Thank you so much! I wasn't aware of the montage capability. I had been stitching together images using photoshop. Talk about tedious! More tutorials, please!
Awesome video, but I had a question. How would I go about analyzing the "brightness" values that you described along a specific line? I was hoping to be able to designate a given line on an image and then be able to generate a chart which would have the brightness on the y axis so that I could see trends along specific lines... Is there a way of doing this all from within ImageJ?
Thank you for the response. I figured it out though by installing the "drag & drop installation" function, then installing your plug-in by simply using this feature. Maybe useful for others who have problems with installation on their Mac.
Thank you for the video. I need to perform cephalometric analysis on a bunch of facial x-rays for which I have to mark two independent lines and check the angle between them.Can you help me in this regard? Thanks in advance!
Excellent! I'm hoping to use imageJ to simulate a virtual learning environment for plant science students. hopefully this will work, I may have questions in due course!
Hi. The easiest way to get imageJ on the mac would be to download ImageJ from the main site and then also download the plugins only bundle from the MBF imageJ website (MBF ImageJ > Installations) from the menu. You then find your imageJ folder on your hard drive and replace all of these folders with the macro and plugin folders you just downloaded from MBF. Another option is to download Fiji ImageJ which is already full of useful plugins and downloads as a single package on a Mac. Good luck.
The Merge/split shortcut can be reached just by going to 'Image'-->'Color' . The menu you reach there has all of the same functions. The only thing missing is the pretty pie graph :(
Hey! Is it possible to detect colored particles and fibers with this program? I mean not just counting the pixels which are colored but to count particles. Thanks in advance :-)
Hello, I watched your video because I'm planning to use ImageJ as a tool for the analysis of data and results of my master's thesis. I would just like to ask some simple questions that I have about using ImageJ: 1) Is there a functionality or option in ImageJ that allows the user to count the number of pixels of a particular color and/or get its percentage from the total number of pixels? For example, I have an image with color A and B, I want to get the percentage of the total number of pixels of color A, or color B. (For simplicity, we can let color A = black, and color B = white) 2) For getting the percentage of total number of pixels, which ImageJ would you recommend for me to download and use, the basic ImageJ that you first showed in the video or the MBF ImageJ which you used in the video? I would really appreciate if you could respond to my queries, it will be a great help. Thanks in advance.
Hello I downloaded (fiji is just) ImageJ, i am trying to cut parts from my 3d viewer but as soon as I select "freehand selection" (or any else selection type) my fiji software crashes and quits on its own (btw i have installed it on my Ubuntu 16.04). Can you please advice me what should i do to resolve this problem. Thanks in advance :)
Hi I hope you can help me. I am analysing Retinal Fundus Photographs which I have taken in high resolution images. I am using NeuronJ plugin to trace the retinal vessels and get a binary image of those traces. However, in NeuronJ it does not allow me to open the images unless it is an 8-Bit image. But when i convert my images into 8-Bit image, it loses a lot of the detail. How could I open my image without it being converted into an 8Bit image where it loses a lot of detail. I hope you can help. Thank you
Hello, thanks for the video. I was trying to download the MBF ImageJ for 64 bit -widows 10 via the site that you mention, but it seems that I have to create an account to oracle in order to do so. Is it any other way?
Hi, ImageJ is a java programme, so doesn't actually have to be installed on a computer, it could even run off a USB stick. It sounds to me as if the programme didn't install properly on your computer. Try uninstalling it and then download either the MBF imageJ bundle or even the Fiji ImageJ bundle. Once installed you should be able to increase the amount of memory ImageJ can use by going to through Edit >Options >Memory and Threads and then increase the memory to whatever you can. Good luck
I can only run your folder if I go directly to the plugins folder and double click on the ij.jar icon. Then it opens Image J, but it only has 128MB of working memory and cannot be adjusted. This is not enough to do anything meaningful with an image besides open 1 file to look at. Is this how it's supposed to run?
HOW WE CAN CALCULATE PERCENTAGE OF CELL POSITIVE FOR EGFR IN IMMUNOHISTOCHEMTRY STAINED IMAGE . I ALSO NEED TO CALCULATE TOTAL NUMBER OF CELL PRESENT IN THE IMAGE? CAN SOMEONE HELP?
Hi, MBF have shut off their webpage, but the even better news is that all of the plugins are still available as a single zip file. Just go to the plugins> collections (imagej.nih.gov/ij/plugins/index.html#collections) and you can get the lot into the latest version of ImageJ or Fiji. There are also instruction of how to install it. Hope that helps.
Thank You for your tutorial. The download of ImageJ microscopy is not available in the site. It will very helpful if you will provide me link to download this file. Thank You. Waiting eagerly for your kind reply.
Good video, I have one question, I have problems with open a image in format TIFF, the software say me that ImageJ can only open 8 and 16 bits/channel images (12), my pictures are 24 bits but I read the manual I undestand that ImageJ can open to 32 bits pictures, Can somebody help me please? Excuse me for bad english