AggreCount is an automated image analysis tool written in the ImageJ macro language based on the FIJI distribution of ImageJ (version 1.52p or later). AggreCount requires dual channel images that have at least immunohistochemical stains for aggregates and nuclei though it supports n-channel images.
AggreCount utilizes the difference of gaussians (DoG) methodology to isolate puncta from immunohistochemical images. DoG allows for the reliable quantification of puncta even when images have uneven background illumination, out of focus fields, or varying fluorescence intensities. AC is ready for analysis out of the box for a large variety of aggregate stains (inclduing ubiquitin stains) though may be modified by users to analyze numerous other punctate structures such as peroxisomes and lysosomes.
AggreCount is ready for batch image analysis allowing for rapid quantification of 100s of images. AC can accept any file type supported by the BioFormats image importer including proprietary image file types such as .nd2. Find all supported formats in the BioFormats documentation
AggreCount uses the watershed-based segmentation algorithm native to FIJI allowing for segmentation of cells without the need of machine learning algorithms and training sets. This segmentation methods allows for separation of cells even when closely packed. Users may change the ‘prominence’ variable that determines local maxima which defines cells using the main settings window.
The AggreCount journal article is now in preprint on BioRx.
AggreCount was developed by Jacob Klickstein in the Raman Lab in 2020. Find more information on the lab, our research, and our members by visiting the lab website here