<div dir="ltr"><div class="gmail_default" style="color:rgb(51,51,153)">Hello Narenda, some points right below that should be of use to you. ~Cheers</div><div class="gmail_default" style="color:rgb(51,51,153)"><br></div><div class="gmail_default" style="color:rgb(51,51,153)">1. Explore the Netstation and EGI documentation, available at their support site or through their customer support.</div><div class="gmail_default" style="color:rgb(51,51,153)">2. See the readme notes within the folders at the EGI ftp site that have their channel locations. You can find these if you google "EEGLAB channel location files" which gives you a list and weblinks of many layouts. You may also log into the EGI customer service website to get all available channel layouts.</div><div class="gmail_default" style="color:rgb(51,51,153)">3. There are two folders of channel layouts at the egi ftp support folder. Make sure you grab "Hydrocel" versions of the layouts you need. The GSN is incorrect unless you recorded with the older GSN nets.</div><div class="gmail_default" style="color:rgb(51,51,153)">4. 128 channels in a layout file means that the channel layout file has 128 channels, and does not include a row of information about the label and location of the reference electrode.</div><div class="gmail_default" style="color:rgb(51,51,153)">If the layout filename has 129 within it, it means that it does not include a row of information about the label and location of the reference electrode.</div><div class="gmail_default" style="color:rgb(51,51,153)">Simialrly for 64 and 64, 256 and 257 channel layout files for hydrocel egi nets.</div><div class="gmail_default" style="color:rgb(51,51,153)">5. For erplab questions, you will likely have success putting a query right on the erplab mailing list.</div><div class="gmail_default" style="color:rgb(51,51,153)"><br></div><div class="gmail_default" style="color:rgb(51,51,153)"><br></div><div class="gmail_default" style="color:rgb(51,51,153)"><br></div><div class="gmail_default" style="color:rgb(51,51,153)"><br></div><div class="gmail_extra"><br><div class="gmail_quote">On Sun, May 10, 2015 at 3:34 AM, Narendra Kumar <span dir="ltr"><<a href="mailto:narendra.linguistics@gmail.com" target="_blank">narendra.linguistics@gmail.com</a>></span> wrote:<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"><div style="font-family:georgia,serif">Hi, </div><div style="font-family:georgia,serif"><br></div><div style="font-family:georgia,serif">I am a very new user to EEGLab and ERPLab toolbox. I have done practice on EEG/ERPLab using the sample data given on the website. I have data recorded using EGI-128 channel system. Following the same steps when I am trying to analyse my data I got stucked in following issues:</div><div style="font-family:georgia,serif"> </div><div style="font-family:georgia,serif"> --- Electrode location file which one to use ? I am using HydrocelGSN net but in the plugins location files GSN128.sfp, GSN129.sfp and GSN Hydrocel257.sfp are available. Electrode location file for GSN Hydrocel 128 is absent.</div><div style="font-family:georgia,serif"><br></div><div style="font-family:georgia,serif"> --- Please clarify when to use GSN128.sfp and GSN129.sfp ?</div><div style="font-family:georgia,serif"><br></div><div style="font-family:georgia,serif"> --- How to assign Binlister to the file ? </div><div style="font-family:georgia,serif"><br></div><div class="gmail_extra"><br clear="all"><div><div><div dir="ltr">Thanks & Regards,<br><br>Narendra Kumar<br>Research Scholar<div>Department of Humanities and Social Sciences</div><div>Indian Institute of Technology Ropar</div><div>Punjab, India - 140001 <br></div><div>Contact No.:- <a href="tel:%2B91-8968945650" value="+918968945650" target="_blank">+91-8968945650</a><br></div><div>Homepage:- <a href="https://www.sites.google.com/site/narendraiitrpr/" target="_blank">https://www.sites.google.com/site/narendraiitrpr</a>/</div><div>Social Networking Sites: - <a href="https://www.facebook.com/narendra.karna.7" target="_blank">Facebook</a>; <a href="https://www.researchgate.net/profile/Narendra_Kumar22/" target="_blank">Researchgate</a><br></div><div><br> <br><br></div></div></div></div>
<br><div class="gmail_quote">On Sun, May 10, 2015 at 12:30 AM, <span dir="ltr"><<a href="mailto:eeglablist-request@sccn.ucsd.edu" target="_blank">eeglablist-request@sccn.ucsd.edu</a>></span> wrote:<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">Send eeglablist mailing list submissions to<br>
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<br>Today's Topics:<br>
<br>
1. Re: Electrode location.... (Makoto Miyakoshi)<br>
2. Re: ICA component rejection (Makoto Miyakoshi)<br>
3. Re: Topography plot in component clusters (Makoto Miyakoshi)<br>
4. Re: ICA component rejection (Makoto Miyakoshi)<br>
5. Re: Regarding PACT (Makoto Miyakoshi)<br>
<br><br>---------- Forwarded message ----------<br>From: Makoto Miyakoshi <<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>><br>To: Gonzalo Rojas Costa <<a href="mailto:gonzalo.rojas.costa@gmail.com" target="_blank">gonzalo.rojas.costa@gmail.com</a>><br>Cc: EEGLAB List <<a href="mailto:eeglablist@sccn.ucsd.edu" target="_blank">eeglablist@sccn.ucsd.edu</a>><br>Date: Fri, 8 May 2015 12:02:26 -0700<br>Subject: Re: [Eeglablist] Electrode location....<br><div dir="ltr">Dear Gonzalo,<div><br></div><div>Are these channels compatible with 10-20 system? In other words, are they Fz, Cz, Pz, etc? If so then you just need to manually enter the channel names and 'look up locs' to let EEGLAB read the template locations.</div><div><br></div><div>Makoto</div></div><div class="gmail_extra"><br><div class="gmail_quote">On Wed, May 6, 2015 at 2:18 PM, Gonzalo Rojas Costa <span dir="ltr"><<a href="mailto:gonzalo.rojas.costa@gmail.com" target="_blank">gonzalo.rojas.costa@gmail.com</a>></span> wrote:<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"><p dir="ltr">Hi:</p>
<p dir="ltr">I have a four electrode EEG data file in EDF format.... I loaded successfully in EEGLAB, but I couldn't load the electrode location.... how can I do it?.... I tried to follow the EEGLAB tutorial instructions...</p>
<p dir="ltr">Sincerely,<br></p>
<p dir="ltr">Gonzalo Rojas Costa</p>
<p dir="ltr">--------------------------------<br>
Gonzalo Rojas Costa<br>
Advanced Medical Image Processing Laboratory<br>
Department of Radiology<br>
Clínica las Condes<br>
Lo Fontecilla 441, Las Condes, Santiago, Chile.<br>
Tel: 56-2-2105170<br>
Cel: 56-9-97771785<br>
<a href="http://www.clc.cl" target="_blank">www.clc.cl</a></p>
<br>_______________________________________________<br>
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For digest mode, send an email with the subject "set digest mime" to <a href="mailto:eeglablist-request@sccn.ucsd.edu" target="_blank">eeglablist-request@sccn.ucsd.edu</a><br></blockquote></div><br><br clear="all"><div><br></div>-- <br><div><div dir="ltr">Makoto Miyakoshi<br>Swartz Center for Computational Neuroscience<br>Institute for Neural Computation, University of California San Diego<br></div></div>
</div>
<br><br>---------- Forwarded message ----------<br>From: Makoto Miyakoshi <<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>><br>To: Mostafa IR <<a href="mailto:mostafa.rouzbahani@gmail.com" target="_blank">mostafa.rouzbahani@gmail.com</a>><br>Cc: EEGLAB List <<a href="mailto:eeglablist@sccn.ucsd.edu" target="_blank">eeglablist@sccn.ucsd.edu</a>><br>Date: Fri, 8 May 2015 12:06:52 -0700<br>Subject: Re: [Eeglablist] ICA component rejection<br><div dir="ltr">Dear Mostafa,<div><br></div><div>First of all, how did you get ICA work on the 5-sec data?</div><div><br></div><div>For the example of efficient and flexible group-level IC rejection, see my wiki page below. </div><div><a href="http://sccn.ucsd.edu/wiki/Backproject_clustered_ICs" target="_blank">http://sccn.ucsd.edu/wiki/Backproject_clustered_ICs</a><br></div><div><br></div><div>Makoto</div></div><div class="gmail_extra"><br><div class="gmail_quote">On Fri, May 8, 2015 at 12:14 AM, Mostafa IR <span dir="ltr"><<a href="mailto:mostafa.rouzbahani@gmail.com" target="_blank">mostafa.rouzbahani@gmail.com</a>></span> wrote:<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"><div>Hi <br><br></div><div>I want reject bad component after ICA analysis. I read the chapter09 , Julie Onton<br>Scott Makeig paper and ... . Except eye artifact the others are very hard to distinguish in other hand my data is very large(360 data set each one 5s without any event) and it's hard to reject all of them manually. I try to use MARA plugins but it need at least 15s of EEG which my data are 5s. Is there any other plugin to help me for bad component rejection automatically?<br><br></div><div>Thank you<br></div></div>
<br>_______________________________________________<br>
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</div>
<br><br>---------- Forwarded message ----------<br>From: Makoto Miyakoshi <<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>><br>To: Shingo Tokimoto <<a href="mailto:tokimoto@mejiro.ac.jp" target="_blank">tokimoto@mejiro.ac.jp</a>><br>Cc: UCSD List EEG <<a href="mailto:eeglablist@sccn.ucsd.edu" target="_blank">eeglablist@sccn.ucsd.edu</a>><br>Date: Fri, 8 May 2015 14:32:32 -0700<br>Subject: Re: [Eeglablist] Topography plot in component clusters<br><div dir="ltr">Dear Shingo,<div><br></div><div>Ok here is a solution for you based on my guess.</div><div><br></div><div><span style="font-size:12.6666669845581px">> Is it impossible to plot topographies of two experimental conditions for a component cluster as we can do in channel pot (for a time-window)?</span><br></div><div><br></div><div>I guess you mean 'to plot <b><i>difference</i></b> topographies of two experimental conditions for a component cluster'. The instruction below is based on this assumption.</div><div><br></div><div>Case 1: The conditions are all within-subject and with the continuous use of an EEG cap.</div><div>Unless each within-subject condition is recorded on different sessions (i.e. apply the EEG cap for one session, remove it, and applied it newly for the next session), independent components should be shared across the conditions. If this is the case, then difference topography is all zero. Therefore, <b>you can't get difference topographies</b>.</div><div><br></div><div>Case 2: The conditions are between-subject (or within-subject but different sessions with different EEG cap application). If this is the case, subtraction of IC scalp maps makes sense. </div><div><br></div><div>How to do it:</div><div><br></div><div>1. Load your STUDY with group differences (i.e. Case 2 mentioned above)</div><div><br></div><div>2. Use my plugin std_envtopo and show whatever envtopo. This is to generate topoall_group under STUDY.cluster(1,X) It looks like this</div><div><br></div><div><div>topoall_group: {{1x14 cell} {1x17 cell}}<br></div></div><div><br></div><div>3. To visualize Group A and Group B in Cluster 5, see my code and result example below</div><div><a href="https://drive.google.com/open?id=0BzTEovh4TOLiflAwREdrZmxsUTBfVFdjR3AyS0pOV3JONEEtTHpwdndwLU9mVXg3cHlITHc&authuser=0" target="_blank">https://drive.google.com/open?id=0BzTEovh4TOLiflAwREdrZmxsUTBfVFdjR3AyS0pOV3JONEEtTHpwdndwLU9mVXg3cHlITHc&authuser=0</a><br></div><div><br></div><div>Let me know if you have any trouble in accessing my Google drive.</div><div><br></div><div>Makoto</div><div><br></div><div><br></div><div><br></div><div><br></div><div class="gmail_extra"><br><div class="gmail_quote">On Tue, May 5, 2015 at 1:23 PM, Makoto Miyakoshi <span dir="ltr"><<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>></span> wrote:<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">Dear Shingo,<div><br></div><div>I don't think it's possible.</div><div>scalp topo generation is relatively straightforward using pop_topoplot() function. I can help you to do this if you are interested in.</div><div><br></div><div>Makoto</div></div><div class="gmail_extra"><div><div><br><div class="gmail_quote">On Thu, Apr 30, 2015 at 3:24 PM, Shingo Tokimoto <span dir="ltr"><<a href="mailto:tokimoto@mejiro.ac.jp" target="_blank">tokimoto@mejiro.ac.jp</a>></span> wrote:<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">Dear EEGLAB experts,<br>
<br>
Is it impossible to plot topographies of two experimental conditions for a component cluster as we can do in channel pot (for a time-window)? Thank you in advance.<br>
<br>
************************************************<br>
Shingo Tokimoto, Ph.D.<br>
in Linguistics and Psychology<br>
Department of Foreign Languages<br>
Mejiro University<br>
4-31-1, Naka-Ochiai, Shinjuku, Tokyo,<br>
161-8539, Japan<br>
<a href="mailto:tokimoto@mejiro.ac.jp" target="_blank">tokimoto@mejiro.ac.jp</a><br>
************************************************<br>
<br>
<br>
_______________________________________________<br>
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</blockquote></div><br><br clear="all"><div><br></div></div></div><span><font color="#888888">-- <br><div><div dir="ltr">Makoto Miyakoshi<br>Swartz Center for Computational Neuroscience<br>Institute for Neural Computation, University of California San Diego<br></div></div>
</font></span></div>
</blockquote></div><br><br clear="all"><div><br></div>-- <br><div><div dir="ltr">Makoto Miyakoshi<br>Swartz Center for Computational Neuroscience<br>Institute for Neural Computation, University of California San Diego<br></div></div>
</div></div>
<br><br>---------- Forwarded message ----------<br>From: Makoto Miyakoshi <<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>><br>To: Mostafa IR <<a href="mailto:mostafa.rouzbahani@gmail.com" target="_blank">mostafa.rouzbahani@gmail.com</a>><br>Cc: EEGLAB List <<a href="mailto:eeglablist@sccn.ucsd.edu" target="_blank">eeglablist@sccn.ucsd.edu</a>><br>Date: Fri, 8 May 2015 14:34:26 -0700<br>Subject: Re: [Eeglablist] ICA component rejection<br><div dir="ltr">Dear Mostafa,<div><br></div><div>> 1)Can I append these 5-sec data together for creating a longer data and after that use the ICA?</div><div><br></div><div>Yes, for ICA longer the data better the decomposition. If possible, use even continuous data.</div><div><br>> 2) If the first question is yes can I separate my data again to 5-sec and use the ICA weights of merged data?<br></div><div><br></div><div>Yes. You can actually epoch the data normally after ICA.</div><div><br></div><div>Makoto</div><div class="gmail_extra"><br><div class="gmail_quote">On Fri, May 8, 2015 at 1:34 PM, Mostafa IR <span dir="ltr"><<a href="mailto:mostafa.rouzbahani@gmail.com" target="_blank">mostafa.rouzbahani@gmail.com</a>></span> wrote:<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">Dear Laura<br>I will be glad to use your plugin and count on your help. <br><br>Dear Makoto<br>Thanks for your link and your advice. I used to make a big mistake about ICA with neglect of data point rule of thumb. <br>I have a new question. My data is about emotions. In my case the person saw a picture for 5-sec and eeg with 16 channels at 512HZ captured. 10 picture with the same content show to the person. <br>1)Can I append these 5-sec data together for creating a longer data and after that use the ICA?<br>2) If the first question is yes can I separate my data again to 5-sec and use the ICA weights of merged data?<br><br>Best Regards<div><div><br><div class="gmail_quote">On Fri, May 8, 2015 at 23:37 Makoto Miyakoshi <<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>> wrote:<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">Dear Mostafa,<div><br></div><div>First of all, how did you get ICA work on the 5-sec data?</div><div><br></div><div>For the example of efficient and flexible group-level IC rejection, see my wiki page below. </div><div><a href="http://sccn.ucsd.edu/wiki/Backproject_clustered_ICs" target="_blank">http://sccn.ucsd.edu/wiki/Backproject_clustered_ICs</a><br></div><div><br></div><div>Makoto</div></div><div class="gmail_extra"><br><div class="gmail_quote"></div></div><div class="gmail_extra"><div class="gmail_quote">On Fri, May 8, 2015 at 12:14 AM, Mostafa IR <span dir="ltr"><<a href="mailto:mostafa.rouzbahani@gmail.com" target="_blank">mostafa.rouzbahani@gmail.com</a>></span> wrote:<br></div></div><div class="gmail_extra"><div class="gmail_quote"><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"><div>Hi <br><br></div><div>I want reject bad component after ICA analysis. I read the chapter09 , Julie Onton<br>Scott Makeig paper and ... . Except eye artifact the others are very hard to distinguish in other hand my data is very large(360 data set each one 5s without any event) and it's hard to reject all of them manually. I try to use MARA plugins but it need at least 15s of EEG which my data are 5s. Is there any other plugin to help me for bad component rejection automatically?<br><br></div><div>Thank you<br></div></div>
<br></blockquote></div></div><div class="gmail_extra"><div class="gmail_quote"><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">_______________________________________________<br>
Eeglablist page: <a href="http://sccn.ucsd.edu/eeglab/eeglabmail.html" target="_blank">http://sccn.ucsd.edu/eeglab/eeglabmail.html</a><br>
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</div></blockquote></div>
</div></div></blockquote></div><br><br clear="all"><div><br></div>-- <br><div><div dir="ltr">Makoto Miyakoshi<br>Swartz Center for Computational Neuroscience<br>Institute for Neural Computation, University of California San Diego<br></div></div>
</div></div>
<br><br>---------- Forwarded message ----------<br>From: Makoto Miyakoshi <<a href="mailto:mmiyakoshi@ucsd.edu" target="_blank">mmiyakoshi@ucsd.edu</a>><br>To: "井澤考史" <<a href="mailto:ko.izawa@gmail.com" target="_blank">ko.izawa@gmail.com</a>><br>Cc: EEGLAB List <<a href="mailto:eeglablist@sccn.ucsd.edu" target="_blank">eeglablist@sccn.ucsd.edu</a>><br>Date: Fri, 8 May 2015 14:50:35 -0700<br>Subject: Re: [Eeglablist] Regarding PACT<br><div dir="ltr">Dear Koji,<div><br></div><div>I tried it but could not replicate the problem. I used Matlab 2014b, EEGLAB 13.x, PACT0.17.</div><div><br></div><div>From your log,</div><div><br></div><div><div style="font-size:13.3333330154419px;color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;line-height:20px">> pop_eegfiltnew() - performing 425 point bandpass filtering.</div></div><div><br></div><div>This does not make sense to me. Looks like your sampling rate is very low, must be around 100Hz? Because the default amplitude frequency cutoff is 100Hz (i.e. amplitude of > 100Hz will be analyzed), your sampling rate should be much higher than 100Hz.</div><div><br></div><div>PACT assumed that the input is ECoG data, which is usually sampled at >= 1000Hz. Please try the data with much higher sampling rate (or upsampling your data to see if it fixes the problem.)</div><div><br></div><div>Makoto</div><div><br></div><div class="gmail_extra"><br><div class="gmail_quote">On Mon, Apr 27, 2015 at 4:27 PM, 井澤考史 <span dir="ltr"><<a href="mailto:ko.izawa@gmail.com" target="_blank">ko.izawa@gmail.com</a>></span> wrote:<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"><div>Dear EEGLAB and PACT team,</div><div><br></div><div>I’m trying to learn the PACT by using eeglab_data.set. But I met some errors as follows. Could you provide any opinion to me?</div><div><br></div><div>My Operation</div><div>- Loaded dataset.</div><div>- Launched "Compute PAC” GUI. </div><div>- No change all parameters value form default and press OK.</div><div><br></div><div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">pop_eegfiltnew() - performing 425 point bandpass filtering.</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">pop_eegfiltnew() - transition band width: 1 Hz</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">pop_eegfiltnew() - passband edge(s): [1 2] Hz</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">pop_eegfiltnew() - cutoff frequency(ies) (-6 dB): [0.5 2.5] Hz</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">pop_eegfiltnew() - filtering the data (zero-phase)</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">firfilt(): |====================| 100%, ETE 00:00</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">Error using pop_eegfiltnew (line 148)</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">Cutoff frequency out of range</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px"><br></div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">Error in pac_man (line 181)</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">EEG_highFreqAmp = pop_eegfiltnew(EEG, hfoAmp(1), hfoAmp(end));</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px"><br></div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">Error in pac_pop_main (line 145)</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">EEG = pac_man(EEG, options{:});</div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px"> </div><div style="color:rgb(40,55,105);font-family:'Lucida Grande','Lucida Sans Unicode',Arial,sans-serif;font-size:13.3333330154419px;line-height:20px">Error while evaluating uimenu Callback</div></div><div><br></div><div><br></div><div>Best regards,</div><div>Koji</div><div><br></div></div>
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