Scores on benchmarks
Model rank shown below is with respect to all public models..113 |
average_vision
rank 376
81 benchmarks |
|
.227 |
behavior_vision
rank 163
43 benchmarks |
|
.512 |
Rajalingham2018-i2n
v2
[reference]
rank 132
|
|
match-to-sample task
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.486 |
Geirhos2021-error_consistency
[reference]
rank 34
17 benchmarks |
|
.800 |
Geirhos2021colour-error_consistency
v1
[reference]
rank 8
|
|
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.544 |
Geirhos2021contrast-error_consistency
v1
[reference]
rank 31
|
|
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.355 |
Geirhos2021cueconflict-error_consistency
v1
[reference]
rank 41
|
|
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.153 |
Geirhos2021edge-error_consistency
v1
[reference]
rank 52
|
|
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.593 |
Geirhos2021eidolonI-error_consistency
v1
[reference]
rank 33
|
|
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.640 |
Geirhos2021eidolonII-error_consistency
v1
[reference]
rank 19
|
|
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.501 |
Geirhos2021eidolonIII-error_consistency
v1
[reference]
rank 36
|
|
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.702 |
Geirhos2021falsecolour-error_consistency
v1
[reference]
rank 16
|
|
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.177 |
Geirhos2021highpass-error_consistency
v1
[reference]
rank 44
|
|
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.410 |
Geirhos2021lowpass-error_consistency
v1
[reference]
rank 44
|
|
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.376 |
Geirhos2021phasescrambling-error_consistency
v1
[reference]
rank 38
|
|
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.380 |
Geirhos2021powerequalisation-error_consistency
v1
[reference]
rank 44
|
|
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.431 |
Geirhos2021rotation-error_consistency
v1
[reference]
rank 24
|
|
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.817 |
Geirhos2021silhouette-error_consistency
v1
[reference]
rank 37
|
|
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.267 |
Geirhos2021sketch-error_consistency
v1
[reference]
rank 42
|
|
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.627 |
Geirhos2021stylized-error_consistency
v1
[reference]
rank 34
|
|
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.493 |
Geirhos2021uniformnoise-error_consistency
v1
[reference]
rank 46
|
|
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.155 |
Baker2022
rank 132
3 benchmarks |
|
.308 |
Baker2022fragmented-accuracy_delta
v1
[reference]
rank 108
|
|
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.156 |
Baker2022frankenstein-accuracy_delta
v1
[reference]
rank 129
|
|
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.000 |
Baker2022inverted-accuracy_delta
v1
[reference]
rank 54
|
|
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.368 |
Ferguson2024
[reference]
rank 172
14 benchmarks |
|
.546 |
Ferguson2024gray_hard-value_delta
v1
[reference]
rank 86
|
|
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.305 |
Ferguson2024lle-value_delta
v1
[reference]
rank 136
|
|
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.608 |
Ferguson2024juncture-value_delta
v1
[reference]
rank 34
|
|
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.952 |
Ferguson2024color-value_delta
v1
[reference]
rank 63
|
|
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.062 |
Ferguson2024round_v-value_delta
v1
[reference]
rank 200
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.148 |
Ferguson2024eighth-value_delta
v1
[reference]
rank 89
|
|
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.576 |
Ferguson2024round_f-value_delta
v1
[reference]
rank 63
|
|
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.242 |
Ferguson2024llh-value_delta
v1
[reference]
rank 151
|
|
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.198 |
Ferguson2024circle_line-value_delta
v1
[reference]
rank 148
|
|
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.518 |
Ferguson2024gray_easy-value_delta
v1
[reference]
rank 69
|
|
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1.0 |
Ferguson2024tilted_line-value_delta
v1
[reference]
rank 1
|
|
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.150 |
Hebart2023-match
v1
rank 157
|
|
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.145 |
BMD2024
rank 128
4 benchmarks |
|
.166 |
BMD2024.dotted_1Behavioral-accuracy_distance
v1
rank 83
|
|
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.083 |
BMD2024.texture_1Behavioral-accuracy_distance
v1
rank 166
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.126 |
BMD2024.texture_2Behavioral-accuracy_distance
v1
rank 129
|
|
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.205 |
BMD2024.dotted_2Behavioral-accuracy_distance
v1
rank 49
|
|
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.158 |
engineering_vision
rank 237
25 benchmarks |
|
.604 |
Geirhos2021-top1
[reference]
rank 67
17 benchmarks |
|
.986 |
Geirhos2021colour-top1
v1
[reference]
rank 44
|
|
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.971 |
Geirhos2021contrast-top1
v1
[reference]
rank 36
|
|
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.195 |
Geirhos2021cueconflict-top1
v1
[reference]
rank 164
|
|
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.212 |
Geirhos2021edge-top1
v1
[reference]
rank 194
|
|
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.453 |
Geirhos2021eidolonI-top1
v1
[reference]
rank 214
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.505 |
Geirhos2021eidolonII-top1
v1
[reference]
rank 147
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.498 |
Geirhos2021eidolonIII-top1
v1
[reference]
rank 158
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.984 |
Geirhos2021falsecolour-top1
v1
[reference]
rank 29
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.487 |
Geirhos2021highpass-top1
v1
[reference]
rank 73
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.481 |
Geirhos2021lowpass-top1
v1
[reference]
rank 62
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.639 |
Geirhos2021phasescrambling-top1
v1
[reference]
rank 88
|
|
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.812 |
Geirhos2021powerequalisation-top1
v1
[reference]
rank 61
|
|
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.780 |
Geirhos2021rotation-top1
v1
[reference]
rank 45
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.544 |
Geirhos2021silhouette-top1
v1
[reference]
rank 76
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.672 |
Geirhos2021sketch-top1
v1
[reference]
rank 59
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.410 |
Geirhos2021stylized-top1
v1
[reference]
rank 94
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.641 |
Geirhos2021uniformnoise-top1
v1
[reference]
rank 40
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.185 |
Hermann2020
[reference]
rank 213
2 benchmarks |
|
.151 |
Hermann2020cueconflict-shape_match
v1
[reference]
rank 173
|
|
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
.219 |
Hermann2020cueconflict-shape_bias
v1
[reference]
rank 217
|
|
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How to use
from brainscore_vision import load_model model = load_model("pnasnet_large") model.start_task(...) model.start_recording(...) model.look_at(...)
Benchmarks bibtex
@article {Rajalingham240614, author = {Rajalingham, Rishi and Issa, Elias B. and Bashivan, Pouya and Kar, Kohitij and Schmidt, Kailyn and DiCarlo, James J.}, title = {Large-scale, high-resolution comparison of the core visual object recognition behavior of humans, monkeys, and state-of-the-art deep artificial neural networks}, elocation-id = {240614}, year = {2018}, doi = {10.1101/240614}, publisher = {Cold Spring Harbor Laboratory}, abstract = {Primates{ extemdash}including humans{ extemdash}can typically recognize objects in visual images at a glance even in the face of naturally occurring identity-preserving image transformations (e.g. changes in viewpoint). A primary neuroscience goal is to uncover neuron-level mechanistic models that quantitatively explain this behavior by predicting primate performance for each and every image. Here, we applied this stringent behavioral prediction test to the leading mechanistic models of primate vision (specifically, deep, convolutional, artificial neural networks; ANNs) by directly comparing their behavioral signatures against those of humans and rhesus macaque monkeys. Using high-throughput data collection systems for human and monkey psychophysics, we collected over one million behavioral trials for 2400 images over 276 binary object discrimination tasks. Consistent with previous work, we observed that state-of-the-art deep, feed-forward convolutional ANNs trained for visual categorization (termed DCNNIC models) accurately predicted primate patterns of object-level confusion. However, when we examined behavioral performance for individual images within each object discrimination task, we found that all tested DCNNIC models were significantly non-predictive of primate performance, and that this prediction failure was not accounted for by simple image attributes, nor rescued by simple model modifications. These results show that current DCNNIC models cannot account for the image-level behavioral patterns of primates, and that new ANN models are needed to more precisely capture the neural mechanisms underlying primate object vision. To this end, large-scale, high-resolution primate behavioral benchmarks{ extemdash}such as those obtained here{ extemdash}could serve as direct guides for discovering such models.SIGNIFICANCE STATEMENT Recently, specific feed-forward deep convolutional artificial neural networks (ANNs) models have dramatically advanced our quantitative understanding of the neural mechanisms underlying primate core object recognition. In this work, we tested the limits of those ANNs by systematically comparing the behavioral responses of these models with the behavioral responses of humans and monkeys, at the resolution of individual images. Using these high-resolution metrics, we found that all tested ANN models significantly diverged from primate behavior. Going forward, these high-resolution, large-scale primate behavioral benchmarks could serve as direct guides for discovering better ANN models of the primate visual system.}, URL = {https://www.biorxiv.org/content/early/2018/02/12/240614}, eprint = {https://www.biorxiv.org/content/early/2018/02/12/240614.full.pdf}, journal = {bioRxiv} } @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} }