*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi, I was wondering whether there is a way to shorten the read out speed of my Andor IXON897 EMCCD camera. I am runnig it with a Labview program and I cannot get faster than ~20ms per image, although I am only reading out one line of 512 pixels (1X512 Pixel image). Settings: Exposition time 0,5 ms External Start Trigger in run till abort mode Franziska |
Vitaly Boyko |
I am looking for a file converter plugin in Image J. In part
***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear All, I am looking for a file converter plugin in Image J. In particular, I would like to convert large >30GB 3D tile data set (ca. 4000x4000x300, xyz) from .lif to .ids/.ics (ideally ICS2) format. Thank you, Vitaly 240-342-6217 |
Cameron Nowell |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Vitaly, There is a built in converter in Fiji (and I assume imageJ) but it won't do ICS format. But the LOCI tools can export to ICS (not ICS2 though). So you could write a simple macro to batch process a folder of files to convert them to ICS. Do you lif files contain multiple experiments? Cheers Cam Cameron J. Nowell Microscopy Manager Centre for Advanced Microscopy Ludwig Institute for Cancer Research Melbourne - Parkville Branch PO Box 2008 Royal Melbourne Hospital Victoria, 3050 AUSTRALIA Office: +61 3 9341 3158 Mobile: +61 422882700 Fax: +61 3 9341 3104 Facility Website Linked In Profile -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Vitaly Boyko Sent: Friday, 17 August 2012 3:57 AM To: [hidden email] Subject: file converter plugin for Image J I am looking for a file converter plugin in Image J. In part ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear All, I am looking for a file converter plugin in Image J. In particular, I would like to convert large >30GB 3D tile data set (ca. 4000x4000x300, xyz) from .lif to .ids/.ics (ideally ICS2) format. Thank you, Vitaly 240-342-6217 |
In reply to this post by Franziska Curdt
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Franziska, You should be able to achieve a faster readout than 20 ms if you read a row rather than a column. It seems that you are reading a 1 x 512 column which means the whole sensor will be read out. However, if you choose a 512 x 1 row, your read out will be significantly reduced. I hope this helps, Orla Hanrahan, Application Specialist, Andor Technology |
Free forum by Nabble | Edit this page |