Skip to content

Latest commit

 

History

History

FIJI

Folders and files

NameName
Last commit message
Last commit date

parent directory

..
 
 
 
 

FIJI User Tutorial

FIJI (https://imagej.net/Fiji) is an image processing package—a "batteries-included" distribution of ImageJ, bundling a lot of plugins which facilitate scientific image analysis.

FIJI can be used to post-process raw X-ray CT images of particles to obtain "cleaned" binary (black/white) stack images. Then the voxel coordinates of the stack images can be exported for constructing the bonded-sphere DEM particle geometry templates as input for LIGGGHTS-INL.

A concise user tutorial is provided.

Import image sequence

File -> Import -> Image Sequence

Crop image sequence (optional)

Select region. Then do Image -> Crop

We recommend saving the cropped image sequence in TIFF and load it again for the following operations. This saves computer memory if the memory limit is a concern.

Decide threshold

Auto local threshold

Only good with high-contrast images. Low-contrast images like those of biomass should not use any automatic thresholding.

Manual threshold

Image -> Adjust -> Threshold

Low-contrast images like those of biomass should require manual thresholding.

Binarize images

Process -> Binary -> Make Binary

Equivalent to auto threshholding. Should not apply to low-contrast images like those of biomass.

Denoise (optional)

Despeckle

Process -> Noise -> Despeckle

Subtract background (optional)

Process -> Subtract Background

Do not subtract background if already binarized.

Check the 3D view (optional)

Plug-ins -> 3D Viewer

Save image stack and image sequence

File -> Save As -> Image Sequence

Export XYZ coordinates and visualize in ParaView

Analyze -> Tools -> Save XY Coordinates (save all slices)