Publication: Rhythmic continuous-time coding in the songbird analog of vocal motor cortex
Rhythmic continuous-time coding in the songbird analog of vocal motor cortex
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Lynch, G. F., Okubo, T. S., Hanuschkin, A., Hahnloser, R. H. R., & Fee, M. S. (2016). Rhythmic continuous-time coding in the songbird analog of vocal motor cortex. Neuron, 90(4), 877–892. https://doi.org/10.1016/j.neuron.2016.04.021
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Songbirds learn and produce complex sequences of vocal gestures. Adult birdsong requires premotor nucleus HVC, in which projection neurons (PNs) burst sparsely at stereotyped times in the song. It has been hypothesized that PN bursts, as a population, form a continuous sequence, while a different model of HVC function proposes that both HVC PN and interneuron activity is tightly organized around motor gestures. Using a large dataset of PNs and interneurons recorded in singing birds, we test several predictions of these models. We find
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- Lynch, Galen F
- Okubo, Tatsuo S
- Hanuschkin, Alexander
- Hahnloser, Richard H R
- Fee, Michale S
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Lynch, G. F., Okubo, T. S., Hanuschkin, A., Hahnloser, R. H. R., & Fee, M. S. (2016). Rhythmic continuous-time coding in the songbird analog of vocal motor cortex. Neuron, 90(4), 877–892. https://doi.org/10.1016/j.neuron.2016.04.021