Benchmarking three simple DNA staining-based image metrics for live-cell tracking of chromatin organization
Quantifying chromatin-state dynamics in living cells remains challenging, in part because most methods require fixation or cell lysis. Here, we introduce two simple DNA image-derived metrics - Diffuse Signal Index (DSI)and 1-Gini - and benchmark them against the coefficient of variation (CV) as fixation-free readouts of chromatin reorganization. Leveraging the pronounced compact-to-decompact chromatin transition of NETosis, we show that all three metrics track progressive chromatin reorganization, with DSI providing the strongest trajectory-level discrimination between NETing and non-NETing cells. All three metrics also correlate with ATAC-see-based chromatin accessibility measurement in fixed cells, supporting their biological interpretability. In dividing cells, the metrics capture mitotic chromatin compaction and post-mitotic decompaction, demonstrating applicability in diverse biological processes. Together, these results provide a practical framework for extracting readouts of chromatin reorganization from routine live-cell DNA staining. We also provide NucMetrics, an open-source ImageJ/Fiji macro toolset for easily computing CV, DSI and 1-Gini.
Authors
- Manasi Sawant (ORCID: https://orcid.org/0000-0002-4465-6891)
- Hawa Racine Thiam (ORCID: https://orcid.org/0000-0002-2381-1442)
- Minwoo Kang (ORCID: https://orcid.org/0000-0002-1982-9818)
- Aidan Tomas Cabral
Institutions
- Chan Zuckerberg Biohub San Francisco (US)
- Stanford University (US)
Publication Details
- Journal
- Nucleus
- Published
- 2026-09-12
- DOI
- https://doi.org/10.1080/19491034.2026.2721777
- Primary Topic
- Genomics and Chromatin Dynamics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- David and Lucile Packard Foundation
- Koret Foundation
- School of Medicine, Stanford University
- Stanford Bio-X