Evidence map›Paper›PMID 36482307›Full record

ArticleBMC bioinformatics2022

ReCSAI: recursive compressed sensing artificial intelligence for confocal lifetime localization microscopy.

Sebastian Reinhard, Dominic A Helmerich, Dominik Boras, Markus Sauer, Philip Kollmannsberger

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Article in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sebastian ReinhardDepartment of Biotechnology and Biophysics, University of Wuerzburg, Am Hubland, 97074, Wuerzburg, Germany.
Dominic A HelmerichDepartment of Biotechnology and Biophysics, University of Wuerzburg, Am Hubland, 97074, Wuerzburg, Germany.
Dominik BorasDepartment of Biotechnology and Biophysics, University of Wuerzburg, Am Hubland, 97074, Wuerzburg, Germany.
Markus SauerDepartment of Biotechnology and Biophysics, University of Wuerzburg, Am Hubland, 97074, Wuerzburg, Germany.
Philip KollmannsbergerCenter for Computational and Theoretical Biology, University of Wuerzburg, Klara-Oppenheimer-Weg 32, 97074, Wuerzburg, Germany. Philip.Kollmannsberger@uni-wuerzburg.de.

Funding

Deutsche Forschungsgemeinschaft KO3715/5-1Deutsche Forschungsgemeinschaft SA829/19-1European Research Council 835102
6 · The paper itself

Abstract

backgroundLocalization-based super-resolution microscopy resolves macromolecular structures down to a few nanometers by computationally reconstructing fluorescent emitter coordinates from diffraction-limited spots. The most commonly used algorithms are based on fitting parametric models of the point spread function (PSF) to a measured photon distribution. These algorithms make assumptions about the symmetry of the PSF and thus, do not work well with irregular, non-linear PSFs that occur for example in confocal lifetime imaging, where a laser is scanned across the sample. An alternative method for reconstructing sparse emitter sets from noisy, diffraction-limited images is compressed sensing, but due to its high computational cost it has not yet been widely adopted. Deep neural network fitters have recently emerged as a new competitive method for localization microscopy. They can learn to fit arbitrary PSFs, but require extensive simulated training data and do not generalize well. A method to efficiently fit the irregular PSFs from confocal lifetime localization microscopy combining the advantages of deep learning and compressed sensing would greatly improve the acquisition speed and throughput of this method.

resultsHere we introduce ReCSAI, a compressed sensing neural network to reconstruct localizations for confocal dSTORM, together with a simulation tool to generate training data. We implemented and compared different artificial network architectures, aiming to combine the advantages of compressed sensing and deep learning. We found that a U-Net with a recursive structure inspired by iterative compressed sensing showed the best results on realistic simulated datasets with noise, as well as on real experimentally measured confocal lifetime scanning data. Adding a trainable wavelet denoising layer as prior step further improved the reconstruction quality.

conclusionsOur deep learning approach can reach a similar reconstruction accuracy for confocal dSTORM as frame binning with traditional fitting without requiring the acquisition of multiple frames. In addition, our work offers generic insights on the reconstruction of sparse measurements from noisy experimental data by combining compressed sensing and deep learning. We provide the trained networks, the code for network training and inference as well as the simulation tool as python code and Jupyter notebooks for easy reproducibility.

Indexed as

Artificial IntelligenceMicroscopyReproducibility of ResultsAICompressed sensingdSTORMFLIMbeeSMLM

Identifiers

PMID36482307
PMCPMC9732995

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.