
| .472 |
Allen2022_fmri_surface.V4-ridge
v1
[reference]
rank 5
|
|
|
||
| .385 |
Hebart2023_fmri.V4-ridgecv
v3
rank 3
|
|
|
||
| .508 |
MajajHong2015.V4-pls
v4
[reference]
rank 267
|
|
|
recordings from
88
sites in
V4
2560 images
|
||
| .562 |
Sanghavi2020.V4-pls
v2
[reference]
rank 158
|
|
|
recordings from
47
sites in
V4
5760 images
|
||
| .477 |
SanghaviJozwik2020.V4-pls
v2
[reference]
rank 89
|
|
|
recordings from
50
sites in
V4
4916 images
|
||
| .209 |
SanghaviMurty2020.V4-pls
v2
[reference]
rank 171
|
|
|
recordings from
46
sites in
V4
300 images
|
||
| .038 |
Coggan2024_fMRI.V4-rdm
v1
rank 114
|
|
|
24 images
|
||
| .324 |
Zerbe2026_fmri.V4
rank 14
3 benchmarks |
|
| .415 |
Zerbe2026_fmri.V4-ood-ridgecv
v1
rank 16
|
|
|
||
| .189 |
Zerbe2026_fmri.V4-rdm-pearson
v1
rank 35
|
|
|
||
| .368 |
Zerbe2026_fmri.V4-tau-ridgecv
v1
rank 8
|
|
|
||
| .201 |
IT
rank 126
16 benchmarks |
|
| .400 |
Allen2022_fmri_surface.IT
rank 43
2 benchmarks |
|
| .261 |
Allen2022_fmri_surface.IT-rdm
v1
[reference]
rank 74
|
|
|
||
| .539 |
Allen2022_fmri_surface.IT-ridge
v1
[reference]
rank 20
|
|
|
||
| .206 |
Bracci2019.anteriorVTC-rdm
v1
rank 195
|
|
|
27 images
|
||
| .341 |
Hebart2023_fmri.IT-ridgecv
v3
rank 10
|
|
|
||
| .385 |
MajajHong2015.IT-pls
v4
[reference]
rank 331
|
|
|
recordings from
168
sites in
IT
2560 images
|
||
| .038 |
MajajHong2015public.IT-reverse_pls
v4
[reference]
rank 95
|
|
|
||
| .409 |
SanghaviJozwik2020.IT-pls
v2
[reference]
rank 245
|
|
|
recordings from
26
sites in
IT
4916 images
|
||
| .302 |
SanghaviMurty2020.IT-pls
v2
[reference]
rank 255
|
|
|
recordings from
29
sites in
IT
300 images
|
||
| .360 |
Coggan2024_fMRI.IT-rdm
v1
rank 133
|
|
|
24 images
|
||
| .176 |
Zerbe2026_fmri.IT
rank 94
3 benchmarks |
|
| .227 |
Zerbe2026_fmri.IT-ood-ridgecv
v1
rank 27
|
|
|
||
| .300 |
Zerbe2026_fmri.IT-tau-ridgecv
v1
rank 42
|
|
|
||
| .387 |
behavior_vision
rank 92
43 benchmarks |
|
| .491 |
Geirhos2021-error_consistency
[reference]
rank 45
17 benchmarks |
|
| .202 |
Geirhos2021colour-error_consistency
v1
[reference]
rank 208
|
|
|
640 images
|
||
| .073 |
Geirhos2021contrast-error_consistency
v1
[reference]
rank 253
|
|
|
800 images
|
||
| .846 |
Geirhos2021cueconflict-error_consistency
v1
[reference]
rank 8
|
|
|
1280 images
|
||
| .705 |
Geirhos2021edge-error_consistency
v1
[reference]
rank 20
|
|
|
160 images
|
||
| .436 |
Geirhos2021eidolonI-error_consistency
v1
[reference]
rank 107
|
|
|
800 images
|
||
| .408 |
Geirhos2021eidolonII-error_consistency
v1
[reference]
rank 120
|
|
|
640 images
|
||
| .359 |
Geirhos2021eidolonIII-error_consistency
v1
[reference]
rank 120
|
|
|
480 images
|
||
| .339 |
Geirhos2021falsecolour-error_consistency
v1
[reference]
rank 125
|
|
|
560 images
|
||
| .353 |
Geirhos2021highpass-error_consistency
v1
[reference]
rank 38
|
|
|
640 images
|
||
| .370 |
Geirhos2021lowpass-error_consistency
v1
[reference]
rank 70
|
|
|
800 images
|
||
| .508 |
Geirhos2021phasescrambling-error_consistency
v1
[reference]
rank 30
|
|
|
640 images
|
||
| .487 |
Geirhos2021powerequalisation-error_consistency
v1
[reference]
rank 38
|
|
|
560 images
|
||
| .475 |
Geirhos2021rotation-error_consistency
v1
[reference]
rank 30
|
|
|
960 images
|
||
| .901 |
Geirhos2021silhouette-error_consistency
v1
[reference]
rank 27
|
|
|
160 images
|
||
| .666 |
Geirhos2021sketch-error_consistency
v1
[reference]
rank 16
|
|
|
800 images
|
||
| .755 |
Geirhos2021stylized-error_consistency
v1
[reference]
rank 10
|
|
|
800 images
|
||
| .472 |
Geirhos2021uniformnoise-error_consistency
v1
[reference]
rank 64
|
|
|
800 images
|
||
| .631 |
Baker2022
rank 35
3 benchmarks |
|
| .691 |
Baker2022fragmented-accuracy_delta
v1
[reference]
rank 79
|
|
|
716 images
|
||
| .220 |
Baker2022frankenstein-accuracy_delta
v1
[reference]
rank 147
|
|
|
716 images
|
||
| .982 |
Baker2022inverted-accuracy_delta
v1
[reference]
rank 19
|
|
|
360 images
|
||
| .513 |
BMD2024
rank 20
4 benchmarks |
|
| .551 |
BMD2024.dotted_1Behavioral-accuracy_distance
v1
rank 19
|
|
|
100 images
|
||
| .304 |
BMD2024.dotted_2Behavioral-accuracy_distance
v1
rank 21
|
|
|
100 images
|
||
| .620 |
BMD2024.texture_1Behavioral-accuracy_distance
v1
rank 20
|
|
|
100 images
|
||
| .577 |
BMD2024.texture_2Behavioral-accuracy_distance
v1
rank 19
|
|
|
100 images
|
||
| .669 |
Ferguson2024
[reference]
rank 12
14 benchmarks |
|
| .320 |
Ferguson2024circle_line-value_delta
v1
[reference]
rank 141
|
|
|
2_way_afc task
48 images
|
||
| 1.0 |
Ferguson2024color-value_delta
v1
[reference]
rank 1
|
|
|
2_way_afc task
48 images
|
||
| .385 |
Ferguson2024convergence-value_delta
v1
[reference]
rank 136
|
|
|
2_way_afc task
48 images
|
||
| 1.0 |
Ferguson2024eighth-value_delta
v1
[reference]
rank 1
|
|
|
2_way_afc task
48 images
|
||
| .845 |
Ferguson2024gray_easy-value_delta
v1
[reference]
rank 26
|
|
|
2_way_afc task
48 images
|
||
| .942 |
Ferguson2024gray_hard-value_delta
v1
[reference]
rank 28
|
|
|
2_way_afc task
48 images
|
||
| .653 |
Ferguson2024half-value_delta
v1
[reference]
rank 104
|
|
|
2_way_afc task
48 images
|
||
| .184 |
Ferguson2024juncture-value_delta
v1
[reference]
rank 122
|
|
|
2_way_afc task
48 images
|
||
| .125 |
Ferguson2024lle-value_delta
v1
[reference]
rank 248
|
|
|
2_way_afc task
48 images
|
||
| 1.0 |
Ferguson2024llh-value_delta
v1
[reference]
rank 1
|
|
|
2_way_afc task
48 images
|
||
| .706 |
Ferguson2024quarter-value_delta
v1
[reference]
rank 52
|
|
|
2_way_afc task
48 images
|
||
| .544 |
Ferguson2024round_f-value_delta
v1
[reference]
rank 92
|
|
|
2_way_afc task
48 images
|
||
| 1.0 |
Ferguson2024round_v-value_delta
v1
[reference]
rank 1
|
|
|
2_way_afc task
48 images
|
||
| .657 |
Ferguson2024tilted_line-value_delta
v1
[reference]
rank 111
|
|
|
2_way_afc task
48 images
|
||
| .528 |
Hebart2023-match
v1
rank 6
|
|
|
1854 images
|
||
| .261 |
Coggan2024_behavior-ConditionWiseAccuracySimilarity
v1
rank 133
|
|
|
22560 images
|
||
| .212 |
engineering_vision
rank 258
25 benchmarks |
|
| .827 |
Geirhos2021-top1
[reference]
rank 7
17 benchmarks |
|
| .997 |
Geirhos2021colour-top1
v1
[reference]
rank 10
|
|
|
640 images
|
||
| .999 |
Geirhos2021contrast-top1
v1
[reference]
rank 2
|
|
|
800 images
|
||
| .500 |
Geirhos2021cueconflict-top1
v1
[reference]
rank 14
|
|
|
1280 images
|
||
| .825 |
Geirhos2021edge-top1
v1
[reference]
rank 21
|
|
|
160 images
|
||
| .564 |
Geirhos2021eidolonI-top1
v1
[reference]
rank 48
|
|
|
800 images
|
||
| .672 |
Geirhos2021eidolonII-top1
v1
[reference]
rank 8
|
|
|
640 images
|
||
| .754 |
Geirhos2021eidolonIII-top1
v1
[reference]
rank 6
|
|
|
480 images
|
||
| .996 |
Geirhos2021falsecolour-top1
v1
[reference]
rank 3
|
|
|
560 images
|
||
| .995 |
Geirhos2021highpass-top1
v1
[reference]
rank 1
|
|
|
640 images
|
||
| .708 |
Geirhos2021lowpass-top1
v1
[reference]
rank 7
|
|
|
800 images
|
||
| .933 |
Geirhos2021phasescrambling-top1
v1
[reference]
rank 4
|
|
|
640 images
|
||
| .989 |
Geirhos2021powerequalisation-top1
v1
[reference]
rank 4
|
|
|
560 images
|
||
| .975 |
Geirhos2021rotation-top1
v1
[reference]
rank 8
|
|
|
960 images
|
||
| .713 |
Geirhos2021silhouette-top1
v1
[reference]
rank 11
|
|
|
160 images
|
||
| .905 |
Geirhos2021sketch-top1
v1
[reference]
rank 22
|
|
|
800 images
|
||
| .664 |
Geirhos2021stylized-top1
v1
[reference]
rank 16
|
|
|
800 images
|
||
| .874 |
Geirhos2021uniformnoise-top1
v1
[reference]
rank 2
|
|
|
800 images
|
||
| .235 |
Hermann2020
[reference]
rank 150
2 benchmarks |
|
| .470 |
Hermann2020cueconflict-shape_match
v1
[reference]
rank 14
|
|
|
||
How to use
from brainscore_vision import load_model
model = load_model("dinov2_vitl14_lc_res336")
model.start_task(...)
model.start_recording(...)
model.look_at(...)
Brain Encoding Response Generator (BERG)
Through the BERG you can easily generate neural responses to images of your choice using any Brain-Score vision model.
For more information on how to use BERG, see the documentation and tutorial.
Benchmarks bibtex
@article{allen_massive_2022,
title = {A massive 7T fMRI dataset to bridge cognitive neuroscience and artificial intelligence},
volume = {25},
issn = {1097-6256},
doi = {10.1038/s41593-021-00962-x},
journal = {Nature Neuroscience},
author = {Allen, Emily J. and St-Yves, Ghislain and Wu, Yihan and Breedlove, Jesse L.
and Prince, Jacob S. and Dowdle, Logan T. and Nau, Matthias and Caron, Brad
and Pestilli, Franco and Charest, Ian and Hutchinson, J. Benjamin
and Naselaris, Thomas and Kay, Kendrick},
year = {2022},
pages = {116--126},
}
@Article{Freeman2013,
author={Freeman, Jeremy
and Ziemba, Corey M.
and Heeger, David J.
and Simoncelli, Eero P.
and Movshon, J. Anthony},
title={A functional and perceptual signature of the second visual area in primates},
journal={Nature Neuroscience},
year={2013},
month={Jul},
day={01},
volume={16},
number={7},
pages={974-981},
abstract={The authors examined neuronal responses in V1 and V2 to synthetic texture stimuli that replicate higher-order statistical dependencies found in natural images. V2, but not V1, responded differentially to these textures, in both macaque (single neurons) and human (fMRI). Human detection of naturalistic structure in the same images was predicted by V2 responses, suggesting a role for V2 in representing natural image structure.},
issn={1546-1726},
doi={10.1038/nn.3402},
url={https://doi.org/10.1038/nn.3402}
}
@article {Marques2021.03.01.433495,
author = {Marques, Tiago and Schrimpf, Martin and DiCarlo, James J.},
title = {Multi-scale hierarchical neural network models that bridge from single neurons in the primate primary visual cortex to object recognition behavior},
elocation-id = {2021.03.01.433495},
year = {2021},
doi = {10.1101/2021.03.01.433495},
publisher = {Cold Spring Harbor Laboratory},
abstract = {Primate visual object recognition relies on the representations in cortical areas at the top of the ventral stream that are computed by a complex, hierarchical network of neural populations. While recent work has created reasonably accurate image-computable hierarchical neural network models of those neural stages, those models do not yet bridge between the properties of individual neurons and the overall emergent behavior of the ventral stream. One reason we cannot yet do this is that individual artificial neurons in multi-stage models have not been shown to be functionally similar to individual biological neurons. Here, we took an important first step by building and evaluating hundreds of hierarchical neural network models in how well their artificial single neurons approximate macaque primary visual cortical (V1) neurons. We found that single neurons in certain models are surprisingly similar to their biological counterparts and that the distributions of single neuron properties, such as those related to orientation and spatial frequency tuning, approximately match those in macaque V1. Critically, we observed that hierarchical models with V1 stages that better match macaque V1 at the single neuron level are also more aligned with human object recognition behavior. Finally, we show that an optimized classical neuroscientific model of V1 is more functionally similar to primate V1 than all of the tested multi-stage models, suggesting room for further model improvements with tangible payoffs in closer alignment to human behavior. These results provide the first multi-stage, multi-scale models that allow our field to ask precisely how the specific properties of individual V1 neurons relate to recognition behavior.HighlightsImage-computable hierarchical neural network models can be naturally extended to create hierarchical {\textquotedblleft}brain models{\textquotedblright} that allow direct comparison with biological neural networks at multiple scales {\textendash} from single neurons, to population of neurons, to behavior.Single neurons in some of these hierarchical brain models are functionally similar to single neurons in macaque primate visual cortex (V1)Some hierarchical brain models have processing stages in which the entire distribution of artificial neuron properties closely matches the biological distributions of those same properties in macaque V1Hierarchical brain models whose V1 processing stages better match the macaque V1 stage also tend to be more aligned with human object recognition behavior at their output stageCompeting Interest StatementThe authors have declared no competing interest.},
URL = {https://www.biorxiv.org/content/early/2021/08/13/2021.03.01.433495},
eprint = {https://www.biorxiv.org/content/early/2021/08/13/2021.03.01.433495.full.pdf},
journal = {bioRxiv}
}
@article{Cavanaugh2002,
author = {Cavanaugh, James R. and Bair, Wyeth and Movshon, J. A.},
doi = {10.1152/jn.00692.2001},
isbn = {0022-3077 (Print) 0022-3077 (Linking)},
issn = {0022-3077},
journal = {Journal of Neurophysiology},
mendeley-groups = {Benchmark effects/Done,Benchmark effects/*Surround Suppression},
number = {5},
pages = {2530--2546},
pmid = {12424292},
title = {{Nature and Interaction of Signals From the Receptive Field Center and Surround in Macaque V1 Neurons}},
url = {http://www.physiology.org/doi/10.1152/jn.00692.2001},
volume = {88},
year = {2002}
}
@article{Freeman2013,
author = {Freeman, Jeremy and Ziemba, Corey M. and Heeger, David J. and Simoncelli, E. P. and Movshon, J. A.},
doi = {10.1038/nn.3402},
issn = {10976256},
journal = {Nature Neuroscience},
number = {7},
pages = {974--981},
pmid = {23685719},
publisher = {Nature Publishing Group},
title = {{A functional and perceptual signature of the second visual area in primates}},
url = {http://dx.doi.org/10.1038/nn.3402},
volume = {16},
year = {2013}
}
@article{Schiller1976,
author = {Schiller, P. H. and Finlay, B. L. and Volman, S. F.},
doi = {10.1152/jn.1976.39.6.1352},
issn = {0022-3077},
journal = {Journal of neurophysiology},
number = {6},
pages = {1334--1351},
pmid = {825624},
title = {{Quantitative studies of single-cell properties in monkey striate cortex. III. Spatial Frequency}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/825624},
volume = {39},
year = {1976}
}
@inproceedings{santurkar2019computer,
title={Computer Vision with a Single (Robust) Classifier},
author={Shibani Santurkar and Dimitris Tsipras and Brandon Tran and Andrew Ilyas and Logan Engstrom and Aleksander Madry},
booktitle={ArXiv preprint arXiv:1906.09453},
year={2019}
}
@article {Majaj13402,
author = {Majaj, Najib J. and Hong, Ha and Solomon, Ethan A. and DiCarlo, James J.},
title = {Simple Learned Weighted Sums of Inferior Temporal Neuronal Firing Rates Accurately Predict Human Core Object Recognition Performance},
volume = {35},
number = {39},
pages = {13402--13418},
year = {2015},
doi = {10.1523/JNEUROSCI.5181-14.2015},
publisher = {Society for Neuroscience},
abstract = {To go beyond qualitative models of the biological substrate of object recognition, we ask: can a single ventral stream neuronal linking hypothesis quantitatively account for core object recognition performance over a broad range of tasks? We measured human performance in 64 object recognition tests using thousands of challenging images that explore shape similarity and identity preserving object variation. We then used multielectrode arrays to measure neuronal population responses to those same images in visual areas V4 and inferior temporal (IT) cortex of monkeys and simulated V1 population responses. We tested leading candidate linking hypotheses and control hypotheses, each postulating how ventral stream neuronal responses underlie object recognition behavior. Specifically, for each hypothesis, we computed the predicted performance on the 64 tests and compared it with the measured pattern of human performance. All tested hypotheses based on low- and mid-level visually evoked activity (pixels, V1, and V4) were very poor predictors of the human behavioral pattern. However, simple learned weighted sums of distributed average IT firing rates exactly predicted the behavioral pattern. More elaborate linking hypotheses relying on IT trial-by-trial correlational structure, finer IT temporal codes, or ones that strictly respect the known spatial substructures of IT ({ extquotedblleft}face patches{ extquotedblright}) did not improve predictive power. Although these results do not reject those more elaborate hypotheses, they suggest a simple, sufficient quantitative model: each object recognition task is learned from the spatially distributed mean firing rates (100 ms) of \~{}60,000 IT neurons and is executed as a simple weighted sum of those firing rates.SIGNIFICANCE STATEMENT We sought to go beyond qualitative models of visual object recognition and determine whether a single neuronal linking hypothesis can quantitatively account for core object recognition behavior. To achieve this, we designed a database of images for evaluating object recognition performance. We used multielectrode arrays to characterize hundreds of neurons in the visual ventral stream of nonhuman primates and measured the object recognition performance of \>100 human observers. Remarkably, we found that simple learned weighted sums of firing rates of neurons in monkey inferior temporal (IT) cortex accurately predicted human performance. Although previous work led us to expect that IT would outperform V4, we were surprised by the quantitative precision with which simple IT-based linking hypotheses accounted for human behavior.},
issn = {0270-6474},
URL = {https://www.jneurosci.org/content/35/39/13402},
eprint = {https://www.jneurosci.org/content/35/39/13402.full.pdf},
journal = {Journal of Neuroscience}}
@misc{Sanghavi_DiCarlo_2021,
title={Sanghavi2020},
url={osf.io/chwdk},
DOI={10.17605/OSF.IO/CHWDK},
publisher={OSF},
author={Sanghavi, Sachi and DiCarlo, James J},
year={2021},
month={Nov}
}
@misc{Sanghavi_Jozwik_DiCarlo_2021,
title={SanghaviJozwik2020},
url={osf.io/fhy36},
DOI={10.17605/OSF.IO/FHY36},
publisher={OSF},
author={Sanghavi, Sachi and Jozwik, Kamila M and DiCarlo, James J},
year={2021},
month={Nov}
}
@misc{Sanghavi_Murty_DiCarlo_2021,
title={SanghaviMurty2020},
url={osf.io/fchme},
DOI={10.17605/OSF.IO/FCHME},
publisher={OSF},
author={Sanghavi, Sachi and Murty, N A R and DiCarlo, James J},
year={2021},
month={Nov}
}
@Article{Kar2019,
author={Kar, Kohitij
and Kubilius, Jonas
and Schmidt, Kailyn
and Issa, Elias B.
and DiCarlo, James J.},
title={Evidence that recurrent circuits are critical to the ventral stream's execution of core object recognition behavior},
journal={Nature Neuroscience},
year={2019},
month={Jun},
day={01},
volume={22},
number={6},
pages={974-983},
abstract={Non-recurrent deep convolutional neural networks (CNNs) are currently the best at modeling core object recognition, a behavior that is supported by the densely recurrent primate ventral stream, culminating in the inferior temporal (IT) cortex. If recurrence is critical to this behavior, then primates should outperform feedforward-only deep CNNs for images that require additional recurrent processing beyond the feedforward IT response. Here we first used behavioral methods to discover hundreds of these `challenge' images. Second, using large-scale electrophysiology, we observed that behaviorally sufficient object identity solutions emerged { extasciitilde}30{ hinspace}ms later in the IT cortex for challenge images compared with primate performance-matched `control' images. Third, these behaviorally critical late-phase IT response patterns were poorly predicted by feedforward deep CNN activations. Notably, very-deep CNNs and shallower recurrent CNNs better predicted these late IT responses, suggesting that there is a functional equivalence between additional nonlinear transformations and recurrence. Beyond arguing that recurrent circuits are critical for rapid object identification, our results provide strong constraints for future recurrent model development.},
issn={1546-1726},
doi={10.1038/s41593-019-0392-5},
url={https://doi.org/10.1038/s41593-019-0392-5}
}
@article{muzellec_reverse_2026,
title = {Reverse predictivity for bidirectional comparison of neural networks and biological brains},
volume = {8},
issn = {2522-5839},
url = {https://doi.org/10.1038/s42256-026-01204-0},
doi = {10.1038/s42256-026-01204-0},
number = {3},
journal = {Nature Machine Intelligence},
author = {Muzellec, Sabine and Kar, Kohitij},
month = mar,
year = {2026},
pages = {474--488},
}
@article{geirhos2021partial,
title={Partial success in closing the gap between human and machine vision},
author={Geirhos, Robert and Narayanappa, Kantharaju and Mitzkus, Benjamin and Thieringer, Tizian and Bethge, Matthias and Wichmann, Felix A and Brendel, Wieland},
journal={Advances in Neural Information Processing Systems},
volume={34},
year={2021},
url={https://openreview.net/forum?id=QkljT4mrfs}
}
@article{BAKER2022104913,
title = {Deep learning models fail to capture the configural nature of human shape perception},
journal = {iScience},
volume = {25},
number = {9},
pages = {104913},
year = {2022},
issn = {2589-0042},
doi = {https://doi.org/10.1016/j.isci.2022.104913},
url = {https://www.sciencedirect.com/science/article/pii/S2589004222011853},
author = {Nicholas Baker and James H. Elder},
keywords = {Biological sciences, Neuroscience, Sensory neuroscience},
abstract = {Summary
A hallmark of human object perception is sensitivity to the holistic configuration of the local shape features of an object. Deep convolutional neural networks (DCNNs) are currently the dominant models for object recognition processing in the visual cortex, but do they capture this configural sensitivity? To answer this question, we employed a dataset of animal silhouettes and created a variant of this dataset that disrupts the configuration of each object while preserving local features. While human performance was impacted by this manipulation, DCNN performance was not, indicating insensitivity to object configuration. Modifications to training and architecture to make networks more brain-like did not lead to configural processing, and none of the networks were able to accurately predict trial-by-trial human object judgements. We speculate that to match human configural sensitivity, networks must be trained to solve a broader range of object tasks beyond category recognition.}
}
@misc{ferguson_ngo_lee_dicarlo_schrimpf_2024,
title={How Well is Visual Search Asymmetry predicted by a Binary-Choice, Rapid, Accuracy-based Visual-search, Oddball-detection (BRAVO) task?},
url={osf.io/5ba3n},
DOI={10.17605/OSF.IO/5BA3N},
publisher={OSF},
author={Ferguson, Michael E, Jr and Ngo, Jerry and Lee, Michael and DiCarlo, James and Schrimpf, Martin},
year={2024},
month={Jun}
}
@article{hermann2020origins,
title={The origins and prevalence of texture bias in convolutional neural networks},
author={Hermann, Katherine and Chen, Ting and Kornblith, Simon},
journal={Advances in Neural Information Processing Systems},
volume={33},
pages={19000--19015},
year={2020},
url={https://proceedings.neurips.cc/paper/2020/hash/db5f9f42a7157abe65bb145000b5871a-Abstract.html}
}