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Biofilm-Viability-Checker

//This macro processes multiple images in a folder, outputting the number of bacteria pixels in the red channel and the green channel respectively to calculate the //viability of a biofilm stained with red and green viability stains. //It also saves overlay images showing the bacteria which have been detected. //See "Supplementary Information" file for details on how to run and implement the macro.

Original Authors

//Sophie Mountcastle (sem093@bham.ac.uk) and Nina Vyas (n.vyas@bham.ac.uk) //University of Birmingham, UK //For queries related to the original code, please contact Dr. Sarah Kuehne (s.a.kuehne@bham.ac.uk).

Modifications by Tinatini Tchatchiashvili

//In this fork, I have made the following modifications: //Updated channel analysis and protocol to work with Calcein AM (green) and TMA-DPH (blue) stains for metabolic activity and membrane integrity. //The original (SYTO9/PI) and modified (CAM/TMA-DPH) versions of the code now output the number of stained pixels instead of percentage values.

//For questions about these modifications, feel free to contact me (Tinatini.tchatchiashvili@med.uni-jena.de) //Jena University Hospital, Am Klinikum 1, 07747 Jena, Germany

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This macro writtin for use with Fiji (ImageJ) processes multiple confocal images of live/dead stained biofilms, outputting the number of bacteria pixels in the red channel and both channels respectively to calculate the viability of the biofilm. It also saves overlay images showing the bacteria which have been detected.

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  • ImageJ Macro 100.0%