Evidence map›Paper›PMID 41339750›Full record

ArticleScientific reports2025

Detecting continuous structural heterogeneity in single molecule localization microscopy data with a point cloud variational auto-encoder.

Sobhan Haghparast, Yi Zhang, Qian Tao, Sjoerd Stallinga, Bernd Rieger

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Sobhan Haghparast *Department of Imaging Physics, Delft University of Technology, Delft, 2628, The Netherlands.
Yi Zhang *Department of Imaging Physics, Delft University of Technology, Delft, 2628, The Netherlands.
Qian TaoDepartment of Imaging Physics, Delft University of Technology, Delft, 2628, The Netherlands.
Sjoerd StallingaDepartment of Imaging Physics, Delft University of Technology, Delft, 2628, The Netherlands.
Bernd RiegerDepartment of Imaging Physics, Delft University of Technology, Delft, 2628, The Netherlands. b.rieger@tudelft.nl.

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek 17046
6 · The paper itself

Abstract

The low degree of labeling and limited photon count of fluorescent emitters in single molecule localization microscopy results in poor quality images of macro-molecular complexes. Particle fusion provides a single reconstruction with high signal-to-noise ratio by combining many single molecule localization microscopy images of the same structure. The underlying assumption of homogeneity is not always valid, heterogeneity can arise due to geometrical shape variations or distinct conformational states. We introduce a Point Cloud Variational Auto-Encoder that works directly on 2D and 3D localization data, to detect multiple modes of variation in such datasets. The computing time is on the order of a few minutes, enabled by the linear scaling with dataset size, and fast network training in just four epochs. The use of lists of localization data instead of pixelated images leads to just minor differences in computational burden between 2D and 3D cases. With the proposed method, we detected radius variation in 2D Nuclear Pore Complex data, height variations in 3D DNA origami tetrahedron data, and both radius and height variations in 3D Nuclear Pore Complex data. In all cases, the detected variations were on the few nanometer scale.

Identifiers

PMID41339750
PMCPMC12796463

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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.