AutoComet: A fully automated algorithm to quickly and accurately analyze comet assays.

Redox Biol

Center for Systems and Therapeutics, Gladstone Institutes, 1650 Owens Street, San Francisco, CA, 94158, USA; Departments of Neurology and Physiology, University of California, San Francisco, San Francisco, CA, 94158, USA. Electronic address:

Published: June 2023

DNA damage is a common cellular feature seen in cancer and neurodegenerative disease, but fast and accurate methods for quantifying DNA damage are lacking. Comet assays are a biochemical tool to measure DNA damage based on the migration of broken DNA strands towards a positive electrode, which creates a quantifiable 'tail' behind the cell. However, a major limitation of this approach is the time needed for analysis of comets in the images with available open-source algorithms. The requirement for manual curation and the laborious pre- and post-processing steps can take hours to days. To overcome these limitations, we developed AutoComet, a new open-source algorithm for comet analysis that utilizes automated comet segmentation and quantification of tail parameters. AutoComet first segments and filters comets based on size and intensity and then filters out comets without a well-connected head and tail, which significantly increases segmentation accuracy. Because AutoComet is fully automated, it minimizes curator bias and is scalable, decreasing analysis time over ten-fold, to less than 3 s per comet. AutoComet successfully detected statistically significant differences in tail parameters between cells with and without induced DNA damage, and was more comparable to the results of manual curation than other open-source software analysis programs. We conclude that the AutoComet algorithm provides a fast, unbiased and accurate method to quantify DNA damage that avoids the inherent limitations of manual curation and will significantly improve the ability to detect DNA damage.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090439PMC
http://dx.doi.org/10.1016/j.redox.2023.102680DOI Listing

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