Cell Counting Using Imagej

Post on 06-Nov-2015

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CELL COUNTING USING IMAGEJ

CELL COUNTING USING IMAGEJParticle counting can be done automatically using ImageJ, a free software for image processing and analysis in Java.

In a few and very simple steps you can count the cells in your biological experimental image.Automatic particle analysis requires the image to be a binary image i.e. black or white. The software needs to know exactly where the edges are to perform morphology measurements. A threshold range is set and pixels in the image whose value lies in this range are converted to black; pixels with values outside this range are converted to white (or vice-versa depending on what the user requests).

The image can be converted to a binary image via the menu command Image/Type/8-bit.In a few and very simple steps you can count the cells in your biological experimental image.

Download WCIF IMAGEJ at link http://www.uhnresearch.ca/facilities/wcif/imagej/installing_imagej.htm Install WCIF IMAGEJ following the website instructions

Open WCIF IMAGEJ

Import Image File. The menu command File/Open will import common file formats(e.g. JPEG, GIF, BMP, PGM, PNG, TIFF) Convert image into a binary image from Image/Type/8-bit Click on Plugins/Particle Analysis/ Nucleus counter, a window opens up

Enter the size range which should be counted

Opt to perform a background correction. We suggest to select this option.

Select the automatic thresholding method. This can be either "Current", "Otsu", Maximum Entropy", "Mixture Modeling" or k-means" clustering. We suggest k-means clustering which can segment an image in to multiple bands. Opt to perform a "Smooth" filter. We suggest mean 3x3 Opt to perform a watershed separation. We suggest to select this option. Opt to add the particles to Region Of Interest (ROI) manager.

Opt for a summary.