<div dir="ltr">Hi Makoto,<div><br></div><div style>You can set those channel names in your biosemi config file. That saves a lot of time. </div><div style>As for me, I'm using 10-20 so I'm not sure of how that translates to 10-5.</div>
<div style>Good luck =)</div></div><div class="gmail_extra"><br><br><div class="gmail_quote">2013/8/12 Makoto Miyakoshi <span dir="ltr"><<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>></span><br>
<blockquote class="gmail_quote" style="margin:0 0 0 .8ex;border-left:1px #ccc solid;padding-left:1ex"><div dir="ltr">Dear Vincent,<div><br></div><div>> If I set the labels to FP1, FP3 etc. instead of A1, A2, etc., I do get coordinates.<br>
</div><div class="gmail_extra"><br></div><div class="gmail_extra">Yes, this is what I experienced too. I guess 'pair channels' does not work if you have non 10-5 channel names.</div>
<div class="gmail_extra"><br></div><div class="gmail_extra">So my personal solution for this kind of dataset is that you chose 5 closet channels (Fz -> ??, Cz -> ??, Pz->??, T7->??, T8->??) and rename them into 10-5 names. Then warp montage using these renamed channels. This is an ugly solution but it still works and better than nothing.</div>
<div class="gmail_extra"><br></div><div class="gmail_extra">Makoto</div><div class="gmail_extra"><br><div class="gmail_quote">2013/8/6 Vincent LeBlanc <span dir="ltr"><<a href="mailto:leblvin@gmail.com" target="_blank">leblvin@gmail.com</a>></span><br>
<blockquote class="gmail_quote" style="margin:0px 0px 0px 0.8ex;border-left-width:1px;border-left-color:rgb(204,204,204);border-left-style:solid;padding-left:1ex"><div dir="ltr">Hi Enzo!<div>If I keep the original labels, it can't find any coordinates. If I set the labels to FP1, FP3 etc. instead of A1, A2, etc., I do get coordinates. However, when I plot their location, some of the channels are off the head. Is that simply an effect of not having a 3D map of their localisation? <br>
</div></div><div><div><div class="gmail_extra"><br><br><div class="gmail_quote">2013/8/5 Enzo Brunetti <span dir="ltr"><<a href="mailto:enzo.brunetti@gmail.com" target="_blank">enzo.brunetti@gmail.com</a>></span><br>
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<div style="word-wrap:break-word">Hi Vincent,<div><br></div><div>eeglab's plugin 'dipfit' offers some head montages including some Biosemi common layouts. When you use Edit/Channel locations, the displayed window offers you to look up the corresponding coordinates for the labels present in the .bdf file. Try clicking 'Ok' in this window to see if it helps you.</div>
<div><br></div><div>Good luck.</div><div><br></div><div><br><div><div>El 05-08-2013, a las 13:51, Vincent LeBlanc <<a href="mailto:leblvin@gmail.com" target="_blank">leblvin@gmail.com</a>> escribió:</div><br><blockquote type="cite">
<div><div><div dir="ltr">Hi to all!<div><br></div><div>I've been trying to correctly enter the BioSemi coordinates into eeglab, to no avail. Using the excel sheet on their website (<a href="http://www.biosemi.com/download/Cap_coords_all.xls" target="_blank">http://www.biosemi.com/download/Cap_coords_all.xls</a>) gives me absurd results when plotting the channel positions.</div>
<div>I'm using the 64 electrodes cap. Does anybody have a clue on where/how I could get those coordinates?</div><div><br></div><div>Thanks in advance =)</div></div></div></div>
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-- <br><div dir="ltr">Makoto Miyakoshi<br>Swartz Center for Computational Neuroscience<br>Institute for Neural Computation, University of California San Diego<br></div>
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