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Description
The Microscopy Image Analysis Tool (MIATool) is a software application designed for the viewing and processing of N-dimensional array of images. At its core is an image viewer which allows the traversal of an N-dimensional array of images. Besides the standard display as pixels of varying intensity values, options are available to view the images as mesh or contour plots. The current version of MIATool supports four different image editing tools which can be used to process the images displayed in the viewer. The intensity adjustment tool provides different ways to modify the pixel intensity values, and the crop tool allows trimming of the images to retain only the portion that is of interest. The two remaining tools - the segmentation tool and the label tool - can be used for manual image segmentation and image labeling.
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Description

Clus-Doc is a software that quantifies both the spatial distribution of a protein as well as its colocalization status. It may be used to quantify signaling activity and protein colocalization at the level of individual proteins.

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Description

The MorphoLeaf application allows you to extract the contour of multiple leaf images and identify their biologically-relevant landmarks. These landmarks are then used to quantify morphological parameters of individual leaves and to reconstruct average leaf shapes. MorphoLeaf is developed by the Modeling and Digital Imaging and the Transcription Factors and Architecture teams of the Institut Jean-Pierre Bourgin, INRA Versailles, France, and the Biophyscis and Development group at RDP, Lyon.

Description

 

In this workflow, you can use MorphoLibJ to generate accurate morphometric measurements

  • First the fibers are segmented by mathematical morphology:
    • for example by using MorphoLibJ:
      • Create a marker image by creating a rough mask with extended regional maxima (similar to Find Max), such that you have one max per fiber
      • Use the marker controlled watershed (in MorpholLibJ/ Segmentation/ marker controlled watershed) : indicate the original grayscale image as the input, Marker will be your maxima image, select None for mask
      • it will create a label mask of your fibers
  •  In MorphoLibJ /analyze/ select Region Morphometry: this will compute different shape factors which are more robust than the ones implemented by default in ImageJ
  • Export the result table created to a csv file
  • Then for example in Matlab or R, you can apply a PCA analysis (Principal component analysis) followed by a k-means with the number of class (clusters) (different fibers type) you want to separate.
  • You can then add this class as a new feature to your csv file.
  • From this you can sort your labelled fibers into these clusters for a visual feedback or further spatial analysis
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hemp analysis
Description

This imageJ/Fiji plugin provides an analysis of the granulometry inside an image by mathematical morphology. It has sevral option for the structuring element to be used, and the size domain to be tested. The output will be both a curve of the remaining content of the image against the growing size of the structuring element, and the corresponding results table that could be then exported. It can deal with grayscale images directly, no need to segment the image first. This plugin can then be used to compare different texture based on some statistical analysis of the produced curve (for exemple comparison of the geometrical means to discriminate 2 textures). It is macro recordable as well. Programming Language: java Processes: successive erosion, dilation, closing or opening -> ANALYSIS User skills: Life Scientist, developers, analysts

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granulometry