Johannes Amon |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Community, just to inform you, we at Carl Zeiss Microscopy just recently launched a fluorescence microscopy app for your iPads, iPhones and iPod touch devices. I was already in contact with George McNamara as the app uses the pubspectra database, similar to our ZEN Smart Setup, and he suggested to post it here so that you are able to have a test-drive and discuss what you like or what you might not like. We are completely open for ideas, so hit the inbox micro- [hidden email], hit me, and of course also feel free to discuss the app here. http://www.zeiss.com/micro-apps The website should give you a good impression about what the app is able to do. We are really curious to learn how it will be received by the scientific community so I'll try to check back regularly and see what you think. Have a nice weekend! Carl Zeiss MicroImaging GmbH Business Unit BioSciences Imaging Software Munich Dr. Johannes Amon [hidden email] |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Sounds great! Do you have the plan to further "push" this project. such as transplanting this software to Android platform? Hao, Xiang --- State Key Laboratory of Modern Optical Instrumentation Zhejiang University, China |
Tim Feinstein-2 |
In reply to this post by Johannes Amon
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Nicely done and well presented. I like the implementation of the spectra viewer. It has some odd missing spectra (Venus/YFP, dTomato) but I assume that can be fixed. No doubt you already know how much demand there is for an iOS/Android data viewer app. I fully understand how challenging that might be, but I imagine that the vast wealth of tele-radiology solutions already out there could provide a useful template. Maybe one of them could be jerry-rigged to work as-is… I hope that this inspires Nikon, Leica and Olympus to answer this with applications of their own. cheers, TF Timothy Feinstein, PhD Postdoctoral Fellow Laboratory for GPCR Biology Dept. of Pharmacology & Chemical Biology University of Pittsburgh, School of Medicine BST W1301, 200 Lothrop St. Pittsburgh, PA 15261 On Jan 13, 2012, at 10:26 AM, Johannes Amon wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Dear Community, > > just to inform you, we at Carl Zeiss Microscopy just recently launched a > fluorescence microscopy app for your iPads, iPhones and iPod touch devices. I > was already in contact with George McNamara as the app uses the pubspectra > database, similar to our ZEN Smart Setup, and he suggested to post it here so > that you are able to have a test-drive and discuss what you like or what you > might not like. We are completely open for ideas, so hit the inbox micro- > [hidden email], hit me, and of course also feel free to discuss the app here. > > http://www.zeiss.com/micro-apps > > The website should give you a good impression about what the app is able to > do. We are really curious to learn how it will be received by the scientific > community so I'll try to check back regularly and see what you think. > > Have a nice weekend! > > Carl Zeiss MicroImaging GmbH > Business Unit BioSciences > Imaging Software Munich > > Dr. Johannes Amon > [hidden email] |
Loralei Dewe-3 |
In reply to this post by Johannes Amon
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I too would prefer it in an Android format. I find the Android to be more useful to me than the Apple types... Loralei Dewe On Fri, Jan 13, 2012 at 7:26 AM, Johannes Amon <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Dear Community, > > just to inform you, we at Carl Zeiss Microscopy just recently launched a > fluorescence microscopy app for your iPads, iPhones and iPod touch > devices. I > was already in contact with George McNamara as the app uses the pubspectra > database, similar to our ZEN Smart Setup, and he suggested to post it here > so > that you are able to have a test-drive and discuss what you like or what > you > might not like. We are completely open for ideas, so hit the inbox micro- > [hidden email], hit me, and of course also feel free to discuss the app > here. > > http://www.zeiss.com/micro-apps > > The website should give you a good impression about what the app is able to > do. We are really curious to learn how it will be received by the > scientific > community so I'll try to check back regularly and see what you think. > > Have a nice weekend! > > Carl Zeiss MicroImaging GmbH > Business Unit BioSciences > Imaging Software Munich > > Dr. Johannes Amon > [hidden email] > |
Gabriel Lapointe-2 |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Great news, I can't wait to try the Android version. Sincerely, logo Gabriel Lapointe, M.Sc. [hidden email] http://gabriellapointe.ca logo On Fri, 2012-01-13 at 08:55 -0800, Loralei Dewe wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > I too would prefer it in an Android format. I find the Android to be more > useful to me than the Apple types... > > Loralei Dewe > > On Fri, Jan 13, 2012 at 7:26 AM, Johannes Amon <[hidden email]> wrote: > > > ***** > > To join, leave or search the confocal microscopy listserv, go to: > > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > > ***** > > > > Dear Community, > > > > just to inform you, we at Carl Zeiss Microscopy just recently launched a > > fluorescence microscopy app for your iPads, iPhones and iPod touch > > devices. I > > was already in contact with George McNamara as the app uses the pubspectra > > database, similar to our ZEN Smart Setup, and he suggested to post it here > > so > > that you are able to have a test-drive and discuss what you like or what > > you > > might not like. We are completely open for ideas, so hit the inbox micro- > > [hidden email], hit me, and of course also feel free to discuss the app > > here. > > > > http://www.zeiss.com/micro-apps > > > > The website should give you a good impression about what the app is able to > > do. We are really curious to learn how it will be received by the > > scientific > > community so I'll try to check back regularly and see what you think. > > > > Have a nice weekend! > > > > Carl Zeiss MicroImaging GmbH > > Business Unit BioSciences > > Imaging Software Munich > > > > Dr. Johannes Amon > > [hidden email] > > |
Johannes Amon |
In reply to this post by Johannes Amon
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** of course I can't tell you any specifics but at the moment we are evaluating a native port to android ICS 4.0. at the end it always comes down to budget so it would help immensely if you'd order some confocals right now ^^ just joking, gonna keep you posted on this project |
Peter Gabriel Pitrone |
In reply to this post by Johannes Amon
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I must say that I like the idea! However, I think that this would be better if Open Microscopy Environment would make a Smart Phone viewer so you wouldn't be limited by what microscope system you acquired the data from to be able to see it. What I think is that the vendors really need to focus on right now is compatibility, but I know that they think it is "Anathema". My $0.02 worth, Pete On Fri, January 13, 2012 4:26 pm, Johannes Amon wrote: | ***** | To join, leave or search the confocal microscopy listserv, go to: | http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy | ***** | | Dear Community, | | just to inform you, we at Carl Zeiss Microscopy just recently launched a | fluorescence microscopy app for your iPads, iPhones and iPod touch | devices. I | was already in contact with George McNamara as the app uses the pubspectra | database, similar to our ZEN Smart Setup, and he suggested to post it here | so | that you are able to have a test-drive and discuss what you like or what | you | might not like. We are completely open for ideas, so hit the inbox micro- | [hidden email], hit me, and of course also feel free to discuss the app | here. | | http://www.zeiss.com/micro-apps | | The website should give you a good impression about what the app is able | to | do. We are really curious to learn how it will be received by the | scientific | community so I'll try to check back regularly and see what you think. | | Have a nice weekend! | | Carl Zeiss MicroImaging GmbH | Business Unit BioSciences | Imaging Software Munich | | Dr. Johannes Amon | [hidden email] | -- Peter Gabriel Pitrone - TechRMS Microscopy/Imaging Specialist Prof. Dr. Pavel Tomancak group Max Planck Institute for Molecular Biology and Genetics Pfotenhauerstr. 108 01307 Dresden "If a straight line fit is required, obtain only two data points." - Anon. |
George McNamara |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Pete, I would match your $0.02 except that PubSpectra is open data access: freely available to you, Zeiss - it has been the source of the spectral Smart Setup in ZEN for years - and other vendors. Many vendors have contributed data, including LfieTech/Invitrogen/Molecular Probes, Chroma, Omega and Semrock, as have academics, including Roger Tsien/Robert Campbell, Jonathan Lindsey (see his photochemcad site). I have told many vendors about the data and encouraged them to include the data in their software. I congratulate Zeiss on their introduction of their iZeiss apps (I personally an not an i kind of guy). The PubSpectra data set can be downloaded in the ZIP file at the top of http://sylvester.org/shared-resources/analytical-imaging/links-forms-documentation/pubspectra-data and the UA graphing site is http://www.spectra.arizona.edu/ - along with additional spectra that Urs Utzinger and Carl Boswell have entered. Type in 2p in the dye field for data at the UA site that is not currently in PubSpectra. Data from the UA site can even be downloaded. I'll go further an encourage OME, ImageJ / ImageJ2 / Fiji / MBF ImageJ, and other imaging developers, to make use of PubSpectra. Finally, I encourage everyone who has fluorescence and fluorescence related spectra (including, but limited to dyes, fluorescent proteins, filters, light sources), to send me data to add to PubSpectra - preferably in the same organization as is in the PubSpectra Excel 2007 (xlsx) file. George On 1/14/2012 7:18 AM, Peter Gabriel Pitrone wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > I must say that I like the idea! > > However, I think that this would be better if Open Microscopy Environment > would make a Smart Phone viewer so you wouldn't be limited by what > microscope system you acquired the data from to be able to see it. > > What I think is that the vendors really need to focus on right now is > compatibility, but I know that they think it is "Anathema". > > My $0.02 worth, > > Pete > > On Fri, January 13, 2012 4:26 pm, Johannes Amon wrote: > | ***** > | To join, leave or search the confocal microscopy listserv, go to: > | http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > | ***** > | > | Dear Community, > | > | just to inform you, we at Carl Zeiss Microscopy just recently launched a > | fluorescence microscopy app for your iPads, iPhones and iPod touch > | devices. I > | was already in contact with George McNamara as the app uses the pubspectra > | database, similar to our ZEN Smart Setup, and he suggested to post it here > | so > | that you are able to have a test-drive and discuss what you like or what > | you > | might not like. We are completely open for ideas, so hit the inbox micro- > | [hidden email], hit me, and of course also feel free to discuss the app > | here. > | > | http://www.zeiss.com/micro-apps > | > | The website should give you a good impression about what the app is able > | to > | do. We are really curious to learn how it will be received by the > | scientific > | community so I'll try to check back regularly and see what you think. > | > | Have a nice weekend! > | > | Carl Zeiss MicroImaging GmbH > | Business Unit BioSciences > | Imaging Software Munich > | > | Dr. Johannes Amon > | [hidden email] > | > > > -- George McNamara, PhD Analytical Imaging Core Facility University of Miami |
Jason Swedlow-2 |
In reply to this post by Peter Gabriel Pitrone
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Pete- Thanks for the suggestion. Given our commitment to open source software, it's unlikely you'll see an iOS App from OME. You can look around the web-- there are lots of opinions, but it's pretty clear that the GPL license conflicts with Apple's distribution mechanisms. We have definitely experimented with clients for mobile browsers (for devs only, http://trac.openmicroscopy.org.uk/ome/browser/ome.git/components/tools/OmeroWeb/omeroweb), but this needs more work to be fully developed. As you might imagine, chasing all the different browser platforms and versions is just too much fun. Android? Hmmmm. In general we prefer cross-platform solutions, but the world is changing rapidly..... if you feel strongly about this, post it on the OME Forums ( http://www.openmicroscopy.org/community/) -- your feedback drives our priorities. Cheers, Jason On Sat, Jan 14, 2012 at 12:18 PM, Peter Gabriel Pitrone <[hidden email]>wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > I must say that I like the idea! > > However, I think that this would be better if Open Microscopy Environment > would make a Smart Phone viewer so you wouldn't be limited by what > microscope system you acquired the data from to be able to see it. > > What I think is that the vendors really need to focus on right now is > compatibility, but I know that they think it is "Anathema". > > My $0.02 worth, > > Pete > > On Fri, January 13, 2012 4:26 pm, Johannes Amon wrote: > | ***** > | To join, leave or search the confocal microscopy listserv, go to: > | http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > | ***** > | > | Dear Community, > | > | just to inform you, we at Carl Zeiss Microscopy just recently launched a > | fluorescence microscopy app for your iPads, iPhones and iPod touch > | devices. I > | was already in contact with George McNamara as the app uses the > pubspectra > | database, similar to our ZEN Smart Setup, and he suggested to post it > here > | so > | that you are able to have a test-drive and discuss what you like or what > | you > | might not like. We are completely open for ideas, so hit the inbox micro- > | [hidden email], hit me, and of course also feel free to discuss the app > | here. > | > | http://www.zeiss.com/micro-apps > | > | The website should give you a good impression about what the app is able > | to > | do. We are really curious to learn how it will be received by the > | scientific > | community so I'll try to check back regularly and see what you think. > | > | Have a nice weekend! > | > | Carl Zeiss MicroImaging GmbH > | Business Unit BioSciences > | Imaging Software Munich > | > | Dr. Johannes Amon > | [hidden email] > | > > > -- > Peter Gabriel Pitrone - TechRMS > Microscopy/Imaging Specialist > Prof. Dr. Pavel Tomancak group > Max Planck Institute for > Molecular Biology and Genetics > Pfotenhauerstr. 108 > 01307 Dresden > > "If a straight line fit is required, obtain only two data points." - Anon. > -- ************************** Wellcome Trust Centre for Gene Regulation & Expression College of Life Sciences MSI/WTB/JBC Complex University of Dundee Dow Street Dundee DD1 5EH United Kingdom phone (01382) 385819 Intl phone: 44 1382 385819 FAX (01382) 388072 email: [hidden email] Lab Page: http://www.lifesci.dundee.ac.uk/gre/staff/jason-swedlow Open Microscopy Environment: http://openmicroscopy.org ************************** |
Jason Swedlow-2 |
In reply to this post by George McNamara
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi- A few comments: George's PubSpectra resource is very nice. The usage and contributions are exactly the kind of thing that can develop using open, shareable, maintained resources. I emphasise 'maintained' as anything like this must be kept up-to-date for it to be at all useful. George has done a great job with it. In OME, we provide many mechanism for storing data. In fact, in our first version of OME-XML, we imagined mechanisms for storing fluorescence spectra. As soon as we saw George's work, we were sooo happy that someone else had taken this on, we presumed that a URL linking to PubSpectra would provide the simplest, most flexible mechanism for storing spectral information. We haven't directly specified this, as we prefer to let users make these choices-- but we can. In our current work, we are moving OMERO to a stable platform in order to focus on delivering more functionality in the clients (only if you really care, http://trac.openmicroscopy.org.uk/ome/milestone/OMERO-Beta4.4). Views of PubSpectra data could certainly be implemented in the future. As always, comments, suggestions, and biting critiques are welcome at http://www.openmicroscopy.org/community/ And....hats off to Zeiss. Very nice app!!! Cheers, Jason On Sat, Jan 14, 2012 at 4:26 PM, George McNamara <[hidden email]>wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy<http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> > ***** > > Hi Pete, > > I would match your $0.02 except that PubSpectra is open data access: > freely available to you, Zeiss - it has been the source of the spectral > Smart Setup in ZEN for years - and other vendors. Many vendors have > contributed data, including LfieTech/Invitrogen/Molecular Probes, Chroma, > Omega and Semrock, as have academics, including Roger Tsien/Robert > Campbell, Jonathan Lindsey (see his photochemcad site). I have told many > vendors about the data and encouraged them to include the data in their > software. I congratulate Zeiss on their introduction of their iZeiss apps > (I personally an not an i kind of guy). > > The PubSpectra data set can be downloaded in the ZIP file at the top of > http://sylvester.org/shared-**resources/analytical-imaging/** > links-forms-documentation/**pubspectra-data<http://sylvester.org/shared-resources/analytical-imaging/links-forms-documentation/pubspectra-data> > > and the UA graphing site is http://www.spectra.arizona.**edu/<http://www.spectra.arizona.edu/>- along with additional spectra that Urs Utzinger and Carl Boswell have > entered. Type in 2p in the dye field for data at the UA site that is > not currently in PubSpectra. Data from the UA site can even be downloaded. > > I'll go further an encourage OME, ImageJ / ImageJ2 / Fiji / MBF ImageJ, > and other imaging developers, to make use of PubSpectra. > > Finally, I encourage everyone who has fluorescence and fluorescence > related spectra (including, but limited to dyes, fluorescent proteins, > filters, light sources), to send me data to add to PubSpectra - preferably > in the same organization as is in the PubSpectra Excel 2007 (xlsx) file. > > > George > > > On 1/14/2012 7:18 AM, Peter Gabriel Pitrone wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy<http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> >> ***** >> >> I must say that I like the idea! >> >> However, I think that this would be better if Open Microscopy Environment >> would make a Smart Phone viewer so you wouldn't be limited by what >> microscope system you acquired the data from to be able to see it. >> >> What I think is that the vendors really need to focus on right now is >> compatibility, but I know that they think it is "Anathema". >> >> My $0.02 worth, >> >> Pete >> >> On Fri, January 13, 2012 4:26 pm, Johannes Amon wrote: >> | ***** >> | To join, leave or search the confocal microscopy listserv, go to: >> | http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy<http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> >> | ***** >> | >> | Dear Community, >> | >> | just to inform you, we at Carl Zeiss Microscopy just recently launched a >> | fluorescence microscopy app for your iPads, iPhones and iPod touch >> | devices. I >> | was already in contact with George McNamara as the app uses the >> pubspectra >> | database, similar to our ZEN Smart Setup, and he suggested to post it >> here >> | so >> | that you are able to have a test-drive and discuss what you like or what >> | you >> | might not like. We are completely open for ideas, so hit the inbox >> micro- >> | [hidden email], hit me, and of course also feel free to discuss the app >> | here. >> | >> | http://www.zeiss.com/micro-**apps <http://www.zeiss.com/micro-apps> >> | >> | The website should give you a good impression about what the app is able >> | to >> | do. We are really curious to learn how it will be received by the >> | scientific >> | community so I'll try to check back regularly and see what you think. >> | >> | Have a nice weekend! >> | >> | Carl Zeiss MicroImaging GmbH >> | Business Unit BioSciences >> | Imaging Software Munich >> | >> | Dr. Johannes Amon >> | [hidden email] >> | >> >> >> >> > > > -- > > > George McNamara, PhD > Analytical Imaging Core Facility > University of Miami > -- ************************** Wellcome Trust Centre for Gene Regulation & Expression College of Life Sciences MSI/WTB/JBC Complex University of Dundee Dow Street Dundee DD1 5EH United Kingdom phone (01382) 385819 Intl phone: 44 1382 385819 FAX (01382) 388072 email: [hidden email] Lab Page: http://www.lifesci.dundee.ac.uk/gre/staff/jason-swedlow Open Microscopy Environment: http://openmicroscopy.org ************************** |
Michael Herron |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** PubSpectra needs Flash so it does not work on iPhone or iPad. Any plans to make it HTML5 compliant? On Saturday, January 14, 2012, Jason Swedlow <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Hi- > > A few comments: > > George's PubSpectra resource is very nice. The usage and contributions > exactly the kind of thing that can develop using open, shareable, > maintained resources. I emphasise 'maintained' as anything like this must > be kept up-to-date for it to be at all useful. George has done a great job > with it. > > In OME, we provide many mechanism for storing data. In fact, in our first > version of OME-XML, we imagined mechanisms for storing fluorescence > spectra. As soon as we saw George's work, we were sooo happy that someone > else had taken this on, we presumed that a URL linking to PubSpectra would > provide the simplest, most flexible mechanism for storing spectral > information. We haven't directly specified this, as we prefer to let users > make these choices-- but we can. In our current work, we are moving OMERO > to a stable platform in order to focus on delivering more functionality in > the clients (only if you really care, > http://trac.openmicroscopy.org.uk/ome/milestone/OMERO-Beta4.4). Views of > PubSpectra data could certainly be implemented in the future. > > As always, comments, suggestions, and biting critiques are welcome at > http://www.openmicroscopy.org/community/ > > And....hats off to Zeiss. Very nice app!!! > > Cheers, > > Jason > > > On Sat, Jan 14, 2012 at 4:26 PM, George McNamara > <[hidden email]>wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy< >> ***** >> >> Hi Pete, >> >> I would match your $0.02 except that PubSpectra is open data access: >> freely available to you, Zeiss - it has been the source of the spectral >> Smart Setup in ZEN for years - and other vendors. Many vendors have >> contributed data, including LfieTech/Invitrogen/Molecular Probes, Chroma, >> Omega and Semrock, as have academics, including Roger Tsien/Robert >> Campbell, Jonathan Lindsey (see his photochemcad site). I have told many >> vendors about the data and encouraged them to include the data in their >> software. I congratulate Zeiss on their introduction of their iZeiss apps >> (I personally an not an i kind of guy). >> >> The PubSpectra data set can be downloaded in the ZIP file at the top of >> http://sylvester.org/shared-**resources/analytical-imaging/** >> links-forms-documentation/**pubspectra-data< > >> >> and the UA graphing site is http://www.spectra.arizona.**edu/< http://www.spectra.arizona.edu/>- along with additional spectra that Urs Utzinger and Carl Boswell have >> entered. Type in 2p in the dye field for data at the UA site that is >> not currently in PubSpectra. Data from the UA site can even be downloaded. >> >> I'll go further an encourage OME, ImageJ / ImageJ2 / Fiji / MBF ImageJ, >> and other imaging developers, to make use of PubSpectra. >> >> Finally, I encourage everyone who has fluorescence and fluorescence >> related spectra (including, but limited to dyes, fluorescent proteins, >> filters, light sources), to send me data to add to PubSpectra - preferably >> in the same organization as is in the PubSpectra Excel 2007 (xlsx) file. >> >> >> George >> >> >> On 1/14/2012 7:18 AM, Peter Gabriel Pitrone wrote: >> >>> ***** >>> To join, leave or search the confocal microscopy listserv, go to: >>> http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy< >>> ***** >>> >>> I must say that I like the idea! >>> >>> However, I think that this would be better if Open Microscopy Environment >>> would make a Smart Phone viewer so you wouldn't be limited by what >>> microscope system you acquired the data from to be able to see it. >>> >>> What I think is that the vendors really need to focus on right now is >>> compatibility, but I know that they think it is "Anathema". >>> >>> My $0.02 worth, >>> >>> Pete >>> >>> On Fri, January 13, 2012 4:26 pm, Johannes Amon wrote: >>> | ***** >>> | To join, leave or search the confocal microscopy listserv, go to: >>> | http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy< >>> | ***** >>> | >>> | Dear Community, >>> | >>> | just to inform you, we at Carl Zeiss Microscopy just recently launched a >>> | fluorescence microscopy app for your iPads, iPhones and iPod touch >>> | devices. I >>> | was already in contact with George McNamara as the app uses the >>> pubspectra >>> | database, similar to our ZEN Smart Setup, and he suggested to post it >>> here >>> | so >>> | that you are able to have a test-drive and discuss what you like or what >>> | you >>> | might not like. We are completely open for ideas, so hit the inbox >>> micro- >>> | [hidden email], hit me, and of course also feel free to discuss the app >>> | here. >>> | >>> | http://www.zeiss.com/micro-**apps <http://www.zeiss.com/micro-apps> >>> | >>> | The website should give you a good impression about what the app is able >>> | to >>> | do. We are really curious to learn how it will be received by the >>> | scientific >>> | community so I'll try to check back regularly and see what you think. >>> | >>> | Have a nice weekend! >>> | >>> | Carl Zeiss MicroImaging GmbH >>> | Business Unit BioSciences >>> | Imaging Software Munich >>> | >>> | Dr. Johannes Amon >>> | [hidden email] >>> | >>> >>> >>> >>> >> >> >> -- >> >> >> George McNamara, PhD >> Analytical Imaging Core Facility >> University of Miami >> > > > > -- > ************************** > Wellcome Trust Centre for Gene Regulation & Expression > College of Life Sciences > MSI/WTB/JBC Complex > University of Dundee > Dow Street > Dundee DD1 5EH > United Kingdom > > phone (01382) 385819 > Intl phone: 44 1382 385819 > FAX (01382) 388072 > email: [hidden email] > > Lab Page: http://www.lifesci.dundee.ac.uk/gre/staff/jason-swedlow > Open Microscopy Environment: http://openmicroscopy.org > ************************** > -- Michael J. Herron, U of MN, Dept. of Entomology [hidden email] 612-624-3688 (office) 612-625-5299 (FAX) |
George McNamara |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Michael, PubSpectra is the open data access project - that is, the Excel file that everyone can freely use. The xlsx file format is XML, though Internet Explorer 8 in Windows takes the lazy way out by simply launching Excel. Perhaps Android and/or iThingies have Excel or useful Excel viewers. My limited experience a couple of years ago with the spreadsheet program in Open Office (for Windows) was that it was lame. You are probably referring to Urs Utzinger's Spectra Database hosted at the University of Arizona, http://www.spectra.arizona.edu/ - non-Flash version(s) are for Urs to respond to. *** I want to encourage everyone to make your data available as Open Data. There are some guidelines: http://pantonprinciples.org/ Science is based on building on, reusing and openly criticising the published body of scientific knowledge. For science to effectively function, and for society to reap the full benefits from scientific endeavours, it is crucial that science data be made open <http://opendefinition.org/>. By open data in science we mean that it is freely available on the public internet permitting any user to download, copy, analyse, re-process, pass them to software or use them for any other purpose without financial, legal, or technical barriers other than those inseparable from gaining access to the internet itself. *To this end data related to published science should be explicitly placed in the public domain.* *Formally, we recommend adopting and acting on the following principles:* 1. Where data or collections of data are published it is critical that they be published with a clear and explicit statement of the wishes and expectations of the publishers with respect to re-use and re-purposing of individual data elements, the whole data collection, and subsets of the collection. This statement should be precise, irrevocable, and based on an appropriate and recognized legal statement in the form of a waiver or license. /When publishing data make an explicit and robust statement of your wishes./ 2. Many widely recognized licenses are not intended for, and are not appropriate for, data or collections of data. A variety of waivers and licenses that are designed for and appropriate for the treatment of data are described here <http://opendefinition.org/licenses#Data>. Creative Commons licenses (apart from CCZero), GFDL, GPL, BSD, etc are NOT appropriate for data and their use is STRONGLY discouraged. /Use a recognized waiver or license that is appropriate for data./ 3. The use of licenses which limit commercial re-use or limit the production of derivative works by excluding use for particular purposes or by specific persons or organizations is STRONGLY discouraged. These licenses make it impossible to effectively integrate and re-purpose datasets and prevent commercial activities that could be used to support data preservation. /If you want your data to be effectively used and added to by others it should be open as defined by the Open Knowledge/Data Definition <http://opendefinition.org/> -- in particular non-commercial and other restrictive clauses should not be used./ 4. Furthermore, in science it is STRONGLY recommended that data, especially where publicly funded, be explicitly placed in the public domain via the use of the Public Domain Dedication and Licence or Creative Commons Zero Waiver. This is in keeping with the public funding of much scientific research and the general ethos of sharing and re-use within the scientific community. /Explicit dedication of data underlying published science into the public domain via PDDL or CCZero is strongly recommended and ensures compliance with both the Science Commons Protocol for Implementing Open Access Data <http://sciencecommons.org/projects/publishing/open-access-data-protocol/> and the Open Knowledge/Data Definition <http://opendefinition.org/>./ See also http://www.arl.org/sparc/opendata/ and http://www.arl.org/sparc/innovator/panton.shtml - in particular the latter explains the Panton in Panton Principles. I've already stated my position (2006 Cytometry paper on PubSpectra and Carl Boswell's first generation UA Graphing site ( http://www.mcb.arizona.edu/ipc/fret/index.html -- which is still available ): "... data is not subject to copyright. Text and commentary about Feist (Feist Publications, Inc. v. Rural Tel. Serv. Co. 1991;499 U.S. 340.) can be found on many legal web sites by doing a Google search. Indeed, the broad availability of the text of [the U.S.] Supreme Court decisions is because they are not subject to copyright. The Feist decision reaffirmed the U.S. Copyright act of 1976 that ''there can be no copyright in facts''. The basis for the Feist decision can be found in the U.S. Constitution." but I appreciate the P.P. folks point about explictly placing the data in the public domain. A place you can send your image data is to http://www.cellimagelibrary.org/ Best wishes, and may all your data be reused, George On 1/14/2012 2:47 PM, Michael Herron wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > PubSpectra needs Flash so it does not work on iPhone or iPad. Any plans to > make it HTML5 compliant? > > On Saturday, January 14, 2012, Jason Swedlow<[hidden email]> wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> Hi- >> >> A few comments: >> >> George's PubSpectra resource is very nice. The usage and contributions >> > are > >> exactly the kind of thing that can develop using open, shareable, >> maintained resources. I emphasise 'maintained' as anything like this must >> be kept up-to-date for it to be at all useful. George has done a great >> > job > >> with it. >> >> In OME, we provide many mechanism for storing data. In fact, in our first >> version of OME-XML, we imagined mechanisms for storing fluorescence >> spectra. As soon as we saw George's work, we were sooo happy that someone >> else had taken this on, we presumed that a URL linking to PubSpectra >> > would > >> provide the simplest, most flexible mechanism for storing spectral >> information. We haven't directly specified this, as we prefer to let >> > users > >> make these choices-- but we can. In our current work, we are moving OMERO >> to a stable platform in order to focus on delivering more functionality in >> the clients (only if you really care, >> http://trac.openmicroscopy.org.uk/ome/milestone/OMERO-Beta4.4). Views of >> PubSpectra data could certainly be implemented in the future. >> >> As always, comments, suggestions, and biting critiques are welcome at >> http://www.openmicroscopy.org/community/ >> >> And....hats off to Zeiss. Very nice app!!! >> >> Cheers, >> >> Jason >> >> >> On Sat, Jan 14, 2012 at 4:26 PM, George McNamara >> <[hidden email]>wrote: >> >> >>> ***** >>> To join, leave or search the confocal microscopy listserv, go to: >>> http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy< >>> > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> > >>> ***** >>> >>> Hi Pete, >>> >>> I would match your $0.02 except that PubSpectra is open data access: >>> freely available to you, Zeiss - it has been the source of the spectral >>> Smart Setup in ZEN for years - and other vendors. Many vendors have >>> contributed data, including LfieTech/Invitrogen/Molecular Probes, Chroma, >>> Omega and Semrock, as have academics, including Roger Tsien/Robert >>> Campbell, Jonathan Lindsey (see his photochemcad site). I have told many >>> vendors about the data and encouraged them to include the data in their >>> software. I congratulate Zeiss on their introduction of their iZeiss apps >>> (I personally an not an i kind of guy). >>> >>> The PubSpectra data set can be downloaded in the ZIP file at the top of >>> http://sylvester.org/shared-**resources/analytical-imaging/** >>> links-forms-documentation/**pubspectra-data< >>> > http://sylvester.org/shared-resources/analytical-imaging/links-forms-documentation/pubspectra-data > >> >>> and the UA graphing site is http://www.spectra.arizona.**edu/< >>> > http://www.spectra.arizona.edu/>- along with additional spectra that Urs > Utzinger and Carl Boswell have > >>> entered. Type in 2p in the dye field for data at the UA site that is >>> not currently in PubSpectra. Data from the UA site can even be >>> > downloaded. > >>> I'll go further an encourage OME, ImageJ / ImageJ2 / Fiji / MBF ImageJ, >>> and other imaging developers, to make use of PubSpectra. >>> >>> Finally, I encourage everyone who has fluorescence and fluorescence >>> related spectra (including, but limited to dyes, fluorescent proteins, >>> filters, light sources), to send me data to add to PubSpectra - >>> > preferably > >>> in the same organization as is in the PubSpectra Excel 2007 (xlsx) file. >>> >>> >>> George >>> >>> >>> On 1/14/2012 7:18 AM, Peter Gabriel Pitrone wrote: >>> >>> >>>> ***** >>>> To join, leave or search the confocal microscopy listserv, go to: >>>> http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy< >>>> > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> > >>>> ***** >>>> >>>> I must say that I like the idea! >>>> >>>> However, I think that this would be better if Open Microscopy >>>> > Environment > >>>> would make a Smart Phone viewer so you wouldn't be limited by what >>>> microscope system you acquired the data from to be able to see it. >>>> >>>> What I think is that the vendors really need to focus on right now is >>>> compatibility, but I know that they think it is "Anathema". >>>> >>>> My $0.02 worth, >>>> >>>> Pete >>>> >>>> On Fri, January 13, 2012 4:26 pm, Johannes Amon wrote: >>>> | ***** >>>> | To join, leave or search the confocal microscopy listserv, go to: >>>> | http://lists.umn.edu/cgi-bin/**wa?A0=confocalmicroscopy< >>>> > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> > >>>> | ***** >>>> | >>>> | Dear Community, >>>> | >>>> | just to inform you, we at Carl Zeiss Microscopy just recently >>>> > launched a > >>>> | fluorescence microscopy app for your iPads, iPhones and iPod touch >>>> | devices. I >>>> | was already in contact with George McNamara as the app uses the >>>> pubspectra >>>> | database, similar to our ZEN Smart Setup, and he suggested to post it >>>> here >>>> | so >>>> | that you are able to have a test-drive and discuss what you like or >>>> > what > >>>> | you >>>> | might not like. We are completely open for ideas, so hit the inbox >>>> micro- >>>> | [hidden email], hit me, and of course also feel free to discuss the app >>>> | here. >>>> | >>>> | http://www.zeiss.com/micro-**apps<http://www.zeiss.com/micro-apps> >>>> | >>>> | The website should give you a good impression about what the app is >>>> > able > >>>> | to >>>> | do. We are really curious to learn how it will be received by the >>>> | scientific >>>> | community so I'll try to check back regularly and see what you think. >>>> | >>>> | Have a nice weekend! >>>> | >>>> | Carl Zeiss MicroImaging GmbH >>>> | Business Unit BioSciences >>>> | Imaging Software Munich >>>> | >>>> | Dr. Johannes Amon >>>> | [hidden email] >>>> | >>>> >>>> >>>> >>>> >>>> >>> >>> -- >>> >>> >>> George McNamara, PhD >>> Analytical Imaging Core Facility >>> University of Miami >>> >>> >> >> >> -- >> ************************** >> Wellcome Trust Centre for Gene Regulation& Expression >> College of Life Sciences >> MSI/WTB/JBC Complex >> University of Dundee >> Dow Street >> Dundee DD1 5EH >> United Kingdom >> >> phone (01382) 385819 >> Intl phone: 44 1382 385819 >> FAX (01382) 388072 >> email: [hidden email] >> >> Lab Page: http://www.lifesci.dundee.ac.uk/gre/staff/jason-swedlow >> Open Microscopy Environment: http://openmicroscopy.org >> ************************** >> >> > -- George McNamara, PhD Analytical Imaging Core Facility University of Miami |
Johannes Amon |
In reply to this post by Peter Gabriel Pitrone
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Peter, right from the beginning we designed our iOS app so that every microscopist independently of the system in his lab is able to use our spectra viewer and can configure all the filters and presets tailored to his very own experimental setup. while Light Lab includes some ZEISS- specific presets (and might include some more in future updates) this is completely for convenience and as a service to users of our systems. we encourage every microscopist to use Light Lab with his own system settings no matter from which vendor your system or filters are. and if I might add, I really fought hard for the free configuration options ^^ in 2012 we have some interesting new projects centered around George's database, so give us a little time here. and please don't be afraid that we'd try to 'own' pubspectra: our main interest lies in establishing a standard database source and format for the whole scientific community together with you. we deeply respect the work George has put into pubspectra and we value the 'open source' spirit behind it. a well-maintained standardized database with an open file format (xml, anybody?) and an easy-to-use open source windows GUI makes our work easier, it makes your work easier, and we don't care too much if it also makes the work of our competitors' easier. stay with us, and have a nice evening! |
Adrian Smith-6 |
In reply to this post by Johannes Amon
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** On 14/01/2012, at 9:01 PM, Johannes Amon wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > of course I can't tell you any specifics but at the moment we are evaluating a native port to > android ICS 4.0. at the end it always comes down to budget so it would help immensely if > you'd order some confocals right now ^^ > > just joking, gonna keep you posted on this project I would love to find a decent resolution calculator that can be used on a smartphone/tablet (iOS preferably for me :) Add in various options for different digitisation approaches (PMT, cameras) with Nyquist shortcuts and it would be real winner… Regards, Adrian Smith Centenary Institute, Sydney, Australia |
Peter Gabriel Pitrone |
In reply to this post by Johannes Amon
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Johannes, I misunderstood the whole concept of the app. I thought it would only work with acquired data, if it is a stand alone spectral viewer than that really is a great idea. Don't forget the light sources!! I also wish you a great weekend and week ahead, Pete On Sun, January 15, 2012 2:00 am, Johannes Amon wrote: | ***** | To join, leave or search the confocal microscopy listserv, go to: | http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy | ***** | | Dear Peter, | | right from the beginning we designed our iOS app so that every | microscopist independently | of the system in his lab is able to use our spectra viewer and can | configure all the filters and | presets tailored to his very own experimental setup. while Light Lab | includes some ZEISS- | specific presets (and might include some more in future updates) this is | completely for | convenience and as a service to users of our systems. | | we encourage every microscopist to use Light Lab with his own system | settings no matter | from which vendor your system or filters are. and if I might add, I really | fought hard for the | free configuration options ^^ | | in 2012 we have some interesting new projects centered around George's | database, so give | us a little time here. and please don't be afraid that we'd try to 'own' | pubspectra: our main | interest lies in establishing a standard database source and format for | the whole scientific | community together with you. we deeply respect the work George has put | into pubspectra | and we value the 'open source' spirit behind it. a well-maintained | standardized database | with an open file format (xml, anybody?) and an easy-to-use open source | windows GUI | makes our work easier, it makes your work easier, and we don't care too | much if it also | makes the work of our competitors' easier. | | stay with us, and have a nice evening! | -- Peter Gabriel Pitrone - TechRMS Microscopy/Imaging Specialist Prof. Dr. Pavel Tomancak group Max Planck Institute for Molecular Biology and Genetics Pfotenhauerstr. 108 01307 Dresden "If a straight line fit is required, obtain only two data points." - Anon. |
John Oreopoulos |
In reply to this post by Adrian Smith-6
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Adrian, there is a fairly good iPhone application that does some of the things you mentioned. It's called ResCalc. John Oreopoulos Research Assistant Spectral Applied Research Richmond Hill, Ontario Canada www.spectral.ca On 2012-01-15, at 1:03 AM, Adrian Smith <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > On 14/01/2012, at 9:01 PM, Johannes Amon wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> of course I can't tell you any specifics but at the moment we are evaluating a native port to >> android ICS 4.0. at the end it always comes down to budget so it would help immensely if >> you'd order some confocals right now ^^ >> >> just joking, gonna keep you posted on this project > > > I would love to find a decent resolution calculator that can be used on a smartphone/tablet (iOS preferably for me :) > > Add in various options for different digitisation approaches (PMT, cameras) with Nyquist shortcuts and it would be real winner… > > Regards, > > Adrian Smith > Centenary Institute, Sydney, Australia |
Tim Feinstein-2 |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi John, ResCalc is a nice app, but it seems to calculate res and nyquist for widefield microscopy only. Am I wrong about that? As it is I use the Nyquist calculator on the SVI site (no commercial interest) but I would love to have something off-line. Cheers, TIm Feinstein Sent from my iPad On Jan 15, 2012, at 10:40 AM, John Oreopoulos <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Adrian, there is a fairly good iPhone application that does some of the things you mentioned. It's called ResCalc. > > John Oreopoulos > Research Assistant > Spectral Applied Research > Richmond Hill, Ontario > Canada > www.spectral.ca > > On 2012-01-15, at 1:03 AM, Adrian Smith <[hidden email]> wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> On 14/01/2012, at 9:01 PM, Johannes Amon wrote: >> >>> ***** >>> To join, leave or search the confocal microscopy listserv, go to: >>> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >>> ***** >>> >>> of course I can't tell you any specifics but at the moment we are evaluating a native port to >>> android ICS 4.0. at the end it always comes down to budget so it would help immensely if >>> you'd order some confocals right now ^^ >>> >>> just joking, gonna keep you posted on this project >> >> >> I would love to find a decent resolution calculator that can be used on a smartphone/tablet (iOS preferably for me :) >> >> Add in various options for different digitisation approaches (PMT, cameras) with Nyquist shortcuts and it would be real winner… >> >> Regards, >> >> Adrian Smith >> Centenary Institute, Sydney, Australia |
There isn't any difference between widefield and confocal resolution in any normal fluorescence mode. Do you really need an app to work out 0.61 lambda/NA? And then to divide by 2.3 to get Nyquist? If you are in multiphoton it's a little more complicated since root 2 (1.414) comes in, but you can just use the formula 0.43 lambda / NA.
Guy Optical Imaging Techniques in Cell Biology by Guy Cox CRC Press / Taylor & Francis http://www.guycox.com/optical.htm ______________________________________________ Guy Cox, MA, DPhil(Oxon), Honorary Associate, Australian Centre for Microscopy & Microanalysis, Madsen Building F09, University of Sydney, NSW 2006 Phone +61 2 9351 3176 Fax +61 2 9351 7682 Mobile 0413 281 861 ______________________________________________ http://www.guycox.net -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Tim Feinstein Sent: Monday, 16 January 2012 4:54 AM To: [hidden email] Subject: Re: Light Lab by Carl Zeiss Microscopy for iOS devices ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi John, ResCalc is a nice app, but it seems to calculate res and nyquist for widefield microscopy only. Am I wrong about that? As it is I use the Nyquist calculator on the SVI site (no commercial interest) but I would love to have something off-line. Cheers, TIm Feinstein Sent from my iPad On Jan 15, 2012, at 10:40 AM, John Oreopoulos <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Adrian, there is a fairly good iPhone application that does some of the things you mentioned. It's called ResCalc. > > John Oreopoulos > Research Assistant > Spectral Applied Research > Richmond Hill, Ontario > Canada > www.spectral.ca > > On 2012-01-15, at 1:03 AM, Adrian Smith <[hidden email]> wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> On 14/01/2012, at 9:01 PM, Johannes Amon wrote: >> >>> ***** >>> To join, leave or search the confocal microscopy listserv, go to: >>> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >>> ***** >>> >>> of course I can't tell you any specifics but at the moment we are evaluating a native port to >>> android ICS 4.0. at the end it always comes down to budget so it would help immensely if >>> you'd order some confocals right now ^^ >>> >>> just joking, gonna keep you posted on this project >> >> >> I would love to find a decent resolution calculator that can be used on a smartphone/tablet (iOS preferably for me :) >> >> Add in various options for different digitisation approaches (PMT, cameras) with Nyquist shortcuts and it would be real winner… >> >> Regards, >> >> Adrian Smith >> Centenary Institute, Sydney, Australia |
John Oreopoulos |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Tim, the ResCalc app assumes a Nyquist sampling rate of 2.3x. As for whether or not one should choose their image pixel size using this sampling factor of 2.3 or something else for confocal or widefield, I would refer the interested reader to the epic discussion on this topic back from 2007 (so as not to have it repeated again!): http://lists.umn.edu/cgi-bin/wa?A2=ind0701&L=CONFOCALMICROSCOPY&D=0&P=15141 John Oreopoulos On 2012-01-15, at 8:08 PM, Guy Cox wrote: > There isn't any difference between widefield and confocal resolution in any normal fluorescence mode. Do you really need an app to work out 0.61 lambda/NA? And then to divide by 2.3 to get Nyquist? If you are in multiphoton it's a little more complicated since root 2 (1.414) comes in, but you can just use the formula 0.43 lambda / NA. > > Guy > > Optical Imaging Techniques in Cell Biology > by Guy Cox CRC Press / Taylor & Francis > http://www.guycox.com/optical.htm > ______________________________________________ > Guy Cox, MA, DPhil(Oxon), Honorary Associate, > Australian Centre for Microscopy & Microanalysis, > Madsen Building F09, University of Sydney, NSW 2006 > > Phone +61 2 9351 3176 Fax +61 2 9351 7682 > Mobile 0413 281 861 > ______________________________________________ > http://www.guycox.net > > > -----Original Message----- > From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Tim Feinstein > Sent: Monday, 16 January 2012 4:54 AM > To: [hidden email] > Subject: Re: Light Lab by Carl Zeiss Microscopy for iOS devices > > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Hi John, > > ResCalc is a nice app, but it seems to calculate res and nyquist for widefield microscopy only. Am I wrong about that? As it is I use the Nyquist calculator on the SVI site (no commercial interest) but I would love to have something off-line. > > Cheers, > > > TIm Feinstein > > Sent from my iPad > > On Jan 15, 2012, at 10:40 AM, John Oreopoulos <[hidden email]> wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> Adrian, there is a fairly good iPhone application that does some of the things you mentioned. It's called ResCalc. >> >> John Oreopoulos >> Research Assistant >> Spectral Applied Research >> Richmond Hill, Ontario >> Canada >> www.spectral.ca >> >> On 2012-01-15, at 1:03 AM, Adrian Smith <[hidden email]> wrote: >> >>> ***** >>> To join, leave or search the confocal microscopy listserv, go to: >>> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >>> ***** >>> >>> On 14/01/2012, at 9:01 PM, Johannes Amon wrote: >>> >>>> ***** >>>> To join, leave or search the confocal microscopy listserv, go to: >>>> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >>>> ***** >>>> >>>> of course I can't tell you any specifics but at the moment we are evaluating a native port to >>>> android ICS 4.0. at the end it always comes down to budget so it would help immensely if >>>> you'd order some confocals right now ^^ >>>> >>>> just joking, gonna keep you posted on this project >>> >>> >>> I would love to find a decent resolution calculator that can be used on a smartphone/tablet (iOS preferably for me :) >>> >>> Add in various options for different digitisation approaches (PMT, cameras) with Nyquist shortcuts and it would be real winner… >>> >>> Regards, >>> >>> Adrian Smith >>> Centenary Institute, Sydney, Australia |
Steffen Dietzel |
In reply to this post by Guy Cox-2
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Well, for my part I wouldn't mind an (Android) app for - z-resolution, prefereably one that includes 2- and 3-photon excitation and - resolution and brightness at various depths under refraction index mismatch conditions (e.g. sample embedded in glycerol instead of immersion oil or underneath a coverslip with a dipping objective). Life isn't always as simple as 0.61 lambda/NA. Even better though than a bunch of apps for various systems would a calculator running in a web browser based on common standards so that it would be accessible on every system. Steffen On 16.01.2012 02:08, Guy Cox wrote: > There isn't any difference between widefield and confocal resolution in any normal fluorescence mode. Do you really need an app to work out 0.61 lambda/NA? And then to divide by 2.3 to get Nyquist? If you are in multiphoton it's a little more complicated since root 2 (1.414) comes in, but you can just use the formula 0.43 lambda / NA. > > Guy > > Optical Imaging Techniques in Cell Biology > by Guy Cox CRC Press / Taylor& Francis > http://www.guycox.com/optical.htm > ______________________________________________ > Guy Cox, MA, DPhil(Oxon), Honorary Associate, > Australian Centre for Microscopy& Microanalysis, > Madsen Building F09, University of Sydney, NSW 2006 > > Phone +61 2 9351 3176 Fax +61 2 9351 7682 > Mobile 0413 281 861 > ______________________________________________ > http://www.guycox.net > -- ------------------------------------------------------------ Steffen Dietzel, PD Dr. rer. nat Ludwig-Maximilians-Universität München Walter-Brendel-Zentrum für experimentelle Medizin (WBex) Head of light microscopy Mail room: Marchioninistr. 15, D-81377 München Building location: Marchioninistr. 27, München-Großhadern |
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