Scores on benchmarks
from scoring API| .238 |
average_vision
rank 156
138 benchmarks |
|
| .032 |
neural_vision
rank 490
77 benchmarks |
|
| .048 |
V1
rank 435
33 benchmarks |
|
| .357 |
Marques2020
[reference]
rank 424
22 benchmarks |
|
| .498 |
V1-orientation
rank 411
7 benchmarks |
|
| .931 |
Marques2020_DeValois1982-pref_or
v1
rank 252
|
|
|
1152 images
|
||
| .797 |
Marques2020_Ringach2002-cv_bandwidth_ratio
v1
rank 259
|
|
|
1152 images
|
||
| .812 |
Marques2020_Ringach2002-opr_cv_diff
v1
rank 301
|
|
|
1152 images
|
||
| .949 |
Marques2020_Ringach2002-or_bandwidth
v1
rank 16
|
|
|
1152 images
|
||
| .514 |
V1-receptive_field_size
rank 285
2 benchmarks |
|
| .638 |
Marques2020_Cavanaugh2002-grating_summation_field
v1
[reference]
rank 245
|
|
|
2304 images
|
||
| .390 |
Marques2020_Cavanaugh2002-surround_diameter
v1
[reference]
rank 281
|
|
|
2304 images
|
||
| .336 |
V1-response_selectivity
rank 419
4 benchmarks |
|
| .594 |
Marques2020_FreemanZiemba2013-texture_sparseness
v1
[reference]
rank 329
|
|
|
450 images
|
||
| .749 |
Marques2020_FreemanZiemba2013-texture_variance_ratio
v1
[reference]
rank 172
|
|
|
450 images
|
||
| .530 |
V1-spatial_frequency
rank 401
3 benchmarks |
|
| .628 |
Marques2020_DeValois1982-peak_sf
v1
rank 284
|
|
|
2112 images
|
||
| .964 |
Marques2020_Schiller1976-sf_selective
v1
[reference]
rank 85
|
|
|
2112 images
|
||
| .621 |
V1-surround_modulation
rank 223
1 benchmark |
|
| .621 |
Marques2020_Cavanaugh2002-surround_suppression_index
v1
[reference]
rank 223
|
|
|
2304 images
|
||
| .025 |
Coggan2024_fMRI.V1-rdm
v1
rank 210
|
|
|
24 images
|
||
| .023 |
V2
rank 504
10 benchmarks |
|
| .135 |
Coggan2024_fMRI.V2-rdm
v1
rank 94
|
|
|
24 images
|
||
| .025 |
V4
rank 512
16 benchmarks |
|
| .245 |
SanghaviMurty2020.V4-pls
v2
[reference]
rank 16
|
|
|
recordings from
46
sites in
V4
300 images
|
||
| .057 |
Coggan2024_fMRI.V4-rdm
v1
rank 103
|
|
|
24 images
|
||
| .033 |
IT
rank 479
18 benchmarks |
|
| .463 |
Coggan2024_fMRI.IT-rdm
v1
rank 103
|
|
|
24 images
|
||
| .444 |
behavior_vision
rank 48
61 benchmarks |
|
| .521 |
Rajalingham2018-i2n
v2
[reference]
rank 136
|
|
|
match-to-sample task
240 images
|
||
| .318 |
Geirhos2021-error_consistency
[reference]
rank 97
17 benchmarks |
|
| .551 |
Geirhos2021colour-error_consistency
v1
[reference]
rank 64
|
|
|
640 images
|
||
| .301 |
Geirhos2021contrast-error_consistency
v1
[reference]
rank 98
|
|
|
800 images
|
||
| .271 |
Geirhos2021cueconflict-error_consistency
v1
[reference]
rank 93
|
|
|
1280 images
|
||
| .107 |
Geirhos2021edge-error_consistency
v1
[reference]
rank 109
|
|
|
160 images
|
||
| .546 |
Geirhos2021eidolonI-error_consistency
v1
[reference]
rank 57
|
|
|
800 images
|
||
| .470 |
Geirhos2021eidolonII-error_consistency
v1
[reference]
rank 92
|
|
|
640 images
|
||
| .465 |
Geirhos2021eidolonIII-error_consistency
v1
[reference]
rank 66
|
|
|
480 images
|
||
| .440 |
Geirhos2021falsecolour-error_consistency
v1
[reference]
rank 95
|
|
|
560 images
|
||
| .059 |
Geirhos2021highpass-error_consistency
v1
[reference]
rank 168
|
|
|
640 images
|
||
| .268 |
Geirhos2021lowpass-error_consistency
v1
[reference]
rank 96
|
|
|
800 images
|
||
| .183 |
Geirhos2021phasescrambling-error_consistency
v1
[reference]
rank 105
|
|
|
640 images
|
||
| .234 |
Geirhos2021powerequalisation-error_consistency
v1
[reference]
rank 89
|
|
|
560 images
|
||
| .195 |
Geirhos2021rotation-error_consistency
v1
[reference]
rank 101
|
|
|
960 images
|
||
| .549 |
Geirhos2021silhouette-error_consistency
v1
[reference]
rank 111
|
|
|
160 images
|
||
| .155 |
Geirhos2021sketch-error_consistency
v1
[reference]
rank 95
|
|
|
800 images
|
||
| .358 |
Geirhos2021stylized-error_consistency
v1
[reference]
rank 106
|
|
|
800 images
|
||
| .253 |
Geirhos2021uniformnoise-error_consistency
v1
[reference]
rank 112
|
|
|
800 images
|
||
| .651 |
Baker2022
rank 31
3 benchmarks |
|
| .670 |
Baker2022fragmented-accuracy_delta
v1
[reference]
rank 84
|
|
|
716 images
|
||
| .374 |
Baker2022frankenstein-accuracy_delta
v1
[reference]
rank 124
|
|
|
716 images
|
||
| .908 |
Baker2022inverted-accuracy_delta
v1
[reference]
rank 31
|
|
|
360 images
|
||
| .241 |
BMD2024
rank 50
4 benchmarks |
|
| .281 |
BMD2024.dotted_1Behavioral-accuracy_distance
v1
rank 40
|
|
|
100 images
|
||
| .182 |
BMD2024.dotted_2Behavioral-accuracy_distance
v1
rank 81
|
|
|
100 images
|
||
| .217 |
BMD2024.texture_1Behavioral-accuracy_distance
v1
rank 90
|
|
|
100 images
|
||
| .283 |
BMD2024.texture_2Behavioral-accuracy_distance
v1
rank 47
|
|
|
100 images
|
||
| .375 |
Ferguson2024
[reference]
rank 247
14 benchmarks |
|
| .291 |
Ferguson2024circle_line-value_delta
v1
[reference]
rank 172
|
|
|
2_way_afc task
48 images
|
||
| .352 |
Ferguson2024color-value_delta
v1
[reference]
rank 237
|
|
|
2_way_afc task
48 images
|
||
| .627 |
Ferguson2024convergence-value_delta
v1
[reference]
rank 77
|
|
|
2_way_afc task
48 images
|
||
| .027 |
Ferguson2024eighth-value_delta
v1
[reference]
rank 270
|
|
|
2_way_afc task
48 images
|
||
| .470 |
Ferguson2024gray_easy-value_delta
v1
[reference]
rank 116
|
|
|
2_way_afc task
48 images
|
||
| .437 |
Ferguson2024gray_hard-value_delta
v1
[reference]
rank 162
|
|
|
2_way_afc task
48 images
|
||
| .155 |
Ferguson2024half-value_delta
v1
[reference]
rank 268
|
|
|
2_way_afc task
48 images
|
||
| .020 |
Ferguson2024juncture-value_delta
v1
[reference]
rank 258
|
|
|
2_way_afc task
48 images
|
||
| .186 |
Ferguson2024lle-value_delta
v1
[reference]
rank 241
|
|
|
2_way_afc task
48 images
|
||
| .643 |
Ferguson2024llh-value_delta
v1
[reference]
rank 115
|
|
|
2_way_afc task
48 images
|
||
| .171 |
Ferguson2024quarter-value_delta
v1
[reference]
rank 217
|
|
|
2_way_afc task
48 images
|
||
| .961 |
Ferguson2024round_f-value_delta
v1
[reference]
rank 20
|
|
|
2_way_afc task
48 images
|
||
| .225 |
Ferguson2024round_v-value_delta
v1
[reference]
rank 249
|
|
|
2_way_afc task
48 images
|
||
| .682 |
Ferguson2024tilted_line-value_delta
v1
[reference]
rank 107
|
|
|
2_way_afc task
48 images
|
||
| .297 |
Hebart2023-match
v1
rank 138
|
|
|
1854 images
|
||
| .476 |
Kato2026
rank 65
18 benchmarks |
|
| .359 |
Kato2026-error_consistency
rank 63
9 benchmarks |
|
| .421 |
Kato2026Ori-error_consistency
v1
rank 49
|
|
|
||
| .755 |
Kato2026Fil-error_consistency
v1
rank 9
|
|
|
||
| .388 |
Kato2026Lin-error_consistency
v1
rank 65
|
|
|
||
| .419 |
Kato2026SilTex-error_consistency
v1
rank 76
|
|
|
||
| .365 |
Kato2026Sil-error_consistency
v1
rank 81
|
|
|
||
| .838 |
Kato2026Tex-error_consistency
v1
rank 47
|
|
|
||
| .008 |
Kato2026LinFil-error_consistency
v1
rank 143
|
|
|
||
| .000 |
Kato2026Sparse-error_consistency
v1
rank 35
|
|
|
||
| .041 |
Kato2026Dense-error_consistency
v1
rank 53
|
|
|
||
| .592 |
Kato2026-accuracy_distance
rank 75
9 benchmarks |
|
| 1.0 |
Kato2026Ori-accuracy_distance
v1
rank 1
|
|
|
||
| .993 |
Kato2026Fil-accuracy_distance
v1
rank 48
|
|
|
||
| .470 |
Kato2026Lin-accuracy_distance
v1
rank 72
|
|
|
||
| .668 |
Kato2026SilTex-accuracy_distance
v1
rank 81
|
|
|
||
| .301 |
Kato2026Sil-accuracy_distance
v1
rank 89
|
|
|
||
| 1.0 |
Kato2026Tex-accuracy_distance
v1
rank 1
|
|
|
||
| .697 |
Kato2026LinFil-accuracy_distance
v1
rank 84
|
|
|
||
| .156 |
Kato2026Sparse-accuracy_distance
v1
rank 77
|
|
|
||
| .042 |
Kato2026Dense-accuracy_distance
v1
rank 78
|
|
|
||
| .768 |
Maniquet2024
rank 27
2 benchmarks |
|
| .831 |
Maniquet2024-confusion_similarity
v1
[reference]
rank 38
|
|
|
13600 images
|
||
| .705 |
Maniquet2024-tasks_consistency
v1
[reference]
rank 45
|
|
|
13600 images
|
||
| .351 |
Coggan2024_behavior-ConditionWiseAccuracySimilarity
v1
rank 105
|
|
|
22560 images
|
||
| .392 |
engineering_vision
rank 105
25 benchmarks |
|
| .736 |
ImageNet-top1
v1
[reference]
rank 94
|
|
|
50000 images
|
||
| .434 |
ImageNet-C-top1
[reference]
rank 78
4 benchmarks |
|
| .349 |
ImageNet-C-noise-top1
v2
[reference]
rank 113
|
|
|
||
| .399 |
ImageNet-C-blur-top1
v2
[reference]
rank 58
|
|
|
||
| .481 |
ImageNet-C-weather-top1
v2
[reference]
rank 84
|
|
|
||
| .507 |
ImageNet-C-digital-top1
v2
[reference]
rank 87
|
|
|
||
| .583 |
Geirhos2021-top1
[reference]
rank 112
17 benchmarks |
|
| .977 |
Geirhos2021colour-top1
v1
[reference]
rank 101
|
|
|
640 images
|
||
| .839 |
Geirhos2021contrast-top1
v1
[reference]
rank 130
|
|
|
800 images
|
||
| .199 |
Geirhos2021cueconflict-top1
v1
[reference]
rank 191
|
|
|
1280 images
|
||
| .238 |
Geirhos2021edge-top1
v1
[reference]
rank 207
|
|
|
160 images
|
||
| .541 |
Geirhos2021eidolonI-top1
v1
[reference]
rank 72
|
|
|
800 images
|
||
| .578 |
Geirhos2021eidolonII-top1
v1
[reference]
rank 60
|
|
|
640 images
|
||
| .583 |
Geirhos2021eidolonIII-top1
v1
[reference]
rank 92
|
|
|
480 images
|
||
| .975 |
Geirhos2021falsecolour-top1
v1
[reference]
rank 57
|
|
|
560 images
|
||
| .375 |
Geirhos2021highpass-top1
v1
[reference]
rank 165
|
|
|
640 images
|
||
| .474 |
Geirhos2021lowpass-top1
v1
[reference]
rank 91
|
|
|
800 images
|
||
| .656 |
Geirhos2021phasescrambling-top1
v1
[reference]
rank 87
|
|
|
640 images
|
||
| .766 |
Geirhos2021powerequalisation-top1
v1
[reference]
rank 114
|
|
|
560 images
|
||
| .680 |
Geirhos2021rotation-top1
v1
[reference]
rank 146
|
|
|
960 images
|
||
| .494 |
Geirhos2021silhouette-top1
v1
[reference]
rank 161
|
|
|
160 images
|
||
| .631 |
Geirhos2021sketch-top1
v1
[reference]
rank 123
|
|
|
800 images
|
||
| .418 |
Geirhos2021stylized-top1
v1
[reference]
rank 111
|
|
|
800 images
|
||
| .488 |
Geirhos2021uniformnoise-top1
v1
[reference]
rank 127
|
|
|
800 images
|
||
| .206 |
Hermann2020
[reference]
rank 205
2 benchmarks |
|
| .254 |
Hermann2020cueconflict-shape_bias
v1
[reference]
rank 207
|
|
|
||
| .157 |
Hermann2020cueconflict-shape_match
v1
[reference]
rank 196
|
|
|
||
How to use
from brainscore_vision import load_model
model = load_model("resnet_101_v1")
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.
Historical trend
Hover the line for a preview; click the chart to pin that month in the sidebar. While pinned, hover does not change it -- use Release or Esc to clear.
Benchmarks BibTeX
@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}
}
@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 {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 {Maniquet2024.04.02.587669,
author = {Maniquet, Tim and de Beeck, Hans Op and Costantino, Andrea Ivan},
title = {Recurrent issues with deep neural network models of visual recognition},
elocation-id = {2024.04.02.587669},
year = {2024},
doi = {10.1101/2024.04.02.587669},
publisher = {Cold Spring Harbor Laboratory},
URL = {https://www.biorxiv.org/content/early/2024/04/10/2024.04.02.587669},
eprint = {https://www.biorxiv.org/content/early/2024/04/10/2024.04.02.587669.full.pdf},
journal = {bioRxiv}
}
@INPROCEEDINGS{5206848,
author={J. {Deng} and W. {Dong} and R. {Socher} and L. {Li} and {Kai Li} and {Li Fei-Fei}},
booktitle={2009 IEEE Conference on Computer Vision and Pattern Recognition},
title={ImageNet: A large-scale hierarchical image database},
year={2009},
volume={},
number={},
pages={248-255},
}
@ARTICLE{Hendrycks2019-di,
title = "Benchmarking Neural Network Robustness to Common Corruptions
and Perturbations",
author = "Hendrycks, Dan and Dietterich, Thomas",
abstract = "In this paper we establish rigorous benchmarks for image
classifier robustness. Our first benchmark, ImageNet-C,
standardizes and expands the corruption robustness topic,
while showing which classifiers are preferable in
safety-critical applications. Then we propose a new dataset
called ImageNet-P which enables researchers to benchmark a
classifier's robustness to common perturbations. Unlike
recent robustness research, this benchmark evaluates
performance on common corruptions and perturbations not
worst-case adversarial perturbations. We find that there are
negligible changes in relative corruption robustness from
AlexNet classifiers to ResNet classifiers. Afterward we
discover ways to enhance corruption and perturbation
robustness. We even find that a bypassed adversarial defense
provides substantial common perturbation robustness.
Together our benchmarks may aid future work toward networks
that robustly generalize.",
month = mar,
year = 2019,
archivePrefix = "arXiv",
primaryClass = "cs.LG",
eprint = "1903.12261",
url = "https://arxiv.org/abs/1903.12261"
}
@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}
}