<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Neto, J.P.a b e</style></author><author><style face="normal" font="default" size="100%">Lopes, G.a e</style></author><author><style face="normal" font="default" size="100%">Frazão, J.a</style></author><author><style face="normal" font="default" size="100%">Nogueira, J.a e</style></author><author><style face="normal" font="default" size="100%">Lacerda, P.a</style></author><author><style face="normal" font="default" size="100%">Baião, P.a</style></author><author><style face="normal" font="default" size="100%">Aarts, A.d</style></author><author><style face="normal" font="default" size="100%">Andrei, A.c</style></author><author><style face="normal" font="default" size="100%">Musa, S.c</style></author><author><style face="normal" font="default" size="100%">Fortunato, E.b</style></author><author><style face="normal" font="default" size="100%">Barquinha, P.b</style></author><author><style face="normal" font="default" size="100%">Kampff, A.R.a e</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Validating silicon polytrodes with paired juxtacellular recordings: Method and dataset</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Neurophysiology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.scopus.com/inward/record.uri?eid=2-s2.0-84984607318&amp;doi=10.1152%2fjn.00103.2016&amp;partnerID=40&amp;md5=ceaa51b527bb23249ca47278d835972f</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">2</style></number><publisher><style face="normal" font="default" size="100%">American Physiological Society</style></publisher><volume><style face="normal" font="default" size="100%">116</style></volume><pages><style face="normal" font="default" size="100%">892-903</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">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 &quot;paired-recordings&quot; 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. © 2016, American Physiological Society. All rights reserved.</style></abstract><notes><style face="normal" font="default" size="100%">cited By 0</style></notes></record></records></xml>