ImageJ Basics

- open source public domain Java image processing and analysis program inspired by NIH Image for the Macintosh. - can be used everywhere with Java (Linux, Mac OS 9, Mac OS X and Windows), -handles several data types and file formats, has an IP toolkit to develop new applets and applications, among other features. -handles Java plugins and macro language (for more details, see presentation

about Image J plugins)

Advantage: Growing numbers of users participate in writing plug-ins for

ImageJ and Fiji.

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Index
-Installing ImageJ (windows) and plugins -Memory settings -Menu and Tools overview p. 3 - 4 p. 5 p. 6

-File menu: Opening, importing, saving files

-Image menu and Image types -Image visualisation/information RGB channel splitting/merging/overlays Stacks -Image Adjustments Brightness/Contrast Threshold Image Crop/Transform/Rotate/Revert

p. 7 - 8
p. 9 - 11 p. 12 p. 13 p. 14 15 p. 16 p. 17 p. 18 p. 19 p. 20 p. 21-22 Imaging

-Image quantification
Calibrating image size/ Scale bars Histogram and line profile ImageJ Region measurements Biology

Installation
Different editions of ImageJ exist: 32bit and 64bit
1. Image J homepage for software and plugin downloads: http://rsbweb.nih.gov/ij/ Wiki: http://imagejdocu.tudor.lu/ Must have java.exe installed to run ImageJ (available with IJ) 2. For a version with pre-installed plugins: The MBF ImageJ collection of plugins and macros http://www.macbiophotonics.ca/imagej/installing_imagej.htm 3. Fiji is a similar software based on ImageJ: http://pacific.mpi-cbg.de/wiki/index.php/Main_Page Obtaining Image J Version information and updating the software:

> Help > About ImageJ - version information > Help > Update ImageJ

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Plugins & Macros

Plugins are additional software modules or code which provide the ability to perform specific tasks. Writing macros using the ImageJ macro language allows you to
string a series of commands together to perform batch operations. These can also be converted to plugins.

Install plugins if required:

Download plugins and Save them in ImageJ Plugin folder (program files) Restart ImageJ: Plugins automatically get placed in the Plugins menu
> There is a list of available plugins here: http://rsb.info.nih.gov/ij/plugins/index.html > There is a plugins collection preorganised in folders available at: http://rsb.info.nih.gov/ij/plugins/collection.html > Many more are available on the website and from other users. Some people have developed their own collections of plugins and bundled them together. McMaster Biophotonics Institute has a great collection for microscopy: http://rsb.info.nih.gov/ij/plugins/mbf-collection.html

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ImageJ memory
Set high memory for optimal use

no more than 70% of max Ram

Edit > Options > Memory

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ImageJ menus and tool bars

Menu bar Tool bar Status bar
(Biophotonics edition)

Region/Measurement tools

Image visualisation and adjustments

Switch to alternative Tool bar themes. Very useful in original ImageJ. Biophotonics edition (shown here) already starts up with a useful Tool bar.

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File menu: Opening, importing, saving files

Drag and drop file to ImageJ menubar to open file Open

microscope image formats: .lei .lsm many image and video formats: .avi .tif

Import -image sequence

Open and manage stacks/movies -many file types and text files/results

Save movies as .avi as compressed jpeg

Drastically reduces file size without quality loss (for presentations for ex.)

Save images as .tif

A JPEG image degrades each time it is opened, edited and resaved.

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Importing OME BIO LOCI & metadata

http://www.loci.wisc.edu/software/bio- formats informs you on types of compatible formats

Open Bio-formats Importer Plugin -to import a wide range of formats -to select meta data to display

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Image Menu
Working with different image types and adjustments can be accessed via the Image Menu or via image adjustment buttons on the second half of the tool bar

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Image type: 8, 16 bit, RGB

Binary image:
For this type of code, each pixel is either black or white because one bit can code for one pixel (0 = black, 1 = white). 1 pixel = 1 bit of memory

Image in gray levels: 8bit or 16bit

If we code each pixel on 2 bits we would have 22 = 4 possibilities (black, dark gray, light gray, white). But this image would have very limited levels.

So in general we use 8 or 16bits:

28 = 256 possibilities (0 - 255 grey levels) 216= 4096 possibilities (0 - 4095 grey levels)

8 bits = 1 octet (1 byte) 16 bits = 2 octets

Multiply number of pixels by number of bits to get memory: 8 bit image: 1000 pixels = 1000 octets = 1 kbyte

Quantification requires 16bit images (bigger window) Tif images dont have 12 bit (usually converted to 16) Acquisition detectors usually only detect in 12 bit!
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Image type: greyscale LUTs, RGB

Pseudocolour in greyscale:
8bit and 12bit greyscale images can be visualised in colour: Use LookUp tables (LUTs): Assigns a range of colour to the grey levels > Either use LUT button on startup tool bar or switch to LUT tool bar by pressing on (Biophotonics edition) The following tool bar appears:

Colour image (RGB): an overlap of 3 pixels 8bit (24 bit total)

Its an additive principle of colours: We can obtain a certain colour by adding 3 primary colours in various proportions: 256x256x256 = more than 16 million colours. Different type of colour coding: RGB, CYMK. RGB: each colour is coded on 1 octet (8bits). Each pixel is a combination of 3 octets (3 x 8 = 24 bits total with Red = 0-255, Green = 0-255, Blue = 0-255. 1 pixel = 3 octets = 24 bits Biology Imaging

Image information & Visualisation

Status Bar = information for cursor position (x,y) and intensity value. Or memory usage

Top of Image = information: Channels Image size (um or pixels) Image type (bits) Image memory Depending on image dimensions, Scroll bars appear at the bottom to scroll across
c: channels z: stack slices t: time frames

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RGB channel splitting/merging/overlays

Image > Color > Merge (overlay)/Split channels
Press once: Merges channels of an RGB stack to one RGB file Press twice: Splits into 3 individual channels Press again: Merges channels back with options as to which channel goes where. Overlay possible with transmitted light images by using the Gray channel. Do not create composite.

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Stacks
Image > Stacks
You need to have a series (time, z, x-y) of images which can be built into a stack. Opeining images as a numbered sequence will automatically create a stack. Compatible with Metamorph stacks. Measuring and analysis tools can be often used to apply to all images in a stack

Convert Images to Stack: converts a set of 2D images that you have opened into a stack. Animate: animates the images in a stack at a rate up to 100 frames per second.

Convert Stack to Images: splits the stack into individual images.

Next Slice/Previous Slice: browsing images can be done using the > and < keys. The
number of the current slice and the total number of slices are displayed in the title bar. You can also use the slider bar in the stack window.

Z Project: simple projection algorithms designed to render 3D images into 2D

projections, allows volume rendering, useful for visualizing the internal structures of 3D images.

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Stacks
For immediate maximum intensity projection (MIP) use this button on the tool bar: Image > Stack > 3D Project: Allows you to project the stack and then rotate it. Orthogonal view: provides an orthogonal (or section) view. Image > Duplicate allows you to save the slice you are viewing as an individual file

Image > Stacks > Movies

Time stamper: allows you to add the time information onto your movie. Zoomify: allows you to make a movie where you zoom in on a particular region.

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Image Adjustments: Brightness/Contrast

Image Adjust > Brightness/Contrast

Or B/C Button on tool bar

Contrast and brightness: use to enhance

images by dynamically changing the lookup table mapping. Click on the brightness slider and drag from side to side. You can also adjust the contrast setting independently.

Brightness - adds or subtracts a constant to

each pixel shift in histogram along x axis but doesnt change the distribution.

DO NOT CLICK on APPLY. This stretches the histogram to fit new min and max values Contrast lower level set (e.g. to 0) and and is not reversible. This affects future higher level set (e.g. to 255) and rest of pixel Measurements!
values adjusted proportionally.

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Image Adjustments: Threshold

Image > Adjust >Threshold
is the simplest method of image segmentation. From a grayscale image, thresholding can be used to create binary images.

Threshold above/below: Individual pixels in an image are marked as

object pixels if their value is greater/lower than some threshold value (assuming an object to be brighter than the background) and as background pixels otherwise.

Threshold inside/outside, when a

pixel value is between two thresholds/vice-versa.

Typically, an object pixel is given a value of 1 while a background pixel is given a value of 0. Finally, a binary image is created by coloring each pixel white or black, depending on a pixel's label. Wikipedia Biology Imaging

Image Crop/Transform/Rotate/Revert
Image >

Crop - You can make selection areas to determine the area to be cropped Rotate - You can also Rotate the image into different angles
All this can be applied to a single image or to all slices of a stack

File > Revert

And revert to the original file (File > Revert or Control-R) To be safe, always click on Image > Duplicate and work on the copy of your image

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Calibrating image size units

Calibrating image size is important for further image processing: -measurements -scale bar Image > Properties Enter unit of length ( m or pixels) Image now shows image size in m

Press scale bar button in tool menu

to add scale bar to single image or all slices of a stack.

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Image histogram and line profile

Histogram: Shows the number of pixels of
each value, regardless of location, and the mean and max values. The log display allows for the visualization of minor components.

Analyse > Histogram Generate list of values by clicking on List.

Line plot: Shows the intensity profile of

pixels along a selection. Select line tool, draw line for profiling Analyse > Plot profile

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ImageJ Region measurements

Area SelectionTools

-Use these tools to create area selections -Location, width and height are displayed in the status bar. (Change properties of selection regions in Edit > Selection > Properties -The contents of an region can be copied, cleared (to white), filled with the current drawing color, outlined (using Edit/Draw), filtered, or measured. > Image > Colors Double click any line tool

Backspace

Arrow keys with ALT Use the small "handles" Holding down Alt

- Edit/Clear -Set the drawing color - Change the line width used by Edit/Draw - to "nudge" a selection one pixel at a time - to resize - forces ellipse circles or rectangles squares

-To create the polygonal selection, click repeatedly with the mouse to create line segments, double click when finish. -Use the wand tool to reposition selections drawn with the rectangle capture tool, oval capture tool, etc. Biology Imaging

ImageJ Region measurements

Measurements can be
managed and logged through the Region of Interest (ROI) Manager available in the Biophotonics ImageJ Version tool bar, or from Image > Analysis > Tools Create regions with the selection tools Click on Add or type t Select Show All so that the regions appear visible Go to More > and choose Measure all In Analyse > Set Measurements: you can decide What type of measurements will appear in the list.

You can save the region measurements (More > Save) And apply them to all stacks or to new images You can also save the results as an excel file.

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