<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Heiney K</submitter><pubmed_abstract>Understanding neuronal communication is fundamental in neuroscience, but there are few methodologies offering detailed analysis for well-controlled conditions. By interfacing microElectrode arrays with microFluidics (μEF devices), it is possible to compartmentalize neuronal cultures with a specified alignment of axons and microelectrodes. This setup allows the extracellular recording of spike propagation with a high signal-to-noise ratio over the course of several weeks. Addressing these μEF devices, we developed an advanced yet easy-to-use publically available computational tool, μSpikeHunter, which provides a detailed quantification of several communication-related properties such as propagation velocity, conduction failure, spike timings, and coding mechanisms. The combination of μEF de</pubmed_abstract><journal>Scientific reports</journal><pagination>5777</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6453950</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>µSpikeHunter: An advanced computational tool for the analysis of neuronal communication and action potential propagation in microfluidic platforms.</pubmed_title><pmcid>PMC6453950</pmcid><pubmed_authors>Aguiar P</pubmed_authors><pubmed_authors>Heiney K</pubmed_authors><pubmed_authors>Neto E</pubmed_authors><pubmed_authors>Lopes CDF</pubmed_authors><pubmed_authors>Lamghari M</pubmed_authors><pubmed_authors>Mateus JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>µSpikeHunter: An advanced computational tool for the analysis of neuronal communication and action potential propagation in microfluidic platforms.</name><description>Understanding neuronal communication is fundamental in neuroscience, but there are few methodologies offering detailed analysis for well-controlled conditions. By interfacing microElectrode arrays with microFluidics (μEF devices), it is possible to compartmentalize neuronal cultures with a specified alignment of axons and microelectrodes. This setup allows the extracellular recording of spike propagation with a high signal-to-noise ratio over the course of several weeks. Addressing these μEF devices, we developed an advanced yet easy-to-use publically available computational tool, μSpikeHunter, which provides a detailed quantification of several communication-related properties such as propagation velocity, conduction failure, spike timings, and coding mechanisms. The combination of μEF de</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Apr</publication><modification>2026-07-17T00:40:32.559Z</modification><creation>2025-05-18T11:07:28.995Z</creation></dates><accession>S-EPMC6453950</accession><cross_references><pubmed>30962522</pubmed><doi>10.1038/s41598-019-42148-3</doi></cross_references></HashMap>