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    <item rdf:about="https://crcns.org/forum/using-datasets/633187280/855897031">        <title>Re: EEG data hc3-vvp01 loading error!</title>        <link>https://crcns.org/forum/using-datasets/633187280/855897031</link>        <description>
 I'm not familiar with the EEGLAB, but I suspect that software is expecting that files with the .eeg extension conforms to a particular format which is different than the .eeg files in the dataset which are probably just binary files containing only data with no metadata.   Try to load the files into matlab arrays without using EEGLAB, maybe using scripts included with the hc-2 dataset. 
 Best wishes, 
 Jeff 
   
  
   
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>jteeters</dc:creator>        <dc:rights></dc:rights>                <dc:date>2020-04-17T05:19:20Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/633187280/559194408">        <title>EEG data hc3-vvp01 loading error!</title>        <link>https://crcns.org/forum/using-datasets/633187280/559194408</link>        <description>
 Hello, 
 I am writing to seek advice from you on the bug when I load the hc3--vvp01 data. I am using this publicity dataset to perform some signal processing tasks. I have used the EEGLAB software (running on Matlab) to load the vvp01 data (.eeg files), and adopted the default parameters configuration. However, when reserving array an unexpected error occurs, saying the required storage (65358 * 6536500 = 3183.0GB) excesses the maximum matrix size. I am not sure what happened. Could you please help me to check and solve this problem?  
   
 Thank you very much for sharing this interesting EEG data~~ 
   
 Best regards, 
   
 Stone 
   
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>Binli</dc:creator>        <dc:rights></dc:rights>                <dc:date>2020-04-15T07:48:05Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/219953310/570528367">        <title>Re: Reading .ang files</title>        <link>https://crcns.org/forum/using-datasets/219953310/570528367</link>        <description>
 Hello, 
   
 This is surprising, my local copy of the file is in the right format. Let me see if something went wrong during data uploading. 
 Best, 
 Adrien 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>apeyrache</dc:creator>        <dc:rights></dc:rights>                <dc:date>2019-05-23T02:39:33Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/219953310/570528366">        <title>Re: Reading .ang files</title>        <link>https://crcns.org/forum/using-datasets/219953310/570528366</link>        <description>
 Dear Adrien, 
 Thanks for the reply.  I was able to open the .ang files. But I don't find the time information in the file (1st column). Do you know how to calculate the time stamps for each angle data?  
 I am looking at session Mouse24-131213. 
 Best, 
 Shyam 
   
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>shyamk</dc:creator>        <dc:rights></dc:rights>                <dc:date>2019-05-21T16:35:58Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/153000545/451568686">        <title>Cannot download ieeg-1 dataset</title>        <link>https://crcns.org/forum/using-datasets/153000545/451568686</link>        <description>
 Hello,  
 I can't download the data of "Fedele T, Burnos S, Boran E, Krayenbühl N, Hilfiker P, Grunwald T, Sarnthein J. Resection of high frequency oscillations predicts seizure outcome in the individual patient. Scientific Reports. 2017;7(1):13836." 
 Please, I need the help , I could not download the data even though my internet connection is good. 
   
 Thanks in advance 
 Best regards 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>Fatma</dc:creator>        <dc:rights></dc:rights>                <dc:date>2021-05-24T21:29:46Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/976211409/124480917">        <title>a question on the single-unit spiking data in ac-3</title>        <link>https://crcns.org/forum/using-datasets/976211409/124480917</link>        <description>
 Dear authors, 
   
 I
 noticed that there are some very short ISIs, as short as 0.015 ms (so 
far I only looked at the first recording, site1-rn1.mat), which makes me
 wonder if the spike-sorting procedure has been validated. I haven't run
 an exhaustive analysis, but very short ISIs seem to be fairly common 
(for 27/31 single units in site1-rn1.mat , the shortest ISI is below 1 
ms). 
   
 Thank you, best regards, 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>fbaroni</dc:creator>        <dc:rights></dc:rights>                <dc:date>2021-10-08T12:46:07Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/267886582/751117108">        <title>[pvc-11] Question regarding recording times in the pvc-11 dataset</title>        <link>https://crcns.org/forum/using-datasets/267886582/751117108</link>        <description>
 Thank you for making this valuable resource publicly available. 
   
 I am analyzing your data to study temporal changes in neural responses. I was unable to find information on the time of day the recordings were made. 
   
 Would it be possible to get the approximate time for the experiments? Even a rough record from lab notes would be very helpful. 
   
 Any information you can provide would be greatly appreciated. 
   
 Thank you. 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>k223314</dc:creator>        <dc:rights></dc:rights>                <dc:date>2025-07-10T08:53:21Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/97053089/472388283">        <title>Re: hc-1 missing data?</title>        <link>https://crcns.org/forum/using-datasets/97053089/472388283</link>        <description>
 I am working specifically with all experiments that used 6-channel linear probes. These include data sets d15711 through d18911. I find discrepancies in the reported times for almost all of the files. It looks like each individual file has 750s of data, focused on synchronized (non-REM like) states during the anesthesia.  
 Thanks again, it would be nice to have confirmation on this. 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>ecmun2002</dc:creator>        <dc:rights></dc:rights>                <dc:date>2021-03-30T15:25:50Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/918330398/480960724">        <title>Re: What is the data voltage scle in hc2 ?</title>        <link>https://crcns.org/forum/using-datasets/918330398/480960724</link>        <description>
 One of the data contributors indicated by email that the answer to this is the same as for: 
 http://crcns.org/forum/using-datasets/495688760#64106314 
   
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>jteeters</dc:creator>        <dc:rights></dc:rights>                <dc:date>2018-10-10T19:51:01Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/190683764/377293746">        <title>Re: vim-4 voxel mappers</title>        <link>https://crcns.org/forum/using-datasets/190683764/377293746</link>        <description>
 Hi Xinyi - the mappers (pixmap/flatmap, voxel to fsaverage left, voxel to fsaverage right) are of different lengths because they are stored as sparse arrays. To load them, you can use  scipy's csr_matrix class  using this set of arguments: csr_array((data, indices, indptr), [shape=(M, N)]). 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>tianjiao</dc:creator>        <dc:rights></dc:rights>                <dc:date>2023-09-01T17:58:37Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/468708876/666822074">        <title>vim-2 How to locate the rois in anatomical space?</title>        <link>https://crcns.org/forum/using-datasets/468708876/666822074</link>        <description>
 The vim-2 dataset provided the rois masks in functional image space, however, how to map the roi to the anatomical space to see its functional responses? 
 The size of functional response is 64*64*18, however, anatomical volume has a size of 240*275*240. So the func should co-register to anat. So, the question arosed, how to map each other? I tried to reach for Nishimoto 2011, and the paper only says 'These data were used to fit a separate encoding model for each voxel located in posterior and ventral occipito-temporal visual cortex', without a precise location of each roi in anatomical space.  
 What should i do to get the location information of each roi in anatomical space? 
   
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>RayChow</dc:creator>        <dc:rights></dc:rights>                <dc:date>2025-10-22T16:48:56Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/976211409/938326811">        <title>Re: a question on the single-unit spiking data in ac-3</title>        <link>https://crcns.org/forum/using-datasets/976211409/938326811</link>        <description>
 Dear Fabiano, 
 Thank you for your interest in the dataset. The spike sorting procedure used in this dataset is a semi-automatic spike sorter based on  Lewicki (1994) . Your characterization of very short ISIs in the dataset being "fairly common" is misleading, since while 27 of 31 single units have "short ISIs", only ~0.5% of all ISIs in that dataset is &lt;1 ms. The manual part of the semi-automatic spike sorting procedure involves a curation of the isolated clusters from the automatic part of the spike sorter, and one of the criteria is indeed that single units cannot have a large percentage of short ISIs. We did not remove spikes that have short ISIs from the curated clusters, but please feel free to do so as you use the dataset. 
 Best, 
 Jermyn 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>szjermyn</dc:creator>        <dc:rights></dc:rights>                <dc:date>2021-10-19T06:37:58Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/235523857/372063370">        <title>how to convert file  with suffix  .eeg to mat file </title>        <link>https://crcns.org/forum/using-datasets/235523857/372063370</link>        <description>
 i want to convert file  with suffix  .eeg to mat file 
 beacuase i want to analysis data in matlab 
can you help me?</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>amin8179</dc:creator>        <dc:rights></dc:rights>                <dc:date>2019-07-09T06:46:37Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/282816360/932649157">        <title>vim-1: EstimatedResponses.mat have some unexpected NaN values.</title>        <link>https://crcns.org/forum/using-datasets/282816360/932649157</link>        <description>
 Hi, there! 
   
 I extracted roi data from EstimatedResponses.mat. I found there are some unexpected Nan values. 
 for subject1's training data, V1 has 1331 voxel; V2 has 2208 voxel; V4 has 1550 voxel; LO has 928 voxel; the total is 6017. 
 for subject2's training data, V1 has 1513 voxel; V2 has 1982 voxel; V4 has 1022 voxel; LO has 358 voxel; the total is 4875. 
 It is in accordance with a study reported — "If we consider only the main afferent pathway of the ventral stream (V1, V2, V4, and LO) then 1786 of 6017 and 768 of 4875 voxels remained for S1 and S2, respectively." (Guclu, U. , &amp; Van Gerven, M. A. J. . (2015). Deep neural networks reveal a gradient in the complexity of neural representations across the ventral stream. The Journal of Neuroence, 35(27).) 
 But there are some NaN values in these data. After voxels which contain NaN values were droped: 
 for subject1's training data, V1 has 1294 voxel; V2 has 2083 voxel; V4 has 1535 voxel; LO has 928 voxel; the total is 5840. 
 for subject2's training data, V1 has 1419 voxel; V2 has 1890 voxel; V4 has 1022 voxel; LO has 358 voxel; the total is 4689. 
 There were many studies used the data. But I didn't remeber any study had reported NaN value existed. 
 So may be there was something wrong with the data? 
 Thank you for your help! 
   
   
   
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>xuhuawei</dc:creator>        <dc:rights></dc:rights>                <dc:date>2020-11-01T09:14:44Z</dc:date>        <dc:type>Comment</dc:type>    </item>
    <item rdf:about="https://crcns.org/forum/using-datasets/632035609/32488148">        <title>Re: fcx-3 data-how to get the MNI coordinates for each electrode</title>        <link>https://crcns.org/forum/using-datasets/632035609/32488148</link>        <description>
 Please find the corrected files attached. 
</description>        <dc:publisher>No publisher</dc:publisher>        <dc:creator>eljohnson</dc:creator>        <dc:rights></dc:rights>                <dc:date>2020-10-20T20:05:18Z</dc:date>        <dc:type>Comment</dc:type>    </item>



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