Evidence map›Paper›PMID 39282368›Full record

ArticlebioRxiv : the preprint server for biology2024

Ultrack: pushing the limits of cell tracking across biological scales.

Jordão Bragantini, Ilan Theodoro, Xiang Zhao, Teun A P M Huijben, Eduardo Hirata-Miyasaki, Shruthi VijayKumar, Akilandeswari Balasubramanian, Tiger Lao, Richa Agrawal, Sheng Xiao and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

5 · Who and what money

Authors and funding

16 authors.

Jordão BragantiniChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0001-7652-2735
Ilan TheodoroChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0003-4019-3380
Xiang ZhaoChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0002-3339-4806
Teun A P M HuijbenChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0002-8984-2882
Eduardo Hirata-MiyasakiChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0002-1016-2447
Shruthi VijayKumarChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0001-6679-1261
Akilandeswari BalasubramanianChan Zuckerberg Biohub, San Francisco, United States.ORCID 0009-0007-7426-6409
Tiger LaoChan Zuckerberg Biohub, San Francisco, United States.ORCID 0009-0005-6793-8102
Richa AgrawalWeill Institute for Cell and Molecular Biology - Cornell University, Ithaca, United States.
Sheng XiaoChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0001-8959-2388
Jan LammerdingWeill Institute for Cell and Molecular Biology - Cornell University, Ithaca, United States.ORCID 0000-0003-4335-8611
Shalin MehtaChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0002-2542-3582
Alexandre X FalcãoInstitute of Computing - State University of Campinas, Campinas, Brazil.ORCID 0000-0002-2914-5380
Adrian JacoboChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0001-9381-6292
Merlin LangeChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0003-0534-4374
Loïc A RoyerChan Zuckerberg Biohub, San Francisco, United States.ORCID 0000-0002-9991-9724

Funding

Nuclear mechanobiology in confined migration (Equipment Supplement 2023)R01GM137605 · NIGMS · CORNELL UNIVERSITY · PI LAMMERDING, JAN · 2020 to 2023
$1.6M
Nuclear mechanobiology in confined migration (equipment supplement 2026)R35GM153257 · NIGMS · CORNELL UNIVERSITY · PI Jan Lammerding · 2024 to 2026
$1.3M
NIGMS NIH HHS R01 GM137605NIGMS NIH HHS R35 GM153257
6 · The paper itself

Abstract

Tracking live cells across 2D, 3D, and multi-channel time-lapse recordings is crucial for understanding tissue-scale biological processes. Despite advancements in imaging technology, achieving accurate cell tracking remains challenging, particularly in complex and crowded tissues where cell segmentation is often ambiguous. We present Ultrack, a versatile and scalable cell-tracking method that tackles this challenge by considering candidate segmentations derived from multiple algorithms and parameter sets. Ultrack employs temporal consistency to select optimal segments, ensuring robust performance even under segmentation uncertainty. We validate our method on diverse datasets, including terabyte-scale developmental time-lapses of zebrafish, fruit fly, and nematode embryos, as well as multi-color and label-free cellular imaging. We show that Ultrack achieves state-of-the-art performance on the Cell Tracking Challenge and demonstrates superior accuracy in tracking densely packed embryonic cells over extended periods. Moreover, we propose an approach to tracking validation via dual-channel sparse labeling that enables high-fidelity ground truth generation, pushing the boundaries of long-term cell tracking assessment. Our method is freely available as a Python package with Fiji and napari plugins and can be deployed in a high-performance computing environment, facilitating widespread adoption by the research community.

Identifiers

PMID39282368
PMCPMC11398427

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.