Literature DB >> 22281297

The statistical analysis of partially confounded covariates important to neural spiking.

Kyle Q Lepage1, Christopher J Macdonald, Howard Eichenbaum, Uri T Eden.   

Abstract

A method is presented capable of disambiguating the relative influence of statistical covariates upon neural spiking activity. The method, an extension of the generalized linear model (GLM) methodology introduced in Truccolo et al. (2005) to analyze neural spiking data, exploits projection operations motivated by a geometry present in the Fisher information of the GLM maximum likelihood parameter estimator. By exploiting these projections, neural activity can be divided into three categories. These three categories, neural activity due solely to a set of covariates of interest, neural activity due solely to a set of uninteresting, or nuisance, covariates, and neural activity that cannot be unequivocally assigned to either set of covariates, can be associated with physical variables such as time, position, head-direction and velocity. This association allows the analysis of neural activity that can, for example, be due solely to temporal influence, irrespective of other, identified, influences. The method is applied in simulation to a rat exploring a temporally modulated place field. A portion of the analysis reported in MacDonald et al. (2011), using the methodology described herein, is reproduced. This analysis demonstrates the temporal bridging of a delay period in a sequential memory task by firing activity of cells present in the rodent hippocampus that cannot be explained by rodent position, head direction or velocity. Copyright Â
© 2012 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Year:  2012        PMID: 22281297      PMCID: PMC3976545          DOI: 10.1016/j.jneumeth.2011.12.021

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  14 in total

1.  Real-time prediction of hand trajectory by ensembles of cortical neurons in primates.

Authors:  J Wessberg; C R Stambaugh; J D Kralik; P D Beck; M Laubach; J K Chapin; J Kim; S J Biggs; M A Srinivasan; M A Nicolelis
Journal:  Nature       Date:  2000-11-16       Impact factor: 49.962

2.  A point process framework for relating neural spiking activity to spiking history, neural ensemble, and extrinsic covariate effects.

Authors:  Wilson Truccolo; Uri T Eden; Matthew R Fellows; John P Donoghue; Emery N Brown
Journal:  J Neurophysiol       Date:  2004-09-08       Impact factor: 2.714

3.  The global record of memory in hippocampal neuronal activity.

Authors:  E R Wood; P A Dudchenko; H Eichenbaum
Journal:  Nature       Date:  1999-02-18       Impact factor: 49.962

4.  Difficulty of visual search modulates neuronal interactions and response variability in the frontal eye field.

Authors:  Jeremiah Y Cohen; Pierre Pouget; Geoffrey F Woodman; Chenchal R Subraveti; Jeffrey D Schall; Andrew F Rossi
Journal:  J Neurophysiol       Date:  2007-09-12       Impact factor: 2.714

5.  Decoding movement trajectories through a T-maze using point process filters applied to place field data from rat hippocampal region CA1.

Authors:  Yifei Huang; Mark P Brandon; Amy L Griffin; Michael E Hasselmo; Uri T Eden
Journal:  Neural Comput       Date:  2009-12       Impact factor: 2.026

6.  The role of CA1 in the acquisition of an object-trace-odor paired associate task.

Authors:  Raymond P Kesner; Michael R Hunsaker; Paul E Gilbert
Journal:  Behav Neurosci       Date:  2005-06       Impact factor: 1.912

7.  Neuronal population coding of movement direction.

Authors:  A P Georgopoulos; A B Schwartz; R E Kettner
Journal:  Science       Date:  1986-09-26       Impact factor: 47.728

8.  Hippocampal "time cells" bridge the gap in memory for discontiguous events.

Authors:  Christopher J MacDonald; Kyle Q Lepage; Uri T Eden; Howard Eichenbaum
Journal:  Neuron       Date:  2011-08-25       Impact factor: 17.173

9.  Hippocampal neurons encode information about different types of memory episodes occurring in the same location.

Authors:  E R Wood; P A Dudchenko; R J Robitsek; H Eichenbaum
Journal:  Neuron       Date:  2000-09       Impact factor: 17.173

10.  Collective dynamics in human and monkey sensorimotor cortex: predicting single neuron spikes.

Authors:  Wilson Truccolo; Leigh R Hochberg; John P Donoghue
Journal:  Nat Neurosci       Date:  2009-12-06       Impact factor: 24.884

View more
  4 in total

1.  Fast maximum likelihood estimation using continuous-time neural point process models.

Authors:  Kyle Q Lepage; Christopher J MacDonald
Journal:  J Comput Neurosci       Date:  2015-03-20       Impact factor: 1.621

2.  Hippocampal "time cells": time versus path integration.

Authors:  Benjamin J Kraus; Robert J Robinson; John A White; Howard Eichenbaum; Michael E Hasselmo
Journal:  Neuron       Date:  2013-05-23       Impact factor: 17.173

3.  During Running in Place, Grid Cells Integrate Elapsed Time and Distance Run.

Authors:  Benjamin J Kraus; Mark P Brandon; Robert J Robinson; Michael A Connerney; Michael E Hasselmo; Howard Eichenbaum
Journal:  Neuron       Date:  2015-11-04       Impact factor: 17.173

4.  Efficient spline regression for neural spiking data.

Authors:  Mehrad Sarmashghi; Shantanu P Jadhav; Uri Eden
Journal:  PLoS One       Date:  2021-10-13       Impact factor: 3.240

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.