1,512 research outputs found
Error Exponents of Low-Density Parity-Check Codes on the Binary Erasure Channel
We introduce a thermodynamic (large deviation) formalism for computing error
exponents in error-correcting codes. Within this framework, we apply the
heuristic cavity method from statistical mechanics to derive the average and
typical error exponents of low-density parity-check (LDPC) codes on the binary
erasure channel (BEC) under maximum-likelihood decoding.Comment: 5 pages, 4 figure
Beyond position weight matrices: nucleotide correlations in transcription factor binding sites and their description
The identification of transcription factor binding sites (TFBSs) on genomic
DNA is of crucial importance for understanding and predicting regulatory
elements in gene networks. TFBS motifs are commonly described by Position
Weight Matrices (PWMs), in which each DNA base pair independently contributes
to the transcription factor (TF) binding, despite mounting evidence of
interdependence between base pairs positions. The recent availability of
genome-wide data on TF-bound DNA regions offers the possibility to revisit this
question in detail for TF binding {\em in vivo}. Here, we use available fly and
mouse ChIPseq data, and show that the independent model generally does not
reproduce the observed statistics of TFBS, generalizing previous observations.
We further show that TFBS description and predictability can be systematically
improved by taking into account pairwise correlations in the TFBS via the
principle of maximum entropy. The resulting pairwise interaction model is
formally equivalent to the disordered Potts models of statistical mechanics and
it generalizes previous approaches to interdependent positions. Its structure
allows for co-variation of two or more base pairs, as well as secondary motifs.
Although models consisting of mixtures of PWMs also have this last feature, we
show that pairwise interaction models outperform them. The significant pairwise
interactions are found to be sparse and found dominantly between consecutive
base pairs. Finally, the use of a pairwise interaction model for the
identification of TFBSs is shown to give significantly different predictions
than a model based on independent positions
Dynamical criticality in the collective activity of a population of retinal neurons
Recent experimental results based on multi-electrode and imaging techniques
have reinvigorated the idea that large neural networks operate near a critical
point, between order and disorder. However, evidence for criticality has relied
on the definition of arbitrary order parameters, or on models that do not
address the dynamical nature of network activity. Here we introduce a novel
approach to assess criticality that overcomes these limitations, while
encompassing and generalizing previous criteria. We find a simple model to
describe the global activity of large populations of ganglion cells in the rat
retina, and show that their statistics are poised near a critical point. Taking
into account the temporal dynamics of the activity greatly enhances the
evidence for criticality, revealing it where previous methods would not. The
approach is general and could be used in other biological networks
A tractable method for describing complex couplings between neurons and population rate
Neurons within a population are strongly correlated, but how to simply
capture these correlations is still a matter of debate. Recent studies have
shown that the activity of each cell is influenced by the population rate,
defined as the summed activity of all neurons in the population. However, an
explicit, tractable model for these interactions is still lacking. Here we
build a probabilistic model of population activity that reproduces the firing
rate of each cell, the distribution of the population rate, and the linear
coupling between them. This model is tractable, meaning that its parameters can
be learned in a few seconds on a standard computer even for large population
recordings. We inferred our model for a population of 160 neurons in the
salamander retina. In this population, single-cell firing rates depended in
unexpected ways on the population rate. In particular, some cells had a
preferred population rate at which they were most likely to fire. These complex
dependencies could not be explained by a linear coupling between the cell and
the population rate. We designed a more general, still tractable model that
could fully account for these non-linear dependencies. We thus provide a simple
and computationally tractable way to learn models that reproduce the dependence
of each neuron on the population rate
Blindfold learning of an accurate neural metric
The brain has no direct access to physical stimuli, but only to the spiking
activity evoked in sensory organs. It is unclear how the brain can structure
its representation of the world based on differences between those noisy,
correlated responses alone. Here we show how to build a distance map of
responses from the structure of the population activity of retinal ganglion
cells, allowing for the accurate discrimination of distinct visual stimuli from
the retinal response. We introduce the Temporal Restricted Boltzmann Machine to
learn the spatiotemporal structure of the population activity, and use this
model to define a distance between spike trains. We show that this metric
outperforms existing neural distances at discriminating pairs of stimuli that
are barely distinguishable. The proposed method provides a generic and
biologically plausible way to learn to associate similar stimuli based on their
spiking responses, without any other knowledge of these stimuli
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