Evidence map›Paper›PMID 35017629›Full record

ArticleCommunications biology2022

Generative adversarial network enables rapid and robust fluorescence lifetime image analysis in live cells.

Yuan-I Chen, Yin-Jui Chang, Shih-Chu Liao, Trung Duc Nguyen, Jianchen Yang, Yu-An Kuo, Soonwoo Hong, Yen-Liang Liu, H Grady Rylander, Samantha R Santacruz and 2 more

Abstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

  1. A Chemigenetic Fluorescence Lifetime Biosensor for Dopamine Sensing.bioRxiv : the preprint server for biology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yuan-I ChenDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Yin-Jui ChangDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Shih-Chu LiaoISS, Inc., 1602 Newton Drive, Champaign, IL, 61822, USA.
Trung Duc NguyenDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Jianchen YangDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Yu-An KuoDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Soonwoo HongDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID http://orcid.org/0000-0002-7618-9052
Yen-Liang LiuMaster Program for Biomedical Engineering, China Medical University, Taichung, 406040, Taiwan.
H Grady RylanderDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Samantha R SantacruzDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Thomas E YankeelovDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID http://orcid.org/0000-0001-6201-3913
Hsin-Chih YehDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA. tim.yeh@austin.utexas.edu.ORCID http://orcid.org/0000-0001-6654-5626

Funding

Developing an ultrafast fluorescence lifetime imaging ophthalmoscopy system for retinal imagingR21EY033106 · NEI · UNIVERSITY OF TEXAS AT AUSTIN · PI YEH, HSIN-CHIH · 2021 to 2022
$399k
Turning a sequence barcode into a spectral barcode for single-cell analysis.R21GM129617 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI FINKELSTEIN, ILYA J, YEH, HSIN-CHIH · 2019 to 2020
$398k
Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RR160005National Science Foundation (NSF) 2041345NEI NIH HHS R21 EY033106NIGMS NIH HHS R21 GM129617Welch Foundation F-1833
6 · The paper itself

Abstract

Fluorescence lifetime imaging microscopy (FLIM) is a powerful tool to quantify molecular compositions and study molecular states in complex cellular environment as the lifetime readings are not biased by fluorophore concentration or excitation power. However, the current methods to generate FLIM images are either computationally intensive or unreliable when the number of photons acquired at each pixel is low. Here we introduce a new deep learning-based method termed flimGANE (fluorescence lifetime imaging based on Generative Adversarial Network Estimation) that can rapidly generate accurate and high-quality FLIM images even in the photon-starved conditions. We demonstrated our model is up to 2,800 times faster than the gold standard time-domain maximum likelihood estimation (TD_MLE) and that flimGANE provides a more accurate analysis of low-photon-count histograms in barcode identification, cellular structure visualization, Förster resonance energy transfer characterization, and metabolic state analysis in live cells. With its advantages in speed and reliability, flimGANE is particularly useful in fundamental biological research and clinical applications, where high-speed analysis is critical.

Indexed as

Deep LearningAlgorithmsCytological TechniquesFluorescent DyesHeLa CellsHumansImage Processing, Computer-AssistedMicroscopy, FluorescenceMolecular ImagingFluorescent Dyes

Identifiers

PMID35017629
PMCPMC8752789

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.