Automated, image-based quantification of peroxisome characteristics with perox-per-cell

Author:

Neal Maxwell L1ORCID,Shukla Nandini2ORCID,Mast Fred D1ORCID,Farré Jean-Claude2ORCID,Pacio Therese M1ORCID,Raney-Plourde Katelyn E2ORCID,Prasad Sumedh2,Subramani Suresh2ORCID,Aitchison John D13ORCID

Affiliation:

1. Center for Global Infectious Disease Research, Seattle Children’s Research Institute , Seattle, WA 98109, United States

2. Department of Molecular Biology, School of Biological Sciences, University of California , San Diego, La Jolla, CA 92093, United States

3. Departments of Pediatrics and Biochemistry, University of Washington , Seattle, WA 98195, United States

Abstract

Abstract Summary perox-per-cell automates cumbersome, image-based data collection tasks often encountered in peroxisome research. The software processes microscopy images to quantify peroxisome features in yeast cells. It uses off-the-shelf image processing tools to automatically segment cells and peroxisomes and then outputs quantitative metrics including peroxisome counts per cell and spatial areas. In validation tests, we found that perox-per-cell output agrees well with manually quantified peroxisomal counts and cell instances, thereby enabling high-throughput quantification of peroxisomal characteristics. Availability and implementation The software is coded in Python. Compiled executables and source code are available at https://github.com/AitchisonLab/perox-per-cell.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

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