Figshare
open access
CC BY-NC 4.0
PSF-Driven Spatiotemporal Blending in Fluorescence Lifetime Imaging Microscopy and Its Mitigation via Mean-Shift Super-Resolution-Based Masking
Fluorescence lifetime imaging microscopy (FLIM) enables quantitative mapping of molecular environments in living systems with high biochemical specificity. However, spatial overlap dictated by the diffraction-limited point spread function (PSF) causes a mixing of temporal signals: photons from neigh
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Aberration sensing in fluorescence microscopy using quantum correlations#1014390
- Phasor-Based Spatio-Spectral Segmentation for Hyperspectral Fluorescence Microscopy.#645270
- SNAPSHOT FIRST AND REFOCUS LATER: LIGHT-FIELD AND FOURIER-DOMAIN POLARIZATION MICROSCOPY FOR MULTIDIMENSIONAL 3D BIOIMAGING#631201
- Fast and Lightweight Network for Single Frame Structured Illumination Microscopy Super-Resolution#634120
- Reconstruction-Aware Cryo-EM Particle Picking#793076
Record · ID 784721
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive