More about neural
coding
William Bialek and
collaborators
Papers
are in chronological order, most recent papers at the top. Numbers refer to a full list of publications for WB.
[103.] Synergy from silence in a combinatorial neural code. E Schneidman, JL Puchalla, RA Harris, W Bialek & MJ Berry II, submitted.
[101.] Entropy and information in neural spike
trains: Progress on the sampling
problem. I Nemenman, W Bialek
& R de Ruyter van Steveninck, Phys Rev E 69, 056111 (2004); physics/0306063.
[98.] Time course of information about motion direction in visual area MT of macaque monkeys. LC Osborne, W Bialek & SG
Lisberger, J Neurosci 24, 3210-3222 (2004).
[93.] Analyzing neural responses to natural
signals: Maximally informative dimensions. T Sharpee, NC Rust & W Bialek, Neural Comp 16,
223-250 (2004).
[92.] Spike sorting in the frequency domain with overlap detection. D Rinberg, W Bialek, H Davidowitz & N Tishby, physics/0306056.
[91.] Synergy, redundancy, and independence
in population codes. E
Schneidman, W Bialek & MJ Berry II, J Neurosci 23, 11539-11553 (2003).
[90.] Network information and connected
correlations. E Schneidman, S Still, MJ Berry II & W Bialek, Phys Rev
Lett 91, 238701
(2003).
[89.] The information content of receptive fields.
TL Adelman, W Bialek & RM Olberg, Neuron 40, 822-833 (2003).
[88.] Computation in single neurons: Hodgkin and Huxley revisited. B
AgŸera y Arcas, AL Fairhall, & W Bialek, Neural Comp 15, 1715-1749 (2003).
[87.] An information theoretic approach to
the functional classification of neurons. E Schneidman, W Bialek, & MJ
Berry II, in Advances in Neural Information Processing 15, S Becker, S Thrun & K Obermayer,
eds, pp 197-204 (MIT Press, Cambridge, 2003).
[82.] Spike timing and the coding of naturalistic
sounds in a central auditory area of songbirds. BD Wright, K Sen, W Bialek,
& AJ Doupe, in Advances in Neural Information Processing 14, TG Dietterich, S Becker & Z Ghahramani, eds, pp
309-316 (MIT Press, Cambridge, 2002).
[58.] Naturalistic stimuli increase the rate and
efficiency of information transmission by primary auditory neurons. F Rieke, DA Bodnar & W Bialek, Proc
R Soc Lond Ser B 262, 259-265 (1995).
[55.] Information flow in sensory neurons. M DeWeese & W Bialek, Il Nuovo Cimento 17D, 733-741 (1995).
This
was a first step in the still incomplete project of constructing a theory for
optimal coding by spiking neurons.
Along the way we introduced some interesting technical tools, such as a
perturbative expansion of the information transmission rate. In addition we took the opportunity to
debunk some misconceptions that surrounded the idea of Òstochastic
resonance.Ó This might also be the
first place here we stated explicitly that the prediction of an optimal coding
theory will necessarily be a code that adapts to the statistics of the sensory
inputs.
[49.] Non-phase-locked auditory
cells and envelope detection. F
Rieke, W Yamada, E Lewis & W Bialek, in Analysis and Modeling of Neural Systems 2, F Eeckman, ed, pp 255-263 (Kluwer
Academic, 1993).
[45.] Coding efficiency and
information rates in sensory neurons.
F Rieke, D Warland & W
Bialek, Europhys Lett 22, 151-156, (1993).
[40.] Real-time coding of
complex sounds in the auditory nerve.
F Rieke, W Yamada, K Moortgat, ER Lewis & W Bialek, in Auditory
Physiology and Perception: Proceedings of the 8th International Conference on
Hearing, Y
Cazals, L Demany, & K Horner, eds, pp 315-322 (Pergamon, 1992).
[33.] Reading between the spikes in the cricket cercal afferent
system. D Warland, M Landolfa, JP
Miller & W Bialek, in Analysis
and Modeling of Neural Systems, F Eeckman, ed, pp 327-333 (Kluwer Academic, 1991).
[25.] Coding and computation with neural spike
trains. W Bialek & A Zee, J. Stat. Phys. 59, 103-115 (1990).
Inspired
in part by the results in the fly, we set out to study the problem of coding
and decoding in simple models of spiking neurons. Probably the most important
result was that there is a large regime in which signals can be decoded by
linear (perturbative) methods even though the encoding is strongly nonlinear.
The small parameter that makes this work is the mean number of spikes per
correlation time of the signal, suggesting that spike trains can be decoded
linearly if they are sparse in the time domain. In Spikes we discuss the evidence that many different neural
systems make use of such a sparse representation, but of course one really wants
a direct experimental answer: Can we decode the spike trains of real neurons
using these theoretical ideas? As an aside, it is worth noting that identifying
a regime where linear decoding can work is really much more general than the
details of the model that we chose to investigate; this is important, since
none of the models we write down are likely to be accurate in detail.
Rereading
the original paper, it is perhaps not so clear that sparseness is the key idea.
A somewhat more explicit discussion is given in later summer school lectures
[29, 84].