1,111 research outputs found
A Semiparametric Bayesian Model for Detecting Synchrony Among Multiple Neurons
We propose a scalable semiparametric Bayesian model to capture dependencies
among multiple neurons by detecting their co-firing (possibly with some lag
time) patterns over time. After discretizing time so there is at most one spike
at each interval, the resulting sequence of 1's (spike) and 0's (silence) for
each neuron is modeled using the logistic function of a continuous latent
variable with a Gaussian process prior. For multiple neurons, the corresponding
marginal distributions are coupled to their joint probability distribution
using a parametric copula model. The advantages of our approach are as follows:
the nonparametric component (i.e., the Gaussian process model) provides a
flexible framework for modeling the underlying firing rates; the parametric
component (i.e., the copula model) allows us to make inference regarding both
contemporaneous and lagged relationships among neurons; using the copula model,
we construct multivariate probabilistic models by separating the modeling of
univariate marginal distributions from the modeling of dependence structure
among variables; our method is easy to implement using a computationally
efficient sampling algorithm that can be easily extended to high dimensional
problems. Using simulated data, we show that our approach could correctly
capture temporal dependencies in firing rates and identify synchronous neurons.
We also apply our model to spike train data obtained from prefrontal cortical
areas in rat's brain
False discovery rate regression: an application to neural synchrony detection in primary visual cortex
Many approaches for multiple testing begin with the assumption that all tests
in a given study should be combined into a global false-discovery-rate
analysis. But this may be inappropriate for many of today's large-scale
screening problems, where auxiliary information about each test is often
available, and where a combined analysis can lead to poorly calibrated error
rates within different subsets of the experiment. To address this issue, we
introduce an approach called false-discovery-rate regression that directly uses
this auxiliary information to inform the outcome of each test. The method can
be motivated by a two-groups model in which covariates are allowed to influence
the local false discovery rate, or equivalently, the posterior probability that
a given observation is a signal. This poses many subtle issues at the interface
between inference and computation, and we investigate several variations of the
overall approach. Simulation evidence suggests that: (1) when covariate effects
are present, FDR regression improves power for a fixed false-discovery rate;
and (2) when covariate effects are absent, the method is robust, in the sense
that it does not lead to inflated error rates. We apply the method to neural
recordings from primary visual cortex. The goal is to detect pairs of neurons
that exhibit fine-time-scale interactions, in the sense that they fire together
more often than expected due to chance. Our method detects roughly 50% more
synchronous pairs versus a standard FDR-controlling analysis. The companion R
package FDRreg implements all methods described in the paper
A Bayesian approach for inferring neuronal connectivity from calcium fluorescent imaging data
Deducing the structure of neural circuits is one of the central problems of
modern neuroscience. Recently-introduced calcium fluorescent imaging methods
permit experimentalists to observe network activity in large populations of
neurons, but these techniques provide only indirect observations of neural
spike trains, with limited time resolution and signal quality. In this work we
present a Bayesian approach for inferring neural circuitry given this type of
imaging data. We model the network activity in terms of a collection of coupled
hidden Markov chains, with each chain corresponding to a single neuron in the
network and the coupling between the chains reflecting the network's
connectivity matrix. We derive a Monte Carlo Expectation--Maximization
algorithm for fitting the model parameters; to obtain the sufficient statistics
in a computationally-efficient manner, we introduce a specialized
blockwise-Gibbs algorithm for sampling from the joint activity of all observed
neurons given the observed fluorescence data. We perform large-scale
simulations of randomly connected neuronal networks with biophysically
realistic parameters and find that the proposed methods can accurately infer
the connectivity in these networks given reasonable experimental and
computational constraints. In addition, the estimation accuracy may be improved
significantly by incorporating prior knowledge about the sparseness of
connectivity in the network, via standard L penalization methods.Comment: Published in at http://dx.doi.org/10.1214/09-AOAS303 the Annals of
Applied Statistics (http://www.imstat.org/aoas/) by the Institute of
Mathematical Statistics (http://www.imstat.org
Fast non-negative deconvolution for spike train inference from population calcium imaging
Calcium imaging for observing spiking activity from large populations of
neurons are quickly gaining popularity. While the raw data are fluorescence
movies, the underlying spike trains are of interest. This work presents a fast
non-negative deconvolution filter to infer the approximately most likely spike
train for each neuron, given the fluorescence observations. This algorithm
outperforms optimal linear deconvolution (Wiener filtering) on both simulated
and biological data. The performance gains come from restricting the inferred
spike trains to be positive (using an interior-point method), unlike the Wiener
filter. The algorithm is fast enough that even when imaging over 100 neurons,
inference can be performed on the set of all observed traces faster than
real-time. Performing optimal spatial filtering on the images further refines
the estimates. Importantly, all the parameters required to perform the
inference can be estimated using only the fluorescence data, obviating the need
to perform joint electrophysiological and imaging calibration experiments.Comment: 22 pages, 10 figure
A hidden Markov model for decoding and the analysis of replay in spike trains
We present a hidden Markov model that describes variation in an animalās position associated with varying levels of activity in action potential spike trains of individual place cell neurons. The model incorporates a coarse-graining of position, which we find to be a more parsimonious description of the system than other models. We use a sequential Monte Carlo algorithm for Bayesian inference of model parameters, including the state space dimension, and we explain how to estimate position from spike train observations (decoding). We obtain greater accuracy over other methods in the conditions of high temporal resolution and small neuronal sample size. We also present a novel, model-based approach to the study of replay: the expression of spike train activity related to behaviour during times of motionlessness or sleep, thought to be integral to the consolidation of long-term memories. We demonstrate how we can detect the time, information content and compression rate of replay events in simulated and real hippocampal data recorded from rats in two different environments, and verify the correlation between the times of detected replay events and of sharp wave/ripples in the local field potential
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