Evidence map›Paper›PMID 40610730›Full record

ArticleNature methods2025

Interpretable representation learning for 3D multi-piece intracellular structures using point clouds.

Ritvik Vasan, Alexandra J Ferrante, Antoine Borensztejn, Christopher L Frick, Philip Garrison, Nathalie Gaudreault, Saurabh S Mogre, Fatwir S Mohammed, Benjamin Morris, Guilherme G Pires and 4 more

Abstract read
In one paragraph

Article in Nature methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Ritvik VasanAllen Institute for Cell Science, Seattle, WA, USA.
Alexandra J FerranteAllen Institute for Cell Science, Seattle, WA, USA.
Antoine BorensztejnAllen Institute for Cell Science, Seattle, WA, USA.
Christopher L FrickAllen Institute for Cell Science, Seattle, WA, USA.
Philip GarrisonAllen Institute for Cell Science, Seattle, WA, USA.
Nathalie GaudreaultAllen Institute for Cell Science, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-9220-5366
Saurabh S MogreAllen Institute for Cell Science, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-3781-5161
Fatwir S MohammedAllen Institute for Cell Science, Seattle, WA, USA.
Benjamin MorrisAllen Institute for Cell Science, Seattle, WA, USA.ORCID http://orcid.org/0009-0001-7670-0797
Guilherme G PiresAllen Institute for Cell Science, Seattle, WA, USA.ORCID http://orcid.org/0009-0006-6660-3092
Daniel SaelidAllen Institute for Cell Science, Seattle, WA, USA.
Susanne M RafelskiAllen Institute for Cell Science, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-1399-5970
Julie A TheriotDepartment of Biology and Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-2334-2535
Matheus P VianaAllen Institute for Cell Science, Seattle, WA, USA. matheus.viana@alleninstitute.org.ORCID http://orcid.org/0000-0001-9288-2108

Funding

Multiscale Analyses of 4D Nucleome Structure and Function by Comprehensive Multimodal Data IntegrationUM1HG011593 · NHGRI · CARNEGIE-MELLON UNIVERSITY · PI ALBER, FRANK, BELMONT, ANDREW STEVEN · 2020 to 2024
$10.4M
NHGRI NIH HHS UM1 HG011593
6 · The paper itself

Abstract

A key challenge in understanding subcellular organization is quantifying interpretable measurements of intracellular structures with complex multi-piece morphologies in an objective, robust and generalizable manner. Here we introduce a morphology-appropriate representation learning framework that uses three-dimensional rotation-invariant autoencoders and point clouds. This framework is used to learn representations of complex shapes that are independent of orientation, compact and interpretable. We apply our framework to intracellular structures with punctate morphologies (for example, DNA replication foci) and polymorphic morphologies (for example, nucleoli). We explore the trade-offs in the performance of this framework compared to image-based autoencoders by performing multi-metric benchmarking across efficiency, generative capability and representation expressivity metrics. We find that the proposed framework, which embraces the underlying morphology of multi-piece structures, can facilitate the unsupervised discovery of subclusters for each structure. We show how this approach can also be applied to phenotypic profiling using a dataset of nucleolar images following drug perturbations.

Indexed as

Image Processing, Computer-AssistedImaging, Three-DimensionalMachine LearningAlgorithmsCell NucleolusHumans

Identifiers

PMID40610730
PMCPMC12240800

What Socratic 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 Socratic graph.