Carlos Lizama |
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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 everybody, I need to a quantification in a z-stack I dont know which is the best way to do it? I was try to do it with image J in 3D reconstruction but my problems is when imageJ and the other software generate the 3d reconstruction it make a average with the fluorescence to generate the 3D reconstruction, And the other thing is I dont know if in imagej is posible select an area in the photo a request the quantiication in all the slides, Because doing the quantification in each slide is really slow and complicate i think. mmm ImageJ has a special tools or plugin to do the quantification? Because I was tried using the tools to select area and then generate histogram or measure options. Thanks Carlos |
Bonnaud, Fabien |
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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 Carlos, Following-up with your previous post about Volocity concerning 3D image visualization, I also confirm you that Volocity provides a complete suite of tools to perform 3D analysis. It allows 3D image segmentation, objects populations analysis, comparison of biological conditions, automatic 3D tracking, 3D co-localization analysis, ratio measurements, FRAP analysis, ... The output can be numerical with analysis and re-analysis of the data, identification of patterns and trends in one or more images, chart edition and export, or visual with snapshots and movies of your images and measurements. The analysis module of Volocity is called Volocity Quantitation. More information about the analysis functions of Volocity can be found here : http://www.perkinelmer.com/pages/020/cellularimaging/training/default.xhtml should you have any specific question or need any further assistance, please do not hesitate to contact me and / or our technical support desk : http://cellularimaging.perkinelmer.com/support/ Sincerely yours, Fabien Bonnaud | Volocity Product Line Leader, Life Sciences & Technology PerkinElmer | For the Better [hidden email] Phone: +33 (0)1 69598407 | Support desk : +44 (0)2 47 66 98 121 16, Av. du Québec Bât. Lys 91140 Villebon sur Yvette www.perkinelmer.com Please consider the environment before printing this e-mail. This e-mail message and any attachments are confidential and proprietary to PerkinElmer, Inc. If you are not the intended recipient of this message, please inform the sender by replying to this email or sending a message to the sender and destroy the message and any attachments. Thank you. -----Message d'origine----- De : Confocal Microscopy List [mailto:[hidden email]] De la part de Carlos Lizama Envoyé : vendredi 6 juillet 2012 04:34 À : [hidden email] Objet : Quantification 3D reconstruction ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi everybody, I need to a quantification in a z-stack I dont know which is the best way to do it? I was try to do it with image J in 3D reconstruction but my problems is when imageJ and the other software generate the 3d reconstruction it make a average with the fluorescence to generate the 3D reconstruction, And the other thing is I dont know if in imagej is posible select an area in the photo a request the quantiication in all the slides, Because doing the quantification in each slide is really slow and complicate i think. mmm ImageJ has a special tools or plugin to do the quantification? Because I was tried using the tools to select area and then generate histogram or measure options. Thanks Carlos |
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