PreprintCC BYbioRxiv
Maximum Likelihood Localization Maps
- 1Leibniz Institute of Photonic Technology, Institute of Physical Chemistry, Frierich Schiller University Jena, Abbe Center of Photonics
Abstract
Single-molecule localization microscopy commonly reconstructs images from estimated emitter coordinates. We calculate maximum-likelihood localization maps (MLLM), a non-iterative approach that evaluates positional likelihood from measured data and a supplied point-spread function. The MLLM of each detected single molecule image is added into a final upsampled image representing the overall molecular probability map, preserving the positional likelihood structure and obviating separate coordinate-based rendering. MLLM calculation is noniterative, fast, supports any calibrated point-spread function, accounts for local background variation, supports two- and three-dimensional reconstruction, and can be calculated in parallel.
Related
- The unreasonable likelihood of being: origin of life, terraforming, and AI
- Brightness demixing for simultaneous multi-target imaging in 3D single-molecule localization microscopy
- A contact-mediated transfer mechanism directs in cis localization and spread of Xist RNA
- Advanced background removal methods in single molecule localization microscopy using scattering networks and SVD
- Mapping of pikachurin heparan sulfate modification to a region dispensable for synaptic localization in photoreceptors
BibTeX
@misc{oshtolagh2026maximum,
title = {{Maximum Likelihood Localization Maps}},
author = {H. Zarei Oshtolagh and R. Foerster and J. Ries and R. Heintzmann},
howpublished = {bioRxiv},
year = {2026},
month = nov,
doi = {10.64898/2026.11.05.764521},
url = {https://www.biorxiv.org/content/10.64898/2026.11.05.764521v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Maximum Likelihood Localization Maps
AU - H. Zarei Oshtolagh
AU - R. Foerster
AU - J. Ries
AU - R. Heintzmann
PY - 2026
DA - 2026/11/05
PB - bioRxiv
DO - 10.64898/2026.11.05.764521
UR - https://www.biorxiv.org/content/10.64898/2026.11.05.764521v1
AB - Single-molecule localization microscopy commonly reconstructs images from estimated emitter coordinates. We calculate maximum-likelihood localization maps (MLLM), a non-iterative approach that evaluates positional likelihood from measured data and a supplied point-spread function. The MLLM of each detected single molecule image is added into a final upsampled image representing the overall molecular probability map, preserving the positional likelihood structure and obviating separate coordinate-based rendering. MLLM calculation is noniterative, fast, supports any calibrated point-spread function, accounts for local background variation, supports two- and three-dimensional reconstruction, and can be calculated in parallel.
ER -