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  Beyond GLMs: A Generative Mixture Modeling Approach to Neural System Identification

Theis, L., Chagas, A., Arnstein, D., Schwarz, C., & Bethge, M. (2013). Beyond GLMs: A Generative Mixture Modeling Approach to Neural System Identification. PLoS Computational Biology, 9(11), 1-9. doi:10.1371/journal.pcbi.1003356.

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Theis, L, Autor           
Chagas , AM, Autor
Arnstein, Dan, Autor           
Schwarz, C, Autor
Bethge, M1, 2, Autor           
Affiliations:
1Research Group Computational Vision and Neuroscience, Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497805              
2Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497794              

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 Zusammenfassung: Generalized linear models (GLMs) represent a popular choice for the probabilistic characterization of neural spike responses. While GLMs are attractive for their computational tractability, they also impose strong assumptions and thus only allow for a limited range of stimulus-response relationships to be discovered. Alternative approaches exist that make only very weak assumptions but scale poorly to high-dimensional stimulus spaces. Here we seek an approach which can gracefully interpolate between the two extremes. We extend two frequently used special cases of the GLM—a linear and a quadratic model—by assuming that the spike-triggered and non-spike-triggered distributions can be adequately represented using Gaussian mixtures. Because we derive the model from a generative perspective, its components are easy to interpret as they correspond to, for example, the spike-triggered distribution and the interspike interval distribution. The model is able to capture complex dependencies on high-dimensional stimuli with far fewer parameters than other approaches such as histogram-based methods. The added flexibility comes at the cost of a non-concave log-likelihood. We show that in practice this does not have to be an issue and the mixture-based model is able to outperform generalized linear and quadratic models.

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 Datum: 2013-11
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1371/journal.pcbi.1003356
BibTex Citekey: TheisCASB2013
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Titel: PLoS Computational Biology
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 9 (11) Artikelnummer: - Start- / Endseite: 1 - 9 Identifikator: eDoc: e1003356