Skip to content


  • Poster presentation
  • Open Access

Computing the inverse of the neurophysiological spike-response transform

  • 1Email author,
  • 1,
  • 2,
  • 2 and
  • 3
BMC Neuroscience200910 (Suppl 1) :P92

  • Published:


  • Standard Method
  • Motor Neuron
  • Muscle Contraction
  • Challenging Problem
  • Synthetic Data
Consider the transform from a discrete spike train to a continuous neurophysiological response such as postsynaptic membrane voltage or muscle contraction. Here we ask about the inverse of this transform: given the response, how can we estimate from it the spike train that produced it? A simple kernel-based model of such a transform is
where t is time (already discretized for practical computation, so that t is the index of a series of time bins), t i is the time of spike i, K is the single-spike response kernel of length N K time bins, A is an amplitude that scales K at each spike time, and R is the overall response to the spike train. In previous work [1, 2], we developed a method to "decode" (1) to find, given the spike times and the response R, simultaneously both K and A. If the spike train is unknown, a spike might hypothetically occur in each time bin t'. In that case, (1) generalizes to the standard convolution
The inverse transform can then be computed using (1) or (2), depending on the circumstances, in at least two ways. If, perhaps from a previous decoding of (1) with a known spike train, we know K, we can use our decoding method, or another standard method, to solve (2) in one step to find from a novel R(t) the corresponding A(t). In datasets with relatively low noise and low spike density, the spikes can then be identified simply as occurring in time bins where A(t) ≠ 0 or, in practice, where A(t) exceeds some threshold. Otherwise, A(t) still reflects the input presented by the spike train, albeit in a more diffuse way. A more challenging problem occurs if K is unknown. Then we can decode (1) to find K and A as previously [1, 2], except iteratively, starting with the assumption that each time bin contains a spike and progressively deleting spikes from those bins that have the smallest values of A. Figure 1 shows an example with synthetic data where this method simultaneously found K and A, reconstructed R, and identified each spike in the train, perfectly. We have used these methods successfully with synthetic data and with the real transforms from motor neuron spikes to postsynaptic membrane voltage and muscle contractions in the cardiac system of the blue crab [3].
Figure 1
Figure 1

Computation of the inverse transform illustrated with synthetic data. A-C, blue: K and values of A at 33 random spike times were used to construct the overall response R. A-C, red: the corresponding solutions found by the iterative decoding of (1) with progressive deletion of candidate spikes. The corresponding blue and red points are in all cases identical; the red points have therefore been shifted right by 1 time bin for visibility. D: log of the fractional mean square error in the reconstruction of R.



Supported by NIH grants NS058017, NS41497, GM08224, and RR03051.

Authors’ Affiliations

Department of Neuroscience, Mount Sinai School of Medicine, New York, NY, USA
Institute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico
Courant Institute of Mathematical Sciences and Center for Neural Science, New York University, New York, NY, USA


  1. Stern E, Fort TJ, Miller MW, Peskin CS, Brezina V: Decoding neurophysiological responses to arbitrary spike trains. Soc Neurosci Abstr. 2006, 491.7.Google Scholar
  2. Stern E, Fort TJ, Miller MW, Peskin CS, Brezina V: Decoding modulation of the neuromuscular transform. Neurocomputing. 2007, 70: 1753-1758. 10.1016/j.neucom.2006.10.117.PubMed CentralPubMedView ArticleGoogle Scholar
  3. Stern E, Fort TJ, Miller MW, Peskin CS, Brezina V: Characterization of the crab cardiac neuromuscular transform. Soc Neurosci Abstr. 2007, 536.1.Google Scholar


© Brezina et al; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd.