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From: Richard F. <fri...@ca...> - 2010-07-12 17:09:46
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Dear Jtreeview Users. Has anyone had success in using Jtreeview with Windows 7. A member of our IT staff had just tried it without success. Thanks and best wishes, Rich ------------------------------------------------------------ Richard A. Friedman, PhD Associate Research Scientist, Biomedical Informatics Shared Resource Herbert Irving Comprehensive Cancer Center (HICCC) Lecturer, Department of Biomedical Informatics (DBMI) Educational Coordinator, Center for Computational Biology and Bioinformatics (C2B2)/ National Center for Multiscale Analysis of Genomic Networks (MAGNet) Room 824 Irving Cancer Research Center Columbia University 1130 St. Nicholas Ave New York, NY 10032 (212)851-4765 (voice) fri...@ca... http://cancercenter.columbia.edu/~friedman/ In Memoriam, George Scithers |
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From: Alok S. <alo...@gm...> - 2010-07-07 23:58:20
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Dear Mara, As far as I know there isn't a particularly easy way. CEL and PCL formats are both simple text formats, and In the past I have written my own perl scripts to translate. The two other things I have heard are 1) Try loading your CEL files in dChip or MeV, and see if they will export to PCL. MeV has a bunch of cluster/JTV functionality built in. 2) Rearrange the files yourself in Excel. You should be able to get the numbers keyed to gene names using the export functions in GCOS. Maybe someone else on the list will get back to you with something easier! On Wed, Jul 7, 2010 at 3:23 PM, <mh...@bu...> wrote: > Hello, I am trying to use Java Treeview with Cluster 3. I am having > trouble getting started. The files I have are .CEL not .CDT or .PCL. > Please help, Thanks, Mara > > > ------------------------------------------------------------------------------ > This SF.net email is sponsored by Sprint > What will you do first with EVO, the first 4G phone? > Visit sprint.com/first -- http://p.sf.net/sfu/sprint-com-first > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users > |
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From: <mh...@bu...> - 2010-07-07 23:37:26
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Hello, I am trying to use Java Treeview with Cluster 3. I am having trouble getting started. The files I have are .CEL not .CDT or .PCL. Please help, Thanks, Mara |
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From: <mh...@bu...> - 2010-07-07 19:23:43
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Hello, I am trying to use Java Treeview with Cluster 3. I am having trouble getting started. The files I have are .CEL not .CDT or .PCL. Please help, Thanks, Mara |
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From: Alok S. <alo...@gm...> - 2010-03-22 14:59:07
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Dear Anna, I'm not sure I fully understand, but there is an "index" attribute that you can set on the "UrlExtractor" and "ArrayUrlExtractor" tags that will specify which header column, or in the case of arrays row to use. For example, <ArrayUrlExtractor index="0" urlTemplate='$url2' isEnabled='1'/> Should tell it to use the "AID" row instead of the "GID" row. Sorry about the delay. Alok On Thu, Mar 18, 2010 at 2:06 PM, Anna Ratner <i_a...@ya...> wrote: > Hi Alok, > > Changing my jtv file to what you suggested i.e.: > > <DocumentConfig> > <UrlExtractor urlTemplate='$url1' isEnabled='1'/> > <ArrayUrlExtractor urlTemplate='$url2' isEnabled='1'/> > </DocumentConfig> > > instead of the previous: > > <ProgramConfig> > <GeneUrlPresets> > <Preset name='Gene' template='$url1' header='*' enabled='true'/> > </GeneUrlPresets> > <ArrayUrlPresets> > <Preset name='Sample' template='$url2' header='*' enabled='true'/> > </ArrayUrlPresets> > </ProgramConfig> > > works and my .jtv file loads the url settings. The only problem now is that > it inserts the "AID" values into the HEADER field instead of "GID" for the > ArrayUrl template, so I still have to manually change the selection in the > drop-down for url settings -> array. How do I specify which values to use > here in my .jtv file. > > Thank you, > Anna > > ------------------------------ > *From:* Alok Saldanha <alo...@gm...> > *To:* Anna Ratner <i_a...@ya...> > *Cc:* jtr...@li... > *Sent:* Thu, March 18, 2010 5:57:49 AM > > *Subject:* Re: [Jtreeview-users] How to load a .jtv url settings file into > TreeViewApplet? > > Dear Anna, > > Most likely the jtv file is being recognized, you can be sure of it by > changing your color (Settings->Pixel Settings, although I just noticed the > Color label is misaligned). There seems to be something funky going on with > the URL Settings, namely they don't seem to be actually written to disk. I > won't have time to look into this further until the weekend, alas Java > Treeview is on the backburner for the time being, warts and all. For now the > best workaround is to close java treeview and manually open the .jtv file > in a text editor. You need to add "urlTemplate" and "isEnabled" attributes > to the UrlExtractor tag which should be a child of DocumentConfig, which is > the root tag of the document. Here is an example to link to google: > > <UrlExtractor urlTemplate="http://www.google.com/search?q=HEADER" > isEnabled="1" /> > > If this doesn't help send me a link to the site with a non-working applet > and I'll take a look. > > Regards, > Alok > > On Wed, Mar 17, 2010 at 9:58 PM, Anna Ratner <i_a...@ya...> wrote: > >> Hi, >> I am using the Jave TreeViewApplet on a web page (thank you for this >> software!) and the problem that I am running into is that it doesn't want to >> take my .jtv file for url settings. I found a previous issue in the archive >> where someone was having a similar problem, but that was eventually fixed >> according to the emails. I write the .jtv file into the same directory as >> the .cdt, .atr, and .gtr files. >> >> <APPLET >> code="edu/stanford/genetics/treeview/applet/ButtonApplet.class" >> archive="$archive" >> width='250' height='50'> >> <PARAM name="cdtFile" value="$tmp_url/cluster$$.cdt"> >> <PARAM name="cdtName" value="with Java TreeView"> >> <PARAM name="styleName" value="linked"> >> <PARAM name="plugins" >> value="edu.stanford.genetics.treeview.plugin.dendroview.DendrogramFactory"> >> </APPLET> >> >> Also, where can I find the documentation for how to specify url settings >> for applets? >> Any help would be appreciated. >> Thank you very much, >> Anna >> >> >> >> ------------------------------------------------------------------------------ >> Download Intel® Parallel Studio Eval >> Try the new software tools for yourself. Speed compiling, find bugs >> proactively, and fine-tune applications for parallel performance. >> See why Intel Parallel Studio got high marks during beta. >> http://p.sf.net/sfu/intel-sw-dev >> _______________________________________________ >> Jtreeview-users mailing list >> Jtr...@li... >> https://lists.sourceforge.net/lists/listinfo/jtreeview-users >> >> > > |
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From: Alok S. <alo...@gm...> - 2010-03-18 13:05:46
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Dear Omer, There is no uninstaller. I recommend that you use a right-click to delete the item from the program menu, and then delete the folder in C:\Program Files\Stanford University\Java TreeView 2010/3/13 Ömer AN <bo...@gm...> > Hey, > > How can I uninstall Java Tree View from my computer? I installed it togeter > with Cluster 3.0 and now i removed Cluster 3.0 but can't do for Tree View. > It is not located in Add/Remove Programs section. Can you explain how to do? > > My OS is Windows XP. > > Thanks in advance... > > > ------------------------------------------------------------------------------ > Download Intel® Parallel Studio Eval > Try the new software tools for yourself. Speed compiling, find bugs > proactively, and fine-tune applications for parallel performance. > See why Intel Parallel Studio got high marks during beta. > http://p.sf.net/sfu/intel-sw-dev > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users > > |
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From: Alok S. <alo...@gm...> - 2010-03-18 12:57:58
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Dear Anna, Most likely the jtv file is being recognized, you can be sure of it by changing your color (Settings->Pixel Settings, although I just noticed the Color label is misaligned). There seems to be something funky going on with the URL Settings, namely they don't seem to be actually written to disk. I won't have time to look into this further until the weekend, alas Java Treeview is on the backburner for the time being, warts and all. For now the best workaround is to close java treeview and manually open the .jtv file in a text editor. You need to add "urlTemplate" and "isEnabled" attributes to the UrlExtractor tag which should be a child of DocumentConfig, which is the root tag of the document. Here is an example to link to google: <UrlExtractor urlTemplate="http://www.google.com/search?q=HEADER" isEnabled="1" /> If this doesn't help send me a link to the site with a non-working applet and I'll take a look. Regards, Alok On Wed, Mar 17, 2010 at 9:58 PM, Anna Ratner <i_a...@ya...> wrote: > Hi, > I am using the Jave TreeViewApplet on a web page (thank you for this > software!) and the problem that I am running into is that it doesn't want to > take my .jtv file for url settings. I found a previous issue in the archive > where someone was having a similar problem, but that was eventually fixed > according to the emails. I write the .jtv file into the same directory as > the .cdt, .atr, and .gtr files. > > <APPLET > code="edu/stanford/genetics/treeview/applet/ButtonApplet.class" > archive="$archive" > width='250' height='50'> > <PARAM name="cdtFile" value="$tmp_url/cluster$$.cdt"> > <PARAM name="cdtName" value="with Java TreeView"> > <PARAM name="styleName" value="linked"> > <PARAM name="plugins" > value="edu.stanford.genetics.treeview.plugin.dendroview.DendrogramFactory"> > </APPLET> > > Also, where can I find the documentation for how to specify url settings > for applets? > Any help would be appreciated. > Thank you very much, > Anna > > > > ------------------------------------------------------------------------------ > Download Intel® Parallel Studio Eval > Try the new software tools for yourself. Speed compiling, find bugs > proactively, and fine-tune applications for parallel performance. > See why Intel Parallel Studio got high marks during beta. > http://p.sf.net/sfu/intel-sw-dev > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users > > |
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From: Anna R. <i_a...@ya...> - 2010-03-18 01:58:30
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Hi,
I am using the Jave TreeViewApplet on a web page (thank you for this software!) and the problem that I am running into is that it doesn't want to take my .jtv file for url settings. I found a previous issue in the archive where someone was having a similar problem, but that was eventually fixed according to the emails. I write the .jtv file into the same directory as the .cdt, .atr, and .gtr files.
<APPLET code="edu/stanford/genetics/treeview/applet/ButtonApplet.class"
archive="$archive"
width='250' height='50'>
<PARAM name="cdtFile" value="$tmp_url/cluster$$.cdt">
<PARAM name="cdtName" value="with Java TreeView">
<PARAM name="styleName" value="linked">
<PARAM name="plugins" value="edu.stanford.genetics.treeview.plugin.dendroview.DendrogramFactory">
</APPLET>
Also, where can I find the documentation for how to specify url settings for applets?
Any help would be appreciated.
Thank you very much,
Anna
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From: Ömer AN <bo...@gm...> - 2010-03-13 14:29:00
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Hey, How can I uninstall Java Tree View from my computer? I installed it togeter with Cluster 3.0 and now i removed Cluster 3.0 but can't do for Tree View. It is not located in Add/Remove Programs section. Can you explain how to do? My OS is Windows XP. Thanks in advance... |
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From: Alok S. <alo...@gm...> - 2010-01-31 14:10:29
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Dear Wendy, This can sometimes happen if the values in your data file are outside of the expected range. You can test this by selecting a few rows on the left side of the screen and letting your mouse linger over the rows on the right hand of the screen (i.e. the zoomed in rows). If the values displayed are larger than 3, the you may need to adjust the contrast settings. To do this, goto Settings->Pixel Settings, and either use the slider or edit the number in the Contrast box. If this doesn't help, you can also send me a zip file containing the cdt and gtr and I'll have a look. -Alok On Sat, Jan 30, 2010 at 7:29 AM, Wendy Qiao <wen...@ut...> wrote: > Dear there, > > > > When I try to cluster, the map is completely red. I think there is some > problem with the clustering algorithms that I used. I tried the most of the > Adjust Data-Cluster combinations in Cluster3.0, but no one works. What may > the possible reason? > > > > Thank you, > > Wendy > > > > > > > ------------------------------------------------------------------------------ > The Planet: dedicated and managed hosting, cloud storage, colocation > Stay online with enterprise data centers and the best network in the > business > Choose flexible plans and management services without long-term contracts > Personal 24x7 support from experience hosting pros just a phone call away. > http://p.sf.net/sfu/theplanet-com > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users > > |
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From: Alok S. <alo...@gm...> - 2010-01-31 13:11:39
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Hi Wendy, it looks like your data is not ratio data, but either count or intensity data. I got good results by logscaling with a center of 6 (this means a starting value x is mapped to y = log2(x / 6), i.e. a value of 6 is mapped to zero, and other values are turned into fold changes relative to 6. To do this, just open Settings->Pixel Settings, got the "LogScale" section below the contrast section, check "Log (base 2)" , and enter 6 as the center. If you clustered the samples, you should have an atr file which will provide an array tree. I strongly recommend you cluster the genes as well, as that will make it much easier to interpret the output. On Sun, Jan 31, 2010 at 7:41 AM, Wendy Qiao <wen...@ut...> wrote: > Hi Alok, > > > > Thank you for your reply. I think my values are too large. There are some > dots appearing after I increase the contrast value to the max (5), but I > still can’t see the map. Is there a way to navigate this? > > > > My cdt file is attach. I do not have a gtr file as I only clustered the > samples. Would that be one of the reason as well? > > > > Thank you . > > Wendy > > > > *From:* Alok Saldanha [mailto:alo...@gm...] > *Sent:* January-31-10 7:22 AM > *To:* Wendy Qiao > *Cc:* jtr...@li... > *Subject:* Re: [Jtreeview-users] Clustering probem > > > > Dear Wendy, > > This can sometimes happen if the values in your data file are outside of > the expected range. You can test this by selecting a few rows on the left > side of the screen and letting your mouse linger over the rows on the right > hand of the screen (i.e. the zoomed in rows). If the values displayed are > larger than 3, the you may need to adjust the contrast settings. To do this, > goto Settings->Pixel Settings, and either use the slider or edit the number > in the Contrast box. > > If this doesn't help, you can also send me a zip file containing the cdt > and gtr and I'll have a look. > > -Alok > > On Sat, Jan 30, 2010 at 7:29 AM, Wendy Qiao <wen...@ut...> > wrote: > > Dear there, > > > > When I try to cluster, the map is completely red. I think there is some > problem with the clustering algorithms that I used. I tried the most of the > Adjust Data-Cluster combinations in Cluster3.0, but no one works. What may > the possible reason? > > > > Thank you, > > Wendy > > > > > > > > ------------------------------------------------------------------------------ > The Planet: dedicated and managed hosting, cloud storage, colocation > Stay online with enterprise data centers and the best network in the > business > Choose flexible plans and management services without long-term contracts > Personal 24x7 support from experience hosting pros just a phone call away. > http://p.sf.net/sfu/theplanet-com > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users > > > |
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From: Wendy Q. <wen...@ut...> - 2010-01-30 13:06:41
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Dear there, When I try to cluster, the map is completely red. I think there is some problem with the clustering algorithms that I used. I tried the most of the Adjust Data-Cluster combinations in Cluster3.0, but no one works. What may the possible reason? Thank you, Wendy |
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From: Alok S. <alo...@gm...> - 2009-10-11 09:03:11
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Hi Meghan, There are basically three options 1) Try Export->Export to Postscript, which will get you a vector graphics file that should look decent when printed. 2) You can try Export->Export to Image to get a rastered image in either png, ppm or gif format. 3) If all else fails, take a screenshot of what you need at close to the right resolution. For options 1 and 2, I found I had to check the preview checkbox and resize the dialog to get the preview to show. Hope this helps, Alok On Sun, Oct 4, 2009 at 5:06 PM, meghan wyse <mm...@gm...> wrote: > How can i save an image of the dendograph to import into a word document? > Thank you > > ------------------------------------------------------------------------------ > Come build with us! The BlackBerry® Developer Conference in SF, CA > is the only developer event you need to attend this year. Jumpstart your > developing skills, take BlackBerry mobile applications to market and stay > ahead of the curve. Join us from November 9-12, 2009. Register now! > http://p.sf.net/sfu/devconf > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users > > |
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From: meghan w. <mm...@gm...> - 2009-10-04 21:06:34
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How can i save an image of the dendograph to import into a word document? Thank you |
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From: wormbuff <wor...@gm...> - 2009-06-24 17:38:51
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I am trying to standardize the Karyoscope images that I exported from Java TreeView. However, I am having difficulty understanding how image dimensions are determined with "Export to Image". It appears that if I resize the main window by dragging the lower right corner, the exported image dimensions are adjusted. The dimensions, however, do not match up with the "Size Width" and "Height" reported in the upper left frame of the main window. Furthermore, if I attempt to adjust the image dimensions either in the width/height boxes in the main window or the window that pops up after clicking on "Export to Image", neither have an effect on the final exported image. Any insight would be greatly appreciated. This is in reference to Java TreeView v1.1.3 under J2RE 1.5.0_19- b02-306 on Mac OS X 10.4.11. |
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From: Alok S. <alo...@gm...> - 2008-10-28 22:58:51
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I am not sure exactly what is causing your problem. It would help if you could email me a stack trace (i.e. run jtv from the command line, when it exits it should print out something to the terminal). Which version of Java are you using? I recommend downloading and installing the version from Sun: http://java.sun.com/javase/downloads/index.jsp You can test what version of java you have by running java -version I put some effort into making it work with gcj, but java runtimes change quick. -Alok On Oct 27, 2008, at 12:57 PM, wp...@CL... wrote: > To Whom It May Concern: > > I have just downloaded/installed the software on Linux and when > I run > the application and register I always get the following error: > > "Could not open URL: > http://lists.sourceforge.net/lists/listinfo/jtreeview-announce" > > And then the program, "disappears" into the background. What > gives? Am > I doing something wrong? Also, whenever I click on the other two > buttons > (Register Later or Do Not Register) the program terminates. > > Regards, > > William P. Taylor II > > ---------------------------------------------------------------------- > --- > This SF.Net email is sponsored by the Moblin Your Move Developer's > challenge > Build the coolest Linux based applications with Moblin SDK & win > great prizes > Grand prize is a trip for two to an Open Source event anywhere in > the world > http://moblin-contest.org/redirect.php?banner_id=100&url=/ > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users |
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From: <wp...@CL...> - 2008-10-27 16:58:03
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To Whom It May Concern: I have just downloaded/installed the software on Linux and when I run the application and register I always get the following error: "Could not open URL: http://lists.sourceforge.net/lists/listinfo/jtreeview-announce" And then the program, "disappears" into the background. What gives? Am I doing something wrong? Also, whenever I click on the other two buttons (Register Later or Do Not Register) the program terminates. Regards, William P. Taylor II |
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From: Alok S. <alo...@gm...> - 2008-05-12 22:16:28
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Dear fine, You don't actually need Java Treeview, you need Cluster 3.0 from http://bonsai.ims.u-tokyo.ac.jp/~mdehoon/software/cluster/software.htm clustering will create a file with a ".gtr" extension that has columns corresponding to Node, Left child, Right Child and height. You will need to parse this to create the tree that you want. I am not aware of a good tool that will do clustering in a web browser if that is what you want, although it would certainly be possible to port from cluster 3.0 (which is open source). Good luck, Alok On Mon, May 12, 2008 at 5:36 PM, fine cur <fi...@ya...> wrote: > Hi, I am trying to use Treeview to generate dendrogram. I have my own > "draw" function written alreay in Adobe Flash. So I do not need a java > JPanel or other GUI program. I just need to use TreeView to compute the > clusters from original data and output a descriptive result something like > the file bellow. Could anyone tell me how to do it? > > --[dendrogram w/ 2 branches and 20 members at h = 10.1] > |--[dendrogram w/ 2 branches and 5 members at h = 3.69] > | |--leaf "17" > | `--[dendrogram w/ 2 branches and 4 members at h = 2.13] > | |--leaf "9" > | `--[dendrogram w/ 2 branches and 3 members at h = 0.352] > | |--leaf "20" > | `--[dendrogram w/ 2 branches and 2 members at h = 0.143] > | |--leaf "18" > | `--leaf "19" > `--[dendrogram w/ 2 branches and 15 members at h = 6.16] > |--leaf "6" > `--[dendrogram w/ 2 branches and 14 members at h = 3.05] > |--[dendrogram w/ 2 branches and 7 members at h = 0.82] > | |--leaf "14" > | `--[dendrogram w/ 2 branches and 6 members at h = 0.356] > | |--[dendrogram w/ 2 branches and 3 members at h = 0.128] > | | |--leaf "15" > | | `--[dendrogram w/ 2 branches and 2 members at h = 0.110] > | | |--leaf "11" > | | `--leaf "12" > | `--[dendrogram w/ 2 branches and 3 members at h = 0.217] > | |--leaf "13" > | `--[dendrogram w/ 2 branches and 2 members at h = 0.117] > | |--leaf "10" > | `--leaf "16" > `--[dendrogram w/ 2 branches and 7 members at h = 1.7] > |--[dendrogram w/ 2 branches and 5 members at h = 0.539] > | |--leaf "7" > | `--[dendrogram w/ 2 branches and 4 members at h = 0.223] > | |--leaf "8" > | `--[dendrogram w/ 2 branches and 3 members at h = 0.183] > | |--leaf "4" > | `--[dendrogram w/ 2 branches and 2 members at h = > 0.107] > | |--leaf "2" > | `--leaf "3" > `--[dendrogram w/ 2 branches and 2 members at h = 0.698] > |--leaf "1" > `--leaf "5" > > ------------------------------ > Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it > now.<http://us.rd.yahoo.com/evt=51733/*http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ> > > ------------------------------------------------------------------------- > This SF.net email is sponsored by: Microsoft > Defy all challenges. Microsoft(R) Visual Studio 2008. > http://clk.atdmt.com/MRT/go/vse0120000070mrt/direct/01/ > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users > > |
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From: fine c. <fi...@ya...> - 2008-05-12 21:36:23
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Hi, I am trying to use Treeview to generate dendrogram. I have my own "draw" function written alreay in Adobe Flash. So I do not need a java JPanel or other GUI program. I just need to use TreeView to compute the clusters from original data and output a descriptive result something like the file bellow. Could anyone tell me how to do it?
--[dendrogram w/ 2 branches and 20 members at h = 10.1]
|--[dendrogram w/ 2 branches and 5 members at h = 3.69]
| |--leaf "17"
| `--[dendrogram w/ 2 branches and 4 members at h = 2.13]
| |--leaf "9"
| `--[dendrogram w/ 2 branches and 3 members at h = 0.352]
| |--leaf "20"
| `--[dendrogram w/ 2 branches and 2 members at h = 0.143]
| |--leaf "18"
| `--leaf "19"
`--[dendrogram w/ 2 branches and 15 members at h = 6.16]
|--leaf "6"
`--[dendrogram w/ 2 branches and 14 members at h = 3.05]
|--[dendrogram w/ 2 branches and 7 members at h = 0.82]
| |--leaf "14"
| `--[dendrogram w/ 2 branches and 6 members at h = 0.356]
| |--[dendrogram w/ 2 branches and 3 members at h = 0.128]
| | |--leaf "15"
| | `--[dendrogram w/ 2 branches and 2 members at h = 0.110]
| | |--leaf "11"
| | `--leaf "12"
| `--[dendrogram w/ 2 branches and 3 members at h = 0.217]
| |--leaf "13"
| `--[dendrogram w/ 2 branches and 2 members at h = 0.117]
| |--leaf "10"
| `--leaf "16"
`--[dendrogram w/ 2 branches and 7 members at h = 1.7]
|--[dendrogram w/ 2 branches and 5 members at h = 0.539]
| |--leaf "7"
| `--[dendrogram w/ 2 branches and 4 members at h = 0.223]
| |--leaf "8"
| `--[dendrogram w/ 2 branches and 3 members at h = 0.183]
| |--leaf "4"
| `--[dendrogram w/ 2 branches and 2 members at h = 0.107]
| |--leaf "2"
| `--leaf "3"
`--[dendrogram w/ 2 branches and 2 members at h = 0.698]
|--leaf "1"
`--leaf "5"
---------------------------------
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From: fangm55555 <fan...@gm...> - 2008-04-26 04:49:07
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Hi, I tried many times, it seems that the latest release of java treeview can't work at all in VISTA. Could you give me some suggestion? Thank you! Ming 2008-04-25 fangm55555 |
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From: Alok S. <alo...@gm...> - 2008-04-06 18:43:13
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Flipping of gene nodes has not yet been implemented. JTV is not very actively developed right now, but since you are the second person to request this, http://sourceforge.net/tracker/index.php? func=detail&aid=1753534&group_id=84593&atid=573301 I will try and find time over the next week or next weekend to implement it. -Alok On Apr 3, 2008, at 1:38 PM, Jan Krzysztof Blusztajn wrote: > Hi, > > I am trying to flip nodes of genes. I select a gene node and use the > "Flip tree node" option under Analysis but this flips the arrays. Is > it possible to flip the gene nodes? > > Many thanks, > > Jan > > > ---------------------------------------------------------------------- > --- > This SF.net email is sponsored by the 2008 JavaOne(SM) Conference > Register now and save $200. Hurry, offer ends at 11:59 p.m., > Monday, April 7! Use priority code J8TLD2. > http://ad.doubleclick.net/clk;198757673;13503038;p?http:// > java.sun.com/javaone > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users |
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From: Jan K. B. <jbl...@bu...> - 2008-04-03 17:40:47
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Hi, I am trying to flip nodes of genes. I select a gene node and use the "Flip tree node" option under Analysis but this flips the arrays. Is it possible to flip the gene nodes? Many thanks, Jan |
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From: Alok S. <alo...@gm...> - 2007-10-29 11:36:43
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Dear Annie, You can adjust the scale using the pixel setttings. Load the ratio =20 data, then go to settings->pixel settings, and then in the contrast =20 section you can enter a contrast value in the box labelled "value" or =20= adjust the slider. Also, you can log transform within treeview now =20 within the settings menu but (embarssingly) I haven' updated JTV on =20 this laptop so I can't tell you exactly what I named the controls, =20 but they're on the same settings panel. There is some slightly out =20 of date documentation here: http://jtreeview.sourceforge.net/docs/JTVUserManual/=20 ch02s04.html#ch2_settings_dcolor Hope this helps. Alok On Oct 28, 2007, at 6:32 PM, Annie Chiu Eng Wong wrote: > Hi there, > > Thank you for the jtreeview software. I am a researcher from the =20 > University of Melbourne and I hope you don=92t mind my abrupt email =20= > asking for some advice. > > > > I have some microarray time point data (log2 transformed signal =20 > intensity level for each gene) that I have clustered using K-mean =20 > clustering implemented in Cluster. I would like to display the =20 > results as a heat map in jtreeview. I realised that the difference =20 > between each time point for each gene is better displayed when =20 > ratio is used instead of the log2 transformed signal intensity =20 > level. I understand this is because the pixel setting is such that =20 > =93red=94 is for positive and =93green=94 is for negative while black = is =20 > for =93zero=94. The scale is not sensitive enough to capture all the =20= > positive value of the signal intensity level. > > > > I wonder whether there is a way that I can change the setting such =20 > that it allows me to display the normalized signal intensity data =20 > in red and green with red denoting high expression while green low =20 > expression. > > > > Your kind attention is very much appreciated and I look forward to =20 > your reply. > > > > Regards, Annie > > > > Annie CE WONG (PhD), > Research Fellow, > Plant Molecular Biology and Biotechnology Laboratory, > ARC Centre of Excellence for Integrative Legume Research, > School of Agriculture and Food Systems, > University of Melbourne, > Parkville, > Victoria 3010, > Australia. > > Tel : 03 8344 5013/6326 > > > > ----------------------------------------------------------------------=20= > --- > This SF.net email is sponsored by: Splunk Inc. > Still grepping through log files to find problems? Stop. > Now Search log events and configuration files using AJAX and a =20 > browser. > Download your FREE copy of Splunk now >> http://get.splunk.com/=20 > _______________________________________________ > Jtreeview-users mailing list > Jtr...@li... > https://lists.sourceforge.net/lists/listinfo/jtreeview-users |
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From: Annie C. E. W. <ac...@un...> - 2007-10-28 22:33:01
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Hi there, Thank you for the jtreeview software. I am a researcher from the University of Melbourne and I hope you don't mind my abrupt email asking for some advice. =20 I have some microarray time point data (log2 transformed signal intensity level for each gene) that I have clustered using K-mean clustering implemented in Cluster. I would like to display the results as a heat map in jtreeview. I realised that the difference between each time point for each gene is better displayed when ratio is used instead of the log2 transformed signal intensity level. I understand this is because the pixel setting is such that "red" is for positive and "green" is for negative while black is for "zero". The scale is not sensitive enough to capture all the positive value of the signal intensity level.=20 =20 I wonder whether there is a way that I can change the setting such that it allows me to display the normalized signal intensity data in red and green with red denoting high expression while green low expression. =20 Your kind attention is very much appreciated and I look forward to your reply. =20 Regards, Annie =20 Annie CE WONG (PhD), Research Fellow, Plant Molecular Biology and Biotechnology Laboratory, ARC Centre of Excellence for Integrative Legume Research, School of Agriculture and Food Systems, University of Melbourne, Parkville, Victoria 3010, Australia. Tel : 03 8344 5013/6326 =20 |
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From: Thorsten O. <tho...@ly...> - 2007-09-18 14:16:02
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Hello, i just wanted to know if there is some chance that you could help us with=20 our problem running a clustering process like considered. Some weeks ago i= =20 sent some archives for explaining more adequately what we're up to do and=20 what's the expectes result. It would be very kind hearing from whether there is support possible or=20 not. Thanks a lot in advance, regards! Thorsten Thorsten Ortjohann Consultant Business Process Management Lynx-Consulting AG Johanniskirchplatz 6 D-33615 Bielefeld Fon: +49 521 5247-0 Fax: +49 521 5247-250 Mobil: +49 175 22 85 490 Company and Management Headquarters: Lynx-Consulting AG, Johanniskirchplatz 6, D-33615 Bielefeld Fon: +49 521 5247-0, Fax: +49 521 5247-250, www.lynx.de Court Registration: Amtsgericht Bielefeld HRB 35946 Members of the Management Board authorised to represent: Peter H=C3=BCsener Chairman of the Supervisory Board: Hans-Joachim Rosowski ---------------------------------------------------------------------------= ------------------------- This e-mail may contain trade secrets or privileged, undisclosed, or otherw= ise confidential information. If you have received this e-mail in error, yo= u are hereby notified that any review, copying, or distribution of it is st= rictly prohibited. Please inform us immediately and destroy the original tr= ansmittal. Thank you for your cooperation.=20 ---------------------------------------------------------------------------= ------------------------- =20 |