*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Dear Coleagues, Last year we upgraded our BX61 with CellSens software and a new DP73 camera. Almost all of our users wants to get multichannel 8 bits color images in ".tif" format and the software cannot get them without exporting each channel separately, which is very time consuming. Multichannel acquisition does not work in 8 bits mode. In my opinion it should be a decision of the user to work with 8 or 16 bits acquisition and also with gray or color images. As an alternative, I've tried to configure a 8 bits multichannel color acquisition with Experiment Manager but the system produce 3 separated .vsi images for each channel and you have to go one by one converting ".vsi" to ".tif" format. I wonder if someone has an alternative way to acquire quickly (one mouse click) multichannel 8 bit color images and generate ".tif" images for each channel? Thank you very much in advance. All the best Juan Luis Ribas -- Juan Luis Ribas Servicio de Microscopía Centro de Investigación, Tecnología e Innovación Universidad de Sevilla Av. Reina Mercedes 4b 41012 Sevilla Tfnos: 954559983 // 628220681 // 12068 http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento |
Hi Juan,
Have you tried the following in CellSens: select Image>Mode>8 bit/Channel menu command to change the image into 8�\bit image. Use File>Save as… menu command to save the image as one image containing multiple channels or use File>Export to>tiff series… command to save the image as multiple images for each channel I do not have access to CellSens right now. I had this notes which I have collected from some web site with me and thought of sharing it with you. Good luck. Sathya Srinivasan ________________________________________ From: Confocal Microscopy List <[hidden email]> on behalf of Juan Luis Ribas <[hidden email]> Sent: December 15, 2015 7:09 AM To: [hidden email] Subject: Exporting 8 bits color .tif images in Cell Sens ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Dear Coleagues, Last year we upgraded our BX61 with CellSens software and a new DP73 camera. Almost all of our users wants to get multichannel 8 bits color images in ".tif" format and the software cannot get them without exporting each channel separately, which is very time consuming. Multichannel acquisition does not work in 8 bits mode. In my opinion it should be a decision of the user to work with 8 or 16 bits acquisition and also with gray or color images. As an alternative, I've tried to configure a 8 bits multichannel color acquisition with Experiment Manager but the system produce 3 separated .vsi images for each channel and you have to go one by one converting ".vsi" to ".tif" format. I wonder if someone has an alternative way to acquire quickly (one mouse click) multichannel 8 bit color images and generate ".tif" images for each channel? Thank you very much in advance. All the best Juan Luis Ribas -- Juan Luis Ribas Servicio de Microscopía Centro de Investigación, Tecnología e Innovación Universidad de Sevilla Av. Reina Mercedes 4b 41012 Sevilla Tfnos: 954559983 // 628220681 // 12068 http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Thank you for all the people that reply, but unfortunately I have to say that at the end all the procedures finished in gray scale images .tif images. Definitevely, it should be named CellNoSens or Cell-nonSens. I wonder if the vendor could argue something about this question. About 50 users in my facility moved to another microscope beside. The companies has to design the software to do the life easier... On the other hand, perhaps some expert in ImageJ could know if there is a plugin in ImageJ that could convert .vsi files to .tif 8 bit color . Best regards Juan Luis Ribas El 16/12/2015 a las 2:09, Sathya Srinivasan escribió: > Hi Juan, > Have you tried the following in CellSens: > > select Image>Mode>8 bit/Channel menu command to change the image into 8‐bit > image. Use File>Save as… menu command to save the image as one image containing multiple channels or use > File>Export to>tiff series… command to save the image as multiple images for each channel > > I do not have access to CellSens right now. I had this notes which I have collected from some web site with me and thought of sharing it with you. Good luck. > > Sathya Srinivasan > > ________________________________________ > From: Confocal Microscopy List <[hidden email]> on behalf of Juan Luis Ribas <[hidden email]> > Sent: December 15, 2015 7:09 AM > To: [hidden email] > Subject: Exporting 8 bits color .tif images in Cell Sens > > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > Dear Coleagues, > Last year we upgraded our BX61 with CellSens software and a new DP73 > camera. Almost all of our users wants to get multichannel 8 bits color > images in ".tif" format and the software cannot get them without > exporting each channel separately, which is very time consuming. > Multichannel acquisition does not work in 8 bits mode. In my opinion it > should be a decision of the user to work with 8 or 16 bits acquisition > and also with gray or color images. > As an alternative, I've tried to configure a 8 bits multichannel color > acquisition with Experiment Manager but the system produce 3 separated > .vsi images for each channel and you have to go one by one converting > ".vsi" to ".tif" format. > I wonder if someone has an alternative way to acquire quickly (one mouse > click) multichannel 8 bit color images and generate ".tif" images for > each channel? > > Thank you very much in advance. > > All the best > Juan Luis Ribas > -- > Juan Luis Ribas > Servicio de Microscopía > Centro de Investigación, Tecnología e Innovación > Universidad de Sevilla > Av. Reina Mercedes 4b > 41012 Sevilla > > Tfnos: 954559983 // 628220681 // 12068 > > http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento -- Juan Luis Ribas Servicio de Microscopía Centro de Investigación, Tecnología e Innovación Universidad de Sevilla Av. Reina Mercedes 4b 41012 Sevilla Tfnos: 954559983 // 628220681 // 12068 http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento |
Ondřej Šebesta |
In reply to this post by jlribas
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Hello Juan Despite you are absolutely right, that Olympus should improve export capabilities of IMHO any of their software, ImageJ is surely able to convert many formats. I do not have personal experience with .vsi files, but I guess Bioformats would import correctly and resave is easy. You can use a macro recorder to get a primitive macro which can do the job for you. Batch process - macro is another usefull tool. Best, Ondrej Sebesta 2015-12-16 14:42 GMT+01:00 Juan Luis Ribas <[hidden email]>: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > Thank you for all the people that reply, but unfortunately I have to say > that at the end all the procedures finished in gray scale images .tif > images. > Definitevely, it should be named CellNoSens or Cell-nonSens. I wonder if > the vendor could argue something about this question. About 50 users in my > facility moved to another microscope beside. The companies has to design > the software to do the life easier... > On the other hand, perhaps some expert in ImageJ could know if there is a > plugin in ImageJ that could convert .vsi files to .tif 8 bit color . > > Best regards > Juan Luis Ribas > > > El 16/12/2015 a las 2:09, Sathya Srinivasan escribió: > >> Hi Juan, >> Have you tried the following in CellSens: >> >> select Image>Mode>8 bit/Channel menu command to change the image into >> 8‐bit >> image. Use File>Save as… menu command to save the image as one image >> containing multiple channels or use >> File>Export to>tiff series… command to save the image as multiple images >> for each channel >> >> I do not have access to CellSens right now. I had this notes which I have >> collected from some web site with me and thought of sharing it with you. >> Good luck. >> >> Sathya Srinivasan >> >> ________________________________________ >> From: Confocal Microscopy List <[hidden email]> on >> behalf of Juan Luis Ribas <[hidden email]> >> Sent: December 15, 2015 7:09 AM >> To: [hidden email] >> Subject: Exporting 8 bits color .tif images in Cell Sens >> >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> Post images on http://www.imgur.com and include the link in your posting. >> ***** >> >> Dear Coleagues, >> Last year we upgraded our BX61 with CellSens software and a new DP73 >> camera. Almost all of our users wants to get multichannel 8 bits color >> images in ".tif" format and the software cannot get them without >> exporting each channel separately, which is very time consuming. >> Multichannel acquisition does not work in 8 bits mode. In my opinion it >> should be a decision of the user to work with 8 or 16 bits acquisition >> and also with gray or color images. >> As an alternative, I've tried to configure a 8 bits multichannel color >> acquisition with Experiment Manager but the system produce 3 separated >> .vsi images for each channel and you have to go one by one converting >> ".vsi" to ".tif" format. >> I wonder if someone has an alternative way to acquire quickly (one mouse >> click) multichannel 8 bit color images and generate ".tif" images for >> each channel? >> >> Thank you very much in advance. >> >> All the best >> Juan Luis Ribas >> -- >> Juan Luis Ribas >> Servicio de Microscopía >> Centro de Investigación, Tecnología e Innovación >> Universidad de Sevilla >> Av. Reina Mercedes 4b >> 41012 Sevilla >> >> Tfnos: 954559983 // 628220681 // 12068 >> >> http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento >> > > -- > Juan Luis Ribas > Servicio de Microscopía > Centro de Investigación, Tecnología e Innovación > Universidad de Sevilla > Av. Reina Mercedes 4b > 41012 Sevilla > > Tfnos: 954559983 // 628220681 // 12068 > > http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento > > -- > <http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento> > Mgr. Ondřej Šebesta > E-mail: > <http://investigacion.us.es/scisi/sgi/servicios/microscopia/equipamiento> > [hidden email] > > Univerzita Karlova v Praze > Přírodovědecká fakulta > Albertov 6, 128 43 Praha 2 > www.natur.cuni.cz > > Charles University in Prague > Faculty of Science > Albertov 6, 128 43 Praha 2 > www.natur.cuni.cz/en > > -- ------------------------------ Pokud je tento e-mail součástí obchodního jednání, Přírodovědecká fakulta Univerzity Karlovy v Praze: a) si vyhrazuje právo jednání kdykoliv ukončit a to i bez uvedení důvodu, b) stanovuje, že smlouva musí mít písemnou formu, c) vylučuje přijetí nabídky s dodatkem či odchylkou, d) stanovuje, že smlouva je uzavřena teprve výslovným dosažením shody na všech náležitostech smlouvy. |
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