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Bayesian Models of Brain and Behaviour

DOI: 10.5402/2012/785791

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This paper presents a review of Bayesian models of brain and behaviour. We first review the basic principles of Bayesian inference. This is followed by descriptions of sampling and variational methods for approximate inference, and forward and backward recursions in time for inference in dynamical models. The review of behavioural models covers work in visual processing, sensory integration, sensorimotor integration, and collective decision making. The review of brain models covers a range of spatial scales from synapses to neurons and population codes, but with an emphasis on models of cortical hierarchies. We describe a simple hierarchical model which provides a mathematical framework relating constructs in Bayesian inference to those in neural computation. We close by reviewing recent theoretical developments in Bayesian inference for planning and control. 1. Introduction This paper presents a review of Bayesian models of brain and behaviour. Overall, the aim of the paper is to review work which relates constructs in Bayesian inference to aspects of behaviour and neural computation, as outlined in Figure 1. This is a very large research area and we refer readers to standard textbooks and other review materials [1–6]. Figure 1: This paper reviews work which relates constructs in Bayesian inference to those in experimental psychology and neuroscience. One of the main ideas to emerge in recent years is that Bayesian inference operates at the level of cortical macrocircuits. These circuits are arranged in a hierarchy which reflects the hierarchical structure of the world around us. The idea that the brain encodes a model of the world and makes predictions about its sensory input is also known as predictive coding [7]. Consider, for example, your immediate environment. It may be populated by various objects such as desks, chairs, walls, trees, and so forth. Generic attributes of this scene and the objects in it will be represented by activity in brain regions near the top of the hierarchy. The connections from higher to lower regions then encode a model of your world, describing how scenes consist of objects, and objects by their features. If a higher level representation is activated, it will activate those lower level representations that encode the presence of, for example, configurations of oriented lines that your brain expects to receive signals about in early visual cortex. At the lowest level of the hierarchy these predictions are compared with sensory input and the difference between them, the prediction error, is propagated back up the

References

[1]  K. Friston, “A theory of cortical responses,” Philosophical Transactions of the Royal Society of London Series B, vol. 360, no. 1456, pp. 815–836, 2005.
[2]  P. Dayan and L. F. Abbott, Theoretical Neuroscience: Computational and Mathematical Modeling of Neural Systems, MIT Press, 2001.
[3]  C. Frith, Making Up the Mind: How the Brain Creates Our Mental World, Wiley-Blackwell, 2007.
[4]  K. Doya, S. Ishii, A. Pouget, and R. Rao, Eds., Bayesian Brain: Probabilistic Approaches to Neural Coding, MIT Press, 2007.
[5]  T. Lochmann and S. Deneve, “Neural processing as causal inference,” Current Opinion in Neurobiology, vol. 21, no. 5, pp. 774–781, 2011.
[6]  J. Fiser, P. Berkes, G. Orbán, and M. Lengyel, “Statistically optimal perception and learning: from behavior to neural representations,” Trends in Cognitive Sciences, vol. 14, no. 3, pp. 119–130, 2010.
[7]  R. P. N. Rao and D. H. Ballard, “Predictive coding in the visual cortex: a functional interpretation of some extra-classical receptive-field effects,” Nature Neuroscience, vol. 2, no. 1, pp. 79–87, 1999.
[8]  P. C. Fletcher and C. D. Frith, “Perceiving is believing: a Bayesian approach to explaining the positive symptoms of schizophrenia,” Nature Reviews Neuroscience, vol. 10, no. 1, pp. 48–58, 2009.
[9]  D. M. Eagleman and T. J. Sejnowski, “Motion integration and postdiction in visual awareness,” Science, vol. 287, no. 5460, pp. 2036–2038, 2000.
[10]  D. Mumford, “On the computational architecture of the neocortex—II the role of cortico-cortical loops,” Biological Cybernetics, vol. 66, no. 3, pp. 241–251, 1992.
[11]  K. Friston, “Learning and inference in the brain,” Neural Networks, vol. 16, no. 9, pp. 1325–1352, 2003.
[12]  K. Friston, “The free-energy principle: a unified brain theory?” Nature Reviews Neuroscience, vol. 11, no. 2, pp. 127–138, 2010.
[13]  D. Wolpert and Z. Ghahramani, “Oxford companion to the mind,” in Bayes Rule in Perception, Action and Cognition, Oxford University Press, 2004.
[14]  R. Bogacz, E. Brown, J. Moehlis, P. Holmes, and J. D. Cohen, “The physics of optimal decision making: a formal analysis of models of performance in two-alternative forced-choice tasks,” Psychological Review, vol. 113, no. 4, pp. 700–765, 2006.
[15]  J. I. Gold and M. N. Shadlen, “Neural computations that underlie decisions about sensory stimuli,” Trends in Cognitive Sciences, vol. 5, no. 1, pp. 10–16, 2001.
[16]  C. M. Bishop, Pattern Recognition and Machine Learning, Springer, 2006.
[17]  J. Pearl, Probabilistic Reasoning in Intelligent Systems: Networks of Plausible Inference, Morgan Kauman, 1988.
[18]  M. Jordan and Y. Weiss, “Graphical models: probabilistic inference,” in The Handbook of Brain Theory and Neural Networks, M. Arbib, Ed., MIT Press, 2002.
[19]  D. George and J. Hawkins, “Towards a mathematical theory of cortical micro-circuits,” PLoS Computational Biology, vol. 5, no. 10, Article ID e1000532, 2009.
[20]  S. Deneve, “Bayesian spiking neurons I: inference,” Neural Computation, vol. 20, no. 1, pp. 91–117, 2008.
[21]  A. Gelman, J. B. Carlin, H. S. Stern, and D. B. Rubin, Bayesian Data Analysis, Chapman and Hall, Boca Raton, Fla, USA, 1995.
[22]  A. Jasra, D. A. Stephens, and C. C. Holmes, “On population-based simulation for static inference,” Statistics and Computing, vol. 17, no. 3, pp. 263–279, 2007.
[23]  S. Gershman E Vul J Tenenbaum, “Perceptual multistability as markov chain monte carlo inference,” in Advances in Neural Information Procesing Systems, vol. 22, 2009.
[24]  D. J. C. Mackay, Information Theory, Inference and Learning Algorithms, Cambridge University Press, Cambridge, UK, 2003.
[25]  M. I. Jordan, Ed., Learning in Graphical Models, MIT Press, 1999.
[26]  M. Beal, Variational algorithms for approximate Bayesian inference [Ph.D. thesis], University College London, 2003.
[27]  P. Dayan, G. E. Hinton, R. M. Neal, and R. S. Zemel, “The Helmholtz machine,” Neural Computation, vol. 7, no. 5, pp. 889–904, 1995.
[28]  K. Friston, “The free-energy principle: a rough guide to the brain?” Trends in Cognitive Sciences, vol. 13, no. 7, pp. 293–301, 2009.
[29]  S. Roweis and Z. Ghahramani, “A unifying review of linear gaussian models,” Neural Computation, vol. 11, no. 2, pp. 305–345, 1999.
[30]  J. Beck, P. Latham, and A. Pouget, “Marginalization in neural circuits with divisive normalization,” The Journal of Neuroscience, vol. 31, no. 43, pp. 15310–15319, 2011.
[31]  T. S. Lee and D. Mumford, “Hierarchical Bayesian inference in the visual cortex,” Journal of the Optical Society of America A, vol. 20, no. 7, pp. 1434–1448, 2003.
[32]  Z. Ghahramani and M. J. Beal, “Propagation algorithms for Variational Bayesian learning,” in Advances in Neural Information Processing Systems, T. K. Leen, T. Dietterich, and V. Tresp, Eds., vol. 13, MIT Press, Cambridge, Mass, USA, 2001.
[33]  J. Daunizeau, K. J. Friston, and S. J. Kiebel, “Variational Bayesian identification and prediction of stochastic nonlinear dynamic causal models,” Physica D, vol. 238, no. 21, pp. 2089–2118, 2009.
[34]  A. Doucet, N. de Freitas, and N. Gordon, Eds., Sequential Monte Carlo Methods in Practice, Springer, 2001.
[35]  M. West and J. Harrison, Eds., Bayesian Forecasting and Dynamic Models, Springer, 1997.
[36]  A. A. Stocker and E. P. Simoncelli, “Noise characteristics and prior expectations in human visual speed perception,” Nature Neuroscience, vol. 9, no. 4, pp. 578–585, 2006.
[37]  R. Gregory, Eye and Brain: The Psychology of Seeing, Oxford University Press, 1998.
[38]  M. O. Ernst and M. S. Banks, “Humans integrate visual and haptic information in a statistically optimal fashion,” Nature, vol. 415, no. 6870, pp. 429–433, 2002.
[39]  D. Green and J. Swets, Signal Detection Theory and Psychophysics, John Wiley & Sons, 1966.
[40]  D. Alais and D. Burr, “The Ventriloquist effect results from near-optimal bimodal integration,” Current Biology, vol. 14, no. 3, pp. 257–262, 2004.
[41]  P. W. Battaglia, R. A. Jacobs, and R. N. Aslin, “Bayesian integration of visual and auditory signals for spatial localization,” Journal of the Optical Society of America A, vol. 20, no. 7, pp. 1391–1397, 2003.
[42]  D. Kersten, P. Mamassian, and A. Yuille, “Object perception as Bayesian inference,” Annual Review of Psychology, vol. 55, pp. 271–304, 2004.
[43]  D. Knill and W. Richards, Perception as Bayesian Inference, Cambridge, UK, 1996.
[44]  W. J. Adams, E. W. Graf, and M. O. Ernst, “Experience can change the “light-from-above” prior,” Nature Neuroscience, vol. 7, no. 10, pp. 1057–1058, 2004.
[45]  A. J. Yu, P. Dayan, and J. D. Cohen, “Dynamics of attentional selection under conflict: toward a rational Bayesian account,” Journal of Experimental Psychology, vol. 35, no. 3, pp. 700–717, 2009.
[46]  Y. S. Liu, A. Yu, and P. Holmes, “Dynamical analysis of bayesian inferencemodels for the eriksen task,” Neural Computation, vol. 21, no. 6, pp. 1520–1553, 2009.
[47]  Y. Weiss, E. P. Simoncelli, and E. H. Adelson, “Motion illusions as optimal percepts,” Nature Neuroscience, vol. 5, no. 6, pp. 598–604, 2002.
[48]  J. Najemnik and W. S. Geisler, “Optimal eye movement strategies in visual search,” Nature, vol. 434, no. 7031, pp. 387–391, 2005.
[49]  J. Najemnik and W. S. Geisler, “Eye movement statistics in humans are consistent with an optimal search strategy,” Journal of Vision, vol. 8, no. 3, article 4, 2008.
[50]  R. Nijhawan, “Motion extrapolation in catching,” Nature, vol. 370, no. 6487, pp. 256–257, 1994.
[51]  K. A. Sundberg, M. Fallah, and J. H. Reynolds, “A motion-dependent distortion of retinotopy in area V4,” Neuron, vol. 49, no. 3, pp. 447–457, 2006.
[52]  R. Soga, R. Akaishi, and K. Sakai, “Predictive and postdictive mechanisms jointly contribute to visual awareness,” Consciousness and Cognition, vol. 18, no. 3, pp. 578–592, 2009.
[53]  T. Bachmann, Psychophysiology of Backward Masking, Nova Science, 1994.
[54]  P. A. Kolers and M. Von Gruenau, “Shape and color in apparent motion,” Vision Research, vol. 16, no. 4, pp. 329–335, 1976.
[55]  D. Dennett, Consciousness Explained, Little, Brown and Company, 1991.
[56]  D. M. Wolpert, Z. Ghahramani, and M. I. Jordan, “An internal model for sensorimotor integration,” Science, vol. 269, no. 5232, pp. 1880–1882, 1995.
[57]  S. S. Shergill, P. H. Bays, C. D. Frith, and D. M. Wotpert, “Two eyes for an eye: the neuroscience of force escalation,” Science, vol. 301, no. 5630, p. 187, 2003.
[58]  K. P. K?rding and D. M. Wolpert, “Bayesian integration in sensorimotor learning,” Nature, vol. 427, no. 6971, pp. 244–247, 2004.
[59]  F. J. G. M. Klaassen and J. R. Magnus, “Are points in tennis independent and identically distributed? Evidence from a dynamic binary panel data model,” Journal of the American Statistical Association, vol. 96, no. 454, pp. 500–509, 2001.
[60]  R. D. Sorkin, C. J. Hays, and R. West, “Signal-detection analysis of group decision making,” Psychological Review, vol. 108, no. 1, pp. 183–203, 2001.
[61]  B. Bahrami, K. Olsen, P. E. Latham, A. Roepstorff, G. Rees, and C. D. Frith, “Optimally interacting minds,” Science, vol. 329, no. 5995, pp. 1081–1085, 2010.
[62]  M. Colombo and P. Series, “Bayes in the brain—on Bayesian modelling in neuroscience,” British Journal for the Philosophy of Science, vol. 63, no. 3, pp. 697–723, 2012.
[63]  N. C. Rust and A. A. Stocker, “Ambiguity and invariance: two fundamental challenges for visual processing,” Current Opinion in Neurobiology, vol. 20, no. 3, pp. 382–388, 2010.
[64]  R. Adams, S. Shipp, and K. Friston, “Predictions not commands: active inference in the motor system”.
[65]  E. Kandel, J. Schwartz, and T. Jessell, Principals of Neural Science, McGraw-Hill, 2000.
[66]  J. Nicholls, A. R. Martin, P. Fuchs, D. Brown, M. Diamond, and D. Weisblat, From Neuron to Brain: A Cellular and Molecular Approach to the Function of the Nervous System, Sinaeur, 2012.
[67]  L. F. Abbott and W. G. Regehr, “Synaptic computation,” Nature, vol. 431, no. 7010, pp. 796–803, 2004.
[68]  J. P. Pfister, P. Dayan, and M. Lengyel, “Synapses with short-term plasticity are optimal estimators of presynaptic membrane potentials,” Nature Neuroscience, vol. 13, no. 10, pp. 1271–1275, 2010.
[69]  S. Kiebel and K. Friston, “Free energy and dendritic self-organization,” Frontiers in Systems Neuroscience, vol. 5, article 80, 2011.
[70]  C. D. Fiorillo, “Towards a general theory of neural computation based on prediction by single neurons,” PLoS ONE, vol. 3, no. 10, Article ID e3298, 2008.
[71]  M. Lengyel, J. Kwag, O. Paulsen, and P. Dayan, “Matching storage and recall: hippocampal spike timing-dependent plasticity and phase response curves,” Nature Neuroscience, vol. 8, no. 12, pp. 1677–1683, 2005.
[72]  M. Lengyel P Dayan, “Uncertainty, phase and oscillatory hippocampal recall,” in Neural Information Processing Systems, 2007.
[73]  S. Deneve, “Bayesian spiking neurons II: learning,” Neural Computation, vol. 20, no. 1, pp. 118–145, 2008.
[74]  D. J. Tolhurst, J. A. Movshon, and A. F. Dean, “The statistical reliability of signals in single neurons in cat and monkey visual cortex,” Vision Research, vol. 23, no. 8, pp. 775–785, 1983.
[75]  P. Hoyer and A. Hyvarinen, “Interpreting neural response variability as monte carlo sampling of the posterior,” in Neural Information Processing Systems 2003, 2003.
[76]  W. J. Ma, J. M. Beck, P. E. Latham, and A. Pouget, “Bayesian inference with probabilistic population codes,” Nature Neuroscience, vol. 9, no. 11, pp. 1432–1438, 2006.
[77]  W. J. Ma, J. M. Beck, and A. Pouget, “Spiking networks for Bayesian inference and choice,” Current Opinion in Neurobiology, vol. 18, no. 2, pp. 217–222, 2008.
[78]  M. Carandini and D. Heeger, “Normalization as a canonical neural computation,” Nature Reviews Neuroscience, vol. 13, no. 1, pp. 51–62, 2012.
[79]  R. Sundareswara and P. R. Schrater, “Perceptual multistability predicted by search model for Bayesian decisions,” Journal of Vision, vol. 8, no. 5, article 12, 2008.
[80]  P. Dayan, “A hierarchical model of binocular rivalry,” Neural Computation, vol. 10, no. 5, pp. 1119–1135, 1998.
[81]  P. Berkes, G. Orbán, M. Lengyel, and J. Fiser, “Spontaneous cortical activity reveals hallmarks of an optimal internal model of the environment,” Science, vol. 331, no. 6013, pp. 83–87, 2011.
[82]  G. Hinton and T. Sejnowski, Eds., Unsupervised Learning: Foundations of Neural Computation, MIT Press, 1999.
[83]  K. Fukushima, “Neocognitron: a self-organizing neural network model for a mechanism of pattern recognition unaffected by shift in position,” Biological Cybernetics, vol. 36, no. 4, pp. 193–202, 1980.
[84]  M. Riesenhuber and T. Poggio, “Hierarchical models of object recognition in cortex,” Nature Neuroscience, vol. 2, no. 11, pp. 1019–1025, 1999.
[85]  S. M. Stringer and E. T. Rolls, “Invariant object recognition in the visual system with novel views of 3D objects,” Neural Computation, vol. 14, no. 11, pp. 2585–2596, 2002.
[86]  D. Mackay, The Epistemological Problem for Automata, Princeton University Press, 1956.
[87]  B. A. Olshausen and D. J. Field, “Emergence of simple-cell receptive field properties by learning a sparse code for natural images,” Nature, vol. 381, no. 6583, pp. 607–609, 1996.
[88]  E. C. Smith and M. S. Lewicki, “Efficient auditory coding,” Nature, vol. 439, no. 7079, pp. 978–982, 2006.
[89]  A. Hyv?rinen and P. O. Hoyer, “A two-layer sparse coding model learns simple and complex cell receptive fields and topography from natural images,” Vision Research, vol. 41, no. 18, pp. 2413–2423, 2001.
[90]  G. E. Hinton, S. Osindero, and Y. W. Teh, “A fast learning algorithm for deep belief nets,” Neural Computation, vol. 18, no. 7, pp. 1527–1554, 2006.
[91]  G. E. Hinton, “Learning multiple layers of representation,” Trends in Cognitive Sciences, vol. 11, no. 10, pp. 428–434, 2007.
[92]  D. J. Felleman and D. C. Van Essen, “Distributed hierarchical processing in the primate cerebral cortex,” Cerebral Cortex, vol. 1, no. 1, pp. 1–47, 1991.
[93]  G. Shepherd, Ed., The Synaptic Organization of the Brain, Oxford University Press, 2004.
[94]  R. Douglas, K. Martin, and D. Whitteridge, “A canonical microcircuit for neocortex,” Neural Computation, vol. 1, pp. 480–488, 1989.
[95]  S. Shipp, “Structure and function of the cerebral cortex,” Current Biology, vol. 17, no. 12, pp. R443–R449, 2007.
[96]  M. M. Mesulam, “From sensation to cognition,” Brain, vol. 121, no. 6, pp. 1013–1052, 1998.
[97]  H. Kennedy and C. Dehay, “Self-organization and interareal networks in the primate cortex,” Progress in Brain Research, vol. 195, pp. 341–360, 2012.
[98]  P. Cisek, “Cortical mechanisms of action selection: the aordance competition hypothesis,” Philosophical Transactions of the Royal Society of London Series B, vol. 362, no. 1485, pp. 1585–1599, 2007.
[99]  S. J. Kiebel, J. Daunizeau, and K. J. Friston, “A hierarchy of time-scales and the brain,” PLoS Computational Biology, vol. 4, no. 11, Article ID e1000209, 2008.
[100]  R. P. N. Rao and D. H. Ballard, “Dynamic model of visual recognition predicts neural response properties in the visual cortex,” Neural Computation, vol. 9, no. 4, pp. 721–763, 1997.
[101]  K. Friston, J. Kilner, and L. Harrison, “A free energy principle for the brain,” Journal of Physiology Paris, vol. 100, no. 1–3, pp. 70–87, 2006.
[102]  L. Abbott, Where Are the Switches on This Thing?Problems in Systems Neuroscience, chapter 23, Oxford University Press, 2006.
[103]  G. B. Ermentrout and D. Terman, Mathematical Foundations of Neuroscience, Springer, 2010.
[104]  J. J. Hopfield and C. D. Brody, “What is a moment? Trasient synchrony as a collective mechanism for spatiotemporal integration,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 3, pp. 1282–1287, 2001.
[105]  K. Doya, “Metalearning and neuromodulation,” Neural Networks, vol. 15, no. 4–6, pp. 495–506, 2002.
[106]  A. J. Yu and P. Dayan, “Uncertainty, neuromodulation, and attention,” Neuron, vol. 46, no. 4, pp. 681–692, 2005.
[107]  C. D. Fiorillo, P. N. Tobler, and W. Schultz, “Discrete coding of reward probability and uncertainty by dopamine neurons,” Science, vol. 299, no. 5614, pp. 1898–1902, 2003.
[108]  K. Friston, T. Shiner, T. FitzGerald et al., “Dopamine, aordance and active inference,” PLOS Computational Biology, vol. 8, no. 1, Article ID e1002327, 2012.
[109]  A. Yu and P. Dayan, “Inference, attention, and decision in a bayesian neural architecture,” in Neural Information Processing Systems, 2005.
[110]  P. R. Corlett, C. D. Frith, and P. C. Fletcher, “From drugs to deprivation: a Bayesian framework for understanding models of psychosis,” Psychopharmacology, vol. 206, no. 4, pp. 515–530, 2009.
[111]  R. Montague, R. Dolan, K. Friston, and P. Dayan, “Computational psychiatry,” Trends in Cognitive Sciences, vol. 16, no. 1, pp. 72–80, 2012.
[112]  D. Bertsekas, Dynamic Programming and Optimal Control, MIT Press, 2001.
[113]  A. Bryson and Y. Ho, Applied Optimal Control, Ginn and Company, 1969.
[114]  R. Sutton and A. Barto, Reinforcement Learning: An Intro, MIT Press, 1998.
[115]  E. Todorov, “Optimality principles in sensorimotor control,” Nature Neuroscience, vol. 7, no. 9, pp. 907–915, 2004.
[116]  J. Diedrichsen, R. Shadmehr, and R. B. Ivry, “The coordination of movement: optimal feedback control and beyond,” Trends in Cognitive Sciences, vol. 14, no. 1, pp. 31–39, 2010.
[117]  H. Attias, “Planning by probabilistic inference,” in Neural Information Processing Systems, 2003.
[118]  M. Toussaint, “Robot trajectory optimization using approximate inference,” in Proceedings of the 26th International Conference On Machine Learning (ICML '09), pp. 1049–1056, June 2009.
[119]  W. Penny, “Forwards and backwards inference for spatial cognition”.
[120]  E. Todorov, “Efficient computation of optimal actions,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 28, pp. 11478–11483, 2009.
[121]  E. Todorov, “General duality between optimal control and estimation,” in Proceedings of the 47th IEEE Conference on Decision and Control (CDC '08), vol. 47, pp. 4286–4292, December 2008.
[122]  J. Findlay and I. Gilchrist, Active Vision: The Psychology of Looking and Seeing, Oxford, UK, 2003.
[123]  K. J. Friston, L. Harrison, and W. Penny, “Dynamic causal modelling,” NeuroImage, vol. 19, no. 4, pp. 1273–1302, 2003.
[124]  M. I. Garrido, J. M. Kilner, S. J. Kiebel, and K. J. Friston, “Evoked brain responses are generated by feedback loops,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 52, pp. 20961–20966, 2007.
[125]  M. Boly, M. I. Garrido, O. Gosseries et al., “Preserved feedforward but impaired top-down processes in the vegetative state,” Science, vol. 332, no. 6031, pp. 858–862, 2011.

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