Evidence map›Paper›PMID 37848439›Full record

ArticleNature communications2023

Deep-LASI: deep-learning assisted, single-molecule imaging analysis of multi-color DNA origami structures.

Simon Wanninger, Pooyeh Asadiatouei, Johann Bohlen, Clemens-Bässem Salem, Philip Tinnefeld, Evelyn Ploetz, Don C Lamb

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  7. Bayesian Nonparametrics for FRET using Realistic Integrative Detectors.bioRxiv : the preprint server for biology · 2025
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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

7 authors.

Simon WanningerDepartment of Chemistry and Center for NanoScience (CeNS) Ludwig-Maximilians-Universität München Butenandtstr. 5-13, 81377, Munich, Germany.ORCID http://orcid.org/0000-0002-9236-4762
Pooyeh AsadiatoueiDepartment of Chemistry and Center for NanoScience (CeNS) Ludwig-Maximilians-Universität München Butenandtstr. 5-13, 81377, Munich, Germany.ORCID http://orcid.org/0000-0001-8433-4494
Johann BohlenDepartment of Chemistry and Center for NanoScience (CeNS) Ludwig-Maximilians-Universität München Butenandtstr. 5-13, 81377, Munich, Germany.ORCID http://orcid.org/0000-0001-7826-9147
Clemens-Bässem SalemDepartment of Chemistry and Center for NanoScience (CeNS) Ludwig-Maximilians-Universität München Butenandtstr. 5-13, 81377, Munich, Germany.
Philip TinnefeldDepartment of Chemistry and Center for NanoScience (CeNS) Ludwig-Maximilians-Universität München Butenandtstr. 5-13, 81377, Munich, Germany.ORCID http://orcid.org/0000-0003-4290-7770
Evelyn PloetzDepartment of Chemistry and Center for NanoScience (CeNS) Ludwig-Maximilians-Universität München Butenandtstr. 5-13, 81377, Munich, Germany. evelyn.ploetz@lmu.de.ORCID http://orcid.org/0000-0003-0922-875X
Don C LambDepartment of Chemistry and Center for NanoScience (CeNS) Ludwig-Maximilians-Universität München Butenandtstr. 5-13, 81377, Munich, Germany. d.lamb@lmu.de.ORCID http://orcid.org/0000-0002-0232-1903

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-molecule experiments have changed the way we explore the physical world, yet data analysis remains time-consuming and prone to human bias. Here, we introduce Deep-LASI (Deep-Learning Assisted Single-molecule Imaging analysis), a software suite powered by deep neural networks to rapidly analyze single-, two- and three-color single-molecule data, especially from single-molecule Förster Resonance Energy Transfer (smFRET) experiments. Deep-LASI automatically sorts recorded traces, determines FRET correction factors and classifies the state transitions of dynamic traces all in ~20-100 ms per trajectory. We benchmarked Deep-LASI using ground truth simulations as well as experimental data analyzed manually by an expert user and compared the results with a conventional Hidden Markov Model analysis. We illustrate the capabilities of the technique using a highly tunable L-shaped DNA origami structure and use Deep-LASI to perform titrations, analyze protein conformational dynamics and demonstrate its versatility for analyzing both total internal reflection fluorescence microscopy and confocal smFRET data.

Indexed as

Deep LearningSingle Molecule ImagingDNAFluorescence Resonance Energy TransferHumansMicroscopyProtein ConformationDNA

Identifiers

PMID37848439
PMCPMC10582187

What OpenQuestion holds

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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.