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Validating silicon polytrodes with paired juxtacellular recordings: method and dataset.


ABSTRACT: Cross-validating new methods for recording neural activity is necessary to accurately interpret and compare the signals they measure. Here we describe a procedure for precisely aligning two probes for in vivo "paired-recordings" such that the spiking activity of a single neuron is monitored with both a dense extracellular silicon polytrode and a juxtacellular micropipette. Our new method allows for efficient, reliable, and automated guidance of both probes to the same neural structure with micrometer resolution. We also describe a new dataset of paired-recordings, which is available online. We propose that our novel targeting system, and ever expanding cross-validation dataset, will be vital to the development of new algorithms for automatically detecting/sorting single-units, characterizing new electrode materials/designs, and resolving nagging questions regarding the origin and nature of extracellular neural signals.

SUBMITTER: Neto JP 

PROVIDER: S-EPMC5002440 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature

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Validating silicon polytrodes with paired juxtacellular recordings: method and dataset.

Neto Joana P JP   Lopes Gonçalo G   Frazão João J   Nogueira Joana J   Lacerda Pedro P   Baião Pedro P   Aarts Arno A   Andrei Alexandru A   Musa Silke S   Fortunato Elvira E   Barquinha Pedro P   Kampff Adam R AR  

Journal of neurophysiology 20160615 2


Cross-validating new methods for recording neural activity is necessary to accurately interpret and compare the signals they measure. Here we describe a procedure for precisely aligning two probes for in vivo "paired-recordings" such that the spiking activity of a single neuron is monitored with both a dense extracellular silicon polytrode and a juxtacellular micropipette. Our new method allows for efficient, reliable, and automated guidance of both probes to the same neural structure with micro  ...[more]

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