Evidence map›Paper›PMID 39975172›Full record

ArticlebioRxiv : the preprint server for biology2025

Training Generalized Segmentation Networks with Real and Synthetic Cryo-ET data.

Carson Purnell, Jessica Heebner, Linh Nguyen, Michael T Swulius, Ryan Hylton, Seth Kabonick, Michael Grillo, Stephanie Grillo, Sergei Grigoryev, Frederick A Heberle and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Carson PurnellPenn State College of Medicine, Hershey, PA.
Jessica HeebnerPenn State College of Medicine, Hershey, PA.
Linh NguyenPenn State College of Medicine, Hershey, PA.
Michael T SwuliusPenn State College of Medicine, Hershey, PA.
Ryan HyltonPenn State College of Medicine, Hershey, PA.
Seth KabonickPenn State College of Medicine, Hershey, PA.
Michael GrilloPenn State College of Medicine, Hershey, PA.
Stephanie GrilloPenn State College of Medicine, Hershey, PA.
Sergei GrigoryevPenn State College of Medicine, Hershey, PA.ORCID 0000-0003-1890-1862
Frederick A HeberleUniversity of Tennessee, Knoxville, TN.
M Neal WaxhamUniversity of Texas Health Science Center, Houston, TX.ORCID 0000-0003-4801-1190
Matthew T SwuliusPenn State College of Medicine, Hershey, PA.

Funding

Coupling of lateral and transverse organization in complex biomembranesR01GM138887 · NIGMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI HEBERLE, FREDERICK A, WAXHAM, M. NEAL · 2020 to 2023
$1.7M
Using cryo-electron tomography and live-cell fluorescent imaging to study the role of cofilin in regulating neuronal filopodial structure and dynamicsR01NS126448 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MATTHEW SWULIUS · 2023 to 2026
$1.6M
NIGMS NIH HHS R01 GM138887NINDS NIH HHS R01 NS126448
6 · The paper itself

Abstract

Deep learning excels at segmenting objects within noisy cryo-electron tomograms, but the approach is typically bottlenecked by access to ground truth training data. To address this issue we have developed CryoTomoSim (CTS), an open-source software package that builds coarse-grained models of macromolecular complexes embedded in vitreous ice and then simulates transmitted electron tilt series for tomographic reconstruction. Using CTS outputs, we demonstrate the effects of key microscope parameters (dose, defocus, and pixel size) on deep learning-based segmentation, and show that including both molecular crowding and diversity within synthetic datasets is key to training cellular segmentation networks from purely synthetic inputs. While very effective as initial models, the accuracy of these networks is currently limited, and real cellular data is necessary to train the most accurate and generalizable U-Nets. Using a co-training approach, we first segment over 100 tomograms from neuronal growth cones to quantify their cytoskeletal distributions and then we build a generalized cellular cryo-ET segmentation network called NeuralSeg that can segment a subset of cellular features in tomograms from all domains of life.

Identifiers

PMID39975172
PMCPMC11838407

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Registered trials

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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.