Slides and readings

EJ Chichilnisky

Suggested Readings

Pillow, J.W., Shlens, J., Paninski, L., Sher, A., Litke, A.M., Chichilnisky, E.J. & Simoncelli, E.P. (2008). Spatio-temporal correlations and visual signalling in a complete neuronal population
Muratore, D.G. & Chichilnisky, E.J. (2019). Artificial Retina: A Future Cellular-Resolution Brain-Machine Interface
Shah, N.P., Brackbill, N., Rhoades, C., Kling, A., Goetz, G., Litke, A.M., Sher, A., Simoncelli, E.P. & A. Chichilnisky, E.J. (2020). Inference of nonlinear receptive field subunits with spike-triggered clustering


John Serences

Slides

Suggested Readings

Sheehan, T.C. & Serences, J.T. (2022). Attractive serial dependence overcomes repulsive neuronal adaptation. PLoS Biology
Henderson, M.M., Serences, J.,T. & Rungratsameetaweemana, N. (2023). Dynamic categorization rules alter representations in human visual cortex
Henderson, M.M., Rademaker, R.L. & Serences, J.T. (2022). Flexible utilization of spatial- and motor- based codes for the storage of visuo-spatial information


Eero Simoncelli

Slides part 1
Slides part 2

Suggested Readings

Barlow, H. B. (1961a). Possible principles underlying the transformations of sensory messages
Barlow, H. B. (1969). Pattern recognition and the responses of sensory neurons
Adelson, E. H. & Bergen J. R. (1991). The Plenoptic Function and the Elements of Early Vision
Wandell, B.A. (1995). Foundations of vision. [Chapter on trichromacy and metamers]
Balas, B., Nakano, L. & Rosenholtz, R. (2009). A summary-statistic representation in peripheral vision explains visual crowding
Freeman, J. & Simoncelli, E.P. (2011). Metamers of the ventral stream
Ziemba, C.M. & Simoncelli, E.P. (2021). Opposing effects of selectivity and invariance in peripheral vision
Zhou, J.Y. Duong, L.R. & Simoncelli, E.P. (2024). A unified framework for perceived magnitude and discriminability of sensory stimuli
Ganguli, D. & Simoncelli, E.P. (2016). Neural and perceptual signatures of efficient sensory coding
Wei, X-X., & Stocker, A.A. (2017). Lawful relation between perceptual bias and discriminability
Berardino, A., Laparra, V., Ballé, J. & Simoncelli, E.P. (2017). Eigen-distortions of hierarchical representations

Code repository Eero’s lab has produced a python library of tools to explore vision models by synthesizing novel informative images. This includes Metamers, Eigendistortions (Berardino 2017), Maximal differentiation (MAD) competition (Wang 2008), and Geodesics (Henaff 2016).

https://github.com/LabForComputationalVision/plenoptic/


Stephanie Palmer

Slides part 1
Slides part 2

1. Efficient coding notes
2. Spike train information notes
3. Probability and Inference

Suggested Readings

Palmer, S.E., Marre, O., Berry, M.J. & Bialek, W. (2015). Predictive information in a sensory population
Salisbury, J.M. & Palmer, S.E. (2016). Optimal prediction in the retina and natural motion statistics
Wang, S., Segev, I., Borst, A. & Palmer, S. (2021). Maximally efficient prediction in the early fly visual system may support evasive flight maneuvers

Extra:
Wang, S., Hoshal, B., de Laittre, E., Marre, O., Berry, M. & Palmer, S. (2022). Learning low-dimensional generalizable natural features from retina using a U-net.
Hoshal, B.D., Holmes, C.M., Bojanek, K., Salisbury, J., Berry, M.J., Marre, O. & Palmer, S.E. (2023). Stimulus invariant aspects of the retinal code drive discriminability of natural scenes


Jonathan Pillow

Slides
GLM Tutorial (Matlab)
GLM Tutorial (Python)

Suggested Readings

Pillow, Shlens, Paninski, Sher, Litke, Chichilnisky & Simoncelli (2008). Spatio-temporal correlations and visual signaling in a complete neuronal population
Park, Meister, Huk & Pillow (2014). Encoding and decoding in parietal cortex during sensorimotor decision-making
Weber & Pillow (2017). Capturing the dynamical repertoire of single neurons with generalized linear models.
Latimer, Rieke & Pillow (2019). Inferring synaptic inputs from spikes with a conductance-based neural encoding model


Jacob Yates

Slides

Suggested Readings

Casile A, Victor, J.D. & Rucci, M. (2019). Contrast sensitivity reveals an oculomotor strategy for temporally encoding space.
Victor, J.D., & Rucci M. (2015). The unsteady eye: an information-processing stage, not a bug
Yates, J.L. et al. (2023). Detailed characterization of neural selectivity in free viewing primates


Lea Duncker

Slides

Suggested Readings

Adelson, E.H. (2000). Lightness Perception and Lightness Illusions. (Chapter in The New Cognitive Neurosciences).
Bishop, C.M. (2006) Mixture Models and EM. (Chapter 9 in Pattern Recognition and Machine Learning).
Cunningham, J.P. & Yu, B.M. (2014). Dimensionality reduction for large-scale neural recordings.
Ernst M.O. & Banks, M.S. (2002). Humans integrate visual and haptic information in a statistically optimal fashion.
Olshausen, B.A. & Field, D.J. (1996). of simple-cell receptive field properties by learning a sparse code for natural Images.


Ruth Rosenholtz

Slides

Suggested Readings

Rosenholtz R. (2016). Capabilities and Limitations of Peripheral Vision
Rosenholtz, R., Huang, J. & Ehinger, K.A. (2012). Rethinking the Role of Top-Down Attention in Vision: Effects Attributable to a Lossy Representation in Peripheral Vision
Rosenholtz, R., Yu, D., & Keshvari, S. (2019). Challenges to pooling models of crowding: Implications for visual mechanisms


Rachel Denison

Slides

Suggested Readings

Recent reviews on dynamic attention:
Denison, R.N. (2024). Visual temporal attention from perception to computation
Nobre, A.C. & van Ede, F. (2023). Attention in flux

If further interested in our normalization model of dynamic attention:
Denison, R.N., Carrasco, M. & Heeger, D.J. A dynamic normalization model of temporal attention
Corresponding Code


Tony Movshon

Slides

Suggested Readings

Vanni et al (2020). Anatomy and Physiology of Macaque Visual Cortical Areas V1, V2, and V5/MT: Bases for Biologically Realistic Models
Adelson & Bergen (1985). Spatiotemporal energy models for the perception of motion
Emerson, Bergen & Adelson (1991). Directionally Selective and the Computation Cat Visual Cortex
Wei (2018). Neural Mechanisms of Motion Processing in the Mammalian Retina
Borst & Groschner (2023). How Flies See Motion
Wienecke, Leong & Clandinin (2018). Linear Summation Underlies Direction Selectivity in Drosophila
Rust et al. (2006). How MT cells analyze the motion of visual patterns


Kate Bonnen

Slides

Suggested Readings

Burge & Bonnen. (2024). Continuous psychophysics: Past, Present, and Future
Muller et al. (2023). Retinal motion statistics during natural locomotion
Bonnen, K., Burge, J., Yates, J., Pillow, J., & Cormack, L.K. (2015). Continuous psychophysics: Target-tracking to measure visual sensitivity
Noel, J.P., Caziot, B., Bruni, S., Fitzgerald, N.E., Avila, E., & Angelaki, D.E. (2021). Supporting generalization in non-human primate behavior by tapping into structural knowledge: Examples from sensorimotor mappings, inference, and decision-making
Matthis, J.S., Yates, J.L., & Hayhoe, M.M. (2018). Gaze and the control of foot placement when walking in natural terrain
Bonnen, K., Matthis, J.S., Gibaldi, A., Banks, M.S., Levi, D.M., & Hayhoe, M. (2021). Binocular vision and the control of foot placement during walking in natural terrain.


Stefan Treue

Slides

Suggested Readings


Emily Cooper

Slides

Suggested Readings

Dayan & Abbott Theoretical Neuroscience textbook population decoding chapter
Manning et al. (2024). Transformations of sensory information in the brain suggest changing criteria for optimality.
Sprague et al. (2015). Stereopsis is adaptive for the natural environment.


Marlene Cohen

Slides

Suggested Readings

This one first:Rust & Cohen (2022). Priority coding in the visual system
See also:Cohen & Kohn (2011). Measuring and interpreting neuronal correlations

I will also touch on some newer methods for analyzing neural population data. People wanting to learn more might find these papers useful:

Sizemore, A.E., Phillips-Cremins, J.E., Ghrist, R. & Bassett, D.S. (2019). The importance of the whole: topological data analysis for the network neuroscientist
Rouse T.C., Ni A.M., Huang C & Cohen M.R. (2021). Topological insights into the neural basis of flexible behavior
Wu-Yan, E., Betzel, R.F., Tang, E., Gu, S., Pasqualetti, F. & Bassett, D.S. (2020). Benchmarking measures of network controllability on canonical graph models


Madineh Sedigh-Sarvestani

Slides

Suggested Readings

Clippingdale, S. & Wilson, R. (1996). Self-similar neural networks based on a Kohonen learning rule.
Konkle, T. & Alvarez, G.A. (2022) A self-supervised domain-general learning framework for human ventral stream representation.
Sedigh-Sarvestani et al. (2021). A sinusoidal transformation of the visual field is the basis for periodic maps in area V2.


Ione Fine

Slides

Suggested Readings

Fine, I. & Boynton, G.M. (2015). Pulse trains to percepts: the challenge of creating a perceptually intelligible world with sigh recovery technologies
Fine, I. & Boynton, G.M. (2023). A virtual patient simulation modeling the neural and perceptual effects of human visual cortical stimulation, from pulse trains to percepts


Emma Alexander

Slides

Suggested Readings

Introductory slides
Adelson, Edward H., and James R. Bergen. The plenoptic function and the elements of early vision. Vol. 2. Cambridge, MA, USA: Vision and Modeling Group, Media Laboratory, Massachusetts Institute of Technology, 1991
Liang, Chia-Kai, Yi-Chang Shih, and Homer H. Chen. “Light field analysis for modeling image formation.” IEEE Transactions on Image Processing 20.2 (2010): 446-460


Jennifer Groh

Slides

Suggested Readings

Groh, J.M., Schmehl, M.N., Caruso V.C., & Tokdar, S.C. (2024). Signal switching may enhance processing power of the brain.
Jun, N.Y. et al. (2022). Coordinated multiplexing of information about separate objects in visual cortex.

And optionally…

Schmehl, M.N. et al. (2024). Multiple objects evoke fluctuating responses in several regions of the visual pathway.
Caruso et al. (2018). Single neurons may encode simultaneous stimuli by switching between activity patterns


Taraz Lee

Suggested Readings

Lee, T., Sellers, J., Jonides, J. & Zhang, H. (2023). The forced-response method: A new chronometric approach to measure conflict processing
Pélisson, D., Alahyane, N., Panouillères, M. & Tilikete, C. (2010). Sensorimotor adaptation of saccadic eye movements.
Polanía, R., Nitsche, M.A. & Ruff, C.C. (2018). Studying and modifying brain function with non-invasive brain stimulation.
Theeuwes, J., Belopolsky, A. & Olivers, C.N.L. (2009). Interactions between working memory, attention, and eye movements.
van Ede, F. (2020). Visual working memory and action: Functional links and bi-directional influences.


Mariam Aly

Slides part 1
Slides part 2

Suggested Readings

Aly M. & Turk-Browne N.B. (2018). Flexible weighting of diverse inputs makes hippocampal function malleable.
Turk-Browne N.B. (2019). The hippocampus as a visual area organized by space and time: A spatiotemporal similarity hypothesis.


Kohitij Kar

Slides

Suggested Readings

Please read in order of priority:

• Priority 1: Kar, K. & DiCarlo, J.J. (2024) The Quest for an Integrated Set of Neural Mechanisms Underlying Object Recognition in Primates.
• Priority 2: Kar, K. (2019). Kubilius, J., Schmidt, K. Issa, E.B., DiCarlo, J.J. (2019). Evidence that recurrent circuits are critical to the ventral stream’s execution of core object recognition behavior.
• Priority 3: Kar, K. & DiCarlo, J.J. (2021) Fast Recurrent Processing via Ventrolateral Prefrontal Cortex Is Needed by the Primate Ventral Stream for Robust Core Visual Object Recognition.
• Priority 4: Tuckute, G., Finzi, D., Margalit, E., Yates, J., Zylberberg, J., Fyshe, A., Chung, S., Fedorenko, E., Kriegeskorte, N., Grill-Spector, K., & Kar, K. (2024). How to optimize neuroscience data utilization and experiment design for advancing primate visual and linguistic brain models?


Lindsey Glickfeld

Slides part 1 (Normalization)Slides part 2 (Data)

Suggested Readings

Barbera, D., Preibe, N.J. & Glickfeld, L.L. (2022). Feedforward mechanisms of cross-orientation interactions in mouse V1
Niell, C.M. & Scanziani M. (2021). How Cortical Circuits Implement Cortical Computations: Mouse Visual Cortex as a Model