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Updated: Sep 14, 2026

A Multilabel Single Molecule Localization Microscopy Protocol for Investigation of Chromatin in the Dense Nuclear Environment
Published on: June 5, 2026
Benchmarking three simple DNA staining-based image metrics for live-cell tracking of chromatin organization
Minwoo Kang1, Aidan Tomas Cabral1, Manasi Sawant1
1Department of Bioengineering, Stanford University, Stanford, CA, USA.
Abstract:
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.

